SPIROCYCLE CONTAINING BICYCLIC HETEROARYL COMPOUNDS RELATED APPLICATION [0001] This application claims benefit of priority to U.S. provisional patent application no. 63/381,034, filed October 26, 2022. The contents of the above-referenced application are incorporated by reference herein in their entirety. FIELD [0002] Provided herein are compounds useful for treatment of light chain amyloidosis. In one embodiment, the compounds are spirocycle containing bicyclic heteroaryl compounds. BACKGROUND [0003] Light chain (LC) amyloidosis (AL amyloidosis) is a progressive and often fatal degenerative disease caused by monoclonal plasma cell proliferation, resulting in an abnormal free light chain (FLC) ratio and conformational changes within involved immunoglobulin light chains (iFLC) after secretion by clonal plasma cells that result in organ toxicity, e.g., cardiomyopathy, nephrotic syndrome and end-stage renal failure. Organ damage remains the major source of mortality and morbidity. Lambda light chains are more often amyloidogenic than the kappa light chains (~80%). The light chain conformational changes also often lead to light chain aggregation, which may also drive proteotoxicity in some post-mitotic tissues. The pathologic mechanisms of disease leading to organ toxicity include both toxicity of amyloidogenic LC and mass effects of deposits, both modulated by misfolded LC concentration. [0004] Light chain amyloidosis patients are treated today by targeting the cancer component of this disease (proliferating clonal plasma cells) employing chemotherapy cocktails typically involving proteasome inhibitors (and, when possible, stem cell transplants), which ideally eliminate the clonal plasma cells secreting full-length light chains. However, complete clonal plasma cell eradication is achieved in only 30-40% of the patients and most eventually relapse. Restoration of organ function in treated patients is highly variable and often incomplete, resulting in poor outcomes. The current hematologic response criteria for AL amyloidosis define complete response (CR) as no evidence of monoclonal protein based on serum and urine immunofixation, as well as achieving a normal FLC ratio. The response criteria do not take the levels of iFLC into consideration. It has been shown that increased levels of iFLCs at the time of normal FLC ratio and complete or very good partial lower overall survival. However, even low levels of amyloidogenic monoclonal FLC can result in organ dysfunction. Moreover, light chain amyloidosis patients exhibiting cardiac involvement are often too sick to tolerate chemotherapy and die within a year of diagnosis. [0005] Thus, there is a need for additional treatments of light chain amyloidosis. SUMMARY [0006] Provided herein are compounds for use in compositions and methods of treatment of light chain amyloidosis (AL amyloidosis). In certain embodiments, the compounds provided herein are light chain kinetic stabilizers. The compounds provided herein are spirocycle containing bicyclic heteroaryl compounds. [0007] In one embodiment, the compounds for use in the compositions and methods provided herein have formula I: e thereof, where R ^{1 2 5 14 1 2} , R , R to R , X , X , X ³ , X ⁴ , m, n, p, s, t and u are as defined herein. [0009] In another embodiment, the compounds for use in the compositions and methods provided herein have formula Ia: hereof, where R ¹ , R ² , R ⁵ to R ¹⁴ , X ¹ , X ² , X ³ , m, n, p, s and t are as defined herein. [0011] In another embodiment, the compounds for use in the compositions and methods provided herein have formula II: thereof, where R ²¹ to R ³⁰ , X ¹¹ , X ¹² , X ¹³ , X ¹⁴ , a, b, c, d, f and g are as defined herein. [0013] In another embodiment, the compounds for use in the compositions and methods provided herein have formula IIa: ve thereof, where R ²¹ to R ³⁰ , X ¹¹ , X ¹² , X ¹³ , a, b, c, d and f are as defined herein. [0015] In one embodiment, provided herein is a method of treating light chain amyloidosis by administering to a subject a compound or composition provided herein. In another embodiment, provided herein is a method of stabilizing immunoglobulin light chains by contacting the immunoglobulin light chains with a compound provided herein. In one embodiment, the immunoglobulin light chains are stabilized in a native conformation thereof. In certain embodiments, the immunoglobulin light chains are dimers. In another embodiment, provided herein is a method of preventing or lessening immunoglobulin light chain misfolding and/or endoproteolysis by contacting the immunoglobulin light chains with a compound provided herein. In another embodiment, provided is a method of maintenance therapy upon recurrence of light chain amyloidosis following primary treatment by administering to a subject a compound or composition provided herein. In another embodiment, provided is a method of combination therapy using a compound or composition provided herein in combination with one or more additional active agents that treat light chain amyloidosis, deplete clonal plasma cells, stabilize immunoglobulin light chains, prevent or lessen immunoglobulin light chain misfolding and/or endoproteolysis, promote clearance of fibrils, or that are effective in maintenance therapy upon recurrence of light chain amyloidosis following primary treatment. I. DEFINITIONS [0016] To facilitate understanding of the disclosure set forth herein, a number of terms are defined below. [0017] Unless defined otherwise, all technical and scientific terms used herein have the same meaning as is commonly understood by one of ordinary skill in the art. All patents, applications, published applications and other publications are incorporated by reference in their entirety. In the event that there is a plurality of definitions for a term herein, those in this section prevail unless stated otherwise. [0018] The singular forms "a," "an," and "the" include plural references, unless the context clearly dictates otherwise. [0019] As used herein "subject" is an animal, such as a mammal, including human, such as a patient. [0020] As used herein, biological activity refers to the in vivo activities of a compound or physiological responses that result upon in vivo administration of a compound, composition or other mixture. Biological activity, thus, encompasses therapeutic effects and pharmacokinetic behavior of such compounds, compositions and mixtures. Biological activities can be observed in in vitro systems designed to test for such activities. [0021] As used herein, pharmaceutically acceptable derivatives of a compound include, but are not limited to, salts, esters, enol ethers, enol esters, acetals, ketals, orthoesters, hemiacetals, hemiketals, acids, bases, clathrates, solvates or hydrates thereof. Such derivatives may be readily prepared by those of skill in this art using known methods for such derivatization. The compounds produced may be administered to animals or humans without substantial toxic effects and either are pharmaceutically active or are prodrugs. Pharmaceutically acceptable salts include, but are not limited to, amine salts, such as but not limited to N,N'-dibenzylethylenediamine, chloroprocaine, choline, ammonia, diethanolamine and other hydroxyalkylamines, ethylenediamine, N-methylglucamine, procaine, N- benzylphenethylamine, 1-para-chlorobenzyl-2-pyrrolidin-1'-ylmethylbenzimidazole, diethylamine and other alkylamines, piperazine and tris(hydroxymethyl)aminomethane; alkali metal salts, such as but not limited to lithium, potassium and sodium; alkali earth metal salts, such as but not limited to barium, calcium and magnesium; transition metal salts, such as but not limited to zinc; and inorganic salts, such as but not limited to, sodium hydrogen phosphate and disodium phosphate; and also including, but not limited to, salts of mineral acids, such as but not limited to hydrochlorides and sulfates; and salts of organic acids, such butyrates, valerates, mesylates, and fumarates. Pharmaceutically acceptable esters include, but are not limited to, alkyl, alkenyl, alkynyl, aryl, aralkyl, and cycloalkyl esters of acidic groups, including, but not limited to, carboxylic acids, phosphoric acids, phosphinic acids, sulfonic acids, sulfinic acids and boronic acids. Pharmaceutically acceptable enol ethers include, but are not limited to, derivatives of formula C=C(OR) where R is alkyl, alkenyl, alkynyl, aryl, aralkyl and cycloalkyl. Pharmaceutically acceptable enol esters include, but are not limited to, derivatives of formula C=C(OC(O)R) where R is hydrogen, alkyl, alkenyl, alkynyl, aryl, aralkyl and cycloalkyl. Pharmaceutically acceptable solvates and hydrates are complexes of a compound with one or more solvent or water molecules, or 1 to about 100, or 1 to about 10, or one to about 2, 3 or 4, solvent or water molecules. [0022] As used herein, treatment means any manner in which one or more of the symptoms of a disease or disorder are ameliorated or otherwise beneficially altered. Treatment also encompasses any pharmaceutical use of the compositions herein, such as use for treating light chain amyloidosis. [0023] As used herein, amelioration of the symptoms of a particular disorder by administration of a particular compound or pharmaceutical composition refers to any lessening, whether permanent or temporary, lasting or transient that can be attributed to or associated with administration of the compound or pharmaceutical composition. [0024] As used herein, and unless otherwise indicated, the terms "manage," "managing" and "management" encompass preventing the recurrence of the specified disease or disorder in a subject who has already suffered from the disease or disorder, and/or lengthening the time that a subject who has suffered from the disease or disorder remains in remission. The terms encompass modulating the threshold, development and/or duration of the disease or disorder, or changing the way that a subject responds to the disease or disorder. [0025] As used herein, the EC50 refers to an amount, concentration or dosage of a particular test compound that achieves 50% of a maximal response in an assay that measures such response. Transient misfolding events in the unstable WIL-FL LC2 enables proteinase K proteolysis, resulting in release of smaller fluorescein-labeled peptides that exhibit decreased fluorescence polarization. Small molecules that bind to and kinetically stabilize WIL-FL LC2 decrease the rate at which the LC is proteolyzed, and therefore maintain the high fluorescence polarization signal longer. [0026] As used herein, fold protection refers to the calculation as described in Example 1 Proteinase K Sensitivity Assay. test compound that achieves a 50% inhibition of a maximal response in an assay that measures such response. [0028] As used herein, the K _d refers to the measured equilibrium dissociation constant between a compound (or ligand) and a protein (or binding domain of a protein). [0029] Where moieties are specified by their conventional chemical formulae, written from left to right, they equally encompass the chemically identical moieties that would result from writing the structure from right to left, e.g., -CH ₂ O- is equivalent to -OCH ₂ -. [0030] The term "alkyl," by itself or as part of another substituent, means, unless otherwise stated, a straight (i.e., unbranched) or branched chain saturated hydrocarbon radical, which can include di- and multivalent radicals, having the number of carbon atoms designated (i.e., C ₁ -C ₁₀ means one to ten carbons). Examples of alkyl groups include, but are not limited to, groups such as methyl, ethyl, n-propyl, isopropyl, n-butyl, t-butyl, isobutyl, sec-butyl, homologs and isomers of, for example, n-pentyl, n-hexyl, n-heptyl, n-octyl, and the like. [0031] The term "alkenyl," by itself or as part of another substituent, means, unless otherwise stated, a straight (i.e., unbranched) or branched chain hydrocarbon radical having one or more carbon-carbon double bonds, which can include di- and multivalent radicals, having the number of carbon atoms designated (i.e., C1-C10 means one to ten carbons). Examples of alkenyl groups include, but are not limited to, vinyl (i.e., ethenyl), 2-propenyl, crotyl, 2-isopentenyl, 2-(butadienyl), 2,4-pentadienyl, 3-(1,4-pentadienyl), and the higher homologs and isomers. [0032] The term "alkynyl," by itself or as part of another substituent, means, unless otherwise stated, a straight (i.e., unbranched) or branched chain hydrocarbon radical having one or more carbon-carbon triple bonds, which can include di- and multivalent radicals, having the number of carbon atoms designated (i.e., C ₁ -C ₁₀ means one to ten carbons). Examples of alkynyl groups include, but are not limited to, ethynyl, 1- and 3-propynyl, 3- butynyl, and the higher homologs and isomers. [0033] The term "alkylene" by itself or as part of another substituent means a divalent radical derived from an alkyl, as exemplified, but not limited, by -CH ₂ CH ₂ CH ₂ CH ₂ -. Typically, an alkyl (or alkylene) group will have from 1 to 24 carbon atoms, including those groups having 10 or fewer carbon atoms. A "lower alkyl" or "lower alkylene" is a shorter chain alkyl or alkylene group, generally having six or fewer carbon atoms. conventional sense, and refer to those alkyl groups attached to the remainder of the molecule via an oxygen atom, an amino group, or a sulfur atom, respectively. [0035] The term "heteroalkyl," by itself or in combination with another term, means, unless otherwise stated, a straight or branched chain hydrocarbon radical, consisting of a heteroatom selected from the group consisting of O, N, P, Si and S, and wherein the nitrogen and sulfur atoms may optionally be oxidized and the nitrogen atom may have an alkyl substituent to fulfill valency and/or may optionally be quaternized. The heteroatom(s) O, N, P, Si and S may be placed at any interior position of the heteroalkyl group. Examples include, but are not limited to, -CH ₂ -CH ₂ -O-CH ₃ , -CH ₂ -CH ₂ -NH-CH ₃ , -CH ₂ -CH ₂ -N(CH ₃ )-CH ₃ , -CH ₂ -S-CH ₂ - CH3, -CH2-CH2-S(O)-CH3, -CH2-CH2-S(O)2-CH3, -CH=CH-O-CH3, -CH2-CH=N-OCH3, and -CH=CH-N(CH ₃ )-CH ₃ . Up to two heteroatoms may be consecutive, such as, for example, - CH2-NH-OCH3 and –CH2-O-Si(CH3)3. Similarly, the term "heteroalkylene" by itself or as part of another substituent means a divalent radical derived from heteroalkyl, as exemplified, but not limited by, -CH2-CH2-S-CH2-CH2- and –CH2-S-CH2-CH2-NH-CH2-. For alkylene and heteroalkylene linking groups, no orientation of the linking group is implied by the direction in which the formula of the linking group is written. For example, the formula –C(O)2R'- represents both –C(O)2R'- and –R'C(O)2-. [0036] The terms "cycloalkyl" and "heterocycloalkyl", by themselves or in combination with other terms, represent, unless otherwise stated, cyclic versions of "alkyl" and "heteroalkyl", respectively, including bicyclic, tricyclic and bridged bicyclic groups. Additionally, for heterocycloalkyl, a heteroatom can occupy the position at which the heterocycle is attached to the remainder of the molecule. Examples of cycloalkyl include, but are not limited to, cyclopentyl, cyclohexyl, 1-cyclohexenyl, 3-cyclohexenyl, cycloheptyl, norbornanyl, bicyclo[2.2.2]octanyl, and the like. Examples of heterocycloalkyl include, but are not limited to, 1-(1,2,5,6-tetrahydropyridyl), 1-piperidinyl, 2-piperidinyl, 3-piperidinyl, 4- morpholinyl, 3-morpholinyl, tetrahydrofuran-2-yl, tetrahydrofuran-3-yl, tetrahydrothien-2-yl, tetrahydrothien-3-yl, 1-piperazinyl, 2-piperazinyl, 1- or 2-azabicyclo[2.2.2]octanyl, and the like. [0037] The terms "halo," by itself or as part of another substituent, means, unless otherwise stated, a fluorine, chlorine, bromine, or iodine atom. Additionally, terms such as "haloalkyl," are meant to include monohaloalkyl and polyhaloalkyl. For example, the term "halo(C1- C ₄ )alkyl" is meant to include, but not be limited to, trifluoromethyl, 2,2,2-trifluoroethyl, 4- chlorobutyl, 3-bromopropyl, and the like. hydrocarbon substituent which can be a single ring or multiple rings (in one embodiment from 1 to 3 rings) which are fused together or linked covalently. [0039] The term "heteroaryl" refers to aryl groups that contain from one to four heteroatoms selected from N, O, and S in the ring(s), wherein the nitrogen and sulfur atoms are optionally oxidized, and the nitrogen atom(s) are optionally quaternized. A heteroaryl group can be attached to the remainder of the molecule through a carbon or heteroatom. Non-limiting examples of aryl and heteroaryl groups include phenyl, 1-naphthyl, 2-naphthyl, 4-biphenyl, 1-pyrrolyl, 2-pyrrolyl, 3-pyrrolyl, 3-pyrazolyl, 2-imidazolyl, 4-imidazolyl, pyrazinyl, 2-oxazolyl, 4-oxazolyl, 5-oxazolyl, 3-isoxazolyl, 4-isoxazolyl, 5-isoxazolyl, 2- thiazolyl, 4-thiazolyl, 5-thiazolyl, 2-furyl, 3-furyl, 2-thienyl, 3-thienyl, 2-pyridyl, 3-pyridyl, 4-pyridyl, 2-pyrimidyl, 4-pyrimidyl, 5-benzothiazolyl, purinyl, 2-benzimidazolyl, 5-indolyl, 1-isoquinolyl, 5-isoquinolyl, 2-quinoxalinyl, 5-quinoxalinyl, 3-quinolyl, and 6-quinolyl. The term "heteroarylium" refers to a heteroaryl group that is positively charged on one or more of the heteroatoms. [0040] The term "oxo" as used herein means an oxygen atom that is double bonded to a carbon atom. [0041] Each of the above terms (e.g., "alkyl," "heteroalkyl," "aryl" and "heteroaryl") are meant to include both substituted and unsubstituted forms of the indicated radical. Non- limiting examples of substituent moieties for each type of radical are provided below. [0042] Substituent moieties for alkyl, heteroalkyl, alkylene, alkenyl, heteroalkylene, heteroalkenyl, alkynyl, cycloalkyl, heterocycloalkyl, cycloalkenyl, and heterocycloalkenyl groups are, in one embodiment, selected from, deuterium, -OR', =O, =NR', =N-OR', -NR'R", -SR', halo, -SiR'R"R"', -OC(O)R', -C(O)R', -CO2R', -CONR'R", -OC(O)NR'R", -NR"C(O)R', -NR'-C(O)NR"R"', -NR"C(O) ₂ R', -NR-C(NR'R"R'")=NR"", -NR-C(NR'R")=NR'", -S(O)R', -S(O)2R', -S(O)2NR'R", -NRSO2R', -CN and –NO2 in a number ranging from zero to the number of hydrogen atoms in such radical. In one embodiment, substituent moieties for cycloalkyl, heterocycloalkyl, cycloalkenyl, and heterocycloalkenyl groups also include substituted and unsubstituted alkyl, substituted and unsubstituted alkenyl, and substituted and unsubstituted alkynyl. R', R", R"' and R"" each in one embodiment independently are hydrogen, substituted or unsubstituted heteroalkyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl, substituted or unsubstituted aryl (e.g., aryl substituted with 1-3 halogens), substituted or unsubstituted alkyl, alkoxy or thioalkoxy groups, or arylalkyl groups. When a compound independently selected as are each R, R , R and R groups when more than one of these groups is present. When R' and R" are attached to the same nitrogen atom, they can be combined with the nitrogen atom to form a 4-, 5-, 6-, or 7-membered ring. For example, -NR'R" is meant to include, but not be limited to, 1-pyrrolidinyl and 4-morpholinyl. From the above discussion of substituent moieties, one of skill in the art will understand that the term "alkyl" is meant to include groups including carbon atoms bound to groups other than hydrogen groups, such as haloalkyl (e.g., -CF ₃ and –CH ₂ CF ₃ ) and acyl (e.g., -C(O)CH3, -C(O)CF3, -C(O)CH2OCH3, and the like). [0043] Substituent moieties for aryl and heteroaryl groups are, in one embodiment, selected from deuterium, halo, substituted and unsubstituted alkyl, substituted and unsubstituted alkenyl, and substituted and unsubstituted alkynyl, -OR', -NR'R", -SR', -SiR'R"R"', -OC(O)R', -C(O)R', -CO2R', -CONR'R", -OC(O)NR'R", -NR"C(O)R', -NR'-C(O)NR"R"', -NR"C(O) ₂ R', -NR-C(NR'R"R'")=NR"", -NR-C(NR'R")=NR'", -S(O)R', -S(O) ₂ R', -S(O)2NR'R", -NRSO2R', -CN and –NO2, -R', -N3, -CH(Ph)2, fluoro(C1-C4)alkoxy, and fluoro(C1-C4)alkyl, in a number ranging from zero to the total number of hydrogens on the aromatic ring system; and where R', R", R"' and R"" are, in one embodiment, independently selected from hydrogen, substituted or unsubstituted alkyl, substituted or unsubstituted heteroalkyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl, substituted or unsubstituted aryl and substituted or unsubstituted heteroaryl. When a compound provided herein includes more than one R group, for example, each of the R groups is independently selected as are each R', R", R'" and R"" groups when more than one of these groups is present. [0044] Two of the substituent moieties on adjacent atoms of an aryl or heteroaryl ring may optionally form a ring of the formula -Q'-C(O)-(CRR') _q -Q''-, wherein Q' and Q'' are independently –NR-, -O-, -CRR'- or a single bond, and q is an integer of from 0 to 3. Alternatively, two of the substituent moieties on adjacent atoms of the aryl or heteroaryl ring may optionally be replaced with a substituent of the formula -A-(CH2)r-B-, wherein A and B are independently –CRR'-, -O-, -NR-, -S-, -S(O)-, -S(O) ₂ -, -S(O) ₂ NR'- or a single bond, and r is an integer of from 1 to 4. One of the single bonds of the new ring so formed may optionally be replaced with a double bond. Alternatively, two of the substituent moieties on adjacent atoms of the aryl or heteroaryl ring may optionally be replaced with a substituent of the formula –(CRR') _u -X'-(CR''R''') _v -, where u and v are independently integers from 0 to 3, and X' is –O-, -NR'-, -S-, -S(O)-, -S(O)2-, or –S(O)2NR'-. The substituent moieties R, R', R" unsubstituted alkyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl, substituted or unsubstituted aryl, and substituted or unsubstituted heteroaryl. [0045] As used herein, the term "heteroatom" or "ring heteroatom" is meant to include oxygen (O), nitrogen (N), sulfur (S), phosphorus (P), and silicon (Si). [0046] As used herein, a prodrug is a compound that upon in vivo administration is metabolized, or otherwise undergoes chemical changes under physiological conditions, by one or more steps or processes or otherwise converted to a biologically, pharmaceutically or therapeutically active form of the compound. Additionally, prodrugs can be converted to a biologically, pharmaceutically or therapeutically active form of the compound by chemical or biochemical methods in an ex vivo environment. For example, prodrugs can be converted to the compounds of the present invention when placed in a transdermal patch reservoir with a suitable enzyme or chemical reagent. [0047] Certain compounds provided herein can exist in unsolvated forms as well as solvated forms, including hydrated forms. In general, the solvated forms are equivalent to unsolvated forms and are encompassed within the scope of the present disclosure. Certain compounds provided herein may exist in multiple crystalline or amorphous forms. In general, all physical forms are equivalent for the uses contemplated herein and are intended to be within the scope of the present disclosure. [0048] Certain compounds provided herein possess asymmetric carbon atoms (optical centers) or double bonds; the racemates, diastereomers, tautomers, geometric isomers and individual isomers are encompassed within the scope of the present disclosure. The compounds provided herein do not include those which are known in the art to be too unstable to synthesize and/or isolate. [0049] The compounds provided herein may also contain unnatural proportions of atomic isotopes at one or more of the atoms that constitute such compounds. For example, the compounds may be radiolabeled with radioactive isotopes, such as for example tritium ( ³ H), iodine-125 ( ¹²⁵ I) or carbon-14 ( ¹⁴ C). All isotopic variations of the compounds provided herein, whether radioactive or not, are encompassed within the scope of the present disclosure. II. COMPOUNDS FOR USE IN COMPOSITIONS AND METHODS [0050] In one embodiment, provided herein is a compound for use in the compositions and methods provided herein having Formula I: e thereof, wherein [0052] n is an integer from 1-4; [0053] p and u are each independently an integer from 1-3; [0054] m, s and t are each independently an integer from 0-3; [0055] X ¹ is a bond, O, NR ³ or CO; [0056] X ² is a bond, CONR ⁴ , SO2NR ⁴ , CO or SO2; [0057] X ³ is bicyclic heteroarylene; [0058] X ⁴ is (CH2)1-2, O(CH2)0-1 or NH(CH2)0-1; [0059] R ¹ is aryl, heteroaryl or heterocycloalkyl; [0060] R ² is cycloalkyl, heterocyclyl, aryl or heteroaryl; [0061] R ³ to R ⁶ , R ¹¹ and R ¹² are each independently H, alkyl or aralkyl; [0062] R ⁷ and R ⁸ are each independently H, alkyl or aralkyl, or together with the carbon atom to which they are attached form cycloalkyl; [0063] R ⁹ and R ¹⁰ are each independently H, OH, alkoxy, alkyl or aralkyl, or R ⁹ and R ¹⁰ together form oxo; and [0064] R ¹³ and R ¹⁴ are each independently H, alkyl or aralkyl, or together with the carbon atom to which they are attached form cycloalkyl. [0065] In another embodiment, X ⁴ is CH ₂ , O or NH. In another embodiment, X ⁴ is CH ₂ . In another embodiment, X ⁴ is O. In another embodiment, X ⁴ is NH. [0066] In another embodiment, u is 1 or 2. In another embodiment, u is 1. In another embodiment, u is 2. [0067] In one embodiment, provided herein is a compound for use in the compositions and methods provided herein having Formula Ia: hereof, wherein [0069] n is an integer from 1-4; [0070] p is an integer from 1-3; [0071] m, s and t are each independently an integer from 0-3; [0072] X ¹ is a bond, O, NR ³ or CO; [0073] X ² is a bond, CONR ⁴ , SO2NR ⁴ , CO or SO2; [0074] X ³ is bicyclic heteroarylene; [0075] R ¹ is aryl, heteroaryl or heterocycloalkyl; [0076] R ² is cycloalkyl, heterocyclyl, aryl or heteroaryl; [0077] R ³ to R ⁶ , R ¹¹ and R ¹² are each independently H, alkyl or aralkyl; [0078] R ⁷ and R ⁸ are each independently H, alkyl or aralkyl, or together with the carbon atom to which they are attached form cycloalkyl; [0079] R ⁹ and R ¹⁰ are each independently H, OH, alkoxy, alkyl or aralkyl, or R ⁹ and R ¹⁰ together form oxo; and [0080] R ¹³ and R ¹⁴ are each independently H, alkyl or aralkyl, or together with the carbon atom to which they are attached form cycloalkyl. [0081] In one embodiment, provided herein is a compound for use in the compositions and methods provided herein having Formula Ia, [0082] or a pharmaceutically acceptable derivative thereof, wherein [0083] n is an integer from 1-4; [0084] p is an integer from 1-3; [0085] m, s and t are each independently an integer from 0-3; [0086] X ¹ is a bond, O, NR ³ or CO; [0087] X ² is a bond, CONR ⁴ , SO ₂ NR ⁴ , CO or SO ₂ ; [0088] X ³ is bicyclic heteroarylene; [0089] R ¹ is aryl, heteroaryl or heterocycloalkyl; [0090] R ² is aryl or heteroaryl; [0091] R ³ to R ⁶ , R ¹¹ and R ¹² are each independently H, alkyl or aralkyl; atom to which they are attached form cycloalkyl; [0093] R ⁹ and R ¹⁰ are each independently H, OH, alkoxy, alkyl or aralkyl, or R ⁹ and R ¹⁰ together form oxo; and [0094] R ¹³ and R ¹⁴ are each independently H, alkyl or aralkyl, or together with the carbon atom to which they are attached form cycloalkyl. [0095] In another embodiment, s and t are each 0, X ² is a bond and the compound for use in the compositions and methods provided herein has Formula Ib: derivative thereof, wherein [0097] n is an integer from 1-4; [0098] p is an integer from 1-3; [0099] m is an integer from 0-3; [0100] X ¹ is a bond, O, NR ³ or CO; [0101] X ³ is bicyclic heteroarylene; [0102] R ¹ is aryl, heteroaryl or heterocycloalkyl; [0103] R ² is heteroaryl; [0104] R ³ , R ⁵ , R ⁶ , R ¹¹ and R ¹⁰ are each independently H, alkyl or aralkyl; [0105] R ⁷ and R ⁸ are each independently H, alkyl or aralkyl, or together with the carbon atom to which they are attached form cycloalkyl; and [0106] R ⁹ and R ¹⁰ are each independently H, OH, alkoxy, alkyl or aralkyl, or R ⁹ and R ¹⁰ together form oxo. [0107] In another embodiment, p and u are each 2, s and t are each 0, X ² is a bond and the compound for use in the compositions and methods provided herein has Formula Ic: erivative thereof, wherein [0109] n is an integer from 1-4; [0110] m is an integer from 0-3; [0111] X ¹ is a bond, O, NR ³ or CO; [0112] X ³ is bicyclic heteroarylene; [0113] R ¹ is aryl, heteroaryl or heterocycloalkyl; [0114] R ² is heteroaryl; [0115] R ³ , R ⁵ and R ⁶ are each independently H, alkyl or aralkyl; [0116] R ⁷ and R ⁸ are each independently H, alkyl or aralkyl, or together with the carbon atom to which they are attached form cycloalkyl; and [0117] R ⁹ and R ¹⁰ are each independently H, OH, alkoxy, alkyl or aralkyl, or R ⁹ and R ¹⁰ together form oxo. [0118] In another embodiment, each of R ⁵ , R ⁶ , R ⁹ and R ¹⁰ are H, p is 2, s and t are each 0, X ² is a bond and the compound for use in the compositions and methods provided herein has Formula Id: ivative thereof, wherein [0120] n is an integer from 1-4; [0121] m is an integer from 0-3; [0122] X ¹ is a bond, O, NR ³ or CO; [0123] X ³ is bicyclic heteroarylene; [0124] R ¹ is aryl, heteroaryl or heterocycloalkyl; [0125] R ² is heteroaryl; [0127] R and R are each independently H or alkyl, or together with the carbon atom to which they are attached form cycloalkyl. [0128] In another embodiment, X ¹ is a bond, each of R ³ to R ⁶ , R ⁹ and R ¹⁰ are H, p is 2, m, s and t are each 0, X ² is a bond and the compound for use in the compositions and methods provided herein has Formula Ie: ptable derivative thereof, wherein [0130] n is 2 or 3; [0131] X ³ is bicyclic heteroarylene; [0132] R ¹ is heterocycloalkyl, optionally substituted with 1-3 substituents each independently selected from alkyl and aryl; and [0133] R ² is heteroaryl. [0134] In another embodiment, the compound for use in the compositions and methods provided herein has Formula If: ative thereof, wherein [0136] n is 2 or 3; [0137] X ³ is bicyclic heteroarylene; [0138] Ar is aryl; [0139] R ² is heteroaryl; and [0140] R ¹⁵ is alkyl. [0141] In another embodiment, the compound for use in the compositions and methods provided herein has the formula:

herein. [0143] In another embodiment, the compound for use in the compositions and methods provided herein has Formula Ig: erivative thereof, wherein [0145] n is 2 or 3; [0146] X ³ is bicyclic heteroarylene; [0147] Ar is aryl; [0148] R ² is heteroaryl; and [0149] R ⁷ and R ⁸ are each independently H or alkyl, or together with the carbon atom to which they are attached form cycloalkyl. [0150] In another embodiment, the compound for use in the compositions and methods provided herein has the formula: erein. [0152] In another embodiment, p and u are is 1, s and t are each 0, X ² is a bond and the compound for use in the compositions and methods provided herein has Formula Ih: derivative thereof, wherein [0154] n is an integer from 1-4; [0155] m is an integer from 0-3; [0156] X ¹ is a bond, O, NR ³ or CO; [0157] X ³ is bicyclic heteroarylene; [0158] R ¹ is aryl, heteroaryl or heterocycloalkyl; [0159] R ² is heteroaryl; [0160] R ³ , R ⁵ and R ⁶ are each independently H, alkyl or aralkyl; [0161] R ⁷ and R ⁸ are each independently H, alkyl or aralkyl, or together with the carbon atom to which they are attached form cycloalkyl; and [0162] R ⁹ and R ¹⁰ are each independently H, OH, alkoxy, alkyl or aralkyl, or R ⁹ and R ¹⁰ together form oxo. [0163] In another embodiment, each of R ⁵ , R ⁶ , R ⁹ and R ¹⁰ are H, p and u are each 1, s and t are each 0, X ² is a bond and the compound for use in the compositions and methods provided herein has Formula Ii: [0165] n is an integer from 14; [0166] m is an integer from 0-3; [0167] X ¹ is a bond, O, NR ³ or CO; [0168] X ³ is bicyclic heteroarylene; [0169] R ¹ is aryl, heteroaryl or heterocycloalkyl; [0170] R ² is heteroaryl; [0171] R ³ is H or alkyl; and [0172] R ⁷ and R ⁸ are each independently H or alkyl, or together with the carbon atom to which they are attached form cycloalkyl. [0173] In another embodiment, R ¹ in Formulae I, Ia, Ib, Ic, Id, Ih or Ii is aryl or heterocycloalkyl. In another embodiment, R ¹ in Formulae I, Ia, Ib, Ic, Id, Ih or Ii is aryl. In another embodiment, R ¹ in Formulae I, Ia, Ib, Ic, Id, Ih or Ii is heterocycloalkyl. [0174] In another embodiment, X ¹ is a bond, each of R ³ to R ⁶ , R ⁹ and R ¹⁰ are H, p and u are each 1, m, s and t are each 0, X ² is a bond and the compound for use in the compositions and methods provided herein has Formula Ij: eptable derivative thereof, wherein [0176] n is 2 or 3; [0177] X ³ is bicyclic heteroarylene; [0178] R ¹ is heterocycloalkyl, optionally substituted with 1-3 substituents each independently selected from alkyl and aryl; and [0179] R ² is heteroaryl. [0180] In another embodiment, the compound for use in the compositions and methods provided herein has Formula Ik: p y p vative thereof, wherein [0183] X is bicyclic heteroarylene; [0184] Ar is aryl; [0185] R ² is heteroaryl; and [0186] R ¹⁵ is alkyl. [0187] In another embodiment, R ¹⁵ is lower alkyl. In another embodiment, R ¹⁵ is methyl or ethyl. In another embodiment, R ¹⁵ is methyl. In another embodiment, R ¹⁵ is ethyl. [0188] In another embodiment, the compound for use in the compositions and methods provided herein has the formula: rein. [0190] In another embodiment, the compound for use in the compositions and methods provided herein has Formula Im: vative thereof, wherein [0192] n is 2 or 3; [0193] X ³ is bicyclic heteroarylene; [0194] Ar is aryl; [0195] R ² is heteroaryl; and [0196] R ⁷ and R ⁸ are each independently H or alkyl, or together with the carbon atom to which they are attached form cycloalkyl. methyl and R is H. In another embodiment, R and R together with the carbon atom to which they are attached form cyclopropyl. [0198] In another embodiment, the compound for use in the compositions and methods provided herein has the formula: in. [0200] In another embodiment, the compound for use in the compositions and methods provided herein has any of the following formulae where the variables are as defined herein: , ,

, ,

, [0202] In another embodiment, X ³ is imidazopyridinylene or triazolopyridinylene, each optionally substituted with alkyl, haloalkyl, hydroxyalkyl or halo. In another embodiment, X ³ is imidazopyridinylene or triazolopyridinylene, each optionally substituted with methyl, halomethyl, hydroxymethyl or halo. In another embodiment, X ³ is triazolopyridinylene, optionally substituted with methyl, halomethyl, hydroxymethyl or halo. In another embodiment, X ³ is imidazopyridinylene, optionally substituted with methyl, halomethyl, hydroxymethyl or halo. In another embodiment, X ³ is 3-methylimidazo[1,2-a]pyridinyl-2,7- structure: . odiment, X ³ has the structure: . ment, provided herein is a compound for use in the compositions and methods provided herein having Formula In: , wherein [0206] n is an integer from 1-4; [0207] p is an integer from 1-3; [0208] m, s and t are each independently an integer from 0-3; [0209] X ¹ is a bond, O, NR ³ or CO; [0210] X ² is a bond, CONR ⁴ , SO ₂ NR ⁴ , CO or SO ₂ ; [0211] R ¹ is aryl or heterocycloalkyl; [0212] R ² is aryl or heteroaryl; [0213] R ³ to R ⁶ , R ¹¹ and R ¹² are each independently H, alkyl or aralkyl; [0214] R ⁷ and R ⁸ are each independently H, alkyl or aralkyl, or together with the carbon atom to which they are attached form cycloalkyl; [0215] R ⁹ and R ¹⁰ are each independently H, OH, alkoxy, alkyl or aralkyl, or R ⁹ and R ¹⁰ together form oxo; [0216] R ¹³ and R ¹⁴ are each independently H, alkyl or aralkyl, or together with the carbon atom to which they are attached form cycloalkyl; and [0218] In another embodiment, the compounds provided herein for use in the compositions and methods provided herein have Formula In, or a pharmaceutically acceptable derivative thereof, wherein: [0219] n is 2 or 3; [0220] p is 2; [0221] m is 0 or 2; [0222] s and t are each 0; [0223] X ¹ is a bond or O; [0224] X ² is a bond; [0225] R ¹ is aryl or heterocycloalkyl, each optionally substituted with 1-3 substituents each independently selected from alkyl and phenyl; [0226] R ² is heteroaryl; [0227] R ³ to R ⁶ , R ¹¹ and R ¹² are each independently H, alkyl or aralkyl; [0228] R ⁷ and R ⁸ are each independently H, alkyl or aralkyl, or together with the carbon atom to which they are attached form cycloalkyl; [0229] R ⁹ and R ¹⁰ are each independently H, OH, alkoxy, alkyl or aralkyl, or R ⁹ and R ¹⁰ together form oxo; [0230] R ¹³ and R ¹⁴ are each independently H, alkyl or aralkyl, or together with the carbon atom to which they are attached form cycloalkyl; and [0231] R ¹⁶ is H, alkyl, haloalkyl, hydroxyalkyl or halo. [0232] In another embodiment, the compounds provided herein for use in the compositions and methods provided herein have Formula In, or a pharmaceutically acceptable derivative thereof, wherein: [0233] n is 2 or 3; [0234] p is 2; [0235] m is 0 or 2; [0236] s and t are each 0; [0237] X ¹ is a bond or O; [0238] X ² is a bond; [0239] R ¹ is aryl or heterocycloalkyl, each optionally substituted with 1-3 substituents each independently selected from alkyl and phenyl; [0240] R ² is heteroaryl; [0241] R ³ to R ⁶ and R ⁸ to R ¹⁴ are each independently H; and [0243] In another embodiment, provided herein is a compound for use in the compositions and methods provided herein having Formula Io: rein [0245] n is an integer from 1-4; [0246] p and u are each independently an integer from 1-3; [0247] m, s and t are each independently an integer from 0-3; [0248] X ¹ is a bond, O, NR ³ or CO; [0249] X ² is a bond, CONR ⁴ , SO2NR ⁴ , CO or SO2; [0250] X ⁴ is (CH ₂ ) _1-2 , O(CH ₂ ) _0-1 or NH(CH ₂ ) _0-1 ; [0251] R ¹ is aryl or heterocycloalkyl; [0252] R ² is cycloalkyl, heterocyclyl, aryl or heteroaryl; [0253] R ³ to R ⁶ , R ¹¹ and R ¹² are each independently H, alkyl or aralkyl; [0254] R ⁷ and R ⁸ are each independently H, alkyl or aralkyl, or together with the carbon atom to which they are attached form cycloalkyl; [0255] R ⁹ and R ¹⁰ are each independently H, OH, alkoxy, alkyl or aralkyl, or R ⁹ and R ¹⁰ together form oxo; [0256] R ¹³ and R ¹⁴ are each independently H, alkyl or aralkyl, or together with the carbon atom to which they are attached form cycloalkyl; and [0257] R ¹⁶ is H, alkyl, haloalkyl, hydroxyalkyl or halo. [0258] In another embodiment, provided herein is a compound having one of the following formulae where the variables are as defined herein: , or . or use in the compositions and methods provided herein having Formula Ip: erein [0261] n is an integer from 1-4; [0262] p is an integer from 1-3; [0263] m, s and t are each independently an integer from 0-3; [0264] X ¹ is a bond, O, NR ³ or CO; [0265] X ² is a bond, CONR ⁴ , SO2NR ⁴ , CO or SO2; [0266] R ¹ is aryl or heterocycloalkyl; [0267] R ² is aryl or heteroaryl; [0268] R ³ to R ⁶ , R ¹¹ and R ¹² are each independently H, alkyl or aralkyl; [0269] R ⁷ and R ⁸ are each independently H, alkyl or aralkyl, or together with the carbon atom to which they are attached form cycloalkyl; [0270] R ⁹ and R ¹⁰ are each independently H, OH, alkoxy, alkyl or aralkyl, or R ⁹ and R ¹⁰ together form oxo; [0271] R ¹³ and R ¹⁴ are each independently H, alkyl or aralkyl, or together with the carbon atom to which they are attached form cycloalkyl; and [0272] R ¹⁶ is H, alkyl, haloalkyl, hydroxyalkyl or halo. and methods provided herein have Formula Ip, or a pharmaceutically acceptable derivative thereof, wherein: [0274] n is 2 or 3; [0275] p is 2; [0276] m is 0 or 2; [0277] s and t are each 0; [0278] X ¹ is a bond or O; [0279] X ² is a bond; [0280] R ¹ is aryl or heterocycloalkyl, each optionally substituted with 1-3 substituents each independently selected from alkyl and phenyl; [0281] R ² is heteroaryl; [0282] R ³ to R ⁶ , R ¹¹ and R ¹² are each independently H, alkyl or aralkyl; [0283] R ⁷ and R ⁸ are each independently H, alkyl or aralkyl, or together with the carbon atom to which they are attached form cycloalkyl; [0284] R ⁹ and R ¹⁰ are each independently H, OH, alkoxy, alkyl or aralkyl, or R ⁹ and R ¹⁰ together form oxo; [0285] R ¹³ and R ¹⁴ are each independently H, alkyl or aralkyl, or together with the carbon atom to which they are attached form cycloalkyl; and [0286] R ¹⁶ is H, alkyl, haloalkyl, hydroxyalkyl or halo. [0287] In another embodiment, the compounds provided herein for use in the compositions and methods provided herein have Formula Ip, or a pharmaceutically acceptable derivative thereof, wherein: [0288] n is 2 or 3; [0289] p is 2; [0290] m is 0 or 2; [0291] s and t are each 0; [0292] X ¹ is a bond or O; [0293] X ² is a bond; [0294] R ¹ is aryl or heterocycloalkyl, each optionally substituted with 1-3 substituents each independently selected from alkyl and phenyl; [0295] R ² is heteroaryl; and [0296] R ³ to R ⁶ and R ⁸ to R ¹⁴ are each independently H; and [0297] R ⁷ and R ¹⁶ are each independently alkyl. formulae where the variables are as defined herein: or compositions and methods provided herein have Formula Iq: [0302] p is an integer from 1-3; [0303] m is an integer from 0-3; [0304] X ¹ is a bond, O, NR ³ or CO; [0305] R ¹ is aryl, heteroaryl or heterocycloalkyl; [0306] R ² is heteroaryl; and [0307] R ³ , R ⁵ , R ⁶ , R ⁹ , R ¹⁰ and R ¹⁶ are each independently H or alkyl; and [0308] R ⁷ and R ⁸ are each independently H or alkyl, or together with the carbon atom to which they are attached form cycloalkyl. [0309] In another embodiment, the compounds for use in the compositions and methods provided herein have one of the following formulae where the variables are as defined herein: , , . provided herein have Formula Ir: [0312] n is an integer from 1-4; [0313] p is an integer from 1-3; [0314] m is an integer from 0-3; [0315] X ¹ is a bond, O, NR ³ or CO; [0316] R ¹ is aryl, heteroaryl or heterocycloalkyl; [0317] R ² is heteroaryl; and [0318] R ³ , R ⁵ , R ⁶ , R ⁹ , R ¹⁰ and R ¹⁶ are each independently H or alkyl; and which they are attached form cycloalkyl. [0320] In another embodiment, he compounds for use in the compositions and methods provided herein have Formula Iq or Ir, wherein: [0321] n is 2 or 3; [0322] p is 2; [0323] m is 0 or 2; [0324] X ¹ is a bond or O; [0325] R ¹ is aryl or heterocycloalkyl, each optionally substituted with 1-3 substituents each independently selected from alkyl and aryl; [0326] R ² is heteroaryl; and [0327] R ⁵ , R ⁶ , R ⁹ , R ¹⁰ and R ¹⁶ are each independently H or alkyl; and [0328] R ⁷ and R ⁸ are each independently H or alkyl, or together with the carbon atom to which they are attached form cycloalkyl. [0329] In another embodiment, the compound has any of Formulae I, Ia, Ib, Ic, Ih, In, Io, Ip, Iq and Ir, where R ⁹ and R ¹⁰ are each independently H, alkyl or aralkyl. In another embodiment, the compound has any of Formulae I, Ia, Ib, Ic, Ih, In, Io, Ip, Iq and Ir where R ⁹ and R ¹⁰ are each independently H, OH, OMe or methyl, or R ⁹ and R ¹⁰ together form oxo. In another embodiment, the compound has any of Formulae I, Ia, Ib, Ic, Ih, In, Io, Ip, Iq and Ir where R ⁹ and R ¹⁰ are each independently H, OH, OMe or methyl. [0330] In another embodiment, the compound has any of Formulae I, Ia, In, Io or Ip, where R ¹³ and R ¹⁴ are each independently H, alkyl or aralkyl. [0331] In another embodiment, the compound has any of Formulae I, Ia, In, Io or Ip, where R ⁹ and R ¹⁰ are each independently H, alkyl or aralkyl; and R ¹³ and R ¹⁴ are each independently H, alkyl or aralkyl. [0332] In another embodiment, Ar is unsubstituted aryl. In another embodiment, Ar is optionally substituted phenyl. In another embodiment, Ar is unsubstituted phenyl. In another embodiment, R ² is heterocyclyl, aryl or heteroaryl. In another embodiment, R ² is aryl or heteroaryl. In another embodiment, R ² is bicyclic or monocyclic heteroaryl. In another embodiment, R ² is piperidinyl, pyridyl, isoxazolyl, triazolyl, tetrazolyl, pyridazinyl, pyrimidinyl, thiadiazolyl, pyrazinyl, pyrazolyl, thiazolyl, oxadiazolyl, triazolopyrazinyl or imidazopyrazinyl, each optionally substituted with C(O)Me, Me, OH, COOH, CF3, F, Cl, CN, NH ₂ , oxo, S(O)(NH)Me, SO ₂ Me, COOEt, CONHMe, COOMe or OMe. In another embodiment, R ² is triazolopyrazinyl or imidazopyrazinyl. In another embodiment, R ² is yl. [0333] In another embodiment, provided herein is a compound for use in the compositions and methods provided herein having Formula II: thereof, wherein: [0335] b is an integer from 1-4; [0336] c and g are each independently an integer from 1-3; [0337] a, d and f are each independently an integer from 0-3; [0338] X ¹¹ is a bond, O, NR ³¹ or CO; [0339] X ¹² is a bond, CONR ³² , SO2NR ³² , CO or SO2; [0340] X ¹³ is bicyclic heteroarylene; [0341] X ¹⁴ is (CH2)2-3, C(O)NH(CH2)0-1 or C(O)(CH2)1-2; [0342] R ²¹ is aryl, heteroaryl or heterocycloalkyl; [0343] R ²² is cycloalkyl, heterocyclyl, aryl or heteroaryl; [0344] R ²³ and R ²⁴ are each independently H, alkyl or aralkyl, or together with the carbon atom to which they are attached form cycloalkyl; and [0345] R ²⁵ and R ²⁶ are each independently H, OH, alkoxy, alkyl or aralkyl, or R ²⁵ and R ²⁶ together form oxo; [0346] R ²⁹ and R ³⁰ are each independently H, alkyl or aralkyl, or together with the carbon atom to which they are attached form cycloalkyl; and [0347] R ²⁷ , R ²⁸ , R ³¹ and R ³² are each independently H, alkyl or aralkyl. [0348] In one embodiment, provided herein is a compound for use in the compositions and methods provided herein having Formula IIa: [0350] b is an integer from 14; [0351] c is an integer from 1-3; [0352] a, d and f are each independently an integer from 0-3; [0353] X ¹¹ is a bond, O, NR ³¹ or CO; [0354] X ¹² is a bond, CONR ³² , SO ₂ NR ³² , CO or SO ₂ ; [0355] X ¹³ is bicyclic heteroarylene; [0356] R ²¹ is aryl, heteroaryl or heterocycloalkyl; [0357] R ²² is cycloalkyl, heterocyclyl, aryl or heteroaryl; [0358] R ²³ and R ²⁴ are each independently H, alkyl or aralkyl, or together with the carbon atom to which they are attached form cycloalkyl; and [0359] R ²⁵ and R ²⁶ are each independently H, OH, alkoxy, alkyl or aralkyl, or R ²⁵ and R ²⁶ together form oxo; [0360] R ²⁹ and R ³⁰ are each independently H, alkyl or aralkyl, or together with the carbon atom to which they are attached form cycloalkyl; and [0361] R ²⁷ , R ²⁸ , R ³¹ and R ³² are each independently H, alkyl or aralkyl. [0362] In one embodiment, provided herein is a compound for use in the compositions and methods provided herein having Formula IIa, or a pharmaceutically acceptable derivative thereof, wherein: [0363] b is an integer from 1-4; [0364] c is an integer from 1-3; [0365] a, d and f are each independently an integer from 0-3; [0366] X ¹¹ is a bond, O, NR ³¹ or CO; [0367] X ¹² is a bond, CONR ³² , SO2NR ³² , CO or SO2; [0368] X ¹³ is bicyclic heteroarylene; [0369] R ²¹ is aryl, heteroaryl or heterocycloalkyl; [0370] R ²² is aryl or heteroaryl; [0371] R ²³ and R ²⁴ are each independently H, alkyl or aralkyl, or together with the carbon atom to which they are attached form cycloalkyl; [0372] R ²⁵ and R ²⁶ are each independently H, OH, alkoxy, alkyl or aralkyl, or R ²⁵ and R ²⁶ together form oxo; [0373] R ²⁹ and R ³⁰ are each independently H, alkyl or aralkyl, or together with the carbon atom to which they are attached form cycloalkyl; and [0374] R ²⁷ , R ²⁸ , R ³¹ and R ³² are each independently H, alkyl or aralkyl. in the compositions and methods provided herein have Formula IIb: le derivative thereof, wherein: [0377] b is an integer from 1-4; [0378] c is an integer from 1-3; [0379] a is an integer from 0-3; [0380] X ¹¹ is a bond, O, NR ³¹ or CO; [0381] X ¹³ is bicyclic heteroarylene; [0382] R ²¹ is aryl, heteroaryl or heterocycloalkyl; [0383] R ²² is heteroaryl; [0384] R ²³ and R ²⁴ are each independently H, alkyl or aralkyl, or together with the carbon atom to which they are attached form cycloalkyl; [0385] R ²⁵ and R ²⁶ are each independently H, OH, alkoxy, alkyl or aralkyl, or R ²⁵ and R ²⁶ together form oxo; and [0386] R ³¹ is H, alkyl or aralkyl. [0387] In another embodiment, c and g are each 2, d and f are each 0, X ¹² is a bond and the compound for use in the compositions and methods provided herein have Formula IIc: rivative thereof, wherein: [0389] b is an integer from 1-4; [0390] a is an integer from 0-3; [0391] X ¹¹ is a bond, O, NR ³¹ or CO; [0392] X ¹³ is bicyclic heteroarylene; [0394] R is heteroaryl; [0395] R ²³ and R ²⁴ are each independently H, alkyl or aralkyl, or together with the carbon atom to which they are attached form cycloalkyl; [0396] R ²⁵ and R ²⁶ are each independently H, OH, alkoxy, alkyl or aralkyl, or R ²⁵ and R ²⁶ together form oxo; and [0397] R ³¹ is H, alkyl or aralkyl. [0398] In another embodiment, the compound for use in the compositions and methods provided herein has Formula IId: derivative thereof, wherein: [0400] b is an integer from 1-4; [0401] a is an integer from 0-3; [0402] X ¹¹ is a bond, O, NR ³¹ or CO; [0403] X ¹³ is bicyclic heteroarylene; [0404] R ²¹ is aryl, heteroaryl or heterocycloalkyl; [0405] R ²² is heteroaryl; [0406] R ²³ and R ²⁴ are each independently H or alkyl, or together with the carbon atom to which they are attached form cycloalkyl; and [0407] R ²⁵ , R ²⁶ and R ³¹ are each independently H or alkyl. [0408] In another embodiment, R ²¹ in Formulae II, IIa, IIb, IIc or IId is aryl or heterocycloalkyl. In another embodiment, R ²¹ in Formulae II, IIa, IIb, IIc or IId is aryl. In another embodiment, R ²¹ in Formulae II, IIa, IIb, IIc or IId is heterocycloalkyl. [0409] In another embodiment, the compound for use in the compositions and methods provided herein has Formula IIe: [0411] b is 2 or 3; [0412] X ¹³ is bicyclic heteroarylene; [0413] R ²¹ is heterocycloalkyl, optionally substituted with 1-3 substituents each independently selected from alkyl and aryl; and [0414] R ²² is heteroaryl. [0415] In another embodiment, the compound for use in the compositions and methods provided herein has Formula IIf: ivative thereof, wherein: [0417] b is 2 or 3; [0418] X ¹³ is bicyclic heteroarylene; [0419] Ar ¹ is aryl; [0420] R ²² is heteroaryl; [0421] R ³³ is alkyl. [0422] In another embodiment, R ³³ is lower alkyl. In another embodiment, R ³³ is methyl or ethyl. In another embodiment, R ³³ is methyl. In another embodiment, R ³³ is ethyl. [0423] In another embodiment, the compound for use in the compositions and methods provided herein has the formula: rein. provided herein has Formula IIg: ivative thereof, wherein: [0427] b is 2 or 3; [0428] X ¹³ is bicyclic heteroarylene; [0429] Ar ¹ is aryl; [0430] R ²² is heteroaryl; [0431] R ²³ and R ²⁴ are each independently H or alkyl, or together with the carbon atom to which they are attached form cycloalkyl. [0432] In another embodiment, R ²³ is alkyl and R ²⁴ is H. In another embodiment, R ²³ is methyl and R ²⁴ is H. In another embodiment, R ²³ and R ²⁴ together with the carbon atom to which they are attached form cyclopropyl. [0433] In another embodiment, the compound for use in the compositions and methods provided herein has the formula: rein. [0435] In another embodiment, b is 2. In another embodiment, b is 3. [0436] In another embodiment, X ¹³ is imidazopyridinylene or triazolopyridinylene, each optionally substituted with alkyl, haloalkyl, hydroxyalkyl or halo. In another embodiment, X ¹³ is imidazopyridinylene or triazolopyridinylene, each optionally substituted with methyl, halomethyl, hydroxymethyl or halo. In another embodiment, X ¹³ is triazolopyridinylene, embodiment, X is imidazopyridinylene, optionally substituted with methyl, halomethyl, hydroxymethyl or halo. In another embodiment, X ¹³ is 3-methylimidazo[1,2-a]pyridinyl-2,7- ene or 8-methyl-[1,2,4]triazolo[1,5-a]pyridinyl-2,6-ene. In another embodiment, X ¹³ has the structure: . odiment, X ¹³ has the structure: . ment, provided herein is a compound for use in the compositions and methods provided herein having Formula IIh: ein [0440] b is an integer from 1-4; [0441] c is an integer from 1-3; [0442] a, d and f are each independently an integer from 0-3; [0443] X ¹¹ is a bond, O, NR ³¹ or CO; [0444] X ¹² is a bond, CONR ³² , SO2NR ³² , CO or SO2; [0445] R ²¹ is aryl, heteroaryl or heterocycloalkyl; [0446] R ²² is aryl or heteroaryl; [0447] R ²³ and R ²⁴ are each independently H, alkyl or aralkyl, or together with the carbon atom to which they are attached form cycloalkyl; together form oxo; [0449] R ²⁹ and R ³⁰ are each independently H, alkyl or aralkyl, or together with the carbon atom to which they are attached form cycloalkyl; and [0450] R ²⁷ , R ²⁸ , R ³¹ and R ³² are each independently H, alkyl or aralkyl; and [0451] R ³⁴ is H, alkyl, haloalkyl, hydroxyalkyl or halo. [0452] In another embodiment, the compounds provided herein for use in the compositions and methods provided herein have Formula IIh, or a pharmaceutically acceptable derivative thereof, wherein: [0453] b is 2 or 3; [0454] c is 2; [0455] a is 0 or 1; [0456] d and f are each 0; [0457] X ¹¹ is a bond or O; [0458] X ¹² is a bond; [0459] R ²¹ is aryl or heterocycloalkyl, each optionally substituted with 1-3 substituents each independently selected from alkyl and phenyl; [0460] R ²² is heteroaryl; [0461] R ²³ and R ²⁴ are each independently H, alkyl or aralkyl, or together with the carbon atom to which they are attached form cycloalkyl; [0462] R ²⁵ and R ²⁶ are each independently H, OH, alkoxy, alkyl or aralkyl, or R ²⁵ and R ²⁶ together form oxo; [0463] R ²⁹ and R ³⁰ are each independently H, alkyl or aralkyl, or together with the carbon atom to which they are attached form cycloalkyl; and [0464] R ²⁷ , R ²⁸ , R ³¹ and R ³² are each independently H, alkyl or aralkyl; and [0465] R ³⁴ is H, alkyl, haloalkyl, hydroxyalkyl or halo. [0466] In another embodiment, the compounds provided herein for use in the compositions and methods provided herein have Formula IIh, or a pharmaceutically acceptable derivative thereof, wherein: [0467] b is 2 or 3; [0468] c is 2; [0469] a is 0 or 1; [0470] d and f are each 0; [0471] X ¹¹ is a bond or O; [0473] R is aryl or heterocycloalkyl, each optionally substituted with 13 substituents each independently selected from alkyl and phenyl; [0474] R ² is heteroaryl; [0475] R ²⁴ to R ³² are each independently H; and [0476] R ²³ and R ³⁴ are each independently alkyl. [0477] In another embodiment, provided herein is a compound for use in the compositions and methods provided herein having Formula IIi: erein [0479] b is an integer from 1-4; [0480] c is an integer from 1-3; [0481] a, d and f are each independently an integer from 0-3; [0482] X ¹¹ is a bond, O, NR ³¹ or CO; [0483] X ¹² is a bond, CONR ³² , SO2NR ³² , CO or SO2; [0484] R ²¹ is aryl, heteroaryl or heterocycloalkyl; [0485] R ²² is aryl or heteroaryl; [0486] R ²³ and R ²⁴ are each independently H, alkyl or aralkyl, or together with the carbon atom to which they are attached form cycloalkyl; [0487] R ²⁵ and R ²⁶ are each independently H, OH, alkoxy, alkyl or aralkyl, or R ²⁵ and R ²⁶ together form oxo; [0488] R ²⁹ and R ³⁰ are each independently H, alkyl or aralkyl, or together with the carbon atom to which they are attached form cycloalkyl; and [0489] R ²⁷ , R ²⁸ , R ³¹ and R ³² are each independently H, alkyl or aralkyl; and [0490] R ³⁴ is H, alkyl, haloalkyl, hydroxyalkyl or halo. [0491] In another embodiment, the compounds provided herein for use in the compositions and methods provided herein have Formula IIi, or a pharmaceutically acceptable derivative thereof, wherein: [0492] b is 2 or 3; [0493] c is 2; [0495] d and f are each 0; [0496] X ¹¹ is a bond or O; [0497] X ¹² is a bond; [0498] R ²¹ is aryl or heterocycloalkyl, each optionally substituted with 1-3 substituents each independently selected from alkyl and phenyl; [0499] R ²² is heteroaryl; [0500] R ²³ and R ²⁴ are each independently H, alkyl or aralkyl, or together with the carbon atom to which they are attached form cycloalkyl; [0501] R ²⁵ and R ²⁶ are each independently H, OH, alkoxy, alkyl or aralkyl, or R ²⁵ and R ²⁶ together form oxo; [0502] R ²⁹ and R ³⁰ are each independently H, alkyl or aralkyl, or together with the carbon atom to which they are attached form cycloalkyl; and [0503] R ²⁷ and R ²⁸ are each independently H, alkyl or aralkyl; and [0504] R ³⁴ is H, alkyl, haloalkyl, hydroxyalkyl or halo. [0505] In another embodiment, the compounds provided herein for use in the compositions and methods provided herein have Formula IIi, or a pharmaceutically acceptable derivative thereof, wherein: [0506] b is 2 or 3; [0507] c is 2; [0508] a is 0 or 1; [0509] d and f are each 0; [0510] X ¹¹ is a bond or O; [0511] X ¹² is a bond; [0512] R ²¹ is aryl or heterocycloalkyl, each optionally substituted with 1-3 substituents each independently selected from alkyl and phenyl; [0513] R ²² is heteroaryl; and [0514] R ²⁴ to R ³⁰ are each independently H; and [0515] R ²³ and R ³⁴ are each independently alkyl. [0516] In another embodiment, the compound for use in the compositions and methods provided herein has Formula IIj: [0518] b is an integer from 1-4; [0519] c is an integer from 1-3; [0520] a is an integer from 0-3; [0521] X ¹¹ is a bond, O, NR ³¹ or CO; [0522] R ²¹ is aryl or heterocycloalkyl; [0523] R ²² is heteroaryl; [0524] R ²³ and R ²⁴ are each independently H, alkyl or aralkyl, or together with the carbon atom to which they are attached form cycloalkyl; [0525] R ²⁵ and R ²⁶ are each independently H, OH, alkoxy, alkyl or aralkyl, or R ²⁵ and R ²⁶ together form oxo; [0526] and [0527] R ³⁴ is H, alkyl, haloalkyl, hydroxyalkyl or halo. [0528] In another embodiment, the compound for use in the compositions and methods provided herein has Formula IIk: [0530] b is an integer from 1-4; [0531] c is an integer from 1-3; [0532] a is an integer from 0-3; [0533] X ¹¹ is a bond, O, NR ³¹ or CO; [0534] R ²¹ is aryl or heterocycloalkyl; [0535] R ²² is heteroaryl; [0536] R ²³ and R ²⁴ are each independently H, alkyl or aralkyl, or together with the carbon atom to which they are attached form cycloalkyl; together form oxo; and [0538] R ³⁴ is H, alkyl, haloalkyl, hydroxyalkyl or halo. [0539] In another embodiment, he compounds for use in the compositions and methods provided herein have Formula IIi or IIj, wherein: [0540] b is 2 or 3; [0541] c is 2; [0542] a is 0 or 1; [0543] X ¹¹ is a bond or O; [0544] R ²¹ is aryl or heterocycloalkyl, each optionally substituted with 1-3 substituents each independently selected from alkyl and aryl; [0545] R ²² is heteroaryl; [0546] R ²³ and R ²⁴ are each independently H, alkyl or aralkyl, or together with the carbon atom to which they are attached form cycloalkyl; [0547] R ²⁵ and R ²⁶ are each independently H, OH, alkoxy, alkyl or aralkyl, or R ²⁵ and R ²⁶ together form oxo; and [0548] R ³⁴ is H, alkyl, haloalkyl, hydroxyalkyl or halo. [0549] In another embodiment, Ar ¹ is unsubstituted aryl. In another embodiment, Ar ¹ is optionally substituted phenyl. In another embodiment, Ar ¹ is unsubstituted phenyl. [0550] In another embodiment, R ²² is bicyclic or monocyclic heteroaryl. In another embodiment, R ²² is triazolopyrazinyl or imidazopyrazinyl. In another embodiment, R ²² is [1,2,4]-triazolo[4,3-a]pyrazin-8-yl, imidazo[1,5-a]pyrazin-8-yl or imidazo[1,2-a]pyrazin-8- yl. [0551] In another embodiment, R ²⁵ and R ²⁶ are each independently H, alkyl or aralkyl. In another embodiment, R ²⁵ and R ²⁶ are each independently H, OH, OMe or methyl, or R ²⁵ and R ²⁶ together form oxo. In another embodiment, R ²⁵ and R ²⁶ are each independently H, OH, OMe or methyl. [0552] In another embodiment, R ²⁹ and R ³⁰ are each independently H, alkyl or aralkyl. [0553] In another embodiment, R ²⁵ and R ²⁶ are each independently H, alkyl or aralkyl, and and R ³⁰ are each independently H, alkyl or aralkyl. [0554] In another embodiment, the compounds for use in the compositions and methods provided herein has the formula: reof, where R ¹ , R ² , R ⁵ -R ¹⁰ , R ¹⁶ , m and p are as defined herein. [0556] In another embodiment, the compounds provided herein for use in the compositions and methods provided herein are those shown in Table 1 below: Compound Structure 1

III. SYNTHESIS OF THE COMPOUNDS [0557] The compounds provided herein may be prepared according to synthetic methods well known to those of skill in the art. In one embodiment, the compounds may be prepared according to Scheme I (Pg = protecting group, Y = leaving group, hal = halogen):

rding to Scheme II (hal = halogen): [ odiment, the compounds may be ng to Scheme III: [0560] The pharmaceutical compositions provided herein contain therapeutically effective amounts of one or more of compounds provided herein and a pharmaceutically acceptable carrier, diluent or excipient. [0561] The compounds can be formulated into suitable pharmaceutical preparations such as solutions, suspensions, tablets, dispersible tablets, pills, capsules, powders, sustained release formulations or elixirs, for oral administration or in sterile solutions or suspensions for ophthalmic or parenteral administration, as well as transdermal patch preparation and dry powder inhalers. Typically, the compounds described above are formulated into pharmaceutical compositions using techniques and procedures well known in the art (see, e.g., Ansel Introduction to Pharmaceutical Dosage Forms, Seventh Edition 1999). [0562] In the compositions, effective concentrations of one or more compounds or pharmaceutically acceptable salts is (are) mixed with a suitable pharmaceutical carrier or vehicle. In certain embodiments, the concentrations of the compounds in the compositions are effective for delivery of an amount, upon administration, that treats, prevents, or ameliorates one or more of the symptoms and/or progression of a disease or disorder disclosed herein. [0563] Typically, the compositions are formulated for single dosage administration. To formulate a composition, the weight fraction of compound is dissolved, suspended, dispersed or otherwise mixed in a selected vehicle at an effective concentration such that the treated condition is relieved or ameliorated. Pharmaceutical carriers or vehicles suitable for administration of the compounds provided herein include any such carriers known to those skilled in the art to be suitable for the particular mode of administration. [0564] In addition, the compounds may be formulated as the sole pharmaceutically active ingredient in the composition or may be combined with other active ingredients. Liposomal suspensions, including tissue-targeted liposomes, such as tumor-targeted liposomes, may also be suitable as pharmaceutically acceptable carriers. These may be prepared according to methods known to those skilled in the art. For example, liposome formulations may be prepared as known in the art. Briefly, liposomes such as multilamellar vesicles (MLV's) may be formed by drying down egg phosphatidyl choline and brain phosphatidyl serine (7:3 molar ratio) on the inside of a flask. A solution of a compound provided herein in phosphate buffered saline lacking divalent cations (PBS) is added and the flask shaken until the lipid film is dispersed. The resulting vesicles are washed to remove unencapsulated compound, pelleted by centrifugation, and then resuspended in PBS. amount sufficient to exert a therapeutically useful effect in the absence of undesirable side effects on the subject treated. The therapeutically effective concentration may be determined empirically by testing the compounds in in vitro and in vivo systems described herein and then extrapolated therefrom for dosages for humans. In some embodiments, the active compound is administered in a method to achieve a therapeutically effective concentration of the drug. In some embodiments, a companion diagnostic (see, e.g., Olsen D and Jorgensen J T, Front. Oncol., 2014 May 16, 4:105, doi: 10.3389/fonC.2014.00105) is used to determine the therapeutic concentration and safety profile of the active compound in specific subjects or subject populations. [0566] The concentration of active compound in the pharmaceutical composition will depend on absorption, tissue distribution, inactivation and excretion rates of the active compound, the physicochemical characteristics of the compound, the dosage schedule, and amount administered as well as other factors known to those of skill in the art. For example, the amount that is delivered is sufficient to ameliorate one or more of the symptoms of a disease or disorder disclosed herein. [0567] In certain embodiments, a therapeutically effective dosage should produce a serum concentration of active ingredient of from about 0.1 ng/mL to about 50-100 µg/mL. In one embodiment, the pharmaceutical compositions provide a dosage of from about 0.001 mg to about 2000 mg of compound per kilogram of body weight per day. Pharmaceutical dosage unit forms are prepared to provide from about 1 mg to about 1000 mg and in certain embodiments, from about 10 to about 500 mg of the essential active ingredient or a combination of essential ingredients per dosage unit form. [0568] The active ingredient may be administered at once or may be divided into a number of smaller doses to be administered at intervals of time. It is understood that the precise dosage and duration of treatment is a function of the disease being treated and may be determined empirically using known testing protocols or by extrapolation from in vivo or in vitro test data. It is to be noted that concentrations and dosage values may also vary with the severity of the condition to be alleviated. It is to be further understood that for any particular subject, specific dosage regimens should be adjusted over time according to the individual need and the professional judgment of the person administering or supervising the administration of the compositions, and that the concentration ranges set forth herein are exemplary only and are not intended to limit the scope or practice of the claimed compositions. described herein or pharmaceutically acceptable salts thereof are mixed with a suitable pharmaceutical carrier or vehicle for systemic, topical or local administration to form pharmaceutical compositions. Compounds are included in an amount effective for ameliorating one or more symptoms of, or for treating, retarding progression, or preventing. The concentration of active compound in the composition will depend on absorption, tissue distribution, inactivation, excretion rates of the active compound, the dosage schedule, amount administered, particular formulation as well as other factors known to those of skill in the art. [0570] The compositions are intended to be administered by a suitable route, including but not limited to oral, parenteral, subcutaneous, intravenous, intramuscular, intraperitoneal, intrathecal, mucosal, dermal, transdermal, buccal, rectal, topical, local, nasal or inhalation. For oral administration, capsules and tablets can be formulated. The compositions are in liquid, semi-liquid or solid form and are formulated in a manner suitable for each route of administration. [0571] Solutions or suspensions used for parenteral, intradermal, subcutaneous, or topical application can include any of the following components: a sterile diluent, such as water for injection, saline solution, fixed oil, polyethylene glycol, glycerin, propylene glycol, dimethyl acetamide or other synthetic solvent; antimicrobial agents, such as benzyl alcohol and methyl parabens; antioxidants, such as ascorbic acid and sodium bisulfite; chelating agents, such as ethylenediaminetetraacetic acid (EDTA); buffers, such as acetates, citrates and phosphates; and agents for the adjustment of tonicity such as sodium chloride or dextrose. Parenteral preparations can be enclosed in ampules, pens, disposable syringes or single or multiple dose vials made of glass, plastic or other suitable material. [0572] In instances in which the compounds exhibit insufficient solubility, methods for solubilizing compounds may be used. Such methods are known to those of skill in this art, and include, but are not limited to, using cosolvents, such as dimethylsulfoxide (DMSO), using surfactants, such as TWEEN®, or dissolution in aqueous sodium bicarbonate. [0573] Upon mixing or addition of the compound(s), the resulting mixture may be a solution, suspension, emulsion or the like. The form of the resulting mixture depends upon a number of factors, including the intended mode of administration and the solubility of the compound in the selected carrier or vehicle. The effective concentration is sufficient for ameliorating the symptoms of the disease, disorder or condition treated and may be empirically determined. animals in unit dosage forms, such as tablets, capsules, pills, powders, granules, sterile parenteral solutions or suspensions, and oral solutions or suspensions, and oil water emulsions containing suitable quantities of the compounds or pharmaceutically acceptable salts thereof. The pharmaceutically therapeutically active compounds and salts thereof are formulated and administered in unit dosage forms or multiple dosage forms. Unit dose forms as used herein refer to physically discrete units suitable for human and animal subjects and packaged individually as is known in the art. Each unit dose contains a predetermined quantity of the therapeutically active compound sufficient to produce the desired therapeutic effect, in association with the required pharmaceutical carrier, vehicle or diluent. Examples of unit dose forms include ampules and syringes and individually packaged tablets or capsules. Unit dose forms may be administered in fractions or multiples thereof. A multiple dose form is a plurality of identical unit dosage forms packaged in a single container to be administered in segregated unit dose form. Examples of multiple dose forms include vials, bottles of tablets or capsules or bottles of pints or gallons. Hence, multiple dose form is a multiple of unit doses which are not segregated in packaging. [0575] Sustained-release preparations can also be prepared. Suitable examples of sustained- release preparations include semipermeable matrices of solid hydrophobic polymers containing the compound provided herein, which matrices are in the form of shaped articles, e.g., films, or microcapsule. Examples of sustained-release matrices include iontophoresis patches, polyesters, hydrogels (for example, poly(2-hydroxyethyl-methacrylate), or poly(vinylalcohol)), polylactides, copolymers of L-glutamic acid and ethyl-L-glutamate, non- degradable ethylene-vinyl acetate, degradable lactic acid-glycolic acid copolymers such as the LUPRON DEPOT™ (injectable microspheres composed of lactic acid-glycolic acid copolymer and leuprolide acetate), and poly-D-(-)-3-hydroxybutyric acid. While polymers such as ethylene-vinyl acetate and lactic acid-glycolic acid enable release of molecules for over 100 days, certain hydrogels release proteins for shorter time periods. When encapsulated compounds remain in the body for a long time, they may denature or aggregate as a result of exposure to moisture at 37° C., resulting in a loss of biological activity and possible changes in their structure. Rational strategies can be devised for stabilization depending on the mechanism of action involved. For example, if the aggregation mechanism is discovered to be intermolecular S--S bond formation through thio-disulfide interchange, stabilization may be achieved by modifying sulfhydryl residues, lyophilizing from acidic solutions, controlling compositions. [0576] Dosage forms or compositions containing active ingredient in the range of 0.005% to 100% with the balance made up from non-toxic carrier may be prepared. For oral administration, a pharmaceutically acceptable non-toxic composition is formed by the incorporation of any of the normally employed excipients, such as, for example pharmaceutical grades of mannitol, lactose, starch, magnesium stearate, talcum, cellulose derivatives, sodium croscarmellose, glucose, sucrose, magnesium carbonate or sodium saccharin. Such compositions include solutions, suspensions, tablets, capsules, powders and sustained release formulations, such as, but not limited to, implants and microencapsulated delivery systems, and biodegradable, biocompatible polymers, such as collagen, ethylene vinyl acetate, polyanhydrides, polyglycolic acid, polyorthoesters, polylactic acid and others. Methods for preparation of these compositions are known to those skilled in the art. The contemplated compositions may contain about 0.001% 100% active ingredient, in certain embodiments, about 0.185% or about 75-95%. [0577] The active compounds or pharmaceutically acceptable salts may be prepared with carriers that protect the compound against rapid elimination from the body, such as time release formulations or coatings. [0578] The compositions may include other active compounds to obtain desired combinations of properties. The compounds provided herein, or pharmaceutically acceptable salts thereof as described herein, may also be advantageously administered for therapeutic or prophylactic purposes together with another pharmacological agent known in the general art to be of value in treating one or more of the diseases or medical conditions referred to hereinabove, such as diseases related to oxidative stress. It is to be understood that such combination therapy constitutes a further aspect of the compositions and methods of treatment provided herein. [0579] Lactose-free compositions provided herein can contain excipients that are well known in the art and are listed, for example, in the U.S. Pharmacopeia (USP) SP (XXI)/NF (XVI). In general, lactose-free compositions contain an active ingredient, a binder/filler, and a lubricant in pharmaceutically compatible and pharmaceutically acceptable amounts. Exemplary lactose-free dosage forms contain an active ingredient, microcrystalline cellulose, pre-gelatinized starch and magnesium stearate. [0580] Further encompassed are anhydrous pharmaceutical compositions and dosage forms containing a compound provided herein. For example, the addition of water (e.g., 5%) is order to determine characteristics such as shelf life or the stability of formulations over time. See, e.g., Jens T. Carstensen, Drug Stability: Principles & Practice, 2d. Ed., Marcel Dekker, NY, N.Y., 1995, pp.379-80. In effect, water and heat accelerate the decomposition of some compounds. Thus, the effect of water on a formulation can be of great significance since moisture and/or humidity are commonly encountered during manufacture, handling, packaging, storage, shipment and use of formulations. [0581] Anhydrous pharmaceutical compositions and dosage forms provided herein can be prepared using anhydrous or low moisture containing ingredients and low moisture or low humidity conditions. Pharmaceutical compositions and dosage forms that comprise lactose and at least one active ingredient that comprises a primary or secondary amine are anhydrous if substantial contact with moisture and/or humidity during manufacturing, packaging, and/or storage is expected. [0582] An anhydrous pharmaceutical composition should be prepared and stored such that its anhydrous nature is maintained. Accordingly, anhydrous compositions are packaged using materials known to prevent exposure to water such that they can be included in suitable formulary kits. Examples of suitable packaging include, but are not limited to, hermetically sealed foils, plastics, unit dose containers (e.g., vials), blister packs and strip packs. A. ORAL DOSAGE FORMS [0583] Oral pharmaceutical dosage forms are either solid, gel or liquid. The solid dosage forms are tablets, capsules, granules, and bulk powders. Types of oral tablets include compressed, chewable lozenges and tablets which may be enteric coated, sugar coated or film coated. Capsules may be hard or soft gelatin capsules, while granules and powders may be provided in non-effervescent or effervescent form with the combination of other ingredients known to those skilled in the art. [0584] In certain embodiments, the formulations are solid dosage forms, such as capsules or tablets. The tablets, pills, capsules, troches and the like can contain any of the following ingredients, or compounds of a similar nature: a binder; a diluent; a disintegrating agent; a lubricant; a glidant; a sweetening agent; and a flavoring agent. [0585] Examples of binders include microcrystalline cellulose, gum tragacanth, glucose solution, acacia mucilage, gelatin solution, sucrose and starch paste. Lubricants include talc, starch, magnesium or calcium stearate, lycopodium and stearic acid. Diluents include, for example, lactose, sucrose, starch, kaolin, salt, mannitol and dicalcium phosphate. Glidants include, but are not limited to, colloidal silicon dioxide. Disintegrating agents include potato starch, bentonite, methylcellulose, agar and carboxymethylcellulose. Coloring agents include, for example, any of the approved certified water-soluble FD and C dyes, mixtures thereof; and water insoluble FD and C dyes suspended on alumina hydrate. Sweetening agents include sucrose, lactose, mannitol and artificial sweetening agents such as saccharin, and any number of spray dried flavors. Flavoring agents include natural flavors extracted from plants such as fruits and synthetic blends of compounds which produce a pleasant sensation, such as, but not limited to peppermint and methyl salicylate. Wetting agents include propylene glycol monostearate, sorbitan monooleate, diethylene glycol monolaurate and polyoxyethylene lauryl ether. Emetic coatings include fatty acids, fats, waxes, shellac, ammoniated shellac and cellulose acetate phthalates. Film coatings include hydroxyethylcellulose, sodium carboxymethylcellulose, polyethylene glycol 4000 and cellulose acetate phthalate. [0586] If oral administration is desired, the compound could be provided in a composition that protects it from the acidic environment of the stomach. For example, the composition can be formulated in an enteric coating that maintains its integrity in the stomach and releases the active compound in the intestine. The composition may also be formulated in combination with an antacid or other such ingredient. [0587] When the dosage unit form is a capsule, it can contain, in addition to material of the above type, a liquid carrier such as a fatty oil. In addition, dosage unit forms can contain various other materials which modify the physical form of the dosage unit, for example, coatings of sugar and other enteric agents. The compounds can also be administered as a component of an elixir, suspension, syrup, wafer, sprinkle, chewing gum or the like. A syrup may contain, in addition to the active compounds, sucrose as a sweetening agent and certain preservatives, dyes and colorings and flavors. [0588] The active materials can also be mixed with other active materials which do not impair the desired action, or with materials that supplement the desired action, such as antacids, H2 blockers, and diuretics. The active ingredient is a compound or pharmaceutically acceptable salt thereof as described herein. Higher concentrations, up to about 98% by weight of the active ingredient may be included. [0589] Pharmaceutically acceptable carriers included in tablets are binders, lubricants, diluents, disintegrating agents, coloring agents, flavoring agents, and wetting agents. Enteric coated tablets, because of the enteric coating, resist the action of stomach acid and dissolve or disintegrate in the neutral or alkaline intestines. Sugar coated tablets are compressed tablets to tablets are compressed tablets which have been coated with a polymer or other suitable coating. Multiple compressed tablets are compressed tablets made by more than one compression cycle utilizing the pharmaceutically acceptable substances previously mentioned. Coloring agents may also be used in the above dosage forms. Flavoring and sweetening agents are used in compressed tablets, sugar coated, multiple compressed and chewable tablets. Flavoring and sweetening agents are especially useful in the formation of chewable tablets and lozenges. [0590] Liquid oral dosage forms include aqueous solutions, emulsions, suspensions, solutions and/or suspensions reconstituted from non-effervescent granules and effervescent preparations reconstituted from effervescent granules. Aqueous solutions include, for example, elixirs and syrups. Emulsions are either oil in-water or water in oil. In some embodiments, the suspension is a suspension of microparticles or nanoparticles. In some embodiments, the emulsion is an emulsion of microparticles or nanoparticles. [0591] Elixirs are clear, sweetened, hydroalcoholic preparations. Pharmaceutically acceptable carriers used in elixirs include solvents. Syrups are concentrated aqueous solutions of a sugar, for example, sucrose, and may contain a preservative. An emulsion is a two-phase system in which one liquid is dispersed in the form of small globules throughout another liquid. Pharmaceutically acceptable carriers used in emulsions are non-aqueous liquids, emulsifying agents and preservatives. Suspensions use pharmaceutically acceptable suspending agents and preservatives. Pharmaceutically acceptable substances used in non- effervescent granules, to be reconstituted into a liquid oral dosage form, include diluents, sweeteners and wetting agents. Pharmaceutically acceptable substances used in effervescent granules, to be reconstituted into a liquid oral dosage form, include organic acids and a source of carbon dioxide. Coloring and flavoring agents are used in all of the above dosage forms. [0592] Solvents include glycerin, sorbitol, ethyl alcohol and syrup. Examples of preservatives include glycerin, methyl and propylparaben, benzoic add, sodium benzoate and alcohol. Examples of non-aqueous liquids utilized in emulsions include mineral oil and cottonseed oil. Examples of emulsifying agents include gelatin, acacia, tragacanth, bentonite, and surfactants such as polyoxyethylene sorbitan monooleate. Suspending agents include sodium carboxymethylcellulose, pectin, tragacanth, Veegum and acacia. Diluents include lactose and sucrose. Sweetening agents include sucrose, syrups, glycerin and artificial sweetening agents such as saccharin. Wetting agents include propylene glycol monostearate, Organic adds include citric and tartaric acid. Sources of carbon dioxide include sodium bicarbonate and sodium carbonate. Coloring agents include any of the approved certified water-soluble FD and C dyes, and mixtures thereof. Flavoring agents include natural flavors extracted from plants such fruits, and synthetic blends of compounds which produce a pleasant taste sensation. [0593] For a solid dosage form, the solution or suspension, in for example propylene carbonate, vegetable oils or triglycerides, is encapsulated in a gelatin capsule. Such solutions, and the preparation and encapsulation thereof, are disclosed in U.S. Pat. Nos.4,328,245; 4,409,239; and 4,410,545. For a liquid dosage form, the solution, e.g., for example, in a polyethylene glycol, may be diluted with a sufficient quantity of a pharmaceutically acceptable liquid carrier, e.g., water, to be easily measured for administration. [0594] Alternatively, liquid or semi solid oral formulations may be prepared by dissolving or dispersing the active compound or salt in vegetable oils, glycols, triglycerides, propylene glycol esters (e.g., propylene carbonate) and other such carriers, and encapsulating these solutions or suspensions in hard or soft gelatin capsule shells. Other useful formulations include, but are not limited to, those containing a compound provided herein, a dialkylated mono- or poly-alkylene glycol, including, but not limited to, 1,2-dimethoxyethane, diglyme, triglyme, tetraglyme, polyethylene glycol-350-dimethyl ether, polyethylene glycol-550- dimethyl ether, polyethylene glycol-750-dimethyl ether wherein 350, 550 and 750 refer to the approximate average molecular weight of the polyethylene glycol, and one or more antioxidants, such as butylated hydroxytoluene (BHT), butylated hydroxyanisole (BHA), propyl gallate, vitamin E, hydroquinone, hydroxycoumarins, ethanolamine, lecithin, cephalin, ascorbic acid, malic acid, sorbitol, phosphoric acid, thiodipropionic acid and its esters, and dithiocarbamates. [0595] Other formulations include, but are not limited to, aqueous alcoholic solutions including a pharmaceutically acceptable acetal. Alcohols used in these formulations are any pharmaceutically acceptable water-miscible solvents having one or more hydroxyl groups, including, but not limited to, propylene glycol and ethanol. Acetals include, but are not limited to, di(lower alkyl) acetals of lower alkyl aldehydes such as acetaldehyde diethyl acetal. [0596] In all embodiments, tablets and capsules formulations may be coated as known by those of skill in the art in order to modify or sustain dissolution of the active ingredient. Thus, phenylsalicylate, waxes and cellulose acetate phthalate. B. INJECTABLES, SOLUTIONS AND EMULSIONS [0597] Parenteral administration, generally characterized by injection, either subcutaneously, intramuscularly or intravenously is also contemplated herein. Injectables can be prepared in conventional forms, either as liquid solutions or suspensions, solid forms suitable for solution or suspension in liquid prior to injection, or as emulsions. In some embodiments, the suspension is a suspension of microparticles or nanoparticles. In some embodiments, the emulsion is an emulsion of microparticles or nanoparticles. Suitable excipients are, for example, water, saline, dextrose, glycerol or ethanol. In addition, if desired, the pharmaceutical compositions to be administered may also contain minor amounts of non-toxic auxiliary substances such as wetting or emulsifying agents, pH buffering agents, stabilizers, solubility enhancers, and other such agents, such as for example, sodium acetate, sorbitan monolaurate, triethanolamine oleate and cyclodextrins. Implantation of a slow release or sustained release system, such that a constant level of dosage is maintained is also contemplated herein. Briefly, a compound provided herein is dispersed in a solid inner matrix, e.g., polymethylmethacrylate, polybutylmethacrylate, plasticized or unplasticized polyvinylchloride, plasticized nylon, plasticized polyethyleneterephthalate, natural rubber, polyisoprene, polyisobutylene, polybutadiene, polyethylene, ethylene-vinylacetate copolymers, silicone rubbers, polydimethylsiloxanes, silicone carbonate copolymers, hydrophilic polymers such as hydrogels of esters of acrylic and methacrylic acid, collagen, cross-linked polyvinylalcohol and cross-linked partially hydrolyzed polyvinyl acetate, that is surrounded by an outer polymeric membrane, e.g., polyethylene, polypropylene, ethylene/propylene copolymers, ethylene/ethyl acrylate copolymers, ethylene/vinylacetate copolymers, silicone rubbers, polydimethyl siloxanes, neoprene rubber, chlorinated polyethylene, polyvinylchloride, vinylchloride copolymers with vinyl acetate, vinylidene chloride, ethylene and propylene, ionomer polyethylene terephthalate, butyl rubber epichlorohydrin rubbers, ethylene/vinyl alcohol copolymer, ethylene/vinyl acetate/vinyl alcohol terpolymer, and ethylene/vinyloxyethanol copolymer, that is insoluble in body fluids. The compound diffuses through the outer polymeric membrane in a release rate controlling step. The percentage of active compound contained in such parenteral compositions is highly dependent on the specific nature thereof, as well as the activity of the compound and the needs of the subject. and intramuscular administrations. Preparations for parenteral administration include sterile solutions ready for injection, sterile dry soluble products, such as lyophilized powders, ready to be combined with a solvent just prior to use, including hypodermic tablets, sterile suspensions ready for injection, sterile dry insoluble products ready to be combined with a vehicle just prior to use and sterile emulsions. The solutions may be either aqueous or nonaqueous. [0599] If administered intravenously, suitable carriers include physiological saline or phosphate buffered saline (PBS), and solutions containing thickening and solubilizing agents, such as glucose, polyethylene glycol, and polypropylene glycol and mixtures thereof. [0600] Pharmaceutically acceptable carriers used in parenteral preparations include aqueous vehicles, nonaqueous vehicles, antimicrobial agents, isotonic agents, buffers, antioxidants, local anesthetics, suspending and dispersing agents, emulsifying agents, sequestering or chelating agents and other pharmaceutically acceptable substances. [0601] Examples of aqueous vehicles include Sodium Chloride Injection, Ringers Injection, Isotonic Dextrose Injection, Sterile Water Injection, Dextrose and Lactated Ringers Injection. Nonaqueous parenteral vehicles include fixed oils of vegetable origin, cottonseed oil, corn oil, sesame oil and peanut oil. Antimicrobial agents in bacteriostatic or fungistatic concentrations must be added to parenteral preparations packaged in multiple dose containers which include phenols or cresols, mercurials, benzyl alcohol, chlorobutanol, methyl and propyl p hydroxybenzoic acid esters, thimerosal, benzalkonium chloride and benzethonium chloride. Isotonic agents include sodium chloride and dextrose. Buffers include phosphate and citrate. Antioxidants include sodium bisulfate. Local anesthetics include procaine hydrochloride. Suspending and dispersing agents include sodium carboxymethylcelluose, hydroxypropyl methylcellulose and polyvinylpyrrolidone. Emulsifying agents include Polysorbate 80 (TWEEN® 80). A sequestering or chelating agent of metal ions include EDTA. Pharmaceutical carriers also include ethyl alcohol, polyethylene glycol and propylene glycol for water miscible vehicles and sodium hydroxide, hydrochloric acid, citric acid or lactic acid for pH adjustment. [0602] The concentration of the pharmaceutically active compound is adjusted so that an injection provides an effective amount to produce the desired pharmacological effect. The exact dose depends on the age, weight and condition of the subject or animal as is known in the art. with a needle. All preparations for parenteral administration must be sterile, as is known and practiced in the art. [0604] Illustratively, intravenous or intraarterial infusion of a sterile aqueous solution containing an active compound is an effective mode of administration. Another embodiment is a sterile aqueous or oily solution or suspension containing an active material injected as necessary to produce the desired pharmacological effect. [0605] Injectables are designed for local and systemic administration. Typically, a therapeutically effective dosage is formulated to contain a concentration of at least about 0.1% w/w up to about 90% w/w or more, such as more than 1% w/w of the active compound to the treated tissue(s). The active ingredient may be administered at once, or may be divided into a number of smaller doses to be administered at intervals of time. It is understood that the precise dosage and duration of treatment is a function of the tissue being treated and may be determined empirically using known testing protocols or by extrapolation from in vivo or in vitro test data. It is to be noted that concentrations and dosage values may also vary with the age of the individual treated. It is to be further understood that for any particular subject, specific dosage regimens should be adjusted over time according to the individual need and the professional judgment of the person administering or supervising the administration of the formulations, and that the concentration ranges set forth herein are exemplary only and are not intended to limit the scope or practice of the claimed formulations. [0606] The compound may be suspended in micronized or other suitable form or may be derivatized to produce a more soluble active product or to produce a prodrug. The form of the resulting mixture depends upon a number of factors, including the intended mode of administration and the solubility of the compound in the selected carrier or vehicle. The effective concentration is sufficient for ameliorating the symptoms of the condition and may be empirically determined. C. LYOPHILIZED POWDERS [0607] Of interest herein are also lyophilized powders, which can be reconstituted for administration as solutions, emulsions and other mixtures. They may also be reconstituted and formulated as solids or gels. [0608] The sterile, lyophilized powder is prepared by dissolving a compound provided herein, or a pharmaceutically acceptable salt thereof, in a suitable solvent. The solvent may contain an excipient which improves the stability or other pharmacological component of the powder or reconstituted solution, prepared from the powder. Excipients that may be used glucose, sucrose or other suitable agent. The solvent may also contain a buffer, such as citrate, sodium or potassium phosphate or other such buffer known to those of skill in the art at, in one embodiment, about neutral pH. Subsequent sterile filtration of the solution followed by lyophilization under standard conditions known to those of skill in the art provides the desired formulation. Generally, the resulting solution will be apportioned into vials for lyophilization. Each vial will contain a single dosage (including but not limited to 10-1000 mg or 100-500 mg) or multiple dosages of the compound. The lyophilized powder can be stored under appropriate conditions, such as at about 4 °C to room temperature. [0609] Reconstitution of this lyophilized powder with water for injection provides a formulation for use in parenteral administration. For reconstitution, about 1-50 mg, about 5- 35 mg, or about 9-30 mg of lyophilized powder, is added per mL of sterile water or other suitable carrier. The precise amount depends upon the selected compound. Such amount can be empirically determined. D. TOPICAL ADMINISTRATION [0610] Topical mixtures are prepared as described for the local and systemic administration. The resulting mixture may be a solution, suspension, emulsion or the like and are formulated as creams, gels, ointments, emulsions, solutions, elixirs, lotions, suspensions, tinctures, pastes, foams, aerosols, irrigations, sprays, suppositories, bandages, dermal patches or any other formulations suitable for topical administration. [0611] The compounds or pharmaceutically acceptable salts thereof may be formulated as aerosols for topical application, such as by inhalation (see, e.g., U.S. Pat. Nos.4,044,126, 4,414,209, and 4,364,923, which describe aerosols for delivery of a steroid useful for treatment of inflammatory diseases, particularly asthma). These formulations for administration to the respiratory tract can be in the form of an aerosol or solution for a nebulizer, or as a microfine powder for insufflation, alone or in combination with an inert carrier such as lactose. In such a case, the particles of the formulation will have diameters of less than 50 microns or less than 10 microns. [0612] The compounds may be formulated for local or topical application, such as for topical application to the skin and mucous membranes, such as in the eye, in the form of gels, creams, and lotions and for application to the eye or for intracisternal or intraspinal application. Topical administration is contemplated for transdermal delivery and also for administration to the eyes or mucosa, or for inhalation therapies. Nasal solutions of the active also be administered. [0613] These solutions, particularly those intended for ophthalmic use, may be formulated as 0.01%-10% isotonic solutions, pH about 5-7, with appropriate salts. E. COMPOSITIONS FOR OTHER ROUTES OF ADMINISTRATION [0614] Other routes of administration, such as topical application, transdermal patches, and rectal administration are also contemplated herein. [0615] For example, pharmaceutical dosage forms for rectal administration are rectal suppositories, capsules and tablets for systemic effect. Rectal suppositories are used herein mean solid bodies for insertion into the rectum which melt or soften at body temperature releasing one or more pharmacologically or therapeutically active ingredients. Pharmaceutically acceptable substances utilized in rectal suppositories are bases or vehicles and agents to raise the melting point. Examples of bases include cocoa butter (theobroma oil), glycerin gelatin, carbowax (polyoxyethylene glycol) and appropriate mixtures of mono, di and triglycerides of fatty acids. Combinations of the various bases may be used. Agents to raise the melting point of suppositories include spermaceti and wax. Rectal suppositories may be prepared either by the compressed method or by molding. An exemplary weight of a rectal suppository is about 2 to 3 grams. [0616] Tablets and capsules for rectal administration are manufactured using the same pharmaceutically acceptable substance and by the same methods as for formulations for oral administration. F. SUSTAINED RELEASE COMPOSITIONS [0617] Active ingredients provided herein can be administered by controlled release means or by delivery devices that are well known to those of ordinary skill in the art. Examples include, but are not limited to, those described in U.S. Pat. Nos.3,845,770; 3,916,899; 3,536,809; 3,598,123; and U.S. Pat. Nos.4,008,719, 5,674,533, 5,059,595, 5,591,767, 5,120,548, 5,073,543, 5,639,476, 5,354,556, 5,639,480, 5,733,566, 5,739,108, 5,891,474, 5,922,356, 5,972,891, 5,980,945, 5,993,855, 6,045,830, 6,087,324, 6,113,943, 6,197,350, 6,248,363, 6,264,970, 6,267,981, 6,376,461, 6,419,961, 6,589,548, 6,613,358, 6,699,500 and 6,740,634, each of which is incorporated herein by reference. Such dosage forms can be used to provide slow or controlled-release of one or more active ingredients using, for example, hydroxypropylmethyl cellulose, other polymer matrices, gels, permeable membranes, osmotic systems, multilayer coatings, microparticles, liposomes, microspheres, or a combination thereof to provide the desired release profile in varying proportions. Suitable controlled- herein, can be readily selected for use with the active ingredients provided herein. [0618] All controlled-release pharmaceutical products have a common goal of improving drug therapy over that achieved by their non-controlled counterparts. In one embodiment, the use of an optimally designed controlled-release preparation in medical treatment is characterized by a minimum of drug substance being employed to cure or control the condition in a minimum amount of time. In certain embodiments, advantages of controlled- release formulations include extended activity of the drug, reduced dosage frequency, and increased subject compliance. In addition, controlled-release formulations can be used to affect the time of onset of action or other characteristics, such as blood levels of the drug, and can thus affect the occurrence of side (e.g., adverse) effects. [0619] Most controlled-release formulations are designed to initially release an amount of drug (active ingredient) that promptly produces the desired therapeutic effect, and gradually and continually release of other amounts of drug to maintain this level of therapeutic or prophylactic effect over an extended period of time. In order to maintain this constant level of drug in the body, the drug must be released from the dosage form at a rate that will replace the amount of drug being metabolized and excreted from the body. Controlled release of an active ingredient can be stimulated by various conditions including, but not limited to, pH, temperature, enzymes, water, or other physiological conditions or compounds. [0620] In certain embodiments, the agent may be administered using intravenous infusion, an implantable osmotic pump, a transdermal patch, liposomes, or other modes of administration. In one embodiment, a pump may be used (see, Sefton, CRC Crit. Ref. Biomed. Eng. 14:201 (1987); Buchwald et al., Surgery 88:507 (1980); Saudek et al., N. Engl. J. Med.321:574 (1989). In another embodiment, polymeric materials can be used. In yet another embodiment, a controlled release system can be placed in proximity of the therapeutic target, i.e., thus requiring only a fraction of the systemic dose (see, e.g., Goodson, Medical Applications of Controlled Release, vol.2, pp.115-138 (1984). [0621] In some embodiments, a controlled release device is introduced into a subject in proximity of the site of inappropriate immune activation or a tumor. Other controlled release systems are discussed in the review by Langer (Science 249:1527-1533 (1990). The active ingredient can be dispersed in a solid inner matrix, e.g., polymethylmethacrylate, polybutylmethacrylate, plasticized or unplasticized polyvinylchloride, plasticized nylon, plasticized polyethyleneterephthalate, natural rubber, polyisoprene, polyisobutylene, polybutadiene, polyethylene, ethylene-vinylacetate copolymers, silicone rubbers, hydrogels of esters of acrylic and methacrylic acid, collagen, cross linked polyvinylalcohol and cross-linked partially hydrolyzed polyvinyl acetate, that is surrounded by an outer polymeric membrane, e.g., polyethylene, polypropylene, ethylene/propylene copolymers, ethylene/ethyl acrylate copolymers, ethylene/vinylacetate copolymers, silicone rubbers, polydimethyl siloxanes, neoprene rubber, chlorinated polyethylene, polyvinylchloride, vinylchloride copolymers with vinyl acetate, vinylidene chloride, ethylene and propylene, ionomer polyethylene terephthalate, butyl rubber epichlorohydrin rubbers, ethylene/vinyl alcohol copolymer, ethylene/vinyl acetate/vinyl alcohol terpolymer, and ethylene/vinyloxyethanol copolymer, that is insoluble in body fluids. The active ingredient then diffuses through the outer polymeric membrane in a release rate controlling step. The percentage of active ingredient contained in such parenteral compositions is highly dependent on the specific nature thereof, as well as the needs of the subject. G. TARGETED FORMULATIONS [0622] The compounds provided herein, or pharmaceutically acceptable salts thereof, may also be formulated to be targeted to a particular tissue, receptor, or other area of the body of the subject to be treated, including liposome-, resealed erythrocyte-, and antibody-based delivery systems. Many such targeting methods are well known to those of skill in the art. All such targeting methods are contemplated herein for use in the instant compositions. For non- limiting examples of targeting methods, see, e.g., U.S. Pat. Nos.6,316,652, 6,274,552, 6,271,359, 6,253,872, 6,139,865, 6,131,570, 6,120,751, 6,071,495, 6,060,082, 6,048,736, 6,039,975, 6,004,534, 5,985,307, 5,972,366, 5,900,252, 5,840,674, 5,759,542 and 5,709,874. [0623] In one embodiment, the antibody-based delivery system is an antibody-drug conjugate ("ADC"), e.g., as described in Hamilton G S, Biologicals, 2015 September, 43(5):318-32; Kim E G and Kim K M, Biomol. Ther. (Seoul), 2015 November, 23(6):493- 509; and Peters C and Brown S, Biosci. Rep., 2015 Jun.12, 35(4) pii: e00225, each of which is incorporated herein by reference. [0624] In one embodiment, liposomal suspensions, including tissue-targeted liposomes, such as tumor-targeted liposomes, may also be suitable as pharmaceutically acceptable carriers. These may be prepared according to methods known to those skilled in the art. For example, liposome formulations may be prepared as described in U.S. Pat. No.4,522,811. Briefly, liposomes such as multilamellar vesicles (MLV's) may be formed by drying down egg phosphatidyl choline and brain phosphatidyl serine (7:3 molar ratio) on the inside of a flask. A solution of a compound provided herein in phosphate buffered saline lacking resulting vesicles are washed to remove unencapsulated compound, pelleted by centrifugation, and then resuspended in PBS. H. ARTICLES OF MANUFACTURE [0625] The compounds or pharmaceutically acceptable salts can be packaged as articles of manufacture containing packaging material, a compound or pharmaceutically acceptable salt thereof provided herein, which is used for treatment, prevention or amelioration of one or more symptoms or progression of a disease or disorder disclosed herein, and a label that indicates that the compound or pharmaceutically acceptable salt thereof is used for treatment, prevention or amelioration of one or more symptoms or progression of a disease or disorder disclosed herein. [0626] The articles of manufacture provided herein contain packaging materials. Packaging materials for use in packaging pharmaceutical products are well known to those of skill in the art. See, e.g., U.S. Pat. Nos.5,323,907, 5,052,558 and 5,033,252. Examples of pharmaceutical packaging materials include, but are not limited to, blister packs, bottles, tubes, inhalers, pumps, bags, vials, containers, syringes, pens, bottles, and any packaging material suitable for a selected formulation and intended mode of administration and treatment. A wide array of formulations of the compounds and compositions provided herein are contemplated. [0627] In certain embodiments, provided herein also are kits which, when used by the medical practitioner, can simplify the administration of appropriate amounts of active ingredients to a subject. In certain embodiments, the kit provided herein includes a container and a dosage form of a compound provided herein, including a single enantiomer or a mixture of diastereomers thereof; or a pharmaceutically acceptable salt, solvate, or prodrug thereof. [0628] In certain embodiments, the kit includes a container comprising a dosage form of the compound provided herein, including a single enantiomer or a mixture of diastereomers thereof; or a pharmaceutically acceptable salt, solvate, or prodrug thereof, in a container comprising one or more other therapeutic agent(s) described herein. [0629] Kits provided herein can further include devices that are used to administer the active ingredients. Examples of such devices include, but are not limited to, syringes, needle- less injectors drip bags, patches, and inhalers. The kits provided herein can also include condoms for administration of the active ingredients. can be used to administer one or more active ingredients. For example, if an active ingredient is provided in a solid form that must be reconstituted for parenteral administration, the kit can comprise a sealed container of a suitable vehicle in which the active ingredient can be dissolved to form a particulate-free sterile solution that is suitable for parenteral administration. Examples of pharmaceutically acceptable vehicles include, but are not limited to: aqueous vehicles, including, but not limited to, Water for Injection USP, Sodium Chloride Injection, Ringer's Injection, Dextrose Injection, Dextrose and Sodium Chloride Injection, and Lactated Ringer's Injection; water-miscible vehicles, including, but not limited to, ethyl alcohol, polyethylene glycol, and polypropylene glycol; and non-aqueous vehicles, including, but not limited to, corn oil, cottonseed oil, peanut oil, sesame oil, ethyl oleate, isopropyl myristate, and benzyl benzoate. V. DOSING [0631] The compounds and pharmaceutical compositions provided herein may be dosed in certain therapeutically or prophylactically effective amounts, certain time intervals, certain dosage forms, and certain dosage administration methods as described below. [0632] In certain embodiments, a therapeutically or prophylactically effective amount of the compound is from about 0.005 to about 1,000 mg per day, from about 0.01 to about 500 mg per day, from about 0.01 to about 250 mg per day, from about 0.01 to about 100 mg per day, from about 0.1 to about 100 mg per day, from about 0.5 to about 100 mg per day, from about 1 to about 100 mg per day, from about 0.01 to about 50 mg per day, from about 0.1 to about 50 mg per day, from about 0.5 to about 50 mg per day, from about 1 to about 50 mg per day, from about 0.02 to about 25 mg per day, from about 0.05 to about 10 mg per day, from about 0.05 to about 5 mg per day, from about 0.1 to about 5 mg per day, or from about 0.5 to about 5 mg per day. [0633] In certain embodiments, the therapeutically or prophylactically effective amount is about 0.1, about 0.2, about 0.5, about 1, about 2, about 3, about 4, about 5, about 6, about 7, about 8, about 9, about 10, about 15, about 20, about 25, about 30, about 40, about 45, about 50, about 60, about 70, about 80, about 90, about 100, or about 150 mg per day. [0634] In one embodiment, the recommended daily dose range of the compound provided herein, or a derivative thereof, for the conditions described herein lie within the range of from about 0.5 mg to about 50 mg per day, in one embodiment given as a single once-a-day dose, or in divided doses throughout a day. In some embodiments, the dosage ranges from about 1 mg to about 50 mg per day. In other embodiments, the dosage ranges from about 0.5 to about 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46, 47, 48, 49 or 50 mg per day. [0635] In a specific embodiment, the recommended starting dosage may be 0.5, 1, 2, 3, 4, 5, 10, 15, 20, 25 or 50 mg per day. In another embodiment, the recommended starting dosage may be 0.5, 1, 2, 3, 4, or 5 mg per day. The dose may be escalated to 15, 20, 25, 30, 35, 40, 45 and 50 mg/day. In a specific embodiment, the compound can be administered in an amount of about 25 mg/day. In a particular embodiment, the compound can be administered in an amount of about 10 mg/day. In a particular embodiment, the compound can be administered in an amount of about 5 mg/day. In a particular embodiment, the compound can be administered in an amount of about 4 mg/day. In a particular embodiment, the compound can be administered in an amount of about 3 mg/day. [0636] In certain embodiments, the therapeutically or prophylactically effective amount is from about 0.001 to about 100 mg/kg/day, from about 0.01 to about 50 mg/kg/day, from about 0.01 to about 25 mg/kg/day, from about 0.01 to about 10 mg/kg/day, from about 0.01 to about 9 mg/kg/day, 0.01 to about 8 mg/kg/day, from about 0.01 to about 7 mg/kg/day, from about 0.01 to about 6 mg/kg/day, from about 0.01 to about 5 mg/kg/day, from about 0.01 to about 4 mg/kg/day, from about 0.01 to about 3 mg/kg/day, from about 0.01 to about 2 mg/kg/day, from about 0.01 to about 1 mg/kg/day, or from about 0.01 to about 0.05 mg/kg/day. [0637] The administered dose can also be expressed in units other than mg/kg/day. For example, doses for parenteral administration can be expressed as mg/m ² /day. One of ordinary skill in the art would readily know how to convert doses from mg/kg/day to mg/m ² /day to given either the height or weight of a subject or both (see, www.fda.gov/cder/cancer/animalframe.htm). For example, a dose of 1 mg/kg/day for a 65 kg human is approximately equal to 38 mg/m ² /day. [0638] In certain embodiments, the amount of the compound administered is sufficient to provide a plasma concentration of the compound at steady state, ranging from about 0.001 to about 500 µM, about 0.002 to about 200 µM, about 0.005 to about 100 µM, about 0.01 to about 50 µM, from about 1 to about 50 µM, about 0.02 to about 25 µM, from about 0.05 to about 20 µM, from about 0.1 to about 20 µM, from about 0.5 to about 20 µM, or from about 1 to about 20 µM. [0639] In other embodiments, the amount of the compound administered is sufficient to provide a plasma concentration of the compound at steady state, ranging from about 5 to or from about 50 to about 100 nM. [0640] As used herein, the term "plasma concentration at steady state" is the concentration reached after a period of administration of a compound provided herein, or a derivative thereof. Once steady state is reached, there are minor peaks and troughs on the time dependent curve of the plasma concentration of the compound. [0641] In certain embodiments, the amount of the compound administered is sufficient to provide a maximum plasma concentration (peak concentration) of the compound, ranging from about 0.001 to about 50 µM, about 0.002 to about 200 µM, about 0.005 to about 100 µM, about 0.01 to about 50 µM, from about 1 to about 50 µM, about 0.02 to about 25 µM, from about 0.05 to about 20 µM, from about 0.1 to about 20 µM, from about 0.5 to about 20 µM, or from about 1 to about 20 µM. [0642] In certain embodiments, the amount of the compound administered is sufficient to provide a minimum plasma concentration (trough concentration) of the compound, ranging from about 0.001 to about 500 µM, about 0.002 to about 200 µM, about 0.005 to about 100 µM, about 0.01 to about 50 µM, from about 1 to about 50 µM, about 0.01 to about 25 µM, from about 0.01 to about 20 µM, from about 0.02 to about 20 µM, from about 0.02 to about 20 µM, or from about 0.01 to about 20 µM. [0643] In certain embodiments, the amount of the compound administered is sufficient to provide an area under the curve (AUC) of the compound, ranging from about 100 to about 100,000 ng*hr/mL, from about 1,000 to about 50,000 ng*hr/mL, from about 5,000 to about 25,000 ng*hr/mL, or from about 5,000 to about 10,000 ng*hr/mL. [0644] The methods provided herein encompass treating a patient regardless of subject's age, although some diseases or disorders are more common in certain age groups. [0645] Depending on the disease to be treated and the subject's condition, the compound provided herein, or a derivative thereof, may be administered by oral, parenteral (e.g., intramuscular, intraperitoneal, intravenous, CIV, intracisternal injection or infusion, subcutaneous injection, or implant), inhalation, nasal, vaginal, rectal, sublingual, or topical (e.g., transdermal or local) routes of administration. The compound provided herein, or a derivative thereof, may be formulated, alone or together, in suitable dosage unit with pharmaceutically acceptable excipients, carriers, adjuvants and vehicles, appropriate for each route of administration. [0646] In one embodiment, the compound provided herein, or a derivative thereof, is administered orally. In another embodiment, the compound provided herein, or a derivative herein, or a derivative thereof, is administered intravenously. [0647] The compound provided herein, or a derivative thereof, can be delivered as a single dose such as, e.g., a single bolus injection, or oral tablets or pills; or over time, such as, e.g., continuous infusion over time or divided bolus doses over time. The compound can be administered repeatedly if necessary, for example, until the subject experiences stable disease or regression, or until the subject experiences disease progression or unacceptable toxicity. For example, stable disease for solid tumors generally means that the perpendicular diameter of measurable lesions has not increased by 25% or more from the last measurement. Response Evaluation Criteria in Solid Tumors (RECIST) Guidelines, Journal of the National Cancer Institute 92(3): 205216 (2000). Stable disease or lack thereof is determined by methods known in the art such as evaluation of patient symptoms, physical examination, visualization of the tumor that has been imaged using X-ray, CAT, PET, or MRI scan and other commonly accepted evaluation modalities. [0648] The compound provided herein, or a derivative thereof, can be administered once daily (QD), or divided into multiple daily doses such as twice daily (BID), three times daily (TID), and four times daily (QID). In addition, the administration can be continuous (i.e., daily for consecutive days or every day), intermittent, e.g., in cycles (i.e., including days, weeks, or months of rest without drug). As used herein, the term "daily" is intended to mean that a therapeutic compound, such as the compound provided herein, or a derivative thereof, is administered once or more than once each day, for example, for a period of time. The term "continuous" is intended to mean that a therapeutic compound, such as the compound provided herein or a derivative thereof, is administered daily for an uninterrupted period of at least 10 days to 52 weeks. The term "intermittent" or "intermittently" as used herein is intended to mean stopping and starting at either regular or irregular intervals. For example, intermittent administration of the compound provided herein or a derivative thereof is administration for one to six days per week, administration in cycles (e.g., daily administration for two to eight consecutive weeks, then a rest period with no administration for up to one week), or administration on alternate days. The term "cycling" as used herein is intended to mean that a therapeutic compound, such as the compound provided herein or a derivative thereof, is administered daily or continuously but with a rest period. In some such embodiments, administration is once a day for two to six days, then a rest period with no administration for five to seven days. daily dose to about a monthly dose. In certain embodiments, administration is once a day, twice a day, three times a day, four times a day, once every other day, twice a week, once every week, once every two weeks, once every three weeks, or once every four weeks. In one embodiment, the compound provided herein, or a derivative thereof, is administered once a day. In another embodiment, the compound provided herein, or a derivative thereof, is administered twice a day. In yet another embodiment, the compound provided herein, or a derivative thereof, is administered three times a day. In still another embodiment, the compound provided herein, or a derivative thereof, is administered four times a day. [0650] In certain embodiments, the compound provided herein, or a derivative thereof, is administered once per day from one day to six months, from one week to three months, from one week to four weeks, from one week to three weeks, or from one week to two weeks. In certain embodiments, the compound provided herein, or a derivative thereof, is administered once per day for one week, two weeks, three weeks, or four weeks. In one embodiment, the compound provided herein, or a derivative thereof, is administered once per day for 4 days. In one embodiment, the compound provided herein, or a derivative thereof, is administered once per day for 5 days. In one embodiment, the compound provided herein, or a derivative thereof, is administered once per day for 6 days. In one embodiment, the compound provided herein, or a derivative thereof, is administered once per day for one week. In another embodiment, the compound provided herein, or a derivative thereof, is administered once per day for two weeks. In yet another embodiment, the compound provided herein, or a derivative thereof, is administered once per day for three weeks. In still another embodiment, the compound provided herein, or a derivative thereof, is administered once per day for four weeks. VI. METHODS OF TREATMENT [0651] Free light chains (FLCs) adopt a well-defined homodimeric structure, wherein the monomers may be covalently linked by an interchain disulfide bond. LC monomers comprise an N-terminal variable (V) domain attached to a C-terminal constant (C) domain. Amyloidogenic FLCs involved in AL patients, are less stable than non-amyloidogenic FLCs, can misfold and misassemble into nonnative species including cross-β-sheet amyloid fibrils, a hallmark of AL amyloidosis. The structure-proteotoxicity relationship is not fully understood but several processes have been described, including destabilization-dependent endoproteolysis that releases amyloidogenic LC fragments. LC fragments including V domains are observed in patient deposits alongside full length LCs. Without being bound by chain conformational excursions at the beginning of the aggregation cascade via kinetic stabilization of FLCs. It is also believed that the compounds provided herein bind to conserved regions of LCs, thereby allowing the compounds to stabilize many immunoglobulin light chains and to be effective in many AL subjects. [0652] Kinetic stabilization of LCs is unlikely to contribute to plasma cell death but could reduce organ proteotoxicity and the progression of AL. Subjects with prominent cardiac involvement currently have few available options for treatment and represent an urgent unmet medical need, as they are often too sick to tolerate chemotherapy. Reduction of organ proteotoxicity could allow the subject to tolerate chemotherapy. Thus, in one embodiment, provided herein is a method of pretreatment of a subject having AL with prominent cardiac involvement with a compound provided herein, followed by chemotherapy. [0653] In another embodiment, provided herein is a method of treating light chain amyloidosis by administering to a subject a compound or composition provided herein. In one embodiment, the subject has light chain amyloidosis and is treatment naïve. In another embodiment, the subject has relapsed or refractory light chain amyloidosis. [0654] In another embodiment, provided herein is a method of stabilizing immunoglobulin light chains by contacting the immunoglobulin light chains with a compound provided herein. In one embodiment, the immunoglobulin light chains are stabilized in a native conformation thereof. In certain embodiments, the immunoglobulin light chains are dimers. Thus, in certain embodiments, provided herein is a method of stabilizing immunoglobulin light chain dimers in a native conformation. As used herein, “native conformation” refers to a conformation of immunoglobulin light chains present in subjects not having light chain amyloidosis. [0655] In another embodiment, provided herein is a method of preventing or lessening immunoglobulin light chain misfolding and/or endoproteolysis by contacting the immunoglobulin light chains with a compound provided herein. [0656] In another embodiment, provided is a method of maintenance therapy upon recurrence of light chain amyloidosis following primary treatment by administering to a subject a compound or composition provided herein. In such embodiments, reemergence of the clonal plasma cells is generally slow, and thus organ toxicity caused by conformationally unstable circulating LC can be minimized by kinetic stabilizer treatment. [0657] The compound provided herein, or a derivative thereof, can also be combined or used in combination with other therapies or therapeutic agents useful in the treatment and/or prevention of light chain amyloidosis. [0658] In one embodiment, provided herein is a method of treating, preventing, or managing light chain amyloidosis, comprising administering to a subject a compound provided herein, or a derivative thereof, in combination with one or more second active agents. In one embodiment, the second active agent is a proteasome inhibitor (e.g., bortezomib, ixazomib, carfilzomib). In another embodiment, the second active agent is a chemotherapeutic agent, including but not limited to alkylating agents (e.g., bendamustine, melphalan, cyclophosphamide), steroids (e.g., dexamethasone), immunomodulatory agents (e.g., thalidomide, lenalidomide, pomalidomide), an anti-CD38 antibody (e.g., daratumumab, isatuximab), an anti-CD20 antibody (e.g., rituximab), an anti-IL-6 antibody (e.g., siltuximab), a UPR activator (e.g., an ATF-6 activator), an antibody-drug-conjugate (e.g., belantamab mafodotin, STI-6129 (sorrentotherapeutics.com)) and/or an anti-amyloid antibody. In another embodiment, the compounds provided herein, or a derivative thereof, are used in combination with stem cell transplant therapy. In further embodiments, the second active agent is selected from those disclosed in PCT Publication Nos. WO 2020/205683, WO 2019/191558, WO 2017/117430 or WO 2021/007594. In another embodiment, the second active agent is a therapeutic agent that promotes clearance of amyloid deposits, such as CAEL-101 (caelumbio.com) or NEOD001 (birtamimab). [0659] In one embodiment, the second active agent is a plasma cell directed therapy, including high-dose cyclophosphamide combined with an anti-thymocyte antibody (e.g., Thymoglobulin®, Atgam®)(with subsequent autologous stem cell transplantation), an immunomodulatory agent (e.g., lenalidomide), a steroid (e.g., dexamethasone), a proteasome inhibitor (e.g., bortezomib), atacicept, or an anti-CD38 antibody (e.g., daratumumab, isatuximab). In another embodiment, the second active agent is a combination of daratumumab, bortezomib, cyclophosphamide and dexamethasone. [0660] As used herein, the term "in combination" includes the use of more than one therapy (e.g., one or more prophylactic and/or therapeutic agents). However, the use of the term "in combination" does not restrict the order in which therapies (e.g., prophylactic and/or therapeutic agents) are administered to a subject with a disease or disorder. A first therapy (e.g., a prophylactic or therapeutic agent such as a compound provided herein, a compound provided herein, e.g., the compound provided herein, or a derivative thereof) can be hours, 6 hours, 12 hours, 24 hours, 48 hours, 72 hours, 96 hours, 1 week, 2 weeks, 3 weeks, 4 weeks, 5 weeks, 6 weeks, 8 weeks, or 12 weeks before), concomitantly with, or subsequent to (e.g., 5 minutes, 15 minutes, 30 minutes, 45 minutes, 1 hour, 2 hours, 4 hours, 6 hours, 12 hours, 24 hours, 48 hours, 72 hours, 96 hours, 1 week, 2 weeks, 3 weeks, 4 weeks, 5 weeks, 6 weeks, 8 weeks, or 12 weeks after) the administration of a second therapy (e.g., a prophylactic or therapeutic agent) to the subject. Triple therapy is also contemplated herein. [0661] Administration of the compound provided herein, or a derivative thereof and one or more second active agents to a subject can occur simultaneously or sequentially by the same or different routes of administration. The suitability of a particular route of administration employed for a particular active agent will depend on the active agent itself (e.g., whether it can be administered orally without decomposing prior to entering the blood stream) and the disease or disorder being treated. [0662] The route of administration of the compound provided herein, or a derivative thereof, is independent of the route of administration of a second therapy. In one embodiment, the compound provided herein, or a derivative thereof, is administered orally. In another embodiment, the compound provided herein, or a derivative thereof, is administered intravenously. Thus, in accordance with these embodiments, the compound provided herein, or a derivative thereof, is administered orally or intravenously, and the second therapy can be administered orally, parenterally, intraperitoneally, intravenously, intraarterially, transdermally, sublingually, intramuscularly, rectally, transbuccally, intranasally, liposomally, via inhalation, vaginally, intraoccularly, via local delivery by catheter or stent, subcutaneously, intraadiposally, intraarticularly, intrathecally, or in a slow release dosage form. In one embodiment, the compound provided herein, or a derivative thereof, and a second therapy are administered by the same mode of administration, orally or by IV. In another embodiment, the compound provided herein, or a derivative thereof, is administered by one mode of administration, e.g., by IV, whereas the second agent is administered by another mode of administration, e.g., orally. [0663] In one embodiment, the second active agent is administered intravenously or subcutaneously and once or twice daily in an amount of from about 1 to about 1000 mg, from about 5 to about 500 mg, from about 10 to about 350 mg, or from about 50 to about 200 mg. The specific amount of the second active agent will depend on the specific agent used, the type of disease being treated or managed, the severity and stage of disease, and the amount of agents concurrently administered to the subject. [0664] One or more second active ingredients or agents can be used together with the compound provided herein, or a derivative thereof, in the methods and compositions provided herein. Second active agents can be large molecules (e.g., proteins) or small molecules (e.g., synthetic inorganic, organometallic, or organic molecules). [0665] Examples of large molecule active agents include, but are not limited to, hematopoietic growth factors, cytokines, and monoclonal and polyclonal antibodies, particularly, therapeutic antibodies to cancer antigens. Typical large molecule active agents are biological molecules, such as naturally occurring or synthetic or recombinant proteins. [0666] In one embodiment, the compound provided herein, or a derivative thereof, can be administered in an amount ranging from about 0.1 to about 150 mg, from about 1 to about 25 mg, or from about 2 to about 10 mg orally and daily alone, or in combination with a second active agent, prior to, during, or after the use of conventional therapy. VIII. EXAMPLES [0667] The examples below are meant to illustrate certain embodiments provided herein, and not to limit the scope of this disclosure. A. ANALYTICAL CONDITIONS [0668] ¹ H NMR CONDITIONS [0669] Instrument Type: AVANCE Ⅲ 400 or AVANCE Ⅲ 400 HD or AVANCE NEO; Probe Type: 5 mm PABBO BB or 5 mm CPP BBO; Frequency (MHz): 400.1300; Temperature (Degree °C): 27. [0670] LCMS METHODS [0671] Method 1: [0672] Instrument: SHIMADZU LCMS-2020; Column: Kinetex EVO C182.1×30 mm, 5 µm; Mobile Phase: A: 0.0375% TFA in water (v/v), B: 0.01875% TFA in Acetonitrile (v/v); Gradient: 0.0 min 5% B→0.8 min 95% B→1.2 min 95% B→1.21 min 5% B→1.55 min 5% B; Flow: 1.5 mL/min; Column Temp: 50 °C; Detector: PDA (220 & 254 nm). Ionization source: ESI. [0673] Method 2: [0674] Instrument: SHIMADZU LCMS-2020; Column: Kinetex EVO C182.1X30 mm, 5 µm; Mobile Phase: A: 0.025% NH3•H2O in water (v/v), B: Acetonitrile; Gradient: 0.0 min 5% B→0.8 min 95% B→1.2 min 95% B→1.21 min 5% B→1.55 min 5% B; Flow: 1.5 mL/min; Column Temp: 50 °C; Detector: PDA (220 & 254 nm). Ionization source: ESI. [0676] Method 1: [0677] Instrument: SHIMADZU LC-20AB; Column: Kinetex C18 LC Column 4.6 × 50 mm, 5 µm; Mobile Phase: A: 0.0375% TFA in water (v/v), B: 0.01875% TFA in Acetonitrile (v/v); Gradient: 0.0 min 10% B→2.40 min 80% B→3.70 min 80% B→3.71 min 10% B→4.00 min 10% B; Flow: 1.5 mL/min; Column Temp: 50 °C; Detector: PDA (220 nm & 215 nm & 254 nm). [0678] Method 2: [0679] Instrument: SHIMADZU LC-20AB; Column: XBridge C18, 2.1 × 50 mm, 5 µm; Mobile Phase: A: 0.025% NH ₃ •H ₂ O in water (v/v), B: Acetonitrile; Gradient: 0.0 min 10% B→4.20 min 80% B→5.30 min 80% B→5.31 min 10% B→6.00 min 10% B; Flow: 0.8 mL/min; Column Temp: 40 °C; Detector: PDA (220 nm & 215 nm & 254 nm). [0680] Method 3: [0681] Instrument: SHIMADZU LC-20AB; Column: XBridge C18, 2.1 × 50 mm, 3.5 µm; Mobile Phase: A: 0.025% NH3•H2O in water (v/v), B: Acetonitrile; Gradient: 0.0 min 30% B→3.00 min 90% B→3.50 min 90% B→3.51 min 30% B→4.00 min 30% B; Flow: 1.2 mL/min; Column Temp: 50 °C; Detector: PDA (220 nm & 215 nm & 254 nm). EXAMPLE 1 [0682] Compound 1: 8-(Imidazo[1,2-a]pyrazin-8-yl)-3-(2-(8-methyl-6-(3-methyl-3- phenylpyrrolidin-1-yl)-[1,2,4]triazolo[1,5-a]pyridin-2-yl)et hyl)-1,3,8- triazaspiro[4.5]decan-2-one

[0684] To a solution of tert-butyl 4-amino-4-carbamoyl-piperidine-1-carboxylate (10.00 g, 41.10 mmol, 1 equiv) in THF (150 mL) was added BH ₃ ^Me ₂ S (10 M, 20.55 mL, 5 equiv) dropwise at 0 °C under N2 atmosphere. The mixture was stirred at 65 °C for 2 h. The mixture was cooled to 0 °C, then methanol (40 mL) was added dropwise, and the mixture was stirred at 60 °C for 12 h. The reaction mixture was concentrated under the reduced pressure to give the title compound (9.4 g, crude) as a yellow oil. [0685] ¹ H NMR (400 MHz, CDCl3): δ 3.71 - 3.65 (m, 2H), 3.31 - 3.17 (m, 4H), 1.46 (s, 9H), 1.41 - 1.37 (m, 4H). [0686] Step 2: tert-butyl 4-(2,2,2-trifluoroacetamido)-4-((2,2,2 trifluoroacetamido)methyl)piperidine-1-carboxylate g, 39.25 mmol, 1 equiv) in DCM (100 mL) was added Et ₃ N (32.78 mL, 235.48 mmol, 6 equiv) and TFAA (16.38 mL, 117.74 mmol, 3 equiv) dropwise at 0 °C. The resulted mixture was stirred at 20 °C for 12 h. The reaction mixture was quenched by water (80 mL) and extracted with DCM (80 mL x 3), the combined organic layers were washed with brine (100 mL x 3), dried, filtered and concentrated to give a residue. The residue was purified by flash silica gel chromatography (SiO2; Petroleum ether : Ethyl acetate = 0:1, Rf = 0.7 ). The crude product was triturated with PE (20 ml) and DCM (2 ml) at 25 °C for 0.5 h. The mixture was filtered, and the cake was dried in vacuum to give the title compound (5.8 g, 35% yield) as a white solid. [0688] ¹ H NMR (400 MHz, CDCl3): δ 7.51 (s, 1H), 6.31 (s, 1H), 3.75 (s, 4H), 3.22 - 3.13 (m, 2H), 2.07 - 2.02 (m, 2H), 1.74 (ddd, J = 14.0, 10.0, 4.2 Hz, 2H), 1.46 (s, 9H). [0689] LC-MS [ESI, M -100 + 1]: 322.0. [0690] Step 3: 2,2,2-trifluoro-N-(4-((2,2,2-trifluoroacetamido)methyl)piper idin-4- yl)acetamide [0691] To a solution of 4-(2,2,2-trifluoroacetamido)-4-((2,2,2- trifluoroacetamido)methyl)piperidine-1-carboxylate (3.00 g, 7.12 mmol, 1 equiv) in DCM (30 mL) was added HCl/dioxane (20.0 mL, 80.00 mmol, 11.23 equiv) at 0 °C. The mixture was stirred at 25 °C for 0.5 h. The reaction solution was concentrated under the reduced pressure to give the title compound (4.10 g, crude, HCl salt) as a yellow oil. [0692] ¹ H NMR (400 MHz, DMSO-d ₆ ): δ 9.65 (t, J = 6.4 Hz, 1H), 9.10 - 9.02 (m, 2H), 8.87 (s, 1H), 3.52 (d, J = 6.4 Hz, 2H), 3.18 (d, J = 13.2 Hz, 2H), 2.82 (q, J = 11.6 Hz, 2H), 2.35 (d, J = 14.8 Hz, 2H), 1.83 - 1.74 (m, 2H). [0693] LC-MS [ESI, M + 1]: 321.9. [0694] Step 4: 2,2,2-trifluoro-N-(1-(imidazo[1,2-a]pyrazin-8-yl)-4-((2,2,2- trifluoroacetamido)methyl)piperidin-4-yl)acetamide [0695] To a solution of 2,2,2-trifluoro-N-(4-((2,2,2-trifluoroacetamido)methyl)piper idin-4- yl)acetamide (3.10 g, 7.12 mmol, 1 equiv, HCl salt ) in DMA (30 mL) was added DIEA (6.2 mL, 35.61 mmol, 5 equiv) and 8-chloroimidazo[1,2-a]pyrazine (1.04 g, 6.77 mmol, 0.95 equiv). The mixture was stirred at 130 °C for 2 h. The mixture was concentrated under the reduced pressure to give a residue. The residue was purified by reversed-phase HPLC (0.1% FA condition, B%: 5%-10%, 20 min) to give the title compound (2.5 g, 74%) as a red gum. Hz, 1H), 6.81 (s, 1H), 4.75 (td, J 14.4 ,4.4 Hz, 2H), 3.82 3.75 (m, 4H), 2.30 (d, J 14.4 Hz, 2H), .9 ( , J .0, 0.0, 3.6 Hz, 2H). [0697] LC-MS [ESI, M + 1]: 439.0. [0698] Step 5: 4-(aminomethyl)-1-(imidazo[1,2-a]pyrazin-8-yl)piperidin-4-am ine [0699] To a solution of 2,2,2-trifluoro-N-(1-(imidazo[1,2-a]pyrazin-8-yl)-4-((2,2,2- trifluoroacetamido)methyl)piperidin-4-yl)acetamide (2.50 g, 5.70 mmol, 1 equiv) in MeOH (100 mL) and H ₂ O (20 mL) was added K ₂ CO ₃ (2.36 g, 17.11 mmol, 3 equiv). The mixture was stirred at 60 °C for 2 h. The reaction mixture was filtered and the filtrate was concentrated under the reduced pressure to give the residue. The residue was purified by flash silica gel chromatography (SiO2; DCM : MeOH = 10:1, Rf = 0.3) to give the title compound (1.20 g, 85%) as a white gum. [0700] ¹ H NMR (400 MHz, DMSO-d6): δ 7.91 (d, J = 1.2 Hz, 1H), 7.87 (d, J = 4.4 Hz, 1H), 7.54 (d, J = 0.8 Hz, 1H), 7.31 (d, J = 4.4 Hz, 1H), 4.61 (d, J = 13.2 Hz, 2H), 3.96 - 3.89 (m, 2H), 2.64 (s, 2H), 1.62 - 1.46 (m, 4H). [0701] LC-MS [ESI, M + 39]: 285.1. [0702] Step 6: O-(mesitylsulfonyl)hydroxylamine [0703] To a solution of ethyl (Z)-N-((mesitylsulfonyl)oxy)acetimidate (20.00 g, 70.09 mmol, 1 equiv) in dioxane (80 mL) was added perchloric acid (54.3 g, 379 mmol, 32.7 mL, 70% purity, 5.40 equiv) dropwise at 0 °C. The mixture was stirred at 0 °C for 0.5 h. Ice-water (200 mL) was added and the reaction mixture was stirred for 30 min. The precipitate was collected by filtration and washed with water (100 mL) to afford the title compound (15.00 g, 99% yield) as a white solid. [0704] Step 7: 1,2-diamino-5-bromo-3-methylpyridin-1-ium 2,4,6- trimethylbenzenesulfonate [0705] To a mixture of 5-bromo-3-methyl-pyridin-2-amine (15.00 g, 80.20 mmol, 1 equiv) in DCM (70 mL) was added a solution of O-(mesitylsulfonyl)hydroxylamine (15.00 g, 69.70 mmol, 0.9 equiv) in DCM (140 mL) dropwise at 0 °C. The mixture was stirred at 0 °C for 0.5 h. The mixture was filtered and the filter cake was collected and dried under the reduced pressure to give the title compound (18.0 g, 55%) as a white solid. [0706] ¹ H NMR (400 MHz, DMSO-d ₆ ): δ 8.37 - 8.22 (m, 1H), 7.83 (d, J = 2.0 Hz, 1H), 7.42 (d, J , , , , 8 (s, 1H), 2.50 (s, 6H), 2.17 (s, 3H), 2.02 (s, 3H). [0707] LC-MS [ESI, M-200 + 1]: 201.8. [0709] To a mixture of 1,2 diamino 5 bromo 3 methylpyridin 1 ium 2,4,6 trimethylbenzenesulfonate (16.00 g, 39.77 mmol, 1 equiv) and NaOH (1.75 g, 43.75 mmol, 1.1 equiv) in MeOH (160 mL) was added methyl 3,3-dimethoxypropanoate (7.07 g, 47.70 mmol, 1.2 equiv). The mixture was stirred at 70 °C for 1 h. The reaction mixture was concentrated under the reduced pressure to give a residue, which was purified by flash silica gel chromatography (ISCO®; 120 g SepaFlash® Silica Flash Column, Eluent of 0~40% Ethyl acetate/Petroleum ether gradient @ 80 mL/min) to give the title compound (1.20 g, 15%) as a yellow solid. [0710] ¹ H NMR (400 MHz, CDCl ₃ ): δ 8.45 (s, 1H), 7.19 (d, J = 1.6 Hz, 1H), 4.96 (dt, J = 6.0, 1.6 Hz, 1H), 3.33 (d, J = 1.2 Hz, 6H), 3.19 (dd, J = 6.0, 1.6 Hz, 2H), 2.55 (s, 3H). [0711] LC-MS [ESI, M - 15 + 1]: 287.6. [0712] Step 9: 2-(2,2-dimethoxyethyl)-8-methyl-6-(3-methyl-3-phenylpyrrolid in-1-yl)- [1,2,4]triazolo[1,5-a]pyridine [0713] A mixture of 6-bromo-2-(2,2-dimethoxyethyl)-8-methyl-[1,2,4]triazolo[1,5- a]pyridine (1.00 g, 3.33 mmol, 1 equiv), 3-methyl-3-phenyl-pyrrolidine (0.81 g, 5.00 mmol, 1.5 equiv), Cs2CO3 (3.26 g, 9.99 mmol, 3 equiv) and 1,3-bis[2,6-bis(1-propylbutyl)phenyl]- 4,5-dichloro-2H-imidazol-1-ium-2-ide;3-chloropyridine;dichlo ropalladium (32 mg, 33 ^mol, 0.01 equiv) in dioxane (20 mL) was degassed and purged with N2 for 3 times, and then the mixture was stirred at 100 °C for 3 h LCMS showed was consumed and desired mass was detected. The reaction mixture was concentrated under reduced pressure to give a residue, which was purified by flash silica gel chromatography (ISCO®; 10 g SepaFlash® Silica Flash Column, Eluent of 0~80% Ethyl acetate/Petroleum ether gradient @ 40mL/min) to give the title compound (0.60 g, 47% yield) as a yellow solid. [0714] ¹ H NMR (400 MHz, CDCl3): δ 7.55 (d, J = 1.6 Hz, 1H), 7.29 - 7.22 (m, 4H), 7.18 - 7.15 (m, 1H), 6.83 (dd, J = 2.4, 1.2 Hz, 1H), 4.97 (t, J = 6.0 Hz, 1H), 3.64 - 3.52 (m, 2H), 3.50 - 3.43 (m, 2H), 3.34 - 3.32 (m, 6H), 3.16 (d, J = 6.0 Hz, 2H), 2.56 - 2.52 (m, 3H), 2.32 - 2.24 (m, 1H), 2.19 - 2.16 (m, 1H), 1.38 (s, 3H). [0715] LC-MS [ESI, M + 1]: 381.4. [0716] Step 10: 2-(8-methyl-6-(3-methyl-3-phenylpyrrolidin-1-yl)-[1,2,4]tria zolo[1,5- a]pyridin-2-yl)acetaldehyde [0717] To a mixture of 2-(2,2-dimethoxyethyl)-8-methyl-6-(3-methyl-3-phenylpyrrolid in- 1-yl)-[1,2,4]triazolo[1,5-a]pyridine (100 mg, 263 ^mol, 1 equiv) in H ₂ O (0.5 mL) was added for 12 h. The reaction mixture was diluted with water (10 mL) and basified with aqueous NaHCO3 till pH=6, the mixture was extracted with DCM (20 mL x 3). The combined organic layers were dried, filtered, and concentrated to give the title compound (80 mg, 91% yield) as a yellow oil. [0718] LC-MS [ESI, M + 18 + 1]: 353.3. [0719] Step 11: 1-(imidazo[1,2-a]pyrazin-8-yl)-4-(((2-(8-methyl-6-(3-methyl- 3- phenylpyrrolidin-1-yl)-[1,2,4]triazolo[1,5-a]pyridin-2-yl)et hyl)amino)methyl)piperidin- 4-amine [0720] To a mixture of 2-(8-methyl-6-(3-methyl-3-phenylpyrrolidin-1-yl)- [1,2,4]triazolo[1,5-a]pyridin-2-yl)acetaldehyde (80 mg, 239 ^mol, 1 equiv), HOAc (14 mg, 239 ^mol, 1 equiv) and 4-(aminomethyl)-1-(imidazo[1,2-a]pyrazin-8-yl)piperidin-4-am ine 7 (58.92 mg, 239.22 ^mol, 1 equiv) in MeOH (1 mL) was added NaBH3CN (45 mg, 717 ^mol, 3 equiv) at 0 °C in three portions. The mixture was stirred at 0 °C for 0.5 h and then 25 °C for 1 h. The reaction mixture was concentrated under the reduced pressure to give a residue, which was diluted with water (10 mL) and basified with aqueous NaHCO3 until pH around 8, the mixture was extracted with DCM (20 mL x 3). The combined organic layers were dried, filtered and concentrated to give a residue, which was purified by prep-TLC (Dichloromethane : Methanol = 10 : 1, R _f = 0.2) to give the title compound (100 mg, 74% yield) as a yellow oil. [0721] LC-MS [ESI, M + 1]: 565.5. [0722] Step 12: 8-(imidazo[1,2-a]pyrazin-8-yl)-3-(2-(8-methyl-6-(3-methyl-3- phenylpyrrolidin-1-yl)-[1,2,4]triazolo[1,5-a]pyridin-2-yl)et hyl)-1,3,8- triazaspiro[4.5]decan-2-one [0723] A mixture of 1-(imidazo[1,2-a]pyrazin-8-yl)-4-(((2-(8-methyl-6-(3-methyl- 3- phenylpyrrolidin-1-yl)-[1,2,4]triazolo[1,5-a]pyridin-2-yl)et hyl)amino)methyl)piperidin-4- amine (100 mg, 177 ^mol, 1 eq) and CDI (230 mg, 1.42 mmol, 8 eq) in DCM (4 mL) was stirred at 40 °C for 12 h. The reaction mixture was concentrated under the reduced pressure. The residue was purified by prep-HPLC (column: Phenomenex luna C18150*25mm* 10µm; mobile phase: (water(FA)-ACN); B%: 25%-55%, 9 min) to give the title compound (8 mg, 7% yield) as an off-white solid. [0724] ¹ H NMR (400 MHz, CDCl3): δ 7.62 (d, J = 2.0 Hz, 1H), 7.55 - 7.49 (m, 3H), 7.38 - 7.34 (m, 5H), 7.28 - 7.24 (m, 1H), 6.93 (s, 1H), 4.59 (s, 1H), 4.37 - 4.32 (m, 2H), 4.19 - 4.06 2H), 3.15 (t, J 6.8 Hz, 2H), 2.61 (s, 3H), 2.42 2.32 (m, 1H), 2.28 2.26 (m, 1H), 1.89 1.82 (m, 4H), 1.47 (s, 3H). [0725] LC-MS [ESI, M + 1]: 591.4. [0726] DSF: ***** (see Example 8) Compound Number Synthesis LC/MS DSF ¹ Compound 2 Similar to Example 1 m/z 5915 [M+H] ⁺ ***** See xampe 8 EXAMPLE 2 [0727] Compound 9: 8-(Imidazo[1,2-a]pyrazin-8-yl)-3-(2-(8-methyl-6-(2- phenylpropoxy)-[1,2,4]triazolo[1,5-a]pyridin-2-yl)ethyl)-1,3 ,8-triazaspiro[4.5]decan-2- one

, y y y ,, , trimethylbenzenesulfonate (10.00 g, 24.90 mmol, 1 equiv) and NaOH (1.19 g, 29.80 mmol, 1.2 equiv) in MeOH (100 mL) was added methyl 3,3-dimethoxypropanoate (4.42 g, 29.80 mmol, 1.2 equiv), then the mixture was stirred at 70 °C for 1 h. The reaction mixture was concentrated under the reduced pressure to give a residue. The residue was purified by flash silica gel chromatography (ISCO®; 120 g SepaFlash® Silica Flash Column, Eluent of 0~40% Ethyl acetate/Petroleum ether gradient @80 mL/min) to afford the title compound (2.60 g, 35%) as a yellow solid. [0730] ¹ H NMR (400 MHz, CDCl3) δ 8.45 (s, 1H), 7.19 (s, 1H), 4.96 (t, J = 4.4 Hz, 1H), 3.33 (d, J = 1.6 Hz, 6H), 3.19 (dd, J = 6.0, 1.6 Hz, 2H), 2.55 (s, 3H). [0731] LC-MS [ESI, M + 1]: 287.9. [0732] Step 2: 2-(2,2-dimethoxyethyl)-8-methyl-6-(2-phenylpropoxy)- [1,2,4]triazolo[1,5-a]pyridine [0733] A mixture of 6-bromo-2-(2,2-dimethoxyethyl)-8-methyl-[1,2,4]triazolo[1,5- a]pyridine (1.00 g, 3.33 mmol, 1 equiv), 2-phenylpropan-1-ol (1.36 g, 9.99 mmol, 3 equiv), Ir[dF(CF3)ppy]2(dtbpy)(PF6) (37 mg, 33 ^mol, 0.01 equiv) and NiCl2.dtbbpy (66 mg, 0.17 mmol, 0.05 equiv), quinuclidine (37 mg, 0.33 mmol, 0.1 equiv), TMP (940 mg, 6.66 mmol, 1.13 mL, 2 equiv) in CH ₃ CN (12 mL) was degassed for three times. The reaction vial was then sealed with parafilm, placed 2 cm away from one blue LED and irradiated at 25 °C for 12 h. The reaction mixture was filtered and the filtrated was concentrated in vacuum. The residue was purified by flash silica gel chromatography (ISCO®; 20 g SepaFlash® Silica Flash Column, Eluent of 20~25% Ethyl acetate/Petroleum ether gradient @ 80 mL/min) to afford the title compound (100 mg, 55%) as a yellow oil. [0734] LC-MS [ESI, M + 1]: 356.4. [0735] Step 3: 2-(8-methyl-6-(2-phenylpropoxy)-[1,2,4]triazolo[1,5-a]pyridi n-2- yl)acetaldehyde [0736] A mixture of 2-(2,2-dimethoxyethyl)-8-methyl-6-(2-phenylpropoxy)- [1,2,4]triazolo[1,5-a]pyridine (130 mg, 0.37 mmol, 1 equiv) and TFA (924 mg, 8.10 mmol, 22 equiv) in water (0.5 mL) was stirred at 25 °C for 12 h. The reaction mixture was diluted with DCM (6 mL), then adjusted the pH to 5 by solid NaHCO3, then the reaction mixture was dried over sodium sulfate, filtered, and concentrated to afford the title compound (112 mg, crude) as a yellow oil. It was used directly for next step. [1,2,4]triazolo[1,5 a]pyridin 2 yl)ethyl)amino)methyl)piperidin 4 amine [0738] To a solution of 2-(8-methyl-6-(2-phenylpropoxy)-[1,2,4]triazolo[1,5-a]pyridi n-2- yl)acetaldehyde (112 mg, 0.36 mmol, 1 equiv) and 4-(aminomethyl)-1-imidazo[1,2- a]pyrazin-8-yl-piperidin-4-amine (89 mg, 0.36 mmol, 1 equiv) in MeOH (2 mL) was added HOAc (22 mg, 0.36 mmol, 1 equiv). The mixture was stirred at 25 °C for 0.5 h, then NaBH3CN (68 mg, 1.09 mmol, 3 equiv) was added at 0 °C. The reaction mixture was stirred at 0 °C for 1 h. The reaction mixture was concentrated in vacuum. The residue was purified by prep-TLC (SiO2, DCM: MeOH = 10:1, Rf = 0.2) to afford the title compound (130 mg, crude) as a yellow oil. [0739] LC-MS [ESI, M + 1]: 540.2. [0740] Step 5: 8-(imidazo[1,2-a]pyrazin-8-yl)-3-(2-(8-methyl-6-(2-phenylpro poxy)- [1,2,4]triazolo[1,5-a]pyridin-2-yl)ethyl)-1,3,8-triazaspiro[ 4.5]decan-2-one [0741] To a solution of 1-(imidazo[1,2-a]pyrazin-8-yl)-4-(((2-(8-methyl-6-(2- phenylpropoxy)-[1,2,4]triazolo[1,5-a]pyridin-2-yl)ethyl)amin o)methyl)piperidin-4-amine (130 mg, 0.24 mmol, 1 equiv) in DCM (5 mL) was added CDI (312 mg, 1.93 mmol, 8 equiv). The reaction mixture was stirred at 40 °C for 2 h. The reaction mixture was concentrated in vacuum. The residue was purified by prep-HPLC (column: Waters Xbridge BEH C18 100*30mm*10µm; mobile phase: (water(NH ₄ HCO ₃ )-ACN); B%: 31%-61%,10min) to afford the title compound (11 mg, 7%) as a white solid. [0742] ¹ H NMR (400 MHz, CDCl ₃ ) δ 7.91 (d, J = 2.0 Hz, 1H), 7.53 (d, J = 0.8 Hz, 1H), 7.51 (d, J 0.8 Hz, 1H), 7.35 - 7.32 (m, 3H), 7.30 - 7.28 (m, 2H), 7.27 - 7.24 (m, 1H), 7.02 (d, J = 0.8 Hz, 1H), 4.81 (s, 1H), 4.37 - 4.25 (m, 2H), 4.19 - 4.10 (m, 2H), 4.09 - 4.03 (m, 1H), 4.00 - 3.95 (m, 1H), 3.72 (t, J = 6.8 Hz, 2H), 3.33 (s, 2H), 3.30 - 3.25 (m, 1H), 3.13 (t, J = 6.8 Hz, 2H), 2.55 (s, 3H), 1.87 - 1.79 (m, 4H), 1.43 (d, J = 7.2 Hz, 3H). [0743] LC-MS [ESI, M + 1]: 566.3. [0744] DSF: ***** (see Example 8) Compound Number Synthesis LC/MS DSF ¹ Compound 19 Similar to Example 2 m/z 531.2 [M+H] Compound 120 Similar to Example 2 m/z 530.4 [M+H] see Examp e 8 EXAMPLE 3 [0745] Compound 14: 8-(Imidazo[1,2-a]pyrazin-8-yl)-3-(2-(3-methyl-7-(1- phenylethoxy)imidazo[1,2-a]pyridin-2-yl)ethyl)-1,3,8-triazas piro[4.5]decane-2,4-dione

cetate [0747] To a solution of methyl 4-bromo-3-oxo-pentanoate (150 mg, 0.72 mmol, 1 equiv) in MeOH (3 mL) was added 4-benzyloxypyridin-2-amine (140 mg, 0.72 mmol, 1 equiv). The reaction mixture was stirred at 25 °C for 2 h. reaction mixture was concentrated, the residue was purified by prep-TLC (SiO2, DCM: MeOH = 10:1, Rf = 0.45) to afford the title compound (60 mg, 27%) as a yellow oil. [0748] ¹ H NMR (400 MHz, CDCl3): δ 7.67 (d, J = 7.2 Hz, 1H), 7.45 - 7.33 (m, 5H), 6.90 (d, J = 2.4 Hz, 1H), 6.62 (dd, J = 7.2, 2.4 Hz, 1H), 5.09 (s, 2H), 3.76 (s, 2H), 3.72 (s, 3H), 2.39 (s, 3H). [0749] LC-MS [ESI, M + 1]: 311.2. [0750] Step 2: methyl 2-(7-hydroxy-3-methylimidazo[1,2-a]pyridin-2-yl)acetate (1.30 g, 4.19 mmol, 1 equiv) in MeOH (20 mL) was added Pd/C (0.50 g, 0.42 mmol, 10% purity, 0.1 equiv). The reaction mixture was stirred at 25 °C for 2 h under H2 (15 Psi). The reaction mixture was filtered and the filtrate was concentrated in vacuum. The residue was purified by flash silica gel chromatography (ISCO®; 25 g SepaFlash® Silica Flash Column, Eluent of 5~12% DCM/MeOH@ 80 mL/min) to afford the title compound (0.75 g, 82%) as a yellow solid. [0752] ¹ H NMR (400 MHz, DMSO-d ₆ ): δ 8.01 (d, J = 6.8 Hz, 1H), 6.60 - 6.59 (m, 1H), 6.55 (dd, J = 7.2, 2.4 Hz, 1H), 3.67 (s, 2H), 3.59 (s, 3H), 2.32 (s, 3H). [0753] LC-MS [ESI, M + 1]: 221.0. [0754] Step 3: methyl 2-(3-methyl-7-(1-phenylethoxy)imidazo[1,2-a]pyridin-2- yl)acetate [0755] To a solution of TMAD (704 mg, 4.09 mmol, 1.5 eq) in THF (10 mL) was added tributylphosphane (827 mg, 4.09 mmol, 1.01 mL, 1.5 eq) at 0 °C during 0.5 h. Then a solution of methyl 2-(7-hydroxy-3-methyl-imidazo[1,2-a]pyridin-2-yl)acetate (600 mg, 2.72 mmol, 1 equiv) and -1-phenylethanol (500 mg, 4.09 mmol, 1.5 equiv) in THF (10 mL) was added. The reaction mixture was stirred at 25 °C for 1.5 h. The reaction mixture was concentrated in vacuum. The residue was purified by flash silica gel chromatography (ISCO®; 25 g SepaFlash® Silica Flash Column, Eluent of 25~30% Ethyl acetate/Petroleum ethergradient @ 80 mL/min) to afford the title compound (230 mg, 26%) as a yellow solid. [0756] ¹ H NMR (400 MHz, CDCl ₃ ): δ 7.56 (d, J = 7.2 Hz, 1H), 7.30 - 7.27 (m, 4H), 7.25 - 7.23 (m, 1H), 6.62 (d, J = 2.4 Hz, 1H), 6.54 (dd, J = 7.2, 2.4 Hz, 1H), 5.24 (q, J = 6.4 Hz, 1H), 3.64 (s, 2H), 3.62 (s, 3H), 2.28 (s, 3H), 1.60 (d, J = 6.4 Hz, 3H). [0757] LC-MS [ESI, M + 1]: 325.1. [0758] Step 4: 2-(3-methyl-7-(1-phenylethoxy)imidazo[1,2-a]pyridin-2-yl)eth an-1-ol [0759] To a solution of methyl 2-[3-methyl-7-[1-phenylethoxy]imidazo[1,2-a]pyridin-2- yl]acetate (175 mg, 0.54 mmol, 1 equiv) in THF (2.5 mL) was added LiBH ₄ (41 mg, 1.89 mmol, 3.5 equiv) at 0 °C. The reaction mixture was stirred at 0 °C for 1 h. The reaction was quenched by H ₂ O (10 mL) slowly and then extracted with EtOAc (10 mL x 3). The combined organic phase was washed with brine (10 mL x 3), dried, filtered and concentrated to give a residue, which was purified by prep-TLC (SiO ₂ , DCM: MeOH = 10:1, R _f = 0.3) to afford the title compound (100 mg, 61%) as a yellow oil. [0760] LC-MS [ESI, M + 1]: 297.1. phenylethoxy)imidazo[1,2 a]pyridin 2 yl)ethyl) 1,3,8 triazaspiro[4.5]decane 2,4 dione [0762] To a solution of TMAD (9 mg, 51 ^mol, 1.5 equiv) in THF (0.5 mL) was added tributylphosphane (10 mg, 51 ^mol, 1.5 equiv). The reaction mixture was stirred at 0 °C for 0.5 h. Then the solution of 2-[3-methyl-7-[1-phenylethoxy]imidazo[1,2-a]pyridin-2- yl]ethanol (10 mg, 34 ^mol, 1 equiv) and 8-imidazo[1,2-a]pyrazin-8-yl-1,3,8- triazaspiro[4.5]decane-2,4-dione (14 mg, 51 ^mol, 1.5 equiv) in THF (0.5 mL) was added. The reaction mixture was stirred at 0 °C for 0.5 h. The reaction mixture was concentrated in vacuum to give a residue, which was purified by prep-HPLC (column: Phenomenex luna C18 150*25mm* 10µm; mobile phase: (water(FA)-ACN); B%: 9%-39%, 9 min) to afford the title compound (0.27 mg, 2%) as a white solid. [0763] ¹ H NMR (400 MHz, CDCl ₃ ): δ 7.68 (d, J = 7.2 Hz, 1H), 7.55 - 7.53 (m, 3H), 7.46 - 7.39 (m, 2H), 7.39 - 7.32 (m, 3H), 7.24 ( s, 1H), 7.07 - 6.94 (m, 1H), 6.72 ( d, J = 7.2 Hz, 1H), 5.96 - 5.73 (m, 1H), 5.44 ( d, J = 5.6 Hz, 1H), 5.05 - 4.86 (m, 2H), 3.94 - 3.77 (m, 4H), 3.07 ( t, J = 6.8 Hz, 2H), 2.36 (s, 3H), 2.16 - 1.98 (m, 4H), 1.27 ( d, J = 4.8 Hz, 3H). [0764] LC-MS [ESI, M + 1]: 565.2. [0765] DSF: ** (see Example 8) Compound Number Synthesis LC/MS DSF ^{1 1} see Example 8 EXAMPLE 4 [0766] Compound 30: 3-(2-hydroxy-2-(8-methyl-6-((1-phenylcyclopropyl)methoxy)- [1,2,4]triazolo[1,5-a]pyridin-2-yl)ethyl)-8-(4-methyl-4H-1,2 ,4-triazole-3-carbonyl)-1,3,8- triazaspiro[4.5]decan-2-one

l-[1,2,4]triazolo[1,5- a]pyridin-2-yl)-2-hydroxyethyl)amino)methyl)piperidine-1-car boxylate [0768] To a solution of 6-bromo-8-methyl-2-(oxiran-2-yl)-[1,2,4]triazolo[1,5-a]pyrid ine (5.00 g, 19.68 mmol, 1 eq) in DMF (50 mL) was added K2CO3 (2.72 g, 19.68 mmol, 1 eq) and tert-butyl 4-amino-4-(aminomethyl)piperidine-1-carboxylate (4.96 g, 21.65 mmol, 1.1 eq). The mixture was stirred at 100 °C for 2 h. LCMS showed the starting material was consumed and the desired product mass was detected. The reaction mixture was filtered and the combined organic phase was concentrated under reduced pressure to produce the title compound (12.30 g, crude) as a yellow oil. [0769] LC-MS [ESI, M+H]: 483.2. [0770] Step 2: tert-butyl 4-amino-4-(((2-(6-bromo-8-methyl-[1,2,4]triazolo[1,5- a]pyridin-2-yl)-2-((tert-butyldimethylsilyl)oxy)ethyl)amino) methyl)piperidine-1- carboxylate [0771] To a solution of tert-butyl 4-amino-4-[[[2-(6-bromo-8-methyl-[1,2,4]triazolo[1,5- a]pyridin-2-yl)-2-hydroxy-ethyl]amino]methyl]piperidine-1-ca rboxylate (12.30 g, 25.44 mmol, 1 eq) in DCM (30 mL) was added imidazole (8.66 g, 127.22 mmol, 5 eq) and TBSCl LCMS showed the starting material was consumed and the desired product mass was detected. The reaction mixture was extracted with DCM, the aqueous phase was extracted with DCM (10 mL x 2). The combined organic phase was washed with brine (10 mL), dried, filtered and concentrated in vacuum to give the title compound (21.00 g, crude) as a yellow oil. [0772] LC-MS [ESI, M+H]: 597.4. [0773] Step 3: tert-butyl 3-(2-(6-bromo-8-methyl-[1,2,4]triazolo[1,5-a]pyridin-2-yl)-2 - ((tert-butyldimethylsilyl)oxy)ethyl)-2-oxo-1,3,8-triazaspiro [4.5]decane-8-carboxylate [0774] To a solution of tert-butyl 4-amino-4-[[[2-(6-bromo-8-methyl-[1,2,4]triazolo[1,5- a]pyridin-2-yl)-2-[tert-butyl(dimethyl)silyl]oxy-ethyl]amino ]methyl]piperidine-1-carboxylate (21.00 g, 35.14 mmol, 1 eq) in DCM (200 mL) was added CDI (28.49 g, 175.68 mmol, 5 eq). The mixture was stirred at 25 °C for 12 h. LCMS showed the starting material was consumed and the desired product mass was detected. The reaction mixture was extracted with DCM, the aqueous phase was extracted with DCM (50 mL x 2). The combined organic phase was washed with brine (30 mL), dried, filtered and concentrated in vacuum to give a crude. The residue was purified by reversed-phase HPLC (neutral condition) to afford the title compound (4.77 g, 20%) as a white solid. [0775] LC-MS [ESI, M+H]: 623.3. [0776] Step 4: tert-butyl 3-(2-((tert-butyldimethylsilyl)oxy)-2-(8-methyl-6-((1- phenylcyclopropyl)methoxy)-[1,2,4]triazolo[1,5-a]pyridin-2-y l)ethyl)-2-oxo-1,3,8- triazaspiro[4.5]decane-8-carboxylate [0777] A mixture of tert-butyl 3-[2-(6-bromo-8-methyl-[1,2,4]triazolo[1,5-a]pyridin-2-yl)- 2-[tert-butyl(dimethyl)silyl]oxy-ethyl]-2-oxo-1,3,8-triazasp iro[4.5]decane-8-carboxylate (3.00 g, 4.81 mmol, 1 eq) tert-butyl 3-[2-(6-bromo-8-methyl-[1,2,4]triazolo[1,5-a]pyridin-2- yl)-2-[tert-butyl(dimethyl)silyl]oxy-ethyl]-2-oxo-1,3,8-tria zaspiro[4.5]decane-8-carboxylate (3 g, 4.81 mmol, 1 eq), (1-phenylcyclopropyl)methanol (3.56 g, 24.05 mmol, 5 eq), bis[3,5- difluoro-2-[5-(trifluoromethyl)-2-pyridyl]phenyl]iridium(1+) ;4-tert-butyl-2-(4-tert-butyl-2- pyridyl)pyridine;hexafluorophosphate (53.97 mg, 48.10 μmol, 0.01 eq), 4-tert-butyl-2-(4-tert- butyl-2-pyridyl)pyridine;dichloronickel (95.72 mg, 240.52 μmol, 0.05 eq), quinuclidine (53.48 mg, 481.03 μmol, 0.1 eq) and 2,2,6,6-tetramethylpiperidine (1.36 g, 9.62 mmol, 1.63 mL, 2 eq) in MeCN (10 mL) was degassed and purged with N2 for 3 times, and then then the reaction vial was then sealed with parafilm, placed 2 cm away from one blue LED and irradiated at 25 °C for 14 h. LCMS showed the starting material was consumed and the mL x 2), washed with brine (40 mL), dried, filtered and concentrated in vacuum to give the crude. The residue was purified by column chromatography (SiO2, Petroleum ether/Ethyl acetate = 0:1, Rf = 0.5) to afford the title compound (1.36 g, 37%) as a brown solid. [0778] LC-MS [ESI, M+H]: 691.3. [0779] ¹ H NMR (400 MHz, CDCl ₃ ) δ = 7.86 (d, J = 2.0 Hz, 1H), 7.43 - 7.37 (m, 2H), 7.31 (t, J = 8.0 Hz, 2H), 7.23 (br d, J = 8.0 Hz, 1H), 7.02 (d, J = 0.8 Hz, 1H), 5.22 (s, 1H), 5.18 (t, J = 6.0 Hz, 1H), 4.00 (s, 2H), 3.73 - 3.64 (m, 1H), 3.63 - 3.54 (m, 1H), 3.39 (td, J = 6.0, 12.8 Hz, 4H), 3.33 - 3.27 (m, 1H), 3.20 (d, J = 8.8 Hz, 1H), 2.54 (s, 3H), 1.64 - 1.59 (m, 2H), 1.55 (br t, J = 5.6 Hz, 2H), 1.45 (s, 9H), 1.04 (br s, 4H), 0.87 (s, 9H), 0.06 (s, 3H), -0.06 (s, 3H) [0780] Step 5: 3-(2-((tert-butyldimethylsilyl)oxy)-2-(8-methyl-6-((1- phenylcyclopropyl)methoxy)-[1,2,4]triazolo[1,5-a]pyridin-2-y l)ethyl)-1,3,8- triazaspiro[4.5]decan-2-one [0781] To a solution of tert-butyl 3-[2-[tert-butyl(dimethyl)silyl]oxy-2-[8-methyl-6-[(1- phenylcyclopropyl)methoxy]-[1,2,4]triazolo[1,5-a]pyridin-2-y l]ethyl]-2-oxo-1,3,8- triazaspiro[4.5]decane-8-carboxylate (1.36 g, 1.97 mmol, 1 eq) in DCM (15 mL) was added TFA (9.21 g, 80.77 mmol, 6.00 mL, 41.04 eq). The mixture was stirred at 25 °C for 0.5 h. LCMS showed the starting material was consumed and the desired product mass was detected. The reaction mixture was added water (10 mL) and adjusted the pH to around 7 by NaHCO3 solution, and then extracted with DCM (20 mL x 2), washed with brine (20 mL), dried, filtered and concentrated under reduced pressure to give the title compound (1.36 g, crude) was obtained as a green solid. [0782] LC-MS [ESI, M+H]: 591.3. [0783] ¹ H NMR (400 MHz, CDCl3) δ = 8.09 (s, 1H), 7.44 - 7.38 (m, 2H), 7.31 (t, J = 7.6 Hz, 2H), 7.24 - 7.19 (m, 1H), 7.07 (d, J = 0.8 Hz, 1H), 5.14 (dd, J = 4.0, 8.6 Hz, 1H), 4.06 - 4.01 (m, 2H), 3.75 - 3.65 (m, 1H), 3.51 - 3.27 (m, 5H), 3.21 (br d, J = 6.0 Hz, 2H), 2.54 (s, 3H), 2.12 - 1.97 (m, 2H), 1.88 (br t, J = 13.6 Hz, 2H), 1.04 (s, 4H), 0.87 - 0.81 (m, 9H), 0.06 (s, 3H), -0.08 (s, 3H). [0784] Step 6: 3-(2-((tert-butyldimethylsilyl)oxy)-2-(8-methyl-6-((1- phenylcyclopropyl)methoxy)-[1,2,4]triazolo[1,5-a]pyridin-2-y l)ethyl)-8-(4-methyl-4H- 1,2,4-triazole-3-carbonyl)-1,3,8-triazaspiro[4.5]decan-2-one [0785] To a solution of 4-methyl-1,2,4-triazole-3-carboxylic acid (11.34 mg, 84.63 μmol, 1 eq) and 3-[2-[tertbutyl(dimethyl)silyl]oxy-2-[8-methyl-6-[(1- phenylcyclopropyl)methoxy][1,2,4]triazolo[1,5-a]pyridin-2-yl ]ethyl]-1,3,8- (64.36 mg, 169.25 μmol, 2 eq) and DIEA (54.69 mg, 423.13 μmol, 73.70 μL, 5 eq). The mixture was stirred at 0 °C for 1 h. LCMS showed the starting material was consumed and desired product mass was detected. The reaction mixture was concentrated in vacuum. The reaction solution was purified by prep-TLC (PE: EtOAc = 0:1) to afford (PE: EtOAc = 0:1, R _f = 0.15) to give the title compound (35 mg, 59%) as a yellow oil. [0786] LC-MS [ESI, M + 1]: 700.5. [0787] Step 7: 3-(2-hydroxy-2-(8-methyl-6-((1-phenylcyclopropyl)methoxy)- [1,2,4]triazolo[1,5-a]pyridin-2-yl)ethyl)-8-(4-methyl-4H-1,2 ,4-triazole-3-carbonyl)-1,3,8- triazaspiro[4.5]decan-2-one [0788] To a solution of 3-[2-[tert-butyl(dimethyl)silyl]oxy-2-[8-methyl-6-[(1- phenylcyclopropyl)methoxy]-[1,2,4]triazolo[1,5-a]pyridin-2-y l]ethyl]-8-(4-methyl-1,2,4- triazole-3-carbonyl)-1,3,8-triazaspiro[4.5]decan-2-one (30mg, 42.86 μmol, 1 eq) in DCM (1 mL) was added 3HF.TEA (494.50 mg, 3.07 mmol, 0.5 mL, 71.57 eq). The mixture was stirred at 25 °C for 1 h. LCMS showed the starting material was consumed and desired product mass was detected. The reaction mixture was added NaHCO3 (aq.) until pH 7 and the reaction mixture was concentrated in vacuum. The reaction solution was purified by prep- HPLC (column: Welch Xtimate C18150x25mmx5µm;mobile phase:[water(FA)- ACN];gradient:20%-50% B over 0 min) to afford the title compound (5.42 mg, 21%) as a white solid. [0789] LC-MS [ESI, M + 1]: 586.4. [0790] ¹ H NMR (400 MHz, CDCl3) δ = 8.16 (br s, 1H), 7.87 (br s, 1H), 7.43 - 7.37 (m, 2H), 7.32 (br t, J = 7.6Hz, 2H), 7.25 - 7.21 (m, 1H), 7.03 (br s, 1H), 5.80 (br s, 1H), 5.18 (br s, 1H), 4.08 (br s, 1H), 4.00 (br s, 3H), 3.88 (s,4H), 3.73 (br s, 3H), 3.41 (br s, 2H), 2.52 (br s, 3H), 1.79 (br s, 4H), 1.04 (s, 4H). [0791] DSF: **** (see Example 8) Compound Number Synthesis LC/MS DSF ¹ Compound 25 Similar to Example 4 m/z 583.2 [M+H] Compound 59 Similar to Example 4 m/z 573.4 [M+H] Compound 133 Similar to Example 4 m/z 611.4 [M+H] p EXAMPLE 5 [0792] Compound 116: (R)-8-([1,2,4]triazolo[4,3-a]pyrazin-8-yl)-3-(2-(8-methyl-6- (2- phenylpropoxy)-[1,2,4]triazolo[1,5-a]pyridin-2-yl)ethyl)-1-o xa-3,8-diazaspiro[4.5]decan- 2-one N N N ^N ethyl-6-(2-phenylpropoxy)- [1,2,4]triazolo[1,5-a]pyridine [0794] To a solution of 6-bromo-2-(2,2-dimethoxyethyl)-8-methyl-[1,2,4]triazolo[1,5- a]pyridine (3.54 g, 11.79 mmol, 1 eq) and (2R)-2-phenylpropan-1-ol (1.61 g, 11.79 mmol, 1 eq) in ACN (150 mL) was added bis[3,5-difluoro-2-[5-(trifluoromethyl)-2- pyridyl]phenyl]iridium(1+);4-tert-butyl-2-(4-tert-butyl-2- pyridyl)pyridine;hexafluorophosphate(132.32 mg, 117.94 μmol, 0.01 eq) , NiCl2 (15.29 mg, 117.94 μmol, 0.01 eq), TMP (3.33 g, 23.59 mmol, 4.00 mL, 2eq) and quinuclidine (131.13 mg, 1.18 mmol, 0.1 eq). The mixture was degassed three times. The reaction vial was sealed with parafilm, placed 2 cm away from one blue LED, and irradiated at 25 °C for 14 h. LCMS showed the starting material was consumed and desired product compound was detected. The reaction mixture was concentrated under reduced pressure to give a residue, which was purified by flash silica gel chromatography (ISCO®; 220 g SepaFlash® Silica Flash Column, Eluent of 30~70% Ethylacetate/Petroleum ethergradient @ 100 mL/min) to give the title compound (1.23 g, 29%) as a light yellow oil. [0795] LC-MS [ESI, M + 1]: 356.1. [0796] ¹ H NMR (400 MHz, CDCl3) δ = 7.91 (d, J = 1.6 Hz, 1H), 7.36 - 7.29 (m, 2H), 7.27 (s, 3H), 7 2 - 6.96 (m, 1H), 5.00 (t, J = 6.0 Hz, 1H), 4.06 - 4.00 (m, 1H), 3.97 - 3.90 (m, 1H), 3.37 (s, 6H), 3.30 - 3.23 (m, 1H), 3.21 (d, J = 6.0 Hz, 2H), 2.54 (s, 3H), 1.40 (d, J = 7.2 Hz, 3H). [0797] Step 2: (R)-2-(8-methyl-6-(2-phenylpropoxy)-[1,2,4]triazolo[1,5-a]py ridin-2- yl)acetaldehyde [0798] To a solution of 2-(2,2-dimethoxyethyl)-8-methyl-6-[(2R)-2-phenylpropoxy]- [1,2,4]triazolo[1,5-a]pyridine (500.00 mg,1.41 mmol, 1 eq) in H ₂ O (0.5 mL) was added TFA (2.30 g, 20.19 mmol, 1.5 mL, 14.35 eq). The reaction mixture was stirred at 25 °C for 12 h. LCMS showed the starting material was consumed completely and the desired product compound was detected. The reaction mixture was added DCM (50 mL) and NaHCO3 (aq.) until pH around 5 and then extracted with DCM (50 mL × 3), washed with brine (10 mL × 3), dried, filtered and concentrated to give the title compound (550.00 mg, crude) as a yellow oil. [0800] Step 3: tert butyl (R) 4 hydroxy 4 (((2 (8 methyl 6 (2 phenylpropoxy) [1,2,4]triazolo[1,5-a]pyridin-2-yl)ethyl)amino)methyl)piperi dine-1-carboxylate [0801] To a solution of 2-[8-methyl-6-[(2R)-2-phenylpropoxy]-[1,2,4]triazolo[1,5- a]pyridin-2-yl]acetaldehyde (550.00 mg, 1.78 mmol, 1 eq) and tert-butyl 4-(aminomethyl)-4- hydroxy-piperidine-1-carboxylate (409.45 mg, 1.78 mmol, 1 eq) in MeOH (8 mL) was added HOAc (106.76 mg, 1.78 mmol, 101.77 μL, 1 eq). Then the solution was added NaBH3CN (167.58 mg, 2.67 mmol, 1.5 eq) at 0 °C to three portions. The reaction mixture was stirred at 0 °C for 2 h. LCMS showed the starting material was consumed completely and desired product compound was detected. The reaction mixture was concentrated in vacuum. The reaction mixture was added H2O (15 mL) and then extracted with DCM (20 mL x 3). The combined organic phase was dried, filtered and concentrated to give a residue, which was purified by prep-TLC (SiO2, DCM: MeOH = 10:1) and the eluted with DCM: MeOH = 10:1 (200 mL) to give the title compound (230.00 mg, 25%) as a yellow oil. [0802] LC-MS [ESI, M + 1]: 524.4. [0803] ¹ H NMR (400 MHz, CDCl3) δ = 7.90 (d, J = 2.0 Hz, 1H), 7.38 - 7.33 (m, 2H), 7.29 (d, J = 7.2 Hz, 3H),7.25 (br s, 1H), 7.03 (s, 1H), 4.08 - 4.04 (m, 1H), 3.97 (dd, J = 7.2, 8.8 Hz, 1H), 3.33 - 3.24 (m, 2H), 3.21 - 3.10 (m, 7H), 3.09 - 3.05 (m, 2H), 2.56 (s, 3H), 1.97 (br dd, J = 2.4, 13.2 Hz, 1H), 1.79 - 1.61 (m, 3H), 1.46 - 1.44 (m, 12H). [0804] Step 4: tert-butyl (R)-3-(2-(8-methyl-6-(2-phenylpropoxy)-[1,2,4]triazolo[1,5- a]pyridin-2-yl)ethyl)-2-oxo-1-oxa-3,8-diazaspiro[4.5]decane- 8-carboxylate [0805] To a solution of tert-butyl 4-hydroxy-4-[[2-[8-methyl-6-[(2R)-2-phenylpropoxy]- [1,2,4]triazolo[1,5-a]pyridin-2-yl]ethylamino]methyl]piperid ine-1-carboxylate (210.00 mg, 401.02 μmol, 1 eq) in ACN (5 mL) was added CDI (520.20 mg, 3.21 mmol, 8 eq). The reaction mixture was stirred at 80 °C for 2 h. LCMS showed the starting material was consumed completely and desired product compound was detected. The reaction mixture was concentrated under reduced pressure to give a residue, which was purified by prep-TLC (SiO2, DCM: MeOH = 10:1, Rf = 0.6) and then eluted with DCM: MeOH =10:1 (100 mL) to give the title compound (180.00 mg, 82%) as a yellow oil. [0806] LC-MS [ESI, M + 1]: 550.4. [0807] Step 5: (R)-3-(2-(8-methyl-6-(2-phenylpropoxy)-[1,2,4]triazolo[1,5-a ]pyridin-2- yl)ethyl)-1-oxa-3,8-diazaspiro[4.5]decan-2-one [0808] To a solution of tert-butyl 3-[2-[8-methyl-6-[(2R)-2-phenylpropoxy]- [1,2,4]triazolo[1,5-a]pyridin-2-yl]ethyl]-2-oxo-1-oxa-3,8-di azaspiro[4.5]decane-8- 6.73 mmol, 0.5 mL, 24.67 eq). The reaction mixture was stirred at 25 C for 0.5 h. LCMS showed the starting material was consumed completely and desired compound was detected. The reaction mixture was concentrated under the reduced pressure to give the desired compound (200.00 mg, crude, TFA) as a yellow oil. [0809] LC-MS [ESI, M + 1]: 450.3. [0810] Step 6: (R)-8-([1,2,4]triazolo[4,3-a]pyrazin-8-yl)-3-(2-(8-methyl-6- (2- phenylpropoxy)-[1,2,4]triazolo[1,5-a]pyridin-2-yl)ethyl)-1-o xa-3,8-diazaspiro[4.5]decan- 2-one [0811] To a solution of 3-[2-[8-methyl-6-[(2R)-2-phenylpropoxy]-[1,2,4]triazolo[1,5- a]pyridin-2-yl]ethyl]-1-oxa-3,8-diazaspiro[4.5]decan-2-one (30.00 mg, 53.23 μmol, 1 eq, TFA) and 8-chloro-[1,2,4]triazolo[4,3-a]pyrazine (8.23 mg, 53.23 μmol, 1 eq) in DMA (0.5 mL) was added DIEA (34.40 mg, 266.16 μmol, 46.36 μL, 5 eq). The mixture was stirred at 100 °C for 1 h. LCMS showed the starting compound was consumed completely and desired product compound was detected. The reaction mixture was filtered to give a residue, which was purified by prep-HPLC (column: Phenomenex luna C18150x25mmx 10µm;mobile phase:[water(FA)-ACN];gradient:34%-64% B over 8 min) to give the title compound (9.21 mg, 30%) as a white solid. [0812] LC-MS [ESI, M + 1]: 568.4. [0813] ¹ H NMR (400 MHz, CDCl3) δ = 8.72 (s, 1H), 7.90 (d, J = 1.8 Hz, 1H), 7.43 (d, J = 4.4 Hz, 1H), 7.38 -7.33 (m, 3H), 7.33 - 7.27 (m, 3H), 7.25 (br s, 1H), 7.05 (s, 1H), 5.17 (br s, 2H), 4.11 - 4.04 (m, 1H), 4.02 - 3.96 (m, 1H), 3.87 - 3.76 (m, 4H), 3.37 (s, 2H), 3.32 - 3.25 (m, 1H), 3.17 (t, J = 6.8 Hz, 2H), 2.56 (s, 3H), 2.09 (br d, J = 13.2 Hz, 2H), 1.86 - 1.79 (m, 2H), 1.44 (d, J = 7.2 Hz, 3H). [0814] DSF: **** (see Example 8) Compound Number Synthesis LC/MS DSF ^{1 1} see Example 8 [0815] Compound 68: 2 (2 hydroxy 4 pyridyl) 7 [2 [8 methyl 6 [(2R) 2 phenylpropoxy]-[1,2,4]triazolo[1,5-a]pyridin-2-yl]propyl]-2, 5,7-triazaspiro[3.4]octan-6- one B _oc ,5- a]pyridine [0817] To a solution of methyl 3,3-dimethoxy-2-methyl-propanoate (7.80 g, 48.09 mmol, 1 eq) and 5-bromo-3-methyl-pyridin-1-ium-1,2-diamine;2,4,6-trimethylbe nzenesulfonate (19.35 g, 48.09 mmol, 1 eq) in MeOH (10 mL) was added NaOH (2.89 g, 72.14 mmol, 1.5 eq). The mixture was stirred at 70 °C for 12 h. LCMS showed the starting material was consumed and desired product mass was detected. To the reaction mixture was added FA until pH=8. The mixture was concentrated in vacuo to give the residue, which was purified by reversed-phase HPLC (0.1% FA condition, Gradient B%, 44% 50min; 44% 70 min) to afford the title compound (2.80 g, 19%) as a yellow solid. [0819] H NMR (400 MHz, CDCl ₃ ) δ 8.52 (s, 1H), 7.35 (s, 1H), 4.80 (d, J 8.0 Hz, 1H), 3.49 (m, 1H), 3.43 (s, 3H), 3.32 (s, 3H), 2.63 (s, 3H), 1.42 (d, J = 7.2 Hz, 3H). [0820] Step 2: 2-(2,2-dimethoxy-1-methyl-ethyl)-8-methyl-6-[(2R)-2-phenylpr opoxy]- [1,2,4]triazolo[1,5-a]pyridine [0821] A mixture of 6-bromo-2-(2,2-dimethoxy-1-methyl-ethyl)-8-methyl- [1,2,4]triazolo[1,5-a]pyridine (2.80 g, 8.91 mmol, 1 eq), (2R)-2-phenylpropan-1-ol (12.14 g, 89.12 mmol, 10 eq) , bis[3,5-difluoro-2-[5-(trifluoromethyl)-2-pyridyl]phenyl]iri dium(1+);4- tert-butyl-2-(4-tert-butyl-2-pyridyl)pyridine;hexafluorophos phate (99.99 mg, 89.12 μmol, 0.01 eq), 4-tert-butyl-2-(4-tert-butyl-2-pyridyl)pyridine;dichloronick el (177.35 mg, 445.61 μmol, 0.05 eq) quinuclidine (99.09 mg, 891.22 μmol, 0.1 eq) and 2,2,6,6- tetramethylpiperidine (2.52 g, 17.82 mmol, 3.03 mL, 2 eq) in MeCN (1 mL) was degassed and purged with N2 for 3 times, the reaction vial was then sealed with parafilm, placed 2 cm away from one blue LED, and irradiated at 25 °C for 14 h. LCMS showedthe starting compound was consumed and desired product mass was detected. The mixture was concentrated in vacuo to give the residue, which was purified by column chromatography (SiO2, Petroleum ether/Ethyl acetate=20/1 to 5/1, Rf=0.7) to afford the title compound (2.20 g, 67%) as yellow oil. [0822] LC-MS [ESI, M + 1]: 370.2. [0823] ¹ H NMR (400 MHz, CDCl3) δ = 7.96 - 7.91 (m, 1H), 7.39 - 7.32 (m, 2H), 7.29 (s, 2H), 7.26 - 7.21 (m, 1H), 7.00 (d, J = 0.8 Hz, 1H), 4.80 (d, J = 7.6 Hz, 1H), 4.09 - 3.93 (m, 2H), 3.50 - 3.38 (m, 4H), 3.35 - 3.22 (m, 4H), 2.57 (s, 3H), 1.42 (t, J = 6.8 Hz, 6H). [0824] Step 3: 2-[8-methyl-6-[(2R)-2-phenylpropoxy]-[1,2,4]triazolo[1,5-a]p yridin-2- yl]propanal [0825] To a solution of 2-(2,2-dimethoxy-1-methyl-ethyl)-8-methyl-6-[(2R)-2- phenylpropoxy]-[1,2,4]triazolo[1,5-a]pyridine (500.00 mg, 1.35 mmol, 1 eq) in H2O (1.5 mL) was added TFA (2.30 g, 20.19 mmol, 1.5 mL, 14.92 eq). The mixture was stirred at 40 °C for 3 h. LCMS showed the starting compound was consumed and desired product mass was detected. The reaction mixture was adjusted to pH 7 with saturated NaHCO ₃ solution, and then extracted with DCM (20 mL x 3). The combined organic layer was washed with brine (10 mL × 3), dried, filtered, and concentrated under pressure to afford the title compound (520 mg, 73%) as a white solid. [0826] LC-MS [ESI, M + 1]: 324.2. [1,2,4]triazolo[1,5 a]pyridin 2 yl]propylamino]methyl]azetidine 1 carboxylate [0828] To a solution of 2-[8-methyl-6-[(2R)-2-phenylpropoxy]-[1,2,4]triazolo[1,5- a]pyridin-2-yl]propanal (437.00 mg, 1.35 mmol, 1 eq) and tert-butyl 3-amino-3- (aminomethyl)azetidine-1-carboxylate (271.97 mg, 1.35 mmol, 1 eq) in MeOH (5 mL) was added NaBH ₃ CN (254.76 mg, 4.05 mmol, 3 eq) and AcOH (284.02 mg, 4.73 mmol, 270.76 μL, 3.5 eq). The mixture was stirred at 0 °C for 1 h. LCMS showed the starting material was consumed and desired product mass was detected. The reaction mixture was added extracted with DCM (3 x 20 mL). The combined organic layers were washed with brine (20 mL), dried, filtered and the filtrate was concentrated in vacuo to afford the title compound (550.00 mg, 80%) as yellow oil. [0829] LC-MS [ESI, M + 1]: 509.2. [0830] Step 5: Tert-butyl 7-[2-[8-methyl-6-[(2R)-2-phenylpropoxy]-[1,2,4]triazolo[1,5- a]pyridin-2-yl]propyl]-6-oxo-2,5,7-triazaspiro[3.4]octane-2- carboxylate [0831] To a solution of tert-butyl 3-amino-3-[[2-[8-methyl-6-[(2R)-2-phenylpropoxy]- [1,2,4]triazolo[1,5-a]pyridin-2-yl]propylamino]methyl]azetid ine-1-carboxylate (550 mg, 1.08 mmol, 1 eq) in DCM (5 mL) was added CDI (701.32 mg, 4.33 mmol, 4 eq). The mixture was stirred at 40 °C for 2 h. LCMS showed the starting material was consumed and desired product mass was detected. The reaction mixture was extracted with DCM (3 x 20 mL). The combined organic layers were washed with brine (20 mL), dried, filtered and the filtrate was concentrated in vacuo to give the residue, which was purified by prep-HPLC (column: Phenomenex luna C18150x25mmx 10µm;mobile phase: [water(FA)-ACN];gradient:47%- 77% B over 10 min) to afford the title compound (80.00 mg, 13%) as a white solid. [0832] LC-MS [ESI, M + 1]: 535.3. [0833] Step 6: 7-[2-[8-methyl-6-[(2R)-2-phenylpropoxy]-[1,2,4]triazolo[1,5- a]pyridin- 2-yl]propyl]-2,5,7-triazaspiro[3.4]octan-6-one [0834] To a solution of tert-butyl 7-[2-[8-methyl-6-[(2R)-2-phenylpropoxy]- [1,2,4]triazolo[1,5-a]pyridin-2-yl]propyl]-6-oxo-2,5,7-triaz aspiro[3.4]octane-2-carboxylate (40.00 mg, 74.82 μmol, 1 eq) in DCM (1 mL) was added TsOH.H ₂ O (42.69 mg, 224.45 μmol, 3 eq). The mixture was stirred at 25 °C for 1 h. LCMS showed the starting material was consumed and desired product mass was detected. The mixture was concentrated in vacuo to afford the title compound (32.50 mg, 100%) as a white solid. [0835] LC-MS [ESI, M + 1]: 435.2. [1,2,4]triazolo[1,5 a]pyridin 2 yl]propyl] 2,5,7 triazaspiro[3.4]octan 6 one (HMP 2145) [0837] To a solution of 7-[2-[8-methyl-6-[(2R)-2-phenylpropoxy]-[1,2,4]triazolo[1,5- a]pyridin-2-yl]propyl]-2,5,7-triazaspiro[3.4]octan-6-one and (2-hydroxy-4-pyridyl) trifluoromethanesulfonate (18.19 mg, 74.79 μmol, 1 eq) in DMF (0.5 mL) was added DIEA (38.67 mg, 299.17 μmol, 52.11 μL, 4 eq). The mixture was stirred at 100 °C for 1 h. LCMS showed the starting material was consumed and desired product mass was detected. The mixture was concentrated in vacuo to give the residue, which was purified by prep-HPLC (column: Phenomenex luna C18150x25mmx10µm;mobile phase: [water(FA)- ACN];gradient:25%-55% B over 10 min) to afford the title compound(11.33 mg, 28%) as a white solid. [0838] LC-MS [ESI, M + 1]: 528.2. [0839] ¹ H NMR (400 MHz, CDCl3) δ = 7.94 (s, 1H), 7.38 - 7.31 (m, 2H), 7.30 (s, 2H), 7.25 (s, 1H), 7.09 (d, J = 6.4 Hz, 1H), 7.03 (s, 1H), 5.49 (d, J = 7.2 Hz, 2H), 5.21 (s, 1H), 4.09 - 4.03 (m, 1H), 4.02 - 3.91 (m, 4H), 3.87 (d, J = 8.4 Hz, 1H), 3.70 - 3.53 (m, 3H), 3.47 (d, J = 9.6 Hz, 1H), 3.42 - 3.34 (m, 1H), 3.32 - 3.24 (m, 1H), 2.56 (s, 3H), 1.43 (t, J = 6.0 Hz, 6H). [0840] DSF: **** (see Example 8) EXAMPLE 7 [0841] Compound 28: (R)-9-([1,2,4]triazolo[4,3-a]pyrazin-8-yl)-2-(2-(8-methyl-6- (3- methyl-3-phenylpyrrolidin-1-yl)-[1,2,4]triazolo[1,5-a]pyridi n-2-yl)ethyl)-2,9- diazaspiro[5.5]undecan-1-one

decane-9-carboxylic acid [0843] To a solution of tert-butyl 1-oxo-2,9-diazaspiro[5.5]undecane-9-carboxylate (2.00 g, 7.45 mmol, 1 eq) in THF (20 mL) was added NaH (298.12 mg, 7.45 mmol, 60% purity, 1 eq) and methyl prop-2-enoate (1.28 g, 14.91 mmol, 1.34 mL, 2 eq) at 0 °C under N2. The mixture was stirred at 25 °C for 2 h. LCMS showed starting material was consumed completely and desired mass was detected. The reaction mixture was quenched by addition H2O (10 mL) and extracted with EtOAc (20 mL x 3). The combined organic layers were washed with brine (20 mL x 1), dried over Na2SO4, filtered and concentrated under reduced pressure to give the desired compound (1.10 g, crude) as a yellow solid. [0844] LC-MS [ESI, M + 1]: 341.2. [0845] Step 2: tert-butyl 2-(2-(6-bromo-8-methyl-[1,2,4]triazolo[1,5-a]pyridin-2- yl)ethyl)-1-oxo-2,9 diazaspiro[5.5]undecane-9-carboxylate [0846] To a solution of 3-(9-tert-butoxycarbonyl-1-oxo-2,9-diazaspiro[5.5]undecan-2- yl)propanoic acid (1.10 g, 2.94 mmol, 1 eq) and 5-bromo-3-methyl-pyridin-1-ium-1,2- diamine; 2,4,6 trimethylbenzenesulfonate (1.77 g, 4.41 mmol, 1.5 eq) in DMF (15 mL) was added HATU (2.23 g, 5.88 mmol, 2 eq) and DIEA (1.90 g, 14.69 mmol, 2.56 mL, 5 eq). The reaction mixture was added H2O (10 mL) and then extracted with EtOAc (15 mL x 5). The combined organic phase was washed with brine (15 mL x 5) dried, filtered and concentrated in vacuum, which was purified by flash silica gel chromatography (ISCO®; 20 g SepaFlash® Silica Flash Column, Eluent of 55~65% Ethyl acetate/Petroleum ethergradient @ 80 mL/min) to afford the desired compound (400 mg, 27%) as a yellow solid. [0847] ¹ H NMR (400 MHz, DMSO-d ₆ ) δ = 9.11 (d, J = 0.8 Hz, 1H), 7.62 (s, 1H), 3.64 - 3.57 (m, 5H), 3.24 (br s, 2H), 2.99(br t, J = 7.2 Hz, 3H), 2.52 - 2.51 (m, 3H), 1.88 - 1.62 (m, 8H), 1.39 (s, 9H). [0848] LC-MS [ESI, M + 1]: 506.3. [1,2,4]triazolo[1,5 a]pyridin 2 yl)ethyl) 1 oxo 2,9 diazaspiro[5.5]undecane 9 carboxylate [0850] To a solution of tert-butyl 2-[2-(6-bromo-8-methyl-[1,2,4]triazolo[1,5-a]pyridin-2- yl)ethyl]-1-oxo-2,9- diazaspiro[5.5]undecane-9-carboxylate (150.00 mg, 296.19 μmol, 1 eq) and (3R)-3-methyl-3-phenyl-pyrrolidine (47.76 mg, 296.19 μmol, 1 eq) in dioxane (3 mL) was added Pd-PEPPSI-IHeptCl (28.81 mg, 29.62 μmol, 0.1 eq) and Cs2CO3 (289.51 mg, 888.56 μmol, 3 eq). The mixture was stirred at 100 °C for 2 h under N ₂ . LCMS showed starting material was consumed and desired mass was detected. The reaction mixture was filtered and the filtrated was concentrated in vacuum, which was purified by prep-TLC (SiO ₂ , Petroleum ether/Ethyl acetate = 0:1, Rf = 0.3) and the eluted with EtOAc (200 mL) to give the desired compound (100.00 mg, 58%) as a yellow oil. [0851] ¹ H NMR (400 MHz, CDCl3) δ = 7.59 (d, J = 2 Hz, 1H), 7.39 - 7.34 (m, 2H), 7.34 - 7.30 (m, 2H), 7.27 -7.23 (m, 1H), 6.91 (s, 1H), 3.83 - 3.74 (m, 4H), 3.59 (d, J = 8.8 Hz, 1H), 3.55 - 3.50 (m, 1H), 3.47 (d, J = 8.8 Hz, 1H), 3.39 (dt, J = 3.6, 8.7 Hz, 1H), 3.26 (br s, 2H), 3.19 - 3.10 (m, 4H), 2.63 - 2.58 (m, 3H), 2.37 (td, J = 8.4, 12.1 Hz, 1H), 2.30 - 2.21 (m, 1H), 1.84 - 1.64 (m, 8H), 1.48 - 1.44 (m, 12H). [0852] LC-MS [ESI, M + 1]: 587.5. [0853] Step 4: (R)-2-(2-(8-methyl-6-(3-methyl-3-phenylpyrrolidin-1-yl)- [1,2,4]triazolo[1,5-a]pyridin-2-yl)ethyl)-2,9-diazaspiro[5.5 ]undecan-1-one [0854] To a solution of tert-butyl 2-[2-[8-methyl-6-[(3R)-3-methyl-3-phenyl-pyrrolidin-1- yl]-[1,2,4]triazolo[1,5-a]pyridin-2-yl]ethyl]-1-oxo-2,9-diaz aspiro[5.5]undecane-9-carboxylate (100.00 mg, 170.43 μmol, 1 eq) in DCM (2 mL) was added HCl/dioxane (4 M, 2 mL, 46.94 eq) .The mixture was stirred at 25 °C for 1 h. LCMS showed starting material was consumed and desired mass was detected. The reaction mixture was concentrated in vacuum, which was purified by prep-HPLC (column: Phenomenex luna C18150x25mmx10µm; mobile phase: [water(HCl)-ACN]; gradient:25%-55% B over 10 min) to give the desired compound (90.00 mg, 99%) as a yellow solid. [0855] ¹ H NMR (400 MHz, DMSO-d ₆ ) δ = 8.93 (br d, J = 1.6 Hz, 1H), 8.66 (br d, J = 4.0 Hz, 1H), 8.08 (s, 1H), 7.53 (s, 1H), 7.41 - 7.33 (m, 4H), 7.27 - 7.21 (m, 1H), 3.66 (br s, 2H), 3.61 (br d, J = 10.0 Hz, 2H), 3.54 (br d, J = 10.0 Hz, 2H), 3.50 (br s, 1H), 3.41 - 3.37 (m, 1H), 3.34 (br t, J = 5.6 Hz, 2H), 2.94 (br d, J = 6.4 Hz, 2H), 3.09 (br d, J = 6.8 Hz, 5H), 2.57 (s, 3H), 2.28 (br t, J = 6.8 Hz, 2H), 1.98 - 1.89 (m, 2H), 1.75 (br t, J = 7.6 Hz, 4H), 1.61 - 1.51 (m, 2H), 1.35 (s,3H). [0857] Step 5: (R) 9 ([1,2,4]triazolo[4,3 a]pyrazin 8 yl) 2 (2 (8 methyl 6 (3 methyl 3 phenylpyrrolidin-1-yl)-[1,2,4]triazolo[1,5-a]pyridin-2-yl)et hyl)-2,9- diazaspiro[5.5]undecan-1-one [0858] To a solution of 2-[2-[8-methyl-6-[(3R)-3-methyl-3-phenyl-pyrrolidin-1-yl]- [1,2,4]triazolo[1,5-a]pyridin-2-yl]ethyl]-2,9-diazaspiro[5.5 ]undecan-1-one (25.00 mg, 47.79 μmol, 1 eq, HCl) and 8-chloro-[1,2,4]triazolo[4,3-a]pyrazine (8.13 mg, 52.57 μmol, 1.1 eq) in DMA (0.5 mL) was added DIEA (30.88 mg, 238.96 μmol, 41.62 μL, 5 eq). The mixture was stirred at 100 °C for 1 h. LCMS showed starting material was consumed and desired mass was detected. The reaction mixture was filtered to give a residue, which was purified by prep- HPLC (column: Phenomenex luna C18150x25mmx10µm;mobile phase: [water(FA)- ACN];gradient:27%-57% B over 10 min) and prep-HPLC (column: Waters xbridge 150x25mmx10µm; mobile phase: [water(NH4OAc)-ACN];gradient:35%-65% B over 10 min) to give Compound 28 (10.09 mg, 34%) as a white gum. [0859] ¹ H NMR (400 MHz, CH3OD) δ = 9.07 (s, 1H), 7.77 - 7.63 (m, 2H), 7.40 - 7.26 (m, 5H), 7.23 - 7.16 (m, 2H),3.84 - 3.73 (m, 4H), 3.58 - 3.50 (m, 3H), 3.44 - 3.32 (m, 5H), 3.07 (t, J = 6.8 Hz, 2H), 2.56 (s, 3H), 2.38 - 2.26 (m,2H), 2.08 (ddd, J = 4, 10.2, 13.9 Hz, 2H), 1.96 - 1.85 (m, 4H), 1.58 (br d, J = 14 Hz, 2H), 1.43 (s, 3H). [0860] LC-MS [ESI, M + 1]: 605.5. [0861] DSF: ***** (see Example 8) Compound Number Synthesis LC/MS DSF ^{1 1} see Example 8 EXAMPLE 8 [0862] Differential Scanning Fluorimetry Assay [0863] The stabilization effects the compounds have on the immunoglobulin light chain protein were quantitively measured using a thermal shift assay. Recombinant amyloidogenic full length light chain protein WIL-FL T46L was produced in E. coli, purified, and used in the assay. The Thermal Shift Protein Stability Kit from Biotium was used and the assay was done in 96-well plates following the manufacturer’s instructions. The protein and compounds were incubated at RT for 30 min before adding the dye and subjected to the thermal shift assay. The thermal stability (Tm) of each sample was then determined using standard curve [Tm] _compound [Tm] _vehicle . [0864] Results [0865] 0-0.5 ⁰C = * [0866] >0.5-1 ⁰C = ** [0867] > 1-1.5 ⁰C = *** [0868] >1.5-2.5 ⁰C = **** [0869] >2.5 °C = ***** [0870] This disclosure is not to be limited in scope by the embodiments disclosed in the examples which are intended as single illustrations of individual aspects, and any equivalents are within the scope of this disclosure. Various modifications in addition to those shown and described herein will become apparent to those skilled in the art from the foregoing description. Such modifications are intended to fall within the scope of the appended claims. [0871] Various references such as patents, patent applications, and publications are cited herein, the disclosures of which are hereby incorporated by reference herein in their entireties.