AU2013203566B2 - Crystalline peptide epoxy ketone protease inhibitors and the synthesis of amino acid keto-epoxides - Google Patents

Abstract

The invention relates to crystalline peptide keto epoxide compounds, methods of their preparation, and related pharmaceutical compositions. This invention also relates to methods for the preparation of amino acid keto-epoxides. Specifically, allylic ketones 5 are stereoselectively converted to the desired keto epoxides.

Description

CRYSTALLINE PEPTIDE EPOXY KETONE PROTEASE INHIBITORS AND THE SYNTHESIS OF AMINO ACID KETO-EPOXIDES

The present application is a divisional application of Australian Application No. 2008307510, which is incorporated in its entirety herein by reference.

Related Applications

This application claims the benefit of priority of U.S. Provisional Patent Application Serial No. 60/997,613 filed on October 4, 2007 and U.S. Provisional Patent Application Serial No. 61/008,987 filed on December 20, 2007, the teachings of which are incorporated by reference in their entirety.

Background of the Invention

In eukaryotes, protein degradation is predominately mediated through the ubiquitin pathway in which proteins targeted for destruction are ligated to the 76 amino acid polypeptide ubiquitin. Once targeted, ubiquitinated proteins then serve as substrates for the 26S proteasome, a multicatalytic protease, which cleaves proteins into short peptides through the action of its three major proteolytic activities. While having a general function in intracellular protein turnover, proteasome-mediated degradation also plays a key role in many processes such as major histocompatibility complex (MHC) class I antigen presentation, apoptosis, cell growth regulation, NF-κΒ activation, antigen processing, and transduction of pro-inflammatory signals.

The 20S proteasome is a 700 kDa cylindrical-shaped multicatalytic protease complex comprised of 28 subunits organized into four rings. In yeast and other eukaryotes, 7 different a subunits form the outer rings and 7 different β subunits comprise the inner rings. The a subunits serve as binding sites for the 19S (PA700) and 1 IS (PA28) regulatory complexes, as well as a physical barrier for the inner proteolytic chamber formed by the two β subunit rings. Thus, in vivo, the proteasome is believed to exist as a 26S particle (“the 26S proteasome”). In vivo experiments have shown that inhibition of the 20S form of the proteasome can be readily correlated to inhibition of 26S proteasome. Cleavage of amino-terminal prosequences of β subunits during particle formation expose amino-terminal threonine residues, which serve as the catalytic nucleophiles. The subunits responsible for catalytic activity in proteasomes thus possess an amino terminal nucleophilic residue, and these subunits belong to the family of N- terminal nucleophile (Ntn) hydrolases (where the nucleophilic N-terminal residue is, for example, Cys, Ser, Thr, and other nucleophilic moieties). This family includes, for_ example, penicillin G acylase (PGA), penicillin V acylase (PVA), glutamine PRPP amidotransferase (GAT), and bacterial glycosylasparaginase. In addition to the ubiquitously expressed β subunits, higher vertebrates also possess three interferon-y-inducible β subunits (LMP7, LMP2 and MECLI), which replace their normal counterparts, X, Y and Z respectively, thus altering the catalytic activities of the proteasome. Through the use of different peptide substrates, three major proteolytic activities have been defined for the eukaryote 20S proteasome: chymotrypsin-like activity (CT-L), which cleaves after large hydrophobic residues; trypsin-like activity (ΤΙ), which cleaves after basic residues; and peptidylglutamyl peptide hydrolyzing activity (PGPH), which cleaves after acidic residues. Two additional less characterized activities have also been ascribed to the proteasome: BrAAP activity, which cleaves after branched-chain amino acids; and SNAAP activity, which cleaves after small neutral amino acids. The major proteasome proteolytic activities appear to be contributed by different catalytic sites, since inhibitors, point mutations in β subunits and the exchange of γ interferon-inducing β subunits alter these activities to various degrees.

What is needed are improved compositions and methods for preparing and formulating proteasome inhibitor(s).

Any discussion of the prior art throughout the specification should in no way be considered as an admission that such prior art is widely known or forms part of common general knowledge in the field.

Summary of the Invention

The invention generally relates to the synthesis of proteasome inhibitors and the preparation and purification of intermediates useful therefor.

According to a first aspect, the present invention provides a crystalline compound having a structure of Formula (II)

(II) and having a melting point of about 211 to about 213 °C.

According to a second aspect, the present invention provides a crystalline compound having a structure of Formula (II)

(II) and having an XRPD pattern substantially as shown in Figure 2.

According to a third aspect, the present invention provides a crystalline compound having a structure of Formula (II)

(II) and having 2Θ values 6.10; 8.10; 9.32; 10.10; 11.00; 12.14; 12.50; 13.64; 13.94; 17.14; 17.52; 18.44; 20.38; 21.00; 22.26; 23.30; 24.66; 25.98; 26.02; 27.84; 28.00; 28.16; 29.98; 30.46; 32.98; 33.22; 34.52; 39.46.

According to a fourth aspect, the present invention provides a crystalline salt of a compound having a structure of Formula (II)

(II) and having a melting point of about 184 to about 188 °C, wherein the salt is a citrate salt.

According to a fifth aspect, the present invention provides a crystalline salt of a compound having a structure of Formula (II)

(II) and having an XRPD pattern substantially as shown in Figure 12, wherein the salt is a citrate salt.

According to a sixth aspect, the present invention provides a crystalline salt of a compound having a structure of Formula (II)

(N) and having 2Θ values 4.40; 7.22; 9.12; 12.36; 13.35; 14.34; 15.54; 16.14; 16.54; 17.00; 18.24; 18.58; 19.70; 19.90; 20.30; 20.42; 21.84; 22.02; 23.34; 23.84; 24.04; 24.08; 24.48; 24.76; 25.48; 26.18; 28.14; 28.20; 28.64; 29.64; 31.04; 31.84; 33.00; 33.20; 34.06; 34.30; 34.50; 35.18; 37.48; 37.90; 39.48, wherein the salt is a citrate salt.

According to a seventh aspect, the present invention provides a phamaceutical composition comprising a crystalline compound of the first aspect and a pharmaceutically acceptable carrier.

According to an eighth aspect, the present invention provides a method for treating a disease or condition selected from cancer, autoimmune disease, graft or transplant-related condition, neurodegenerative disease, fibrotic-associated condition, ischemic-related conditions, infection (viral, parasitic or prokaryotic) and diseases associated with bone loss, comprising administering a crystalline compound of the first aspect or a phamaceutical composition of the third aspect.

According to a ninth aspect, the present invention provides use of a crystalline compound of the first aspect for the manufacture of a medicament for treating a disease or condition selected from cancer, autoimmune disease, graft or transplant-related condition, neurodegenerative disease, fibrotic-associated condition, ischemic-related conditions, infection (viral, parasitic or prokaryotic) and diseases associated with bone loss.

Unless the context clearly requires otherwise, throughout the description and the claims, the words “comprise”, “comprising”, and the like are to be construed in an inclusive sense as opposed to an exclusive or exhaustive sense; that is to say, in the sense of “including, but not limited to”.

Another aspect of the invention relates to crystalline compounds having a structure of Formula (I) or a pharmaceutically acceptable salt thereof,

I wherein X is Ο, NH, or N-alkyl, preferably O; Y is NH, N-alkyl, 0, orC(R9)2, preferably N-alkyl, 0, orC(R9)2; Z is 0 or C(R9)2, preferably C(R9)2; R1, R2, R3, and R4 are hydrogen; 5 6 7 8 9 each of R , R , R , R , and R is independently selected from hydrogen, Ci^alkyl, C|_6hydroxyalkyl, C|_6alkoxyalkyl, aryl, and C^aralkyl, each of which is optionally substituted with a group selected from alkyl, amide, amine, carboxylic acid or a pharmaceutically acceptable salt thereof, carboxyl ester, thiol, and thioether, preferably R , R , R , and R are independently selected from Ct.6alkyl, Cj^hydroxyalkyl, and C(_ 6aralkyl and each R9 is hydrogen, more preferably, R6 and Rs are independently C|.ealkyl, R5 and R7 are independently C;_f,aralkyi and each R9 is H; m is an integer from 0 to 2; and n is an integer from 0 to 2, preferably 0 or 1.

Another aspect of the invention relates to a crystalline compound of Formula (III)

(III) wherein X is any suitable counterion.

Another aspect of this invention relates to methods for the synthesis of amino acid keto-epoxides according to scheme (I)

(I) wherein R1 is selected from a protecting group or a further chain of amino acids, which itself may be optionally substituted, preferably a protecting group, most preferably an electron withdrawing protecting group; R2 is selected from hydrogen and Ci-ealkyl; R3 is selected from hydrogen, C^aUcyi, C|_6alkoxyalkyl, heterocyclyl, aryl, heteroaryl, C|_6heteroaralkyl, and C|.6aralkyl; and wherein the method comprises a stereoselective epoxidation under epoxidizing conditions, preferably an aqueous sodium hypochlorite (bleach) or calcium hypochlorite solution in the presence of a cosolvent selected from pyridine, acetonitrile, dimethylformamide (DMF), dimethylsulfoxide (DMSO), N-methylpyrrolidine (NMP), dimethylacetamide (DMA), tetrahydrofuran (THF), and nitromethane.

Brief Description of the Figures

Figure 1 shows a DSC (differential scanning calorimetry) thermogram of crystalline compound 1.

Figure 2 shows an XRPD (X-ray powder diffraction) pattern of crystalline compound 1.

Figure 3 shows a TG thermogram of crystalline compound 1.

Figure 4 shows a DSC thermogram of amorphous compound 1 compared to a DSC thermogram of crystalline compound 1.

Figure 5 shows an XRPD pattern of amorphous compound 1 compared to the XRPD pattern of crystalline compound 1.

Figure 6 shows a TG thermogram of amorphous compound t compared to the TG pattern of crystalline compound 1.

Figure 7 shows a DSC curve of an amorphous sample of compound 1.

Figure 8 shows the XRPD pattern of amorphous compound 1.

Figure 9 shows a DSC curve of a crystalline compound F.

Figure 10 shows an XRPD pattern of a crystalline compound F.

Figure 11 shows a DSC curve of a crystalline citrate salt of compound 1.

Figure 12 shows an XRPD pattern of a crystalline citrate salt of compound 1.

Detailed Description of the Invention

In certain embodiments, the invention relates to crystalline compounds having a structure of Formula (I) or a pharmaceutically acceptable salt thereof,

I wherein X is Ο, NH, or N-alkyl, preferably O; Y is NH, N-alkyl, O, or C(R9)2, preferably N-alkyl, O, or C(R9)2; Z is O or C(R9)2, preferably C(R9)2; R1, R2, R3, and R4 are hydrogen; each of R5, R9, R7, R8, and R9 is independently selected from hydrogen, C|.6alkyl, Ci^hydroxyalkyl, C|.6alkoxyalkyl, aryl, and C|.6aralkyl, each of which is optionally substituted with a group selected from alkyl, amide, amine, carboxylic acid or a pharmaceutically acceptable salt thereof, carboxyl ester, thiol, and thioether, preferably R3, R6, R7, and Rx are independently selected from C|.6alkyl, Ci-ehydroxyalkyl, and C|. 6aralkyl and each R is hydrogen, more preferably, R and R' are independently Cj^alkyl, R5 and R7 are independently C|_6aralkyl and each R9 is H; m is an integer from 0 to 2; and n is an integer from 0 to 2, preferably 0 or 1.

In certain embodiments, X is O and R1, R2, R3, and R4 are all the same, preferably R1, R2, R3, and R4 are all hydrogen. In certain such embodiments, R5, R6, R7, and R8 are independently selected from Ci-^alkyl, Ci^hydroxyalkyl, and C|.6aralkyl, more preferably, R6 and Rs are independently Ci^alkyl and R5 and R7 are independently C|. 6aralkyl.

In certain preferred embodiments, X is O, R1, R2. R\ and R4 are all hydrogen, R6 Q # C , Ί and R are both isobutyl, R is phenylethyl, and R is phenylmethyl. r £ η ο

In certain embodiments, R , R , R , and R are independently selected from hydrogen, Ci^alkyl, Q-ehydroxyalkyl, C|_6alkoxyalkyl, aryl, and C^aralkyl, each of which is optionally substituted with a group selected from alkyl, amide, amine, carboxylic acid or a pharmaceutically acceptable salt thereof, carboxyl ester, thiol, and thioether. In certain embodiments, at least one of R and R is C|.&aralkyl substituted with alkyl, more preferably substituted with perhaloalkyl. In certain such embodiments, R7 is Ci^aralkyl substituted with trifluoromethyl.

In certain embodiments, Y is selected from N-alkyl, O, and CH2. In certain such embodiments, Z is CH2, and m and n are both 0. In certain alternative such embodiments, Z is CH2, m is 0, and n is 2 or 3. In yet another alternative such embodiments, Z is O, m is 1, and n is 2.

In certain embodiments, the invention relates to a crystalline compound of Formula (II)

(II)

In certain embodiments, the invention relates to a method for the preparation of a crystalline compound of Formula (I) or (II), comprising one or more of: (i) preparing the amorphous compound, e.g., according to U.S. Patent No. 7,232,818; (ii) dissolving the amorphous compound in an organic solvent; (iii) bringing the solution to supersaturation to cause formation of crystals; and (iv) isolating the crystals, e.g., by filtering the crystals, by decanting fluid from the crystals, or by any other suitable separation technique. In certain embodiments, preparation further comprises inducing crystallization. In certain embodiments, preparation further comprises washing the filtered crystals, e.g., with a solvent or non-solvent fluid. In certain embodiments, preparation further comprises drying, preferably under reduced pressure, such as under vacuum pressure.

In certain embodiments, the invention relates to a method for the preparation of a crystalline compound of Formula (I) or (II), comprising one or more of: (i) preparing a solution of the amorphous compound, which compound may be prepared according to, for example, U.S. Patent No. 7,232,818, in an organic solvent; (ii) bringing the solution to supersaturation to cause formation of crystals; and (iii) isolating the crystals, e.g., by filtering the crystals, by decanting fluid from the crystals, or by any other suitable separation technique. In certain embodiments, preparation further comprises inducing crystallization. In certain embodiments, preparation further comprises washing the filtered crystals, e.g., with a solvent or non-solvent fluid. In certain embodiments, preparation further comprises drying, preferably under reduced pressure, such as under vacuum pressure.

In certain embodiments, the amorphous compound may be dissolved in an organic solvent selected from acetonitrile, methanol, ethanol, ethyl acetate, isopropanol, isopropyl acetate, isobuty! acetate, butyl acetate, propyl acetate, methylethyl ketone, methylisobutyl ketone, and acetone, or any combination thereof. In certain embodiments, the amorphous compound may be dissolved in an organic solvent selected from acetonitrile, methanol, ethanol, ethyl acetate, isopropyl acetate, methylethyl ketone, and acetone, or any combination thereof. In certain embodiments, the amorphous compound may be dissolved in an organic solvent selected from acetonitrile, methanol, ethanol, ethyl acetate, methylethylketone, or any combination thereof. In certain embodiments, the organic solvent or solvents may be combined with water.

In certain embodiments, bringing the solution to supersaturation comprises the addition of an anti-solvent, such as water or another polar liquid miscible with the organic solvent, allowing the solution to cool, reducing the volume of the solution, or any combination thereof. In certain embodiments, bringing the solution to supersaturation comprises adding an anti-solvent, cooling the solution to ambient temperature or lower, and reducing the volume of the solution, e.g., by evaporating solvent from the solution.

In certain embodiments, allowing the solution to cool may be passive (e.g., allowing the solution to stand at ambient temperature) or active (e.g., cooling the solution in an ice bath or freezer).

In certain embodiments, the method further comprises inducing precipitation or crystallization. In certain embodiments inducing precipitation or crystallization comprises secondary nucleation, wherein nucleation occurs in the presence of seed crystals or interactions with the environment (crystallizer walls, stirring impellers, sonication, etc.).

In certain embodiments, washing the crystals comprises washing with a liquid selected from anti-solvent, acetonitrile, methanol, ethanol, ethyl acetate, methylethyl ketone, acetone, or a combination thereof. Preferably the crystals are washed with a combination of anti-solvent and the organic solvent. In certain embodiments, the antisolvent is water.

In certain embodiments, washing the crystals comprises washing the crystalline compound of Formula (II) with methanol and water.

In certain embodiments, a crystalline compound of Formula (II) is substantially pure. In certain embodiments, the melting point of the crystalline compound of Formula (II) is in the range of about 200 to about 220 °C, about 205 to about 215 °C, about 211 to about 213 °C, or even about 212 °C.

In certain embodiments, the DSC of a crystalline compound of Formula (II) has a sharp endothermic maximum at about 2! 2 °C, e.g., resulting from melting and decomposition of the crystalline form as shown in Figure 1.

In certain embodiments, the X-ray powder pattern of a crystalline compound of Formula (II) is (Θ-2Θ°): 6.10; 8.10; 9.32; 10.10; 11.00; 12.14; 122.50; 13.64; 13.94; 17.14; 17.52; 18.44; 20.38; 21.00; 22.26; 23.30; 24.66; 25.98; 26.02; 27.84; 28.00; 28.16; 29.98; 30.46; 32.98; 33.22; 34.52; 39.46 as shown in Figure 2.

In certain embodiments, the TG thermogram of a crystalline compound of Formula (11) exhibits from 0.0 to 0.1% weight loss in the temperature range of 25 to 200 °C as shown in Figure 3.

In certain embodiments, a crystalline compound of Formula (II) is not solvated (e.g., the crystal lattice does not comprise molecules of a solvent). In certain alternative embodiments, a crystalline compound of Formula (II) is solvated.

In certain embodiments, the invention relates to a method for the preparation of an amorphous compound of Formula (II) comprising one or more of (i) dissolving the crystalline compound in an organic solvent; (ii) bringing the solution to supersaturation to cause formation of crystals; and (iii) isolating the crystals, e.g., by filtering the crystals, by decanting fluid from the crystals, or by any other suitable separation technique. In certain embodiments, preparation further comprises inducing precipitation. In certain embodiments, preparation further comprises washing the amorphous compound. In certain embodiments, the method further comprises drying, preferably under reduced pressure, such as under vacuum pressure. In certain embodiments, the invention relates to a crystalline salt of a compound of Formula (I) or (II), wherein the salt counterion is selected from bromide, chloride, sulfate, phosphate, nitrate, acetate, trifluoroacetate, citrate, mcthanesulfonate, valerate, oleate, palmitate, stearate, laurate, benzoate, lactate, succinate, tosylate, malonate, maleate, fiimarate, succinate, tartrate, mesylate, 2-hydroxyethansulfonate, and the like. In certain such embodiments, the salt counterion is selected from citrate, tartrate, trifluoroacetate, methanesulfonate, toluenesulfonatc, chloride, and bromide, preferably citrate.

In certain embodiments, the invention relates to a method for the preparation of a crystalline salt of a compound of Formula (II), comprising one or more of: (i) preparing the amorphous compound e.g., according to U.S. Patent No. 7,232,818; (ii) dissolving the amorphous compound in an organic solvent; (iii) bringing the solution to supersaturation to cause formation of crystals; and (iv) isolating the crystals, e.g., by filtering the crystals, by decanting fluid from the crystals, or by any other suitable separation technique. In certain embodiments, preparation further comprises inducing crystallization. In certain embodiments, preparation further comprises washing the crystals, e.g., with a solvent or non-solvent fluid. In certain embodiments, preparation further comprises drying, preferably under reduced pressure, such as under vacuum pressure.

In certain embodiments, the invention relates to a method for the preparation of a crystalline salt of a compound of Formula (II), comprising one or more of (i) preparing a solution of a compound of Formula (11) in an organic solvent; (ii) adding a suitable acid; (iii) bringing the solution to supersaturation to cause formation of crystals; and (iv) isolating the crystals, e.g., by filtering the crystals, by decanting fluid from the crystals, or by any other suitable separation technique. In certain embodiments, preparation further comprises inducing crystallization. In certain embodiments, preparation further comprises washing the crystals, e.g., with a solvent or non-solvent fluid. In certain embodiments, preparation further comprises drying, preferably under reduced pressure. such as under vacuum pressure. In certain embodiments where the salt is less soluble in a solvent than the free base, adding the acid to a solution may itself be sufficient to bring the solution to supersaturation.

In certain embodiments, the salt counterion is selected from selected from bromide, chloride, sulfate, phosphate, nitrate, acetate, trifluoroacetate, citrate, methanesulfonate, valerate, oleate, palmitate, stearate, laurate, benzoate, lactate, succinate, tosylate, malonate, maleate, fumarate, succinate, tartrate, mesylate, 2-hydroxyethansulfonate, and the like. In certain such embodiments, the salt counterion is selected from citrate, tartrate, trifluoroacetate, methanesulfonate, toluenesulfonate, chloride, and bromide, preferably citrate.

In certain embodiments, the organic solvent is selected from THF, acetonitrile, ether, and MTBE, or any combination thereof, preferably THF or acetonitrile, or a combination thereof.

In certain embodiments, a crystalline citrate salt of a compound of Formula (II) is substantially pure. In certain embodiments, the melting point of the crystalline citrate salt of a compound of Formula (II) is in the range of about 180 to about 190 °C or even about 184 to about 188 °C.

In certain embodiments, the DSC of a crystalline citrate salt of a compound of Fonnula (II) has a sharp endothermic maximum at about 187 °C, e.g., resulting from melting and decomposition of the crystalline form as shown in Figure 11.

In certain embodiments, the X-ray powder pattern of a crystalline citrate salt of a compound of Fonnula (II) is (Θ-2Θ°): 4.40; 7.22; 9.12; 12.36; 13.35; 14.34; 15.54; 16.14; 16.54; 17.00; 18.24; 18.58; 19.70; 19.90; 20.30; 20.42; 21.84; 22.02; 23.34; 23.84; 24.04; 24.08; 24.48; 24.76; 25.48; 26.18; 28.14; 28.20; 28.64; 29.64; 31.04; 31.84; 33.00; 33.20; 34.06; 34.30; 34.50; 35.18; 37.48; 37.90; 39.48 as shown in Figure 12.

In certain embodiments, the invention relates to a crystalline compound of Fonnula (III) (III)

wherein X is any suitable counterion.

In certain embodiments, X is a counterion selected from bromide, chloride, sulfate, phosphate, nitrate, acetate, trifluoroacetate, citrate, methanesulfonate, valerate, oleate, palmitate, stearate, laurate, benzoate, lactate, succinate, tosylate, malonate, maleate, fumarate, succinate, tartrate, mesylate, 2-hydroxyethansulfonate, and the like. (See, for example, Berge et al. (1977) “Pharmaceutical Salts”, J. Pharm. Sci. 66: 1-19.)

In certain embodiments X is selected from trifluoroacetate, methanesulfonate, toluenesulfonate, acetate, chloride, and bromide, preferably trifluoroacetate. in certain embodiments, the invention relates to a method for the preparation of a crystalline compound of Formula (III) comprising one or more of: (i) preparing a compound of Formula (IV), e.g., according to Bioorg. Med. Chem. Letter 1999, 9, 2283-88 or U.S. Patent Application 2005-0256324, wherein PG is a suitable protecting group (e.g., Boc or Cbz)

(IV) (ii) dissolving the compound of Formula (IV) in an organic solvent; (iii) adding a suitable acid; (iv) bringing the solution to supersaturation to cause formation of crystals; and (v) isolating the crystals, e.g., by filtering the crystals, by decanting fluid from the crystals, or by any other suitable separation technique. In certain embodiments, preparation further comprises inducing crystallization. In certain embodiments, preparation further comprises washing the crystals, e.g., with a solvent or non-solvent fluid. In certain embodiments, preparation further comprises drying, preferably under reduced pressure, such as under vacuum pressure.

In certain embodiments, the invention relates to a method for the preparation of a crystalline compound of Formula (III), comprising one or more of: (i) preparing a solution of an amorphous compound of Formula (IV), e.g., according to Bioorg. Med. Chem. Letter 1999, 9, 2283-88 or U.S. Patent Application 2005-0256324, in an organic solvent, wherein PG is a suitable protecting group (e.g., Boc or Cbz).

(IV) (ii) bringing the solution to supersaturation to cause formation of crystals; and (iii) isolating the crystals, e.g., by filtering the crystals, by decanting fluid from the crystals, or by any other suitable separation technique. In certain embodiments, preparation further comprises inducing crystallization. In certain embodiments, preparation further comprises washing the crystals, e.g., with a solvent or non-solvent fluid. In certain embodiments, preparation further comprises drying, preferably under reduced pressure, such as under vacuum pressure. in certain embodiments the acid is selected from hydrobromic, hydrochloric, sulfuric, phosphoric, nitric, acetic, trifluoroacetic, citric, methanesuifonic, valeric, oleaic, palmitic, stearic, lauric, benzoic, lactic, succinic, p-toluenesulfonic, citric, malonic, maleic, fumaric, succinic, tartaric, methanesuifonic, 2-hydroxyethanesulfonic, and the like. Preferably the acid is trifluoroacetic acid.

In certain embodiments, X is a counterion selected from hydrobromide, hydrochloride, sulfate, phosphate, nitrate, acetate, trifluoroacetate, citrate, methanesulfonate, valerate, oleate, palmitate, stearate, laurate, benzoate, lactate, succinate, tosylate, malonate, maleate, fumarate, succinate, tartrate, mesylate, 2-hydroxyethansulfonate, and the like. (See, for example, Berge et al. (1977) "Pharmaceutical Salts", J. Pharm. Sci. 66: 1-19.) In certain embodiments, X is selected from trifluoroacetate, methanesulfonate, toluenesulfonate, acetate, chloride, and bromide, preferably trifluoroacetate.

In certain embodiments, the compound of Formula (IV) may be dissolved in an organic solvent selected from dichloromethane, ethyl acetate, isopropyl acetate, isobutyl acetate, butyl acetate, propyl acetate, diethyl ether, methyl tert-butyl ether (MTBE), or any combination thereof. In certain embodiments, the organic solvent is selected from dichloromethane, ethyl acetate, MTBE, or any combination thereof, preferably either dichloromethane and MTBE or ethyl acetate and MTBE.

In certain embodiments, bringing the solution to supersaturation comprises the addition of an anti-solvent, such as hexanes or heptanes or another liquid miscible with the organic solvent, allowing the solution to cool, reducing the volume of the solution, or any combination thereof. In certain embodiments, bringing the solution to supersaturation comprises adding an anti-solvent, cooling the solution to ambient temperature or lower, and reducing the volume of the solution, e.g., by evaporating solvent from the solution. In certain embodiments, the anti-solvent is hexanes or heptanes, preferably heptanes.

In certain embodiments, washing the crystals comprises washing with a liquid selected from anti-solvent, ethyl acetate, dichloromethane, or a combination thereof. Preferably the crystals are washed with anti-solvent, preferably heptanes.

In certain embodiments, the DSC of a crystalline compound of Formula (III) has a sharp endothermic maximum at about 137 °C, e.g., resulting from melting and decomposition of the crystalline form as shown in Figure 9.

In certain embodiments, the X-ray powder pattern of a crystalline compound of Formula (II) is (Θ-2Θ°): 8.84; 15.18; 15.32; 16.20; 16.82; 17.66; 18.26; 19.10; 21.20; 22.58; 23.06; 23.52; 25.32; 26.58; 28.60; 30.08; 30.48; 30.84; 32.20; 36.14; 37.12 as shown in Figure 10.

In certain embodiments, a crystalline compound of Formula (111) is not solvated (e.g., the crystal lattice does not comprise molecules of a solvent). In certain alternative embodiments, a crystalline compound of Formula (111) is solvated.

In certain embodiments, the invention relates to a method for the preparation of a crystalline compound of Formula (11), comprising one or more of (i) preparing a solution of compound of Formula (IV) wherein PG is a suitable protecting group (e.g., Boc or Cbz), in a first organic solvent

(IV) (ii) adding a suitable acid; (iii) bringing the solution to supersaturation to cause formation of crystals; (iv) isolating the crystals to provide a crystalline compound of Formula (III); (v) reacting the crystalline compound of Formula (III)

(III) wherein X is any suitable counterion, with a compound of Formula (V)

(V) to provide a compound of Formula (II); (vi) preparing a solution of the compound of Fonnula (II) in a second organic solvent; (vii) bringing the solution to supersaturation to cause formation of crystals; and (viii) isolating the crystals to provide a crystalline compound of Fonnula (II), e.g., by filtering the crystals, by decanting, or by any other suitable separation technique. In certain embodiments, preparation further comprises inducing crystallization. In certain embodiments, preparation further comprises washing the crystals, e.g., with a solvent or non-solvent fluid. In certain embodiments, preparation further comprises drying, preferably under reduced pressure, such as under vacuum pressure.

In certain embodiments, the acid is selected from hydrobromic, hydrochloric, sulfuric, phosphoric, nitric, acetic, trifluoroacetic, citric, methanesulfonic, valeric, oleaic, palmitic, stearic, lauric, benzoic, lactic, succinic, p-toluenesulfonic, citric, malonic, maleic, fumaric, succinic, tartaric, methanesulfonic, 2-hydroxyethansulfonic, and the like. Preferably the acid is trifluoroacetic acid.

In certain embodiments, X is a counterion selected from hydrobromide, hydrochloride, sulfate, phosphate, nitrate, acetate, trifluoroacetate, citrate, methanesulfonate, valerate, oleate, palmitate, stearate, laurate, benzoate, lactate, succinate, tosylate, malonate, maleate, fumarate, succinate, tartrate, mesylate, 2-hydroxyethanesulfonate, and the like. (See, for example, Berge et al. (1977) “Pharmaceutical Salts”, J. Pharm. Sci. 66: 1-19.) In certain embodiments, X is selected from trifluoroacetate, methanesulfonate, toluenesulfonate, acetate, chloride, and bromide, preferably trifluoroacetate.

In certain embodiments, the first organic solvent is selected from dichloromethane, ethyl acetate, isopropyl acetate, isobutyl acetate, butyl acetate, propyl acetate, diethyl ether, methyl tert-butyl ether (MTBE), or any combination thereof. In certain embodiments, the organic solvent is selected from dichloromethane, ethyl acetate, MTBE, or any combination thereof, preferably either dichloromethane and MTBE or ethyl acetate and MTBE.

In certain embodiments, the second organic solvent is selected from acetonitrile, methanol, ethanol, ethyl acetate, isopropanol, isopropyl acetate, isobutyl acetate, butyl acetate, propyl acetate, methylethyl ketone, methylisobutyl ketone, and acetone, or any combination thereof. In certain embodiments, the amorphous compound may be dissolved in an organic solvent selected from acetonitrile, methanol, ethanol, ethyl acetate, acetone, or any combination thereof. In certain embodiments, the organic solvent or solvents may be combined with water.

In certain embodiments, preparation further comprises washing the crystals of either or both of Formula (II) or (III). In certain embodiments, washing the crystals of a compound of Formula (II) comprises washing with a liquid selected from anti-solvent, acetonitrile, methanol, ethanol, ethyl acetate, acetone, or a combination thereof.

Preferably the crystals of a compound of Formula (II) are washed with a combination of anti-solvent and the organic solvent. In certain embodiments, washing the crystals comprises washing the crystalline compound of Formula (II) with methanol and water. In certain embodiments, washing the crystals of a compound of Formula (111) comprises washing with a liquid selected from anti-solvent, ethyl acetate, dichloromethane, or a combination thereof. Preferably the crystals of a compound of Formula (111) are washed with anti-solvent, preferably heptanes.

In certain embodiments, preparation further comprises drying the crystals of either or both of Formula (II) or (III), preferably under reduced pressure, such as under vacuum pressure.

In certain embodiments, the invention relates to a pharmaceutical composition comprising a crystalline compound of Formula (I) or (II) and a pharmaceutically acceptable carrier. In certain embodiments, the pharmaceutical composition is selected from tablets, capsules, and injections.

This invention also relates to methods for the synthesis of epoxyketones, such as formulae (III) and (IV) above. Thus, in another aspect, the invention provides a method for preparing amino acid keto-epoxides according to scheme (1)

(I) wherein R1 is selected from a protecting group or a further chain of amino acids, which itself may be optionally substituted, preferably a protecting group, most preferably an electron withdrawing protecting group; R is selected from hydrogen and Chalky); and R3 is selected from hydrogen, C|.6alkyl, C|.6alkoxyalkyl, heterocyclyl, aryl, heteroaryl, C|.6heteroaralkyl, and Ci.earalkyl; and wherein the method comprises a stereoselective epoxidation under epoxidizing conditions, preferably an aqueous sodium hypochlorite(bleach) or calcium hypochlorite solution in the presence of a cosolvent selected from pyridine, acetonitrile, DMF, DMSO, NMP, DMA, THF, and nitromethane.

In certain embodiments, the cosolvent is selected from NMP and pyridine, preferably pyridine.

In certain embodiments, the epoxidation is performed using aqueous sodium hypochlorite in the presence of a cosolvent selected from pyridine, acetonitrile, DMF, DMSO, NMP, DMA, THF, and nitromethane, preferably NMP or pyridine, more preferably pyridine. In certain embodiments, the epoxidation is performed using a 10% aqueous sodium hypochlorite solution. In certain embodiments, the epoxidation is performed using a 10% aqueous sodium hypochlorite solution in the presence of pyridine. In certain embodiments, the epoxidation is performed using a calcium hypochlorite solution in the presence of NMP.

In certain embodiments, R1 is selected from a protecting group or a further chain of amino acids, which itself may be optionally substituted. In certain such embodiments, R1 is a protecting group, preferably an electron withdrawing protecting group.

In certain embodiments, R1 is selected from /-butoxy carbonyl (Boc), benzoyl (Bz), fluoren-9-ylmethoxycarbonyl (Fmoc), trichloroethoxycarbonyl (Troc), and benzyloxy carbonyl (Cbz). In certain such embodiments, R1 is selected from t-butoxy carbonyl (Boc), benzoyl (Bz), trichloroethoxycarbonyl (Troc), and benzyloxy carbonyl (Cbz), preferably Cbz or Boc. in certain preferred embodiments, R1 is Boc.

In certain embodiments, R3 is selected from hydrogen, C|.6alkyl, C^alkoxyalkyl, hetcrocyclyl, aryl, heteroaryl, Cj.fiheteroaralkyl, and Ci-taralkyl. In preferred embodiments, R3 is Chalky!, preferably isobutyl. In certain preferred embodiments, R3 is Cj-earalkyl, preferably phenylmethyi, 4-hydroxyphenylmethyl, or 2-phenylethyl.

In certain embodiments, the stereoselective epoxidation is performed under conditions that do not result in significant epimerization of the carbon bearing R3, such that there is less than 10%, less than 5%, less than 2%, or even less than 1% epimerization of the carbon bearing R3. In certain embodiments, the stereoselective epoxidation is performed such that the product is greater than about 90%, greater than 95%, greater than 98%, or even greater than 99% diastereomerically pure.

In certain embodiments, the epoxidation is performed at a temperature in the range of about -15 °C to about 10 °C, about -10 °C to about 5 °C, or even about -5 °C to about 0 °C.

In certain embodiments, the compounds in scheme I have the following stereochemistry

In certain embodiments, the stereoselective epoxidation is performed such that the product is greater than about 90%, greater than 95%, greater than 98%, or even greater than 99% diastereomerically pure.

The use of various N-protecting groups, e.g., the benzyloxy carbonyl group or the t-butyloxycarbonyl group (Boc), various coupling reagents, e.g., dicyclohexylcarbodiimide (DCC), 1,3-diisopropylcarbodiimide (D1C), 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide (EDC), N-hydroxyazabenzotriazole (HATU), carbonyldiimidazole, or 1-hydroxybenzotriazole monohydrate (HOBT), and various cleavage conditions: for example, trifluoracetic acid (TFA), HC1 in dioxane, hydrogenation on Pd/C in organic solvents (such as methanol or ethyl acetate), boron tris(trifluoroacetate), and cyanogen bromide, and reaction in solution with isolation and purification of intermediates are well-known in the art of peptide synthesis, and are equally applicable to the preparation of the subject compounds (Greene, T.W.; Wuts, P.G.M. Protective Groups in Organic Synthesis, 3,d ed.; Wiley: New York, 1999).

In certain embodiments, the amino acid keto-epoxide may be further modified by deprotection of the amine, if applicable, and coupling with a chain of amino acids. Methods for the coupling of such fragments are well known in the art (Elofsson, M., et al. (1999) Chemistiy & Biology, 6:811-822; Elofsson, M., et al (1999) Chemistry & Biology. 6:811 -822). In a preferred embodiment, the chain of amino acids comprises one to three amino acids.

In certain embodiments, the chain of amino acids has a structure of formula (VI) or a pharmaceutically acceptable salt thereof

(VI) wherein each A is independently selected from C=0, C=S, and SO2, preferably C=0; or A is optionally a covalent bond when adjacent to an occurrence of Z; L is absent or is selected from C=0, C=S, and SO2, preferably L is absent or C=0; M is absent or is C|-i2alkyl, preferably C1 .«alkyl; Q is absent or is selected from Ο, NH, and N-C|.6alkyl, preferably Q is absent, O, or NH, most preferably Q is absent or O; X is COOH or an activated form thereof, preferably X is COOH, COC1, or CON(Me)(OMe), most preferably X is COOH or COC1; Y is absent or is selected from O, NH, N-C|.6alkyl, S, SO, SO2, CHOR17, and CHCO2R17; each Z is independently selected from O, S, NH, and N-C|.6alkyl, preferably O; or Z is optionally a covalent bond when adjacent to an occurrence of A; R5, R6, and R7 are each independently selected from Ci.6alkyl, C|.6hydroxyalkyl, C|. 6alkoxyalkyl, aryl, and C|.6aralkyl, any of which is optionally substituted with one or more of amide, amine, carboxylic acid (or a salt thereof), ester (including C|. 6aikyl and C|-salkyl ester and aryl ester), thiol, or thioether substituents; R9 is N(Rl0)LQRn; R10, R12, and R13 are independently selected from hydrogen, OH, and C|_6alkyl, preferably, R10 is selected from hydrogen, OH, and C|_6alkyl, and R12 and R13 are independently selected from hydrogen and Ci_6alkyl, preferably hydrogen; R11 is selected from hydrogen, C|_6alkyl, C|.6alkenyi, C|.6alkynyl, aryl, C|-6aralkyl, heteroaryl, Ci^heteroaralkyl, RI5ZAZ-C|.8alkyl-, RlsZ-C|-8alkyl-, (R1 sO)(Rl60)P(=0)0-C,_8alkyl-ZAZ-C |.8alkyl-, RI5ZAZ-C,.8alkyl-ZAZ-C,. 8alkyl-, heterocyclylMZAZ-C, 8atkyl-, (Rl50)(Rl60)P(=0)0-C,.8alkyl-, (RI7)2N-C|.|7alkyl-, (Rl7)3N+-C|-i2alkyl-, heterocyclylM-, carbocyclylM-, RlsS02C|.8alkyl-, and Ri8S02NH; preferably Chalky!, C|.6alkenyl, Ci.ealkynyl, aryl, C|.6aralkyl, heteroaryl, Ci-eheteroaralkyl, RI5ZA-C|.8alkyl-, RlsZ-C|.8alkyl-, (Rl50)(R,60)P(=0)0-C,.8alkyl-ZAZ-C,.salkyl-, (Rl50)(R160)P(=0)0-C,.8alkyl-Z-C|_salkyl-, RI5ZA-C|.8alkyl-ZAZ-C|.8alkyl-, heterocyclylMZAZ-C|.8alkyl-, (Rl50)(Rl60)P(=0)0-C,.8alkyl-, (RI7)2N-C,.salkyl-, (RI7)3N+-C,.salkyl-, heterocyclylM-, carbocyclylM-, R18S02Ci.salkyl-, and RI8SC>2NH, wherein each occurrence of Z and A is independently other than a covalent bond; or R10 and Rn together are C|.6alkyl-Y-C|.6alkyl, Ci_6alkyl-ZAZ-C|-6alkyl, ZAZ-C|.6alkyl-ZAZ-C|.6alkyl, ZAZ-Ci-6alkyl-ZAZ, or C|.6alkyl-A, thereby forming a ring; preferably C|.2alkyl-Y-C|.2alkyl, Ci.2alkyl-ZA-C|.2alkyl, A-C|.2alkyl-ZA-C|. 2alkyl, A-Ci^alkyl-A, or Ci^alkyl-A, wherein each occurrence of Z and A is independently other than a covalent bond; R15 and R16 are independently selected from hydrogen, metal cation, Ci^alkyl, C|. 6alkenyl, C|.6alkynyl, aryl, heteroaryl, C|.6aralkyl, and C|.6heteroaralkyl, preferably from hydrogen, metal cation, and Chalky!, or R1'-' and R16 together are Ci.^alkyl, thereby forming a ring; each R17 is independently selected from hydrogen and Ci^alkyl, preferably Ci^alkyl; R is independently selected from hydrogen, OH, C|.6alkyl, C|.6alkenyl, C^alkynyl, carbocyclyl, heterocyclyl, aryl, heteroaryl, C|.6aralkyl, and Ci^heteroaralkyl; provided that in any occurrence of the sequence ZAZ, at least one member of the sequence must be other than a covalent bond.

In some embodiments, R5, R6, and R7 are selected from C|.6alkyl or Ci^aralkyl.

In preferred embodiments, R6 is Ci-ealkyl and R5 and R7 are Ci_6aralkyl. In the most preferred embodiment, R is isobutyl, R" is 2-phenylethyl, and R is phenylmethyl.

In certain embodiments, L and Q are absent and R11 is selected from C|.6alkyl, C|-ealkenyl, C|_6alkynyl, C|.6aralkyl, and Ci^heteroaralkyl. In certain such embodiments, R10 is C|.6alkyl and R11 is selected from butyl, allyl, propargyl, phenylmethyl, 2-pyridyl, 3-pyridyl, and 4-pyridyl.

In other embodiments, L is SOi, Q is absent, and R11 is selected from CYaalkyl and aryl. In certain such embodiments, R11 is selected from methyl and phenyl.

In certain embodiments, L is C=0 and R11 is selected from Ci^alkyl, C|.6alkcnyl, C|.6alkynyl, aryl, C|.6aralkyl, heteroaryl, Ci^heteroaralkyl, RLlZA-C|.8alkyl-, RISZ-C|. salkyl-, (Rl50)(Rl60)P(=0)0-C|.salkyl-, (Rls0)(Rl60)P(=0)0-C|.8alkyl-ZAZ-C|-8alkyl-, (Rl50)(Rl60)P(=0)0-C,.8alkyl-Z-C,-8alkyl-, RI5ZA-Cl8alkyl-ZAZ-Ci.salkyl-, heterocyclylMZAZ-C|.8alkyl-, (RI7)2N-C|.8alkyl-, (RI7)3N+-C|.8alkyl-, heterocyclylM-, ΙΟ ΙΟ carbocyclylM-, R SO2C1 -galkyl-, and R SCbNH-, wherein each occurrence of Z and A is independently other than a covalent bond. In certain embodiments, L is C=0, Q is absent, and R11 is H.

In certain embodiments, R10 is Cuealkyl, R11 is C|-6alkyl, Q is absent, and L is C=0. In certain such embodiments, R11 is ethyl, isopropyl, 2,2,2-trifluoroethyl, or 2-(methylsulfonyl)ethyl.

In other embodiments, L is C=0, Q is absent, and R11 is C|.6aralkyl. In certain such embodiments, R11 is selected from 2-phenylethyl, phenylmethyl, (4-methoxyphenyl)methyl, (4-chlorophenyl)methyl, and (4-fluorophenyl)methyl.

In other embodiments, L is C=0, Q is absent, R10 is C|.6alkyl, and R11 is aryl. In certain such embodiments, R11 is substituted or unsubstituted phenyl.

In certain embodiments, L is C=0, Q is absent or Ο, n is 0 or 1, and R11 is -(CH2)ncarbocyclyl. In certain such embodiments, R11 is cyclopropyl or cyclohexyl.

In certain embodiments, L and A are C=0, Q is absent, Z is Ο, n is an integer from 1 to 8 (preferably 1), and R11 is selected from RI5ZA-C|_8alkyl-, Rl8Z-Ci-galkyl-, R15ZA-C|.8aIkyI-ZAZ-Ci.8alkyI-,(Rls0)(Rl60)P(=0)0-C|.8alky!-ZAZ-C|-8alkyl-, (Rl:>0)(Rl60)P(=0)0-Ci-8alkyl-Z-Ci.8aiky]-, and heterocyclylMZAZ-Ci_salkyl-, wherein each occurrence of A is independently other than a covalent bond. In certain such embodiments, R7 is heterocyclylMZAZ-Ci.galkyl- where heterocycly! is substituted or unsubstituted oxodioxolenyi or N(RI3)(R13), wherein R12 and R13 together are C|_6alkyl-Y-C|_6alkyl, preferably Ci^alkyl-Y-Cioalkyl, thereby forming a ring. in certain preferred embodiments, L is C=0, Q is absent, n is an integer from 1 to 8, and R11 is selected from (Rl50)(Rl60)P(=0)0-C|_salkyl-, (R'^NCi-gaikyl, (Rl7)3N+(CH2)ir, and heterocyclyl-M-. In certain such embodiments, R11 is -Ci-8alkyIN(Rl7)2 or-C|.8alkylN+(Rl7)3, where R17 is C|-6alkyl. In certain other such embodiments, R11 is heterocyclylM-, where heterocyclyl is selected from morpholino, piperidino, piperazino, and pyrrolidino.

In certain embodiments, L is OO. R10 is C|.6aikyl, Q is selected from O and NH and R11 is selected from Cj-ealkyl, cycloalkyl-M, C|-6aralkyl, and C|.6heteroaralkyl. In other embodiments, L is C=0, R10 is C|.6alkyl, Q is selected from 0 and NH, and R11 is

Ci^alkyl, where C|.6alkyl is selected from methyl, ethyl, and isopropyl. In further embodiments, L is C=0, R10 is C|.6alkyl, Q is selected from O and NH and R11 is C|. ^aralkyl, where aralkyl is phenylmethyl. In other embodiments, L is C=0, R10 is C|. ealkyl, Q is selected from O and NH, and R11 is Ci^heteroaralkyl, where heteroaralkyl is (4-pyridyl)methyl.

In certain embodiments, L is absent or is C=0, and R10 and R11 together are C|. 6alkyl-Y-C|_f,alkyl, C|_6alkyl-ZA-C|.6alkyl, or Ci^alkyl-A, wherein each occurrence of Z and A is independently other than a covalent bond, thereby forming a ring. In certain preferred embodiments, L is C=0, Q and Y are absent, and R10 and R11 together are C|. 3alkyl-Y-C|.3alkyl. In another preferred embodiment, L and Q are absent, and R10 and R11 together are C|.3alkyl-Y-C|.3alkyl. In another preferred embodiment, L is 0=0, Q is absent, Y is selected from NH and N-C|.6alkyl, and R10 and R11 together are Qoalkyl-Y-Cioalkyl. In another preferred embodiment, L is C=0, Y is absent, and R10 and R11 together are C|.3alkyl-Y-C|_3alkyl. In another preferred embodiment, L and A are OO, and Rin and Rn together are C|.2atkyl-ZA-C].2alkyl. In another preferred embodiment, L and A are C=0 and RH1 and R11 together are C2-3alkyl-A.

In certain embodiments, the chain of amino acids has a structure of formula (VII)

(VII) wherein each A is independently selected from 0=0, 0=S, and SO2, preferably 0=0; or A is optionally a covalent bond when adjacent to an occurrence of Z; each B is independently selected from C=0, C=S, and SO?, preferably 0=0; D is absent or is C|.$alkyl; G is selected from O, NH, and N-C|_6alkyl; K is absent or is selected from 0=0. C=S, and S02, preferably K is absent or is 0=0; L is absent or is selected from C=0. C=S. and 502, preferably L is absent or 0=0; M is absent or is C|.8alkyl; Q is absent or is selected from Ο, NH, and N-Ci^alkyl, preferably Q is absent, 0, or NH, most preferably Q is absent; X is COOH or an activated form thereof, preferably X is COOH, C0C1, or CON(Me)(OMe), most preferably X is COOH or COC1; each V is independently absent or is selected from 0, S, NH, and N-C|_6alkyl, preferably V is absent or O; W is absent or is independently selected from O, S, NH, and N-C|.6alkyl, preferably O; Y is absent or is selected from 0, NH, N-C|.6alkyl, S, SO, SO2, CHOR17, and CHCO2R17; each Z is independently selected from O, S, NH, and N-C|.6alkyl, preferably O; or Z is optionally a covalent bond when adjacent to an occurrence of A; R5, R6, and R7 are each independently selected from Ci^alkyl, Ci^hydroxyalkyl, C|. ^alkoxyalkyl, aryl, C^aralkyl, and R16DVK.OC|_3alkyl-, wherein at least one of R? and R7 is Rl6DVKOC,.3alkyl-; R9 is N(R,0)LQR“; R10 is selected from hydrogen, OH, and Ci^alkyl, preferably hydrogen or C|_6alkyl; R11 is a further chain of amino acids, hydrogen, a protecting group, aryl, or heteroaryl, any of which is optionally substituted with halogen, carbonyl, nitro, hydroxy, aryl, C|.5alkyl; or R11 is selected from C|.ealkyl, C].6alkenyl, C|.6alkynyl, Ci^aralkyl, C,.6heteroaralkyl, RI2ZAZ-C|.8alkyi-, R15ZAZ-C,.8alkyl-, (Rl20)(Rl30)P(=0)0-C|-saIkyl-ZAZ-C|.8alkyl-, RI2ZAZ-C|.8alkyl-ZAZ-C|.8alkyl-, heterocyclylMZAZ-C,.8alkyl-, (Rl20)(Rl30)P(=0)0-C,-iialkyl-, (RI4)2N-C,.8alkyl-, (RI4)3N+-C,. 8alkyl-, heterocyclylM-, carbocyclylM-, ΡΙ:!3θ2θμ83^]-, and RI:,S02NH; or R10 and R11 together are C|.6alkyl-Y-C|.6alkyl, C|_6alkyl-ZAZ-C|_6alkyl, ZAZ-C|_6alkyl-ZAZ-C|.6alkyl, ZAZ-C|.6alkyl-ZAZ, or C|_6alkyl-ZAZ; R12 and R13 are independently selected from hydrogen, metal cation, C|.ealkyl, C|. 6alkenyl, Ci-ealkynyl, aryl, heteroaryl, C|_6aralkyl, and C|.6heteroaralkyl, preferably from hydrogen, metal cation, and Ci-talkyl, or R12 and Rlj together are Ci.ealkyl, thereby forming a ring; each R14 is independently selected from hydrogen and C|.6alkyl, preferably Ci^alkyl; each R15 is independently selected from hydrogen, OR14, Ci^alkyl, Ci^alkenyl, C|. 6alkynyl, carbocyclyl, heterocyclyl, aryl, heteroaryl, C|.6aralkyl, and C|. 6heteroaralkyl; R16 is selected from hydrogen, (RI70)(RIS0)P(=0)W-, Ri7GB-, heterocyclyl-, (RI9)2N-, (R19)3N+-, RI9S02GBG-, and Rl7GBC|.salkyl- where the C|.galkyl moiety is optionally substituted with OH, Ci-galkylW (optionally substituted with halogen, preferably fluorine), aryl, heteroaryl, carbocyclyl, heterocyclyl, and C|.6aralkyl, preferably at least one occurrence of R16 is other than hydrogen; R and R are independently selected from hydrogen, metal cation, C|.6alkyl, C|. 6alkenyl, C|-6alkynyl, aryl, heteroaryl, C|.6aralkyl, and Ci_6heteroaralkyl, preferably from hydrogen, metal cation, and C|_6alkyl, or R17 and R18 together are C|-6alkyl, thereby forming a ring; and each R19 is independently selected from hydrogen, OR14, C|.6alkyl, C|.6alkenyl, C|. talkynyl, carbocyclyl, heterocyclyl, aryl, heteroaryl, C|.(,aralkyl, and C|. 6heteroaralkyl; and D, G, V, K, and W are selected such that there are no O-O, N-O, S-N, or S-0 bonds.

In certain embodiments, R , R , and R are each independently selected from C|. 6alkyl, Ci-ehydroxyalkyl, C|-6alkoxyalkyl, aryl, C|.6aralkyl, and Rl6DVKOC|_3alkyl-wherein at least one of R3 and R7 is R^DVKOCi^alkyl-. In preferred embodiments, one of R5 and R7 is C|.6aralkyl and the other is Rl6DVKOC|.3alkyl-, and R6 is independently C|.6alkyl. In the most preferred embodiment, one of R5 and R7 is 2-phenylethyl or phenylmethyl and the other is Rl6DVKOCH2- or Rl6DVKO(CH3)CH-, and R6 is isobutyl.

In certain embodiments, each Rl3 is independently selected from hydrogen, C|. 6alkyl, Ci-ealkenyl, C|.6alkynyl, carbocyclyl, heterocyclyl, aryl, heteroaryl, C|.6aralkyl, and Ci_6heteroaralkyl.

In certain embodiments, each R19 is independently selected from hydrogen, C| 6alkyl, Ci .«alkenyl, Ct.6alkynyl, carbocyclyl, heterocyclyl, aryl, heteroaryl, C|.6aralkyl, and Ci^heteroaralkyl.

In certain embodiments, L and Q are absent and R11 is selected from hydrogen, a further chain of amino acids, Ci^acyl, a protecting group, aryl, heteroaryl, C|_6alkyl, C|. 6alkenyl, Ci^alkynyl, C|.6aralkyl, and C|.6heteroaralkyl. In certain such embodiments, R10 is Ci-ealkyl and R11 is selected from butyl, allyl, propargyl, phenylmethyl, 2-pyridyl, 3-pyridyl, and 4-pyridyl.

In other embodiments, L is SO2, Q is absent, and R11 is selected from C^alkyl and aryl. In certain such embodiments, R11 is selected from methyl and phenyl.

In certain embodiments, L is C=0 and R11 is selected from Ci-ealkyl, Ci^alkenyl, Ci^alkynyl, aryl, C ^aralkyl, heteroaryl, C|.6heteroaralkyl, R,2ZA-C|.8alkyl-, RISZ-C|. salkyl-,(Rl20)(Rl30)P(=0)0-C|.8alkyl-, (Rl20)(R130)P(=0)0-C,.8alkyl-ZAZ-C,.8alkyl-, (Ri20)(R1i0)P(=0)0-Ci.8alkyl-Z-C|.8alkyl-, RI2ZA-C,.8alkyl-ZAZ-C|.8alkyl-, heterocycIylMZAZ-Ci.8alkyl-, (R14)?N-C|.8alkyl-, (RI4)3N+-C|.8alkyl-, heterocyclylM-, carbocyclylM-, Rl5S02Cj.8alkyl-, and R^SO^NH-. In certain embodiments, L is 0=0, Q is absent, and R11 is H.

In certain embodiments, R10 is Ci-$alkyl, R11 is C|.6alkyl, Q is absent, and L is 0=0. In certain such embodiments, R11 is ethyl, isopropyl, 2,2,2-trifluoroethyl, or 2-(methylsulfonyl)ethyl.

In other embodiments, L is C=0, Q is absent, and R11 is C|.6aralkyl. In certain such embodiments, R11 is selected from 2-phenylethyl, phenylmethyl, (4-methoxyphenyl)methyl, (4-chlorophenyI)methyl, and (4-fluorophenyl)methyl.

In other embodiments, L is 0=0, Q is absent, R10 is C^alkyl, and R11 is aryl. In certain such embodiments, R11 is substituted or unsubstituted phenyl.

In certain embodiments. L is 0=0, Q is absent or O, and R11 is -(CH2)ncarbocyclyl. In certain such embodiments, R11 is cyclopropyl or cyclohexyl.

In certain embodiments, L and A are 0=0, Q is absent, Z is O, and Rn is selected from Rl2ZA-C|-8alkyl-, Rl5Z-C,.8alkyl-, Rl2ZA-C,-8alkyl-ZAZ-C,.salkyl-; (Rl20)(Rl30)P(=0)0-C,.8alkyl-ZAZ-C,_8alkyl-, (Rl20)(R,30)P(=0)0-C,.8alkyl-Z-C,. salkyl-, and heterocyclylMZAZ-C|.8alkyl-. In certain such embodiments. R11 is heterocyc!ylMZAZ-C|.8aikyl- where heterocyclyl is substituted or unsubstituted oxodioxolenyl or N(R20)(R21), wherein R20 and R21 together are C|.6alkyl-Y-C|-6alkyl, preferably C|_3alkyl-Y-C|.3alkyl, thereby forming a ring.

In certain preferred embodiments, L is C=0, Q is absent, and Rn is selected from (Rl20)(Rl30)P(=0)0-CN8alkyI-, (Rl4)2NC,.gaikyI, (Rl4)3N+(CH2)n-, and heterocyclyl-iVk In certain such embodiments, R11 is-C|_salkylN(R14)2 or-C|.8alkylN+(Rl4)3, where R14 is Ci^alkyl. In certain other such embodiments, R11 is heterocyclylM-, where heterocyclyl is selected from morpholino, piperidino, piperazino, and pyrrolidino.

In certain embodiments, L is C=0, R10 is C|.6alkyl, Q is selected from O and NH and R11 is selected from Ci.ealkyl, cycloalkyl-M, Ci-6araalkyl, and Ci^heteroaraalkyl. In other embodiments, L is C=0, R10 is Ci^alkyl, Q is selected from O and NH, and R11 is Ci^alkyl, where Ci^alkyl is selected from methyl, ethyl, and isopropyl. In further embodiments, L is C=0, Rlu is Ci-ealkyl, Q is selected from O and NH and R11 is C>. 6aralkyl, where aralkyl is phenylmethyl. In other embodiments, L is C=0, R10 is Ci. 6alkyl, Q is selected from O and NH, and R11 is C|.6heteroaralkyl, where heteroaralkyl is (4-pyridyl)mcthyl.

In certain embodiments, L is absent or is 0=0, and R10 and R11 together are C|. 6alkyl-Y-C|.6alkyl, C|-6alky]-ZA-C[_6aikyi, or C|_6alkyl-A, thereby forming a ring. In certain preferred embodiments, L is 0=0, Q and Y are absent, and R10 and R11 together are C|_3alkyl-Y-C(.3alkyl. In another preferred embodiment, L and Q are absent, and R10 and R11 together are C|.3alkyl-Y-Ci-3alkyl. In another preferred embodiment, L is C=0, Q is absent, Y is selected from NH and N-Ci-ealkyl, and R10 and R11 together are C|. 3alkyl-Y-C|_3aikyl. In another preferred embodiment, L is 0=0, Y is absent, and R10 and R11 together are Qoalkyl-Y-Cioalkyl. jn another preferred embodiment, L and A are 0=0, and R10 and R11 together are Ci_2alkyl-ZA-C|.2alkyl. In another preferred embodiment, L and A are 0=0 and R10 and R11 together are C7-3alkyl-A.

In certain embodiments, R16 is (RI70)(RIS0)P(=0)W-. In certain such embodiments, D, V, K, and W are absent. In other such embodiments, V and K. are absent, D is C|.galkyl, and W is O. In yet other such embodiments, D is C|.galkyl, K is 0=0, and V and W are O.

In certain embodiments, R16 is R,7GB-. In preferred embodiments, B is C=0, G is 0, D is Ci-salkyl, V is 0, and K. is C=0.

In certain embodiments, R16 is heterocyclyl-. In preferred such embodiments, D is Ci.galkyl. In certain such embodiments, V is Ο, K is C=0, and heterocyclyl is oxodioxolenyl. In other such embodiments, V is absent, K is absent or is C=0, and heterocyclyl is N(R20)(R21), where R20 and R21 together are J-T-J, J-WB-J, or B-J-T-J, T is absent or is selected from O, NR17, S, SO, SO2, CHOR19, CHCO2R17, 0=0, CF2, and CHF, and J is absent or is Ci^alkyl.

In certain embodiments, R16 is (RI9)2N- or (RI9)3N+-, and preferably V is absent.

In preferred such embodiments, D is Ci.galkyl and K is absent or C=0. In certain embodiments where V is absent and R16 is (RI9)2N-, D is absent K is absent or is C=0, preferably K is C=0.

In certain embodiments, RK> is RI9S02GBG-. In preferred such embodiments, B is 0=0, D, V, and K are absent, and G is NH or NCi.ealkyl.

In certain embodiments, R16 is Rl7GBC|.gaIkyl-. In preferred embodiments, B is C=0, G is 0, and the C|_galkyl moiety is optionally substituted with OH, Ci.galkyl (optionally substituted with halogen, preferably fluorine), Ci-salkylW, aryl, heteroaryl, carbocyclyl, heterocyclyl, and C|.6aralkyl. In certain such embodiments, the C1 -salkyl moiety is an unsubstituted, mono-, or disubstituted Cialkyl.

In certain embodiments, the chain of amino acids has a structure of formula (VIII) or (IX) or a pharmaceutically acceptable salt thereof

(VIII) (IX) wherein each Ar is independently an aromatic or heteroaromatic group optionally substituted with 1 to 4 substituents; L is absent or is selected from C=0, C=S, and SO2, preferably SO2 or C=0; X is COOH or an activated form thereof, preferably X is COOH, C0C1, or CON(Me)(OMe), most preferably X is COOH or C0C1; Y is absent or is selected from C=0 and SO2; Z is absent or is Chalky!; R5 and R6 are each independently selected from Ci^alkyl, Ci-ehydroxyalkyl, C|_6alkoxyalkyl, aryl, and C|.6aralkyl, any of which is optionally substituted with one or more of amide, amine, carboxylic acid (or a salt thereof), ester (including C^alkyl ester, C|.5alkyl ester, and aryl ester), thiol, or thioether substituents; R9isN(Rl0)L-Z-Rn; R10 is selected from hydrogen, OH, Ci-taralkyl-Y-, and C|.6alkyl-Y-, preferably hydrogen; II· 12 R is selected from hydrogen, OR , C|_6alkenyl, Ar-Υ-, carbocyclyl, and heterocyclyl; and 12 R “ is selected from hydrogen, C|-6alkyl, and C|_6aralkyl, preferably hydrogen.

In certain embodiments, L is selected from C=0, C=S, and SO2, preferably SO2 or c=o.

In certain embodiments, R10 is selected from hydrogen, OH, C|_6aralkyl, and C|. 6atkyl, preferably hydrogen.

In certain embodiments, R11 is selected from hydrogen, Cj^alkenyl, Ar-Y-, carbocyclyl, and heterocyclyl. in certain embodiments, Rs and R6 are each independently selected from C|.6alkyl, Cj-fthydroxyalkyl, and Cj^aralkyl. In preferred such embodiments, R5 is Ci.^alkyl and R6 is C|-caraikyl. In more preferred such embodiments, R3 is isobutyl and R6 is phenylmethyl.

In certain embodiments, R10 is hydrogen, L is C=0 or SO2, R11 is Ar-Υ-, and each Ar is independently selected from phenyl, indolyl, benzofuranyl, naphthyl, quinolinyl, quinolonyi, thienyl, pyridyl, pyrazyl, and the like. In certain such embodiments, Ar may be substituted with Ar-Q-, where Q is selected from a direct bond, -Ο-, and C^alkyl. In certain other such embodiments where Z is Ci ealkyl, Z may be substituted, preferably with Ar, e.g., phenyl.

In certain embodiments, R10 is hydrogen, Z is absent, L is 0=0 or SO2, and R11 is selected from Ar-Y and heterocyclyl. In certain preferred such embodiments. heterocyclyl is selected from chromonyl, chromanyl, morpholino, and piperidinyl. In certain other preferred such embodiments, Ar is selected from phenyl, indolyl, benzofuranyl, naphthyl, quinolinyl, quinolonyl, thienyl, pyridyl, pyrazyl, and the like.

In certain embodiments, R10 is hydrogen, L is C=0 or SO2, Z is absent, and R11 is C|.6alkenyl, where C|.6alkenyl is a substituted vinyl group where the substituent is preferably an aryl or heteroaryl group, more preferably a phenyl group optionally substituted with one to four substituents.

In certain embodiments, R12 is selected from hydrogen and C|.6alkyl. In certain 12 preferred such embodiments, R is selected from hydrogen and methyl. In more preferred such embodiments, R12 is hydrogen.

In certain preferred embodiments, the chain of amino acids has a structure of formula (X)

(X) X is COOH or an activated form thereof, preferably X is COOH, COC1, or CON(Me)(OMe), most preferably X is COOH or COC1; f Z τ R , R , and R are independently selected from Ci^alkyl, C|_e,hydroxyalkyl, C|. ealkoxyalkyl, aryl, and Cj.earalkyl, each of which is optionally substituted with a group selected from amide, amine, carboxylic acid or a pharmaceutically acceptable salt thereof, carboxyl ester, thiol, and thioether, preferably R6 is C|-6alkyl and R5 and R7 are C|_ 6aralkyl, most preferably, R6 is isobutyl, R3 is 2-phenylethyl, and R7 is phenyhnethyl; R9 is a further chain of amino acids, hydrogen, C|.6acyl, a protecting group, aryl, or heteroaryl, where substituents include halogen, carbonyl, nitro, hydroxy, aryl, and C|. 5alkyl, preferably R9 is C|_6acyl, most preferably R9 is acetyl.

In certain preferred embodiments, the chain of amino acids has a structure of formula (XI) or a pharmaceutically acceptable salt thereof, (XI)

wherein L is absent or is selected from -COi or -C(=S)0; X is COOH or an activated form thereof, preferably X is COOH, COC1, or CON(Me)(OMe), most preferably X is COOH or COC1; Y is NH, N-alkyl, O, or C(R9)2, preferably N-alkyl, O, or C(R9)2; Z is O or C(Rt,)2, preferably C(Rl>)?; R , R , and R are independently selected from hydrogen and a group of formula (XII), preferably, R1, R2, and R3 are all the same, more preferably R1, R2, and R3 are all hydrogen;

(XII) each R5, R6, R7, and R° is independently selected from hydrogen, C|.6alkyl, Ct_ fthydroxyalkyl, C|.6alkoxyalkyl, aryl, and C|.&aralkyl, each of which is optionally substituted with a group selected from alkyl, amide, amine, carboxylic acid or a pharmaceutically acceptable salt thereof, carboxyl ester, thiol, and thioether, preferably R , R , and R are independently selected from Chalky!, Ci.ehydroxyalkyl, and C|_ 6araikyi and each R9 is hydrogen, more preferably, R6 is C^alkyl, R5 and R' are independently C].ftaralkyl and each R9 is H; R10 and R11 are independently selected from hydrogen and C|.ealkyl, or R10 and R11 together form a 3- to 6-membered carbocyclic or heterocyclic ring; R12 and R,J are independently selected from hydrogen, a metal cation, Ci-ealkyl, and C(^aralkyl, or R12 and R13 together represent Chalky), thereby forming a ring; m is an integer from 0 to 2; and n is an integer from 0 to 2, preferably 0 or 1.

In certain embodiments, X is O and R1, R2, and R3 are all the same, preferably R1, R2, and R3 are all hydrogen. In certain such embodiments, R5, R6, and R7 are independently selected from Ci^alkyl, C|.6hydroxyalkyl, and Ci^aralkyl, more preferably, R6 is Ci-6alkyl and R5 and R7 are independently C|.6aralkyl.

In certain preferred embodiments, R1, R2, and R3 are all hydrogen, R6 and R8 are both isobutyl, R is phenylethyl, and R is phenylmethyl.

In certain embodiments, R5, R6, and R7 are independently selected from hydrogen, Ci^alkyl, Ci^hydroxyalkyl, C|.6alkoxyalkyl, aryl, and Ci^aralkyl, each of which is optionally substituted with a group selected from alkyl, amide, amine, carboxylic acid or a pharmaceutically acceptable salt thereof, carboxyl ester, thiol, and thioether. In certain embodiments, at least one of R and R is Ci^aralkyl substituted with alkyl, more preferably substituted with perhaloalkyl. In certain such embodiments, R7 is Ci^aralkyl substituted with trifluoromethyl.

In certain embodiments, Y is selected from N-alkyl, O, and CH2. In certain such embodiments, Z is CH2, and m and n are both 0. In certain alternative such embodiments, Z is CH2, m is 0, and n is 2 or 3. In yet another alternative such embodiments, Z is O, m is 1, and n is 2.

In certain preferred embodiments, the chain of amino acids has a structure of formula (XIII)

(XIII) wherein each Ar is independently an aromatic or heteroaromatic group optionally substituted with 1 to 4 substituents; each A is independently selected from C=0, C=S, and SO2, preferably C=0; or A is optionally a covalent bond when adjacent to an occurrence ofZ; B is absent or is N(R9)R10, preferably absent; L is absent or is selected from C=0, C=S, and SO2, preferably SO2 or 0=0; M is absent or is Ci.^alkyl, preferably C|.galkyl; Q is absent or is selected from Ο, NH, and N-C|.6alkyl; X is COOH or an activated form thereof, preferably X is COOH, C0C1, or CON(Me)(OMe), most preferably X is COOH or C0C1; Y is absent or is selected from C=0 and S02; each Z is independently selected from 0, S, NH, and N-Ci-ealkyl, preferably O; or Z is optionally a covalent bond when adjacent to an occurrence of A; R1 is selected from H, -C|.6alkyl-B, Ci.shydroxyalky!, Ci^alkoxyalkyl, aryl, and C1 ^aralkyl; R2 is selected from aryl, Ci^araikyl, heteroaryl, and C|.(,heteroaralkyl; R4 is N(R5)L-Q-R6; R5 is selected from hydrogen, OH, C|^aralkyl, and C|.6alkyi, preferably hydrogen; R6 is selected from hydrogen, Ci^alkyl, Q^alkenyl, Ci-^alkynyl, Ar-Y-, carbocyclyl, heterocyclyl, an N-terminal protecting group, aryl, C ^aralkyl, heteroaryl, C|.6heteroaralkyl, RnZAZ-Ci_salkyl-, Rt4Z-C,.ga!kyl-, (R1'0){Ri20)P(=0)0-C|.8aikyl-ZAZ-C|.galkyl-, R1 'ZAZ-Cj.galkyl-ZAZ-Ci.galkyl-, heterocyclylMZAZ-C|.galkyl-, (Rll0)(Rl20)P(=0)0-C1.galkyl-,(R'3)2N-CM2alkyl-,(Rl3)3N^CM2alkyl-, heterocyclylM-, carbocyclylM-, R^SO^Ci.galkyl-, and RI4S02NH; preferably an N-capping group, more preferably t-butoxycarbonyl or benzyloxycarbonyl; or R5 and R6 together are Ci-6alkyl-Y-C|.6alkyl, C|.6alkyl-ZAZ-C|.6alkyl, ZAZ-C|. 6alkyl-ZAZ-C|-6alkyl, ZAZ-Ci.6alkyl-ZAZ, or C|.6alkyl-A, thereby forming a ring; R7 is selected from hydrogen, Ci^alkyl, and C|.6aralkyl, preferably hydrogen; R9 is selected from hydrogen, OH, and Ci^alkyl, preferably Ci^alkyl; and R10 is an N-tenninal protecting group; R11 and R12 are independently selected from hydrogen, metal cation, Chalky], C|. ealkenyl, C|.6alkynyl, aryl, heteroaryl, C|.6aralkyl, and C|.6heteroaralkyl. preferably from hydrogen, metal cation, and C|_6alkyl, or R11 and R12 together are C|.6alkyl, thereby forming a ring; each R13 is independently selected from hydrogen and Chalky!, preferably (¾. 6alkyl; and R14 is independently selected from hydrogen, Cj-ealkyl, Ci-ealkenyl, C|.6alkynyl, carbocyclyl, heterocyclyl, aryl, heteroaryl, Ci-6aralkyl, and C|.6heteroaralkyl; provided that in any occurrence of the sequence ZAZ, at least one member of the sequence must be other than a covalent bond.

In certain embodiments, R1 is selected from -C|.6alkyl-B and C|.6aralkyl. In certain such embodiments, R1 is substituted with one or more substituents selected from hydroxy, halogen, amide, amine, carboxylic acid (or a salt thereof), ester (including C|_ ealkyl ester, Ci.salkyl ester, and aryl ester), thiol, or thioether. In certain preferred such embodiments, R1 is substituted with one or more substituents selected from carboxylic acid and ester. In certain embodiments, R1 is selected from methyl, ethyl, isopropyl, carboxymethyl, and benzyl. In certain embodiments R1 is -Ci^alkyl-B and Ci^aralkyl.

In certain preferred such embodiments, B is absent. λ

In certain embodiments, R is selected from C| ^aralkyl and C|.6heteroaralkyl. In certain such embodiments, R2 is selected from Ci^alkyl-phenyl, Ci^alkyl-indolyl, Ci-6alkyl-thienyl, C|.6alkyl-thiazolyl, and C|_6alkyl-isothiazolyl, wherein the alkyl moiety may contain six, five, four, three, two, or one carbon atoms, preferably one or two. In certain such embodiments, R2 is substituted with one or more substituents selected from hydroxy, halogen, amide, amine, carboxylic acid (or a salt thereof), ester (including C|. 6alkyl ester, Ci^alkyl ester, and aryl ester), thiol, or thioether. In certain such embodiments, R2 is substituted with a substituent selected from alkyl, trihaloalkyl, y alkoxy, hydroxy, or cyano. In certain such embodiments, R" is selected from C|.6alkyl-phenyl and Ci^alkyl-indolyl. In certain preferred such embodiments, R2 is selected from

R = H or any suitable protecting group wherein D is selected from H, OMe, OBu1, OH, CN, CF3 and CH3. In certain embodiments D is selected from H, OMe, OH, CN, CF3 and CH3.

In certain preferred such embodiments where D is attached to a six-membered ring, D is attached at the 4-position relative to the point of attachment, preferably excluding embodiments where the 4-position of the ring is occupied by the nitrogen of a pyridine ring.

In certain embodiments, R5 is hydrogen, L is C=0 or SO2, R6 is Ar-Υ-, and each Ar is independently selected from phenyl, indolyl, benzofiiranyl, naphthyl, quinolinyl, quinolonyl, thienyl, pyridyl, pyrazyl, and the like. In certain such embodiments, Ar may be substituted with Ar-Ε-, where E is selected from a direct bond, -Ο-, and Cnealkyl. In certain other such embodiments where Q is C|-6alkyl, Q may be substituted, preferably with Ar, e.g., phenyl.

In certain embodiments, R5 is hydrogen, Q is absent, L is C=0 or SO?, and R6 is selected from Ar-Y and heterocyclyl. In certain preferred such embodiments, heterocyclyl is selected from chromonyl, chromanyl, morpholino, and piperidinyl. In certain other preferred such embodiments, Ar is selected from phenyl, indolyl, benzofuranyl, naphthyl, quinolinyl, quinolonyl, thienyl, pyridyl, pyrazyl, and the like.

In certain embodiments, R^ is hydrogen. L is C=0 or SO2, Q is absent, and R6 is Ci^alkenyl, where Ci^alkenyl is a substituted vinyl group where the substituent is preferably an aryl or heteroaryl group, more preferably a phenyl group optionally substituted with one to four substituents.

In certain embodiments, L and Q are absent and R6 is selected from Chalky!, C ^alkenyl, C|.6alkynyl, C|.6aralkyl, and C|.6heteroaralkyl. In certain such embodiments, R5 is Cj-ealkyl and R6 is selected from butyl, allyl, propargyl, phenylmethyl, 2-pyridyl, 3-pyridyl, and 4-pyridyl.

In other embodiments, L is S02, Q is absent, and R6 is selected from C|.6alkyl and aryl. In certain such embodiments, R6 is selected from methyl and phenyl.

In certain embodiments, L is C=0 and R6 is selected from Chalky!, C]^alkenyl, Ci-calkynyl, aryl, C|-6aralkyl, heteroaryl, Ci^heteroaralkyl, R1'ZA-C|.8alkyl-, Rl4Z-C,.8alkyl-, (R"0)(Rl20)P(=0)0-C,.8alkyl-, (R1 'OXR^COP^COO-Cualkyl-ZAZ-C|.8alkyl-, (R110)(R l20)P(=0)0-Ci.8alkyl-Z-Ci.8alkyl-, R1 lZA-C,.8alkyl-ZAZ-C,_8alkyl-, heterocyclylMZAZ-C|.8alkyl-, (RI3)2N-C|_8alkyl-, (R1 ')3N+-C|.8alkyl-, heterocyclylM-, carbocyclylM-, Rl4S02C|_8alkyl-, and Rl4S02NH-, wherein each occurrence of Z and A is independently other than a covalent bond. In certain embodiments, L is OO, Q is absent, and R6 is H.

In certain embodiments, R5 is Ci^alkyl, R6 is C|.6alkyl, Q is absent, and L is C=0. In certain such embodiments, R6 is ethyl, isopropyl, 2,2,2-trifluoroethyl, or 2-(mcthylsulfonyl)cthyl.

In other embodiments, L is C=0, Q is absent, and R6 is C|-(,aralkyl. In certain such embodiments, R6 is selected from 2-phenylethyl, phenylmethyl, (4-methoxyphenyl)methyl, (4-chlorophenyl)methyl, and (4-fluorophcnyl)methyl.

In other embodiments, L is C=0, Q is absent, R5 is Cj-^alkyl, and Rf’ is aryl. In certain such embodiments, R6 is substituted or unsubstituted phenyl.

In certain embodiments, L is C=0, Q is absent, and R6 is selected from heteroaryl and Ci^heteroaralkyl. In certain such embodiments, R6 is heteroaryl selected from pyrrole, furan, thiophene, imidazole, isoxazole, oxazole, oxadiazole, thiazole, thiadiazolc, triazole, pyrazole, pyridine, pyrazine, pyridazine and pyrimidine. In certain alternative such embodiments, R6 is C|-6hcteroaralkyl selected from pyrrolylmethyl, furanylmethyl, thienylmethyl, imidazolylmethyl, isoxazolylmethyl, oxazolylmethyl, oxadiazolyhnethyl, thiazolylmethyl, thiadiazolylmethyl, triazolylmethyl, pyrazolylmethyl, pyridylmethyl, pyrazinylmethyl, pyridazinylmethyl and pyrimidinylmethyl.

In certain embodiments, L is C=0, Q is absent or O, and R6 is carbocyclylM-, wherein M is Co-ialkyl. In certain such embodiments, R6 is cyclopropyl or cyclohexyl.

In certain embodiments, L and A are C=0, Q is absent, Z is Ο, M is C|_8alkyl, preferably methylene, and R6 is selected from R1‘ΖΑ-Ci.galkyl-, Rl4Z-C|.8alkyi-, RnZA-C,.8alkyl-ZAZ-C,.8alkyl-, (R110)(R,20)P(=0)0-C,.8alkyl-ZAZ-C,.8alkyl-, (Rn0)(Rl20)P(=0)0-C|_8alkyl-Z-C|_8alkyI-, and heterocyclylMZAZ-C|.8alkyl-, wherein each occurrence of A is independently other than a covalent bond. In certain such embodiments, R6 is heterocyclylMZAZ-C|.8alkyl- where heterocyclyl is substituted or unsubstituted oxodioxolenyl or N(RI6)(R17), wherein R16 and R17 together are C|_6alkyl* Y-Ci-fialkyl, preferably C|-3aikyl-Y-C|.3aIkyl, thereby forming a ring.

In certain preferred embodiments, L is C=0, Q is absent, M is C|.8alkyl, and R6 is selected from (R1 'QXR^OJP^OP-C^alkyl-, (R13)2NC|.8alkyl, (RI3)3N+C,.8alkyl-, and heterocyclyl-M-. In certain such embodiments, R6 is (Rl3)2NC|_8alkyl or (RI3)3N+C|_ 8alkyl-, where R13 is Chalky], In certain other such embodiments, R6 is heterocyclylM-, where heterocyclyl is selected from morpholino, piperidino, piperazino, and pyrrolidino.

In certain embodiments, L is OO, R5 is C|.6alkyl, Q is selected from O and NH and R6 is selected from Chalky!, cycloalkyl-M, C|-6aralkyl, and Ci-eheteroaralkyl. In other embodiments, L is C=Os R5 is C|.6alkyl, Q is selected from O and NH, and R6 is C|_ 6alkyl, where C|.6alkyl is selected from methyl, ethyl, and isopropyl. In further embodiments, L is C=0, R5 is Ci^alkyl, Q is selected from O and NH and R6 is C(. 6aralkyl, where aralkyl is phenylmethyl. In other embodiments, L is C=0, R5 is C|.6alkyl, Q is selected from O and NH, and R6 is Cneheteroaralkyl, where heteroaralkyl is (4-pyridyl)methyi.

In certain embodiments, L is absent or is C=0, and R5 and R6 together are C|. 6alkybY-C|-6alkyl, C|.6alkyl-ZA-C|.6alkyl, or C|-6alkyl-A, wherein each occurrence of Z and A is independently other than a covalent bond, thereby forming a ring. In certain preferred embodiments, L is C=0, Q and Y are absent, and R and R together are C|. 3aIkyl-Y-C|_3alkyl. In another preferred embodiment, L and Q are absent, and R3 and R6 together are C|-3alkyl-Y-C|-3alkyl. In another preferred embodiment, L is C=0, Q is absent, Y is selected from NH and N-C|-6alkyl, and R3 and R6 together are C|.3alkyl-Y-C|.3alkyl. In another preferred embodiment, L is C=0, Y is absent, and R3 and R6 together are C|_3alkyl-Y-C|_3alkyl. In another preferred embodiment, L and A are C=0, and R5 and R6 together are C|.2alkyl-ZA-C|_2alkyl. In another preferred embodiment, L and A are C=0 and R5 and R6 together are C2-3alkyl-A.

In certain embodiments, R7 is selected from hydrogen and C|.6alkyl. In certain preferred such embodiments, R7 is selected from hydrogen and methyl. In more preferred n such embodiments, R is hydrogen.

In certain embodiments, R2 and R3 are each independently Ci-saralkyl, and R1 is selected from C|_6alkyl, Ci.6hydroxyaIkyl, C|-6alkoxyalkyl, aryl, and C|_6aralkyl, any of which is optionally substituted with one or more of amide, amine, carboxylic acid (or a salt thereof), ester (including C|-6alkyl ester, Cj.salkyl ester, and aryl ester), thiol, or thioether substituents.

In certain preferred embodiments, the chain of amino acids has a structure of formula (XIV)

(XIV) each Ar is independently an aromatic or heteroaromatic group optionally substituted with 1 to 4 substituents; each A is independently selected from C=0, C=S, and SO?, preferably C=0; or A is optionally a covalent bond when adjacent to an occurrence of Z; L is absent or is selected from C=0, C=S, and SO?, preferably SO? or C=0; M is absent or is C|.|?alkyl, preferably Cugalkyl; Q is absent or is selected from Ο, NH, and N-C|.6alkyl; X is COOH or an activated form thereof, preferably X is COOH, COC1, or CON(Me)(OMe), most preferably X is COOH or COCI; Y is absent or is selected from C=0 and SO?; each Z is independently selected from O, S, NH, and N-C|.6alkyl, preferably O; or Z is optionally a covalent bond when adjacent to an occurrence of A; R is selected from aryl, Ci^aralkyl, heteroaryl, and C|.6heteroaralkyl; R4 is N(RS)L-Q-R6; R^ is selected from hydrogen, OH, C^aralkyl, and Ci-^alkyl, preferably hydrogen; R6 is selected from hydrogen, Chalky], Ci-talkeny], Gi^alkynyl, Ar-Y-, carbocyclyl, heterocyclyl, an N-terminal protecting group, aryl, C|.6aralkyl, heteroaryl, C|.6heteroaralkyl, R^ZAZ-Ci-galkyl-* Rl4Z-C,.8alkyl-, (R1 l0)(R,20)P(=0)0-C,.galkyl-ZAZ-Ci_salkyl-, R1 'ZAZ-C|-8alkyl-ZAZ-Ci.8alkyl-, heterocyclylMZAZ-C|.salkyl-, (Rn0)(R!20)P(=0)0-C|-gaikyl-, (Rl3)2N-CM2alkyl-, (Rn)3N+-CM2alkyl-, heterocyctylM-, carbocyclylM-, Rl4S02C|.8alkyl-, and R14S02NH; preferably an N-capping group, more preferably t-butoxycarbonyl or benzyloxycarbonyl; or R3 and R6 together are C|-6alkyl-Y-C|.6alkyl, C|.6alkyl-ZAZ-C|_6alkyl, ZAZ-C|_ f,a!kyl-ZAZ'C!-6a!kyl, ZAZ-Ci^alkyl-ZAZ, or C|.6alkyl-A, thereby fonning a ring;

Ry is selected from hydrogen, OH, and Ci-talkyl, preferably Ci^alkyl; and R10 is an N-terminal protecting group;

Rn and R12 are independently selected from hydrogen, metal cation, C|.6alkyl, Cj. 6aikenyl, C]_6alkynyi, aryl, heteroaryl, Gj-earalkyl, and Ci^heteroaralkyl, preferably from hydrogen, metal cation, and C|.6alkyl, or R11 and R12 together are Ci.^alkyl, thereby forming a ring; each R13 is independently selected from hydrogen and C|.6alkyl, preferably C|. 6alkyl; and R14 is independently selected from hydrogen, Chalky), Ci^alkenyl, C|.6alkynyl, carbocyclyl, heterocyclyl, aryl, heteroaryl, Cj^aralkyl, and Ci_6heteroaralkyl;

Rls is selected from hydrogen, C|.6alkyl, Ci^hydroxyalkyl, C|.6alkoxy, -C(0)0Ci-6alkyl, -C(0)NHC|.6alkyl, and C^aralkyl, preferably Ci-ealkyl and C|. 6hydroxyalkyl, more preferably methyl, ethyl, hydroxymethyl, and 2-hydroxyethyl; provided that in any occurrence of the sequence ZAZ, at least one member of the sequence must be other than a covalent bond.

In certain embodiments, R2 is selected from Ci^aralkyl and C|_6heteroaralkyl. In certain such embodiments, R2 is selected from Ci.6alkyl-phenyl, C|-6alkyl-indolyl, C|. 6alkyl-thienyl, C|.6alkyl-thiazolyl, and Ci.ealkyl-isothiazolyl, wherein the alkyl moiety may contain six, five, four, tliree, two, or one carbon atoms, preferably one or two. In certain such embodiments, R2 is substituted with one or more substituents selected from hydroxy, halogen, amide, amine, carboxylic acid (or a salt thereof), ester (including C|. ealkyl ester, C|_5alkyl ester, and aryl ester), thiol, or thioether. In certain such embodiments, R2 is substituted with a substituent selected from alkyl, trihaloalkyl, alkoxy, hydroxy, or cyano. In certain such embodiments, R2 is selected from Cj -ealkyl-phenyi and C|.6alkyl-indolyl. In certain preferred such embodiments, R2 is selected from

R = H or any suitable protecting group wherein D is selected from H, OMe, OBu1, OH, CN, CFj and CH3. In certain embodiments D is selected from H, OMe, OH, CN, CF3 and CH3.

In certain preferred such embodiments where D is attached to a six-membered ring, D is attached at the 4-position relative to the point of attachment, preferably excluding embodiments where the 4-position of the ring is occupied by the nitrogen of a pyridine ring.

In certain embodiments, R5 is hydrogen, L is C=0 or SO?, R6 is Ar-Υ-, and each Ar is independently selected from phenyl, indolyl, benzofuranyl, naphthyl, quinolinyl, quinolonyl, thienyl, pyridyl, pyrazyl, and the like. In certain such embodiments, Ar may be substituted with Ar-E-, where E is selected from a direct bond, -0-, and Ci-6alkyl. In certain other such embodiments where Q is Ci-ealkyl, Q may be substituted, preferably with Ar, e.g., phenyl.

In certain embodiments, R5 is hydrogen, Q is absent, L is C=0 or SO2, and R6 is selected from Ar-Y and heterocyclyl. In certain preferred such embodiments, heterocyclyl is selected from chromonyl, chromanyl, morpholino, and piperidinyl. In certain other preferred such embodiments, Ar is selected from phenyl, indolyl, benzofuranyl, naphthyl, quinolinyl, quinolonyl, thienyl, pyridyl, pyrazyl, and the like.

In certain embodiments, R5 is hydrogen, L is C=0 or SO2, Q is absent, and R6 is C|.6alkenyl, where Ci^alkenyl is a substituted vinyl group where the substituent is preferably an aryl or heteroaryl group, more preferably a phenyl group optionally substituted with one to four substituents.

In certain embodiments, L and Q are absent and R(’ is selected from C|.6alkyl, Ci^alkenyl, Ci^alkynyl, C|.6aralkyi, and C|_6heteroaralkyl. In certain such embodiments, R5 is Ci^alkyl and R6 is selected from butyl, allyl, propargyl, phenylmethyl, 2-pyridyl, 3-pyridyl, and 4-pyridyl.

In other embodiments, L is SO2, Q is absent, and R6 is selected from C|.6alkyl and aryi. In certain such embodiments, R6 is selected from methyl and phenyl.

In certain embodiments, L is C=0 and R6 is selected from C|_6alkyl, C|_6alkenyl, C|.6alkynyl, aryl, C|.(,aralkyl, heteroaryl, Ct_6heteroaralkyl, R1’ZA-C|-galkyl-, Rl4Z-C|.8aIkyl-,{R"0)(Rl20)P(=0)0-C,.8alkyl·, (Rll0)(Rl20)P(=0)0-C,.8alkyl-ZAZ-C|.galkyl-,(R"0)(RI20)P(=0)0-C,.8alkyl-Z-C,.8alkyl-, R1 'ZA-C^alkyl-ZAZ-C,.«alkyl-, heterocycly!MZAZ-C|_«alkyl-, (R'^N-Ci-galkyl-, (Rlj)3N+-C|.«alkyl-, heterocyclylM-, carbocyclylM-, R14S02C|.«alkyl-, and RI4S02NH-, wherein each occurrence of Z and A is independently other than a covalent bond. In certain embodiments, L is C=0, Q is absent, and R6 is H.

In certain embodiments, Rs is Chalky!, R6 is Cι-ealkyl, Q is absent, and L is C=0. In certain such embodiments, R6 is ethyl, isopropyl, 2,2,2-trifluoroethyl, or 2-(methylsulfonyl)ethyl.

In other embodiments, L is C=0, Q is absent, and R6 is C|.baralkyl. In certain such embodiments, R6 is selected from 2-phenylethyl, phenylmethyl, (4-methoxyphenyl)methyl, (4-chlorophenyl)methyl, and (4-fluoropheny!)methyl.

In other embodiments, L is C=0, Q is absent, R5 is C|_6alkyl, and R6 is aryl. In certain such embodiments, R6 is substituted or unsubstituted phenyl.

In certain embodiments, L is C=0, Q is absent, and R6 is selected from heteroaryl and Ci^heteroaralkyl. In certain such embodiments, R6 is heteroaryl selected from pyrrole, furan, thiophene, imidazole, isoxazole, oxazole, oxadiazole, thiazole, thiadiazole, triazole, pyrazole, pyridine, pyrazine, pyridazine and pyrimidine. In certain alternative such embodiments, R6 is C|-6heteroaralkyl selected from pyrrolylmethyl, furanylmethyl, thienylmethyl, imidazolylmethyl, isoxazolylmethyl, oxazolylmethyl, oxadiazolylmethyl, thiazolylmethyl, thiadiazolylmethyl, triazolylmethyl, pyrazolylmethyl, pyridylmethyl, pyrazinylmethyl, pyridazinylmethyl and pyrimidinylmethyl.

In certain embodiments, L is 0=0, Q is absent or O, and R6 is carbocyclylM-, wherein M is C0-ialkyl. In certain such embodiments, R6 is cyclopropyl or cyclohexyl.

In certain embodiments, L and A are C=0, Q is absent, Z is Ο, M is C|.8alkyl, preferably methylene, and R6 is selected from R1 'ZA-C|_8alkyl-, Rl4Z-C|-8alkyl-, RnZA-C|.8alkyl-ZAZ-C,.8alkyl-, (R1 l0)(Rl20)P(=0)0-C,.8alkyl-ZAZ-C,.8alkyl-, (Rn0)(Rl20)P(=:0)0-C|.8alkyl-Z-C|.8alkyl-, and heterocycIylMZAZ-Ct_8alkyl-, wherein each occurrence of A is independently other than a covalent bond. In certain such embodiments, Rfi is heterocyclylMZAZ-C|.8aikyl- where heterocyclyl is substituted or unsubstituted oxodioxolenyl or N(RI6)(R17), wherein R16 and R17 together are C|_6alkyl-Y-C|_6alkyl, preferably Ci.3alkyl-Y-C|.3alkyl, thereby forming a ring.

In certain preferred embodiments, L is C=0, Q is absent, M is C|.8alkyl, and R6 is selected from (R1'0)(Rl20)P(=0)0-C|.8alkyl-, (Rl3)2NC|.8alkyl, (RI3)3N+C|.8alkyl-, and heterocyclyl-M-. In certain such embodiments, R6 is (Rl3)2NC|.8alkyl or (RI3)3N+C|. 8alkyl-, where R13 is C|.6alkyl. In certain other such embodiments, R6 is heterocyclylM-, where heterocyclyl is selected from morpholino, piperidino, piperazino, and pyrrolidino.

In certain embodiments, L is C=0, R3 is C|.6alkyl, Q is selected from 0 and NH and R6 is selected from C|.6alkyl, cycloalkyl-M, C|.6aralkyl, and C|.6heteroaralkyl. In other embodiments, L is C=0, R5 is C^alkyl, Q is selected from O and NH, and R6 is C|. 6alkyl, where Chalky! is selected from methyl, ethyl, and isopropyl. In further embodiments, L is C=0, R3 is C|.6alkyl, Q is selected from O and NH and R6 is Cs. earalkyl, where aralkyl is phenyl methyl. In other embodiments. L is C=0, R3 is C|.6alkyl, Q is selected from O and NH, and R6 is Ci^heteroaralkyl, where heteroaralkyl is (4-pyridyl)methyl.

In certain embodiments, L is absent or is C=0, and R5 and R6 together are C|. 6alkyl-Y-C|.6alkyl, C|-6alkyNZA-C|.6alkyl, or Ci_6alkyl-A, wherein each occurrence of Z and A is independently other than a covalent bond, thereby forming a ring. In certain preferred embodiments, L is C=0, Q and Y are absent, and R5 and R6 together are C|. 3alkyl-Y-Ci-3alkyl. In another preferred embodiment, L and Q are absent, and R5 and R6 together are Cioalkyl-Y-Cioalkyl. In another preferred embodiment, L is C=0, Q is absent, Y is selected from NH and N-Ci-ealkyl, and R5 and R6 together are C|.3alkyl-Y-Cioalkyl. In another preferred embodiment, L is C=0, Y is absent, and R? and R6 together are Ci.3alkyl-Y-Cioalkyl. In another preferred embodiment, L and A are C=0, and R^ and R6 together are C|_2alkyl-ZA-Ct-2a!ky]. In another preferred embodiment, L and A are C=0 and R5 and R6 together are C2-3alkyl-A.

In certain embodiments, R2 is Ci^aralkyl, and R1 is selected from Ci-aalkyl, C|. 6hydroxyalkyl, Ci^alkoxyaikyl, aryl, and C|.6aralkyl, any of which is optionally substituted with one or more of amide, amine, carboxylic acid (or a salt thereof), ester (including Chalky! ester, C|_salkyl ester, and aryl ester), thiol, or thioether substituents.

In certain preferred embodiments, the chain of amino acids has a structure of formula (XV)

(XV) wherein L is selected from C=0, C=S, and SO?, preferably C=0; X is COOH or an activated form thereof, preferably X is COOH, COC1, or CON(Me)(OMe), most preferably X is COOH or COC1; Z is absent. Ci^alkyl, C|.6alkoxy, or NR, e.g., absent, Chalky), or C|.6alkoxy, preferably absent; R is selected from H and Chalky!, preferably H or CH3; R1 and R2 are each independently selected from hydrogen, C|.6alkyl, C2-6alkenyl, C2-6alkynyl, C|.6hydroxyalkyl, Ci^alkoxyalkyl, aryl, Ci^aralkyl, heteroaryl, heterocyclyl, C|.6heterocycloalkyl, Ci^heteroaralkyl, carbocyclyl, and Cj^carbocyclolalkyl; R4 is selected from hydrogen, C|.6aralkyl, and C]_6alkyl;

Rs is heteroaryl; and R6 is selected from hydrogen, C|.6alkyl, and C|.6aralkyl.

In certain embodiments, R and R“ are independently selected from hydrogen, C|. 6alkyl, C|-6hydroxyalkyl, Ci^alkoxyalkyl, C|.6aralkyl, C|.6heterocycloa!kyl, C|. eheteroaralkyl, and Ci^carbocyclolalkyl. In certain embodiments, R1 and R2 are independently Ci^alkyl selected from methyl, ethyl, propyl, isopropyl, butyl, sec-butyl, Ι2·ι and isobutyl. In certain embodiments, R and R are independently C|.6hydroxyalkyl. In I Λ certain preferred such embodiments, R and R‘ are independently selected from hydroxymethyl and hydroxyethyl, preferably hydroxymethyl. In certain embodiments, R1 and R are independently Ci^alkoxyalkyl. In certain such embodiments, R and R are independently selected from methoxymethyl and methoxyethyl, preferably methoxymethyl. In certain embodiments, R and R are independently C|_6heteroaralkyl. In certain such embodiments, R and R* are independently selected from imidazolylmethyl, pyrazolylmethyl, and thiazolylmethyl, and pyridylmethyl, preferably imidazol-4-ylmethyl, thiazol-4-ylmethyl, 2-pyridylmethyl, 3-pyridylmethyl, or 4-pyridylmethyl. In certain embodiments, R and R are independently C|.6aralkyl. In certain such embodiments, R and R" are are independently selected from phenylmethyl (benzyl) and phenylethyl, preferably phenylmethyl. In certain embodiments, R and R are independently Ci-ecarbocycloalkyl. In certain such embodiments R1 is cyclohexylmethyl. in certain embodiments R and R" are different. In certain embodiments, R1 and R2 are the same.

In certain embodiments, at least one of R1 and R2 is selected from C|. (,hydroxyalkyl and Ci^alkoxyalkyl. In certain such embodiments, at least one of R1 and R2 is alkoxyalkyl. In certain such embodiments, at least one of R1 and R2 is selected from methoxymethyl and methoxyethyl.

In certain embodiments, R4 and R6 are independently selected from hydrogen and methyl, preferably hydrogen.

In certain embodiments, R5 is a 5- or 6-membered heteroaryl. In certain such embodiments, R5 is selected from isoxazole, isothiazole, fiiran, thiophene, oxazole, thiazole, pyrazole, or imidazole, preferably isoxazole, furan, or thiazole.

In certain embodiments, R5 is a bicyclic heteroaryl. In certain such embodiments bicyclic heteroaryl is selected from benzisoxazole, benzoxazole, benzothiazole, benzisothiazole.

In certain embodiments, L is C=0, Z is absent, and R5 is a l,3-thiazol-5-yl or 1,3-thiazol-4-yl. In certain such embodiments, when the thiazole is substituted, it is substituted at least at the 2-position. In other such embodiments, R5 is an unsubstituted 1,3-thiazol-5-yl or l,3-thiazol-4-yl.

In certain embodiments, L is C=0, Z is absent, and Rs is a substituted 1,3-thiazol-5-yl. In certain such embodiments, R5 is l,3-thiazol-5-yl substituted with a substituent selected from Ci^alkyl, C|_6aikoxy, C|.6alkoxyalkyl, Ci.6hydroxyaikyl, carboxylic acid, aminocarboxylate, Cj.eaikylaminocarboxylate, (C|.6alkyl)2aminocarboxylate, C|. ^alkylcarboxylate, Ci^heteroaralkyl, Ci.f,aralkyl, C|.6heterocycloalkyl, and Cj. ficarbocycloalkyl. In certain preferred such embodiments, R is l,3-thiazol-5-yl substituted with a substituent selected from methyl, ethyl, isopropyl, and cyclopropylmethyl.

In certain embodiments, L is C=0, Z is absent, and R5 is a substituted 1,3-thiazol-4-yl. In certain such embodiments, R5 is l,3-thiazol-4-yl substituted with a substituent selected from C|.6alkyl, C|.6aIkoxy, C|.f,alkoxyalkyl, Ci^hydroxyalkyl, carboxylic acid, aminocarboxylate, C|.6alkylaminocarboxylate, (C|.6alkyl)2aminocarboxylate, C|. 6alkylcarboxylate, C|-6heteroaralkyl, C|.6aralkyl, Ci^heterocycloalkyl, and C|. 6carbocycloalkyl. In certain preferred such embodiments, R? is 1,3-thiazol-4-yl substituted with a substituent selected from methyl, ethyl, isopropyl, and cyclopropylmethyl.

In certain embodiments, L is C=0, Z is absent, and R^ is an isoxazol-3-yl or isoxazol-5-yl. In certain preferred such embodiments, when the isoxazol-3-yl is substituted, it is substituted at least at the 5-position. In certain preferred embodiments, when the isoxazol-5-yl is substituted, it is substituted at least at the 3-position.

In certain embodiments, L is C=0, Z is absent, and R5 is an unsubstituted isoxazol-3-yi.

In certain embodiments, L is C=0, Z is absent, and R5 is a substituted isoxazol-3-yl. In certain such embodiments, R5 is isoxazo!-3-yl substituted with a substituent selected from Ci^alkyl, C|.6alkoxy, C|_6alkoxyaIkyl, C|_6hydroxyalkyl, carboxylic acid, aminocarboxylate, Ci^alkylaminocarboxylate, (Ci_6alkyl)2aminocarboxylate, C|. 6alkylcarboxylate, C|-6heteroaralkyl, Ci.6aralkyl, Ci.fiheterocycloalkyl, and C|. 6carbocycloalkyl. In certain preferred such embodiments R5 is isoxazole-3-yl substituted with a substituent selected from methyl, ethyl, isopropyl, and cyclopropylmethyl.

In certain embodiments L is C=0, Z is absent, and Rs is isoxazol-3-yl substituted with a 4- to 6-membcrcd nitrogen-containing Ci.eheterocycloalkyl. In certain such embodiments, R5 is isoxazol-3-yl substituted with azetidinylmethyl, preferably azetidin-1-ylmethyl. In certain alternative such embodiments, L is C=0, Z is absent, and R5 is isoxazol-3-yl substituted with

, wherein W is O, NR, or CH2, and R is H or C|.6alkyl. In certain such embodiments, W is O.

In certain embodiments, L is C=0, Z is absent, and R" is isoxazol-3-yl substituted with 5-membered nitrogen-containing C|.6heteroaralkyl, such as pyrazolylmethyl, imidazolylmethyl, triazol-5-ylmethyl, preferably l,2,4-triazol-5-ylmethyl.

In certain embodiments, L is C=0, Z is absent, and R5 is isoxazol-3-yl substituted with C|_6alkoxy or C^alkoxyalkyl, preferably methoxy, ethoxy, methoxymethyl, or methoxyethyl.

In certain embodiments, L is C=0, Z is absent, and Rs is isoxazol-3-yI substituted with Ci^hydroxyalkyl, preferably hydroxymethyl or hydroxyethyl.

In certain embodiments, L is C=0, Z is absent, and R'^ is isoxazol-3-yl substituted with a carboxylic acid, aminocarboxylate, C|-6alkyiaminocarboxylate, (C|. f,alkyl)2aminocarboxylate, or Ci-oalkylcarboxylate. In certain such embodiments, RJ is substituted with methyl carboxyiate or ethyl carboxylate, preferably methyl carboxylate.

In certain embodiments, L is C=0, Z is absent, and R3 is an unsubstituted isoxazol-5-yl.

In certain embodiments, L is C=0, Z is absent, and R5 is a substituted isoxazol-5-yl. In certain such embodiments, R5 is isoxazoI-5-yl substituted with a substituent selected from Ci.6alkyl, Ci-ealkoxy, C|.6alkoxyalkyl, C|.6hydroxyalkyl, carboxylic acid, aminocarboxylate, C].6alkylaminocarboxylate, (C|.6alkyl)2aminocarboxylate, C|. 6alkylcarboxylate, C|.6heteroaralkyl, C|_6aralkyl, CTeheterocycloalkyl, and C|. ecarbocycloalkyl In certain preferred such embodiments R3 is isoxazole-5-yl substituted with a substituent selected from methyl, ethyl, isopropyl, and cyclopropylmethyl.

In certain embodiments L is C=0, Z is absent, and R5 is isoxazol-5-yl substituted with a 4- to 6-membered nitrogen-containing C|_6heterocycloalkyl. In certain such embodiments, R3 is isoxazol-5-yl substituted with azetidinylmethyl, preferably azetidin-1-ylmethyl. In certain alternative such embodiments, L is C=0, Z is absent, and R3 is isoxazol-5-yl substituted with

, wherein W is O, NR, or CH2, and R is H or C|_6alkyl. In certain such embodiments, W is O.

In certain embodiments, L is C=0, Z is absent, and R3 is isoxazol-5-yl substituted with 5-membered nitrogen-containing Cj-ohcteroaralkyl, such as pyrazolylmethyl, imidazolylmethyl, triazol-5-ylmethyl, preferably 1,2,4-triazol-5-ylmethyl.

In certain embodiments, L is C=0, Z is absent, and R5 is isoxazol-5-yl substituted with Ci^alkoxy or Ci^alkoxyaikyl, preferably methoxy, ethoxy, methoxymethyl, or methoxyethyl.

In certain embodiments, L is C=0, Z is absent, and R5 is isoxazol-5-yl substituted with C|_6hydroxyalkyl, preferably hydroxymethyl or hydroxyethyl.

In certain embodiments, L is C=0, Z is absent, and R3 is isoxazol-5-yl substituted with a carboxylic acid, aminocarboxylate, C|.6alkylaminocarboxylate, (C|. 6alkyl)?aminocarboxylate, or C|_6alkylcarboxylate. In certain such embodiments, R3 is substituted with methyl carboxylate or ethyl carboxylate, preferably methyl carboxylate.

In certain embodiments, Z is NR, preferably NH.

Uses of Enzyme Inhibitors

Orderly protein degradation is crucial to the maintenance of normal cell functions, and the proteasome is integral to the protein degradation process. The proteasome controls the levels of proteins that are important for cell-cycle progression and apoptosis in normal and malignant cells; for example, cyclins, caspases, BCL2 and nF-kB (Kumatori et ah, Proc. Natl. Acad. Sci. USA (1990) 87:7071-7075; Almond et al., Leukemia (2002) 16: 433-443). Thus, it is not surprising that inhibiting proteasome activity can translate into therapies to treat various disease states, such as malignant, non-malignant and autoimmune diseases, depending on the cells involved.

Both in vitro and in vivo models have shown that malignant cells, in general, are susceptible to proteasome inhibition. In fact, proteasome inhibition has already been validated as a therapeutic strategy for the treatment of multiple myeloma. This could be due, in part, to the highly proliferative malignant cell's dependency on the proteasome system to rapidly remove proteins (Rolfe et al., J. Mol. Med. (1997) 75:5-17; Adams, Nature (2004) 4: 349-360). Therefore, certain embodiments of the invention relate to a method of treating cancers comprising administering to a subject in need of such treatment an effective amount of the proteasome inhibitor compound disclosed herein.

As used herein, the term “cancer” includes, but is not limited to, blood born and solid tumors. Cancer refers to disease of blood, bone, organs, skin tissue and the vascular system, including, but not limited to, cancers of the bladder, blood, bone, brain, breast, cervix, chest, colon, endrometrium, esophagus, eye, head, kidney, liver, lung, lymph nodes, mouth, neck, ovaries, pancreas, prostate, rectum, renal, skin, stomach, testis, throat, and uterus. Specific cancers include, but are not limited to, leukemia (acute lymphocytic leukemia (ALL), acute lyeiogenous leukemia (AML), chronic lymphocytic leukemia (CLL), chronic myelogenous leukemia (CML), hairy cell leukemia), mature B ceil neoplasms (small lymphocytic lymphoma, B cell prolymphocytic leukemia, lymphoplasmacytic lymphoma (such as Waldenstrdm’s macroglobulinemia), splenic marginal zone lymphoma, plasma cell myeloma, plasmacytoma, monoclonal immunoglobulin deposition diseases, heavy chain diseases, extranodal marginal zone B cell lymphoma (MALT lymphoma), nodal marginal zone B cell lymphoma (NMZL), follicular lymphoma, mantle cell lymphoma, diffuse B cell lymphoma, mediastinal (thymic) large B cell lymphoma, intravascular large B cell lymphoma, primary effusion lymphoma and Burkitt lymphoma/Ieukemia), mature T cell and natural killer (NK) cell neoplasms (T cell prolymphocytic leukemia, T ceil large granular lymphocytic leukemia, aggressive NK cel! leukemia, adult T cell leukemia/lymphoma, extranodal NK/T cell lymphoma, enteropathy-type T cell lymphoma, hepatosplenic T cell lymphoma, blastic NK cell lymphoma, mycosis fungoides (Sezary syndrome), primary cutaneous anaplastic large cell lymphoma, lymphomatoid papulosis, angioimmunoblastic T cell lymphoma, unspecified peripheral T cell lymphoma and anaplastic large cell lymphoma), Hodgkin lymphoma (nodular sclerosis, mixed celluarity, lymphocyte-rich, lymphocyte depleted or not depleted, nodular lymphocyte-predominant), myeloma (multiple myeloma, indolent myeloma, smoldering myeloma), chronic myeloproliferative disease, myelodysplastic/myeloproliferative disease, myelodysplastic syndromes, immunodeficiency-associated lymphoproliferative disorders, histiocytic and dendritic cell neoplasms, mastocytosis, chondrosarcoma, Ewing sarcoma, fibrosarcoma, malignant giant cell tumor, myeloma bone disease, osteosarcoma, breast cancer (hormone dependent, hormone independent), gynecological cancers (cervical, endometrial, fallopian tube, gestational trophoblastic disease, ovarian, peritoneal, uterine, vaginal and vulvar), basal cell carcinoma (BCC), squamous cell carcinoma (SCC), malignant melanoma, dermatofibrosarcoma protuberans, Merkel cell carcinoma, Kaposi’s sarcoma, astrocytoma, pilocytic astrocytoma, dysembryoplastic neuroepithelial tumor, oligodendrogliomas, ependymoma, glioblastoma multiformc, mixed gliomas, oligoastrocytomas, medulloblastoma, retinoblastoma, neuroblastoma, germinoma, teratoma, malignant mesothelioma (peritoneal mesothelioma, pericardial mesothelioma, pleural mesothelioma), gastro-entero-pancreatic or gastroenteropancreatic neuroendocrine tumor (GEP-NET), carcinoid, pancreatic endocrine tumor (PET), colorectal adenocarcinoma, colorectal carcinoma, aggressive neuroendocrine tumor, leiomyosarcomamucinous adenocarcinoma, Signet Ring cell adenocarcinoma, hepatocellular carcinoma, cholangiocarcinoma, hepatoblastoma, hemangioma, hepatic adenoma, focal nodular hyperplasia (nodular regenerative hyperplasia, hamartoma), non-small cell lung carcinoma (NSCLC) (squamous cell lung carcinoma, adenocarcinoma, large cell lung carcinoma), small cell lung carcinoma, thyroid carcinoma, prostate cancer (hormone refractory, androgen independent, androgen dependent, hormone-insensitive), and soft tissue sarcomas (fibrosarcoma, malignant fibrous hystiocytoma, dermatofibrosarcoma, liposarcoma, rhabdomyosarcoma leiomyosarcoma, hemangiosarcoma, synovial sarcoma, malignant peripheral nerve sheath tumor/neurofibrosarcoma, extraskeletal osteosarcoma).

Many tumors of the haematopoietic and lymphoid tissues are characterized by an increase in cell proliferation, or a particular type of cell. The chronic myeloproliferative diseases (CMPDs) are clonal haematopoietic stem cel! disorders characterized by proliferation in the bone marrow of one or more of the myeloid lineages, resulting in increased numbers of granulocytes, red blood cells and /or platelets in the peripheral blood. As such, the use of proteasome inhibitors for the treatment of such diseases is attractive and being examined (Cilloni et al., Haematologica (2007) 92: 1124-1229). CMPD can include chronic myelogenous leukaemia, chronic neutrophilic leukaemia, chronic eosinophilic leukaemia, polycythaemia vera, chronic idiopathic myelofibrosis, essential thrombocythaemia and unclassifiable chronic myeloproliferative disease. An aspect of the invention is the method of treating CMPD comprising administering to a subject in need of such treatment an effective amount of the proteasome inhibitor compound disclosed herein.

Myelodisplastic/myeloproliferative diseases, such as chronic myelomonocytic leukaemia, atypical chronic myeloid leukemia, juvenile myelomonocytic leukaemia and unclassifiable myelodysplastic/myeloproliferative disease, are characterized by hypercellularity of the bone marrow due to proliferation in one or more of the myeloid lineages. Inhibiting the proteasome with the composition described herein, can serve to treat these myelodisplatic/myeioproliferative diseases by providing a subject in need of such treatment an effective amount or the composition.

Myelodysplastic syndromes (MDS) refer to a group of hematopoietic stem cell disorders characterized by dysplasia and ineffective haematopoiesis in one or more of the major myeloid cell lines. Targeting NF-kB with a proteasome inhibitor in these hematologic malignancies induces apoptosis, thereby killing the malignant cell (Braun et al. Cell Death and Differentiation (2006) 13:748-758). A further embodiment of the invention is a method to treat MDS comprising administering to a subject in need of such treatment an effective amount of the compound disclosed herein. MDS includes refractory anemia, refractory anemia with ringed sideroblasts, refractory cytopenia with multilineage dysplasia, refractory anemia with excess blasts, unclassifiable myelodysplastic syndrome and myelodysplastic syndrome associated with isolated del(5q) chromosome abnormality.

Mastocytosis is a proliferation of mast cells and their subsequent accumulation in one or more organ systems. Mastocytosis includes, but is not limited to, cutaneous mastocytosis, indolent systemic mastocytosis (ISM), systemic mastocytosis with associated clonal haematological non-mast-cell-lineage disease (SM-AHNMD), aggressive systemic mastocytosis (ASM), mast cell leukemia (MCL), mast cell sarcoma (MCS) and extrcutaneous mastocytoma. Another embodiment of the invention is a method to treat mastocytosis comprising administering an effect amount of the compound disclosed herein to a subject diagnosed with mastocytosis.

The proteasome regulates NF-κΒ, which in turn regulates genes involved in the immune and inflammatory response. For example, NF-κΒ is required for the expression of the immunoglobulin light chain κ gene, the IL-2 receptor α-chain gene, the class I major histocompatibility complex gene, and a number of cytokine genes encoding, for example, IL-2, IL-6, granulocyte colony-stimulating factor, and IFN-β (Palombella et al., Cell (1994) 78:773-785). Thus, in certain embodiments, the invention relates to methods of affecting the level of expression of IL-2, MHC-I, IL-6, TNFa, IFN-β or any of the other previously-mentioned proteins, each method comprising administering to a subject an effective amount of a proteasome inhibitor composition disclosed herein. In certain embodiments, the invention includes a method of treating an autoimmune disease in a mammal comprising administering a therapeutically effective amount of the compound described herein. An “autoimmune disease1’ herein is a disease or disorder arising from and directed against an individual’s own tissues. Examples of autoimmune diseases or disorders include, but are not limited to, inflammatory responses such as inflammatory skin diseases including psoriasis and dermatitis (e.g. atopic dermatitis); systemic scleroderma and sclerosis; responses associated with inflammatory bowel disease (such as Crohn's disease and ulcerative colitis); respiratory distress syndrome (including adult respiratory distress syndrome; ARDS); dermatitis; meningitis; encephalitis; uveitis; colitis; glomerulonephritis; allergic conditions such as eczema and asthma and other conditions involving infiltration of T cells and chronic inflammatory responses; atherosclerosis; leukocyte adhesion deficiency; rheumatoid arthritis; systemic lupus erythematosus (SLE); diabetes mellitus (e.g. Type I diabetes mellitus or insulin dependent diabetes mellitis); multiple sclerosis; Reynaud's syndrome; autoimmune thyroiditis; allergic encephalomyelitis; Sjorgen's syndrome; juvenile onset diabetes; and immune responses associated with acute and delayed hypersensitivity mediated by cytokines and T-lymphocytes typically found in tuberculosis, sarcoidosis, polymyositis, granulomatosis and vasculitis; pernicious anemia (Addison's disease); diseases involving leukocyte diapedesis; central nervous system (CNS) inflammatory disorder; multiple organ injury syndrome; hemolytic anemia (including, but not limited to cryoglobinemia or Coombs positive anemia); myasthenia gravis; antigen-antibody complex mediated diseases; anti-glomerular basement membrane disease; antiphospholipid syndrome; allergic neuritis; Graves' disease; Lambert-Eaton myasthenic syndrome; pemphigoid bullous; pemphigus; autoinimune polyendocrinopathies; Reiter's disease; stiff-man syndrome; Beheet disease; giant cell arteritis; immune complex nephritis; IgA nephropathy; IgM polyneuropathies; immune thrombocytopenic purpura (ITP) or autoimmune thrombocytopenia.

The immune system screens for autologous cells that are virally infected, have undergone oncogenic transformation or present unfamiliar peptides on their surface. Intracellular proteolysis generate small peptides for presentation to T-lymphocytes to induce MHC class 1-mediated immune responses. Thus, in certain embodiments, the invention relates to a method of using the compound as an immunomodulatory agent for inhibiting or altering antigen presentation in a cell, comprising exposing the cell (or administering to a subject) to the compound described herein. Specific embodiments include a method of treating graft or transplant-related diseases, such as graft-versus-host disease or host versus-graft disease in a mammal, comprising administering a therapeutically effective amount of the compound described herein. The term "graft" as used herein refers to biological material derived from a donor for transplantation into a recipient. Grafts include such diverse material as, for example, isolated cells such as islet cells; tissue such as the amniotic membrane of a newborn, bone marrow, hematopoietic precursor cells, and ocular tissue, such as comeal tissue; and organs such as skin, heart, liver, spleen, pancreas, thyroid lobe, lung, kidney, tubular organs (e.g., intestine, blood vessels, or esophagus). The tubular organs can be used to replace damaged portions of esophagus, blood vessels, or bile duct. The skin grafts can be used not only for bums, but also as a dressing to damaged intestine or to close certain defects such as diaphragmatic hernia. The graft is derived from any mammalian source, including human, whether from cadavers or living donors. In some cases, the donor and recipient is the same mammal.

Preferably the graft is bone marrow or an organ such as heart and the donor of the graft and the host are matched for HLA class II antigens.

Histiocytic and dendritic cell neoplasms are derived from phagocytes and accessory cells, which have major roles in the processing and presentation of antigens to lymphocytes. Depleting the proteasome content in dendritic cells has been shown to alter their antigen-induced responses (Chapatte et al. Cancer Res. (2006) 66:5461-5468).

Thus, another embodiment of the invention comprises administering an effective amount of the composition disclosed herein to a subject with histiocytic or dendritic cell neoplasm. Histiocytic and dindritirc cell neoplasms include histiocytic sarcoma, Langerhans cell histiocytosis, Langerhans cell sarcoma, interdigitating dendritic cell sarcoma/tumor, follicular dendritic cell sarcoma/tumor and non-specified dendritic cell sarcoma.

Inhibition of the proteasome has been shown to be beneficial to treat diseases whereby a cell type is proliferating and immune disorders; thus, an embodiment of the invention includes the treatment of lymphoproliferative diseases (LPD) associated with primary immune disorders (PID) comprising administering an effective amount of the disclosed compound to a subject in need thereof. The most common clinical settings of immunodeficiency associated with an increased incidence of lymphoproliferative disorders, including B-cell and T-ccll neoplasms and lymphomas, are primary immunodeficiency syndromes and other primary immune disorders, infection with the human immunodeficiency virus (HIV), iatrogenic immunosuppression in patients who have received solid organ or bone marrow allografts, and iatrogenis immunosuppression associated with methotrexate treatment. Other PIDs commonly associated with LPDs, but not limited to, are ataxia telangiectasia (AT), Wiskott-Aldrich syndrome (WAS), common variable immunodeficiency (CVID), severe combined immunodeficiency (SCID), X-linked lymphoproliferative disorder (XLP), Nijmegen breakage syndrome (NBS), hyper-IgM syndrome, and autoimmune lymphoproliferative syndrome (ALPS).

Additional embodiments of the invention relate to methods for affecting the proteasome-dependent regulation of oncoproteins and methods of treating or inhibiting cancer growth, each method comprising exposing a cell (m vivo, e.g., in a subject, or in vitro) to the proteasome inhibitor composition disclosed herein. HPV-16 and HPV-18-derived E6 proteins stimulate ATP-and ubiquitin-dependent conjugation and degradation of p53 in crude reticulocyte lysates. The recessive oncogene p53 has been shown to accumulate at the nonpermissive temperature in a cell line with a mutated thermolabile E1. Elevated levels of p53 may lead to apoptosis. Examples of proto-oncoproteins degraded by the ubiquitin system include c-Mos, c-Fos, and c-Jun. In certain embodiments, the invention relates to a method for treating p53-related apoptosis, comprising administering to a subject an effective amount of a proteasome inhibitor composition disclosed herein.

Another aspect of the invention relates to the use of proteasome inhibitor compositions disclosed herein for the treatment of neurodegenerative diseases and conditions, including, but not limited to, stroke, ischemic damage to the nervous system, neural trauma (e.g., percussive brain damage, spinal cord injury, and traumatic damage to the nervous system), multiple sclerosis and other immune-mediated neuropathies (e.g., Guillain-Barre syndrome and its variants, acute motor axonal neuropathy, acute inflammatory demyelinating polyneuropathy, and Fisher Syndrome), HIV/AIDS dementia complex, axonomy, diabetic neuropathy, Parkinson’s disease, Huntington's disease, multiple sclerosis, bacterial, parasitic, fungal, and viral meningitis, encephalitis, vascular dementia, multi-infarct dementia, Lewy body dementia, frontal lobe dementia such as Pick’s disease, subcortical dementias (such as Huntington or progressive supranuclear palsy), focal cortical atrophy syndromes (such as primary aphasia), metabolic-toxic dementias (such as chronic hypothyroidism or B12 deficiency), and dementias caused by infections (such as syphilis or chronic meningitis).

Alzheimer's disease is characterized by extracellular deposits of β-amyloid protein (β-ΑΡ) in senile plaques and cerebral vessels. β-ΑΡ is a peptide fragment of 39 to 42 amino acids derived from an amyloid protein precursor (APP). At least three isoforms of APP are known ¢695, 751, and 770 amino acids). Alternative splicing of mRNA generates the isoforms; normal processing affects a portion of the β-ΑΡ sequence, thereby preventing the generation of β-ΑΡ. It is believed that abnormal protein processing by the proteasome contributes to the abundance of β-ΑΡ in the Alzheimer brain. The APP-processing enzyme in rats contains about ten different subunits (22 kDa-32 kDa). The 25 kDa subunit has an N-terminal sequence of X-Gln-Asn-Pro-Met-X-Thr-Gly-Thr-Ser. which is identical to the β-subunit of human macropain (Kojima, S. et ah, Fed. Fur.

Biochem. Soc., (1992) 304:57-60). The APP-processing enzyme cleaves at the Gin15— Lys16 bond; in the presence of calcium ion, the enzyme also cleaves at the Met-1—Asp1 bond, and the Asp1—Ala2 bonds to release the extracellular domain of β-ΑΡ.

One aspect of the invention, therefore, relates to a method of treating Alzheimer's disease, comprising administering to a subject an effective amount of the proteasome inhibitor composition disclosed herein. Such treatment includes reducing the rate of β-ΑΡ processing, reducing the rate of β-ΑΡ plaque formation, reducing the rate of β-ΑΡ generation, and reducing the clinical signs of Alzheimer's disease.

Fibrosis is the excessive and persistent formation of fibrous connective tissue resulting from the hyperproliferative growth of fibroblasts and is associated with activation of the TGF-β signaling pathway. Fibrosis involves extensive deposition of extracellular matrix and can occur within virtually any tissue or across several different tissues. Normally, the level of intracellular signaling protein (Smad) that activate transcription of target genes upon TGF-β stimulation is regulated by proteasome activity (Xu et al., 2000). However, accelerated degradation of the TGF-β signaling components has been observed in fibrotic conditions, such as cystic fibrosis, injection fibrosis, endomyocardial fibrosis, idiopathic pulmonary fibrosis, myelofibrosis, retroperitoneal fibrosis, progressive massive fibrosis, nephrogenic systemic fibrosis. Other conditions that are often associated with fibrosis include cirrhosis, diffuse parenchymal lung disease, post-vasectomy pain syndrome, tuberculsis, sickle-cell anemia and rheumatoid arthritis. An embodiment of the invention is the method of treating a fibrotic or fibrotic-associated condition comprising administering an effective amount of the composition described herein to a subject in need of such treatment.

The treatment of burn victims is often hampered by fibrosis, thus, in certain embodiments, the invention relates to the topical or systemic administration of the inhibitors to treat bums. Wound closure following surgery is often associated with disfiguring scars, which may be prevented by inhibition of fibrosis. Thus, in certain embodiments, the invention relates to a method for the prevention or reduction of scarring.

Overproduction of lipopolysaccharide (LPS)-induced cytokines such as TNFct is considered to be central to the processes associated with septic shock. Furthermore, it is generally accepted that the first step in the activation of cells by LPS is the binding of LPS to specific membrane receptors. The a- and β-subunits of the 20S proteasome complex have been identified as LPS-binding proteins, suggesting that the LPS-induced signal transduction may be an important therapeutic target in the treatment or prevention of sepsis (Qureshi, N. et al., J. Immun. (2003) 171: 1515-1525). Therefore, in certain embodiments, the proteasome inhibitor composition may be used for the inhibition of TNFa to prevent and/or treat septic shock.

Ischemia and reperfusion injury results in hypoxia, a condition in which there is a deficiency of oxygen reaching the tissues of the body. This condition causes increased degradation of Ικ-Βα, thereby resulting in the activation of NF-κΒ (Koong et al., 1994).

It has been demonstrated that the severity of injury resulting in hypoxia can be reduced with the administration of a proteasome inhibitor (Gao et al., 2000; Bao et al., 2001; Pye et al., 2003). Therefore, certain embodiments of the invention relate to a method of treating an ischemic condition or reperfusion injury comprising administering to a subject in need of such treatment an effective amount of the proteasome inhibitor compound disclosed herein. Examples of such conditions or injuries include, but are not limited to, acute coronary syndrome (vulnerable plaques), arterial occlusive disease (cardiac, cerebral, peripheral arterial and vascular occlusions), atherosclerosis (coronary sclerosis, coronary artery disease), infarctions, heart failure, pancreatitis, myocardial hypertrophy, stenosis, and restenosis. NF-κΒ also binds specifically to the HIV-enhancer/promoter. When compared to the Nef of mac239, the HIV regulatory protein Nef of pbj 14 differs by two amino acids in the region which controls protein kinase binding. It is believed that the protein kinase signals the phosphorylation of IkB, triggering IkB degradation through the ubiquitin-proteasome pathway. After degradation, NF-κΒ is released into the nucleus, thus enhancing the transcription of HIV (Cohen, J., Science, (1995) 267:960). In certain embodiments, the invention relates to a method for inhibiting or reducing HIV infection in a subject, or a method for decreasing the level of viral gene expression, each method comprising administering to the subject an effective amount of the proteasome inhibitor composition disclosed herein.

Viral infections contribute to the pathology of many diseases. Heart conditions such as ongoing myocarditis and dilated cardiomyopathy have been linked to the coxsackievirus B3. In a comparative whole-genome microarray analyses of infected mouse hearts, specific proteasome subunits were uniformly up-regulated in hearts of mice which developed chronic myocarditis (Szalay et al, Am J Pathol 168:1542-52, 2006). Some viruses utilize the ubiquitin-proteasome system in the viral entry step where the virus is released from the endosome into the cytosol. The mouse hepatitis virus (MHV) belongs to the Coronaviridae family, which also includes the severe acute respiratory syndrome (SARS) coronvirus. Yu and Lai (J Virol 79:644-648, 2005) demonstrated that treatment of cells infected with MHV with a proteasome inhibitor resulted in a decrease in viral replication, correlating with reduced viral titer as compared to that of untreated cells. The human hepatitis B virus (HBV), a member of the Hepadnaviridae virus family, likewise requires virally encoded envelop proteins to propagate. Inhibiting the proteasome degradation pathway causes a significant reduction in the amount of secreted envelope proteins (Simsek et al, J Virol 79:12914-12920, 2005). In addition to HBV, other hepatitis viruses (A, C, D and E) may also utilize the ubiquitin-proteasome degradation pathway for secretion, morphogenesis and pathogenesis. Accordingly, in certain embodiments, the invention relates to a method for treating viral infection, such as SARS or hepatitis A, B, C, D and E, comprising contacting a cell with (or administering to a subject) an effective amount of the compound disclosed herein.

In certain embodiments, the disclosed compositions may be useful for the treatment of a parasitic infection, such as infections caused by protozoan parasites. The proteasome of these parasites is considered to be involved primarily in cell differentiation and replication activities (Paugam et al., Trends Parasitol. 2003, 19(2): 55-59). Furthermore, entamoeba species have been shown to lose encystation capacity when exposed to proteasome inhibitors (Gonzales, et al., Arch. Med. Res. 1997, 28, Spec No: 139-140). In certain such embodiments, the administrative protocols for the proteasome inhibitor compositions are useful for the treatment of parasitic infections in humans caused by a protozoan parasite selected from Plasmodium sps. (including P. falciparum, P. vivax, P. malariae, and P. ovale, which cause malaria), Trypanosoma sps. (including T. cruzi, which causes Chagas1 disease, and T. brucei which causes African sleeping sickness), Leishmania sps. (including L. amazonesis, L. donovani, L. infantum, L. mexicana, etc.), Pneumocystis carinii (a protozoan known to cause pneumonia in AIDS and other immunosuppressed patients), Toxoplasma gondii, Entamoeba histolytica,

Entamoeba invadens, and Giardia lamblia. In certain embodiments, the disclosed proteasome inhibitor compositions are useful for the treatment of parasitic infections in animals and livestock caused by a protozoan parasite selected from Plasmodium hermani, Cryptosporidium sps., Echinococcus granulosus, Eimeria tenella, Sarcocystis neurona, and Neurospora crassa. Other compounds that act as proteasome inhibitors in the treatment of parasitic diseases are described in WO 98/10779, which is incorporated herein in its entirety.

In certain embodiments, the proteasome inhibitor compositions inhibit proteasome activity in a parasite without recovery in red blood cells and white blood cells. In certain such embodiments, the long half-life of blood cells may provide prolonged protection with regard to therapy against recurring exposures to parasites. In certain embodiments, the proteasome inhibitor compositions may provide prolonged protection with regard to chemoprophylaxis against future infection.

Prokaryotes have what is equivalent to the eukaryote 20S proteasome particle. Albeit, the subunit composition of the prokaryote 20S particle is simpler than that of eukaryotes, it has the ability to hydrolyze peptide bonds in a similar maimer. For example, the nucleophilic attack on the peptide bond occurs through the threonine residue on the N-terminus of the β-subunits. Thus, an embodiment of this invention relates to a method of treating prokaryotic infections, comprising administering to a subject an effective amount of the proteasome inhibitor composition disclosed herein. Prokaryotic infections may include diseases caused by either mycobacteria (such as tuberculosis, leprosy or Buruli Ulcer) or archaebacteria.

It has also been demonstrated that inhibitors that bind to the 20S proteasome stimulate bone formation in bone organ cultures. Furthermore, when such inhibitors have been administered systemically to mice, certain proteasome inhibitors increased bone volume and bone formation rates over 70% (Garrett, I. R. et al., J. Clin. Invest. (2003) 111: 1771-1 782), therefore suggesting that the ubiquitin-proteasome machinery regulates osteoblast differentiation and bone formation. Therefore, the disclosed proteasome inhibitor composition may be useful in the treatment and/or prevention of diseases associated with bone loss, such as osteoporosis.

Thus, in certain embodiments, the invention relates to a method for treating a disease or condition selected from cancer, autoimmune disease, graft or transplant-related condition, neurodegenerative disease, fibrotic-associated condition, ischemic-related conditions, infection (viral, parasitic or prokaryotic) and diseases associated with bone loss, comprising administering a crystalline compound of Formula (II).

Compounds prepared as described herein can be administered in various forms, depending on the disorder to be treated and the age, condition, and body weight of the patient, as is well known in the art. For example, where the compounds are to be administered orally, they may be formulated as tablets, capsules, granules, powders, or syrups; or for parenteral administration, they may be formulated as injections (intravenous, intramuscular, or subcutaneous), drop infusion preparations, or suppositories. For application by the ophthalmic mucous membrane route, they may be formulated as eye drops or eye ointments. These formulations can be prepared by conventional means, and if desired, the active ingredient may be mixed with any conventional additive or excipient, such as a binder, a disintegrating agent, a lubricant, a corrigent, a solubilizing agent, a suspension aid, an emulsifying agent, a coating agent, a cyclodextrin, and/or a buffer. Although the dosage will vary depending on the symptoms, age and body weight of the patient, the nature and severity of the disorder to be treated or prevented, the route of administration and the form of the drug, in general, a daily dosage of from 0.01 to 2000 mg of the compound is recommended for an adult human patient, and this may be administered in a single dose or in divided doses. The amount of active ingredient which can be combined with a carrier material to produce a single dosage form will generally be that amount of the compound which produces a therapeutic effect.

The precise time of administration and/or amount of the composition that will yield the most effective results in terms of efficacy of treatment in a given patient will depend upon the activity, pharmacokinetics, and bioavailability of a particular compound, physiological condition of the patient (including age, sex, disease type and stage, general physical condition, responsiveness to a given dosage, and type of medication), route of administration, etc. However, the above guidelines can be used as the basis for fine-tuning the treatment, e.g., determining the optimum time and/or amount of administration, which will require no more than routine experimentation consisting of monitoring the subject and adjusting the dosage and/or timing.

The phrase “pharmaceutically acceptable” is employed herein to refer to those ligands, materials, compositions, and/or dosage forms which are, within the scope of sound medical judgment, suitable for use in contact with the tissues of human beings and animals without excessive toxicity, irritation, allergic response, or other problem or complication, commensurate with a reasonable benefit/risk ratio.

The phrase “pharmaceutically acceptable carrier” as used herein means a pharmaceutically acceptable material, composition, or vehicle, such as a liquid or solid filler, diluent, excipient, solvent or encapsulating material. Each carrier must be “acceptable” in the sense of being compatible with the other ingredients of the formulation and not injurious to the patient. Some examples of materials which can serve as pharmaceutically acceptable carriers include: (1) sugars, such as lactose, glucose, and sucrose; (2) starches, such as com starch, potato starch, and substituted or unsubstituted β-cyclodextrin; (3) cellulose, and its derivatives, such as sodium carboxymethyl cellulose, ethyl cellulose, and cellulose acetate; (4) powdered tragacanth; (5) malt; (6) gelatin; (7) talc; (8) excipients, such as cocoa butter and suppository waxes; (9) oils, such as peanut oil, cottonseed oil, safflower oil, sesame oil, olive oil, com oil, and soybean oil; (10) glycols, such as propylene glycoi; (11) polyols, such as glycerin, sorbitol, mannitol, and polyethylene glycol; (12) esters, such as ethyl oleate and ethyl laurate; (13) agar; (14) buffering agents, such as magnesium hydroxide and aluminum hydroxide; (15) alginic acid; (16) pyrogen-free water; (17) isotonic saline; (18) Ringer's solution; (19) ethyl alcohol; (20) phosphate buffer solutions; and (21) other non-toxic compatible substances employed in pharmaceutical formulations. In certain embodiments, pharmaceutical compositions of the present invention are non-pyrogenic, i.e., do not induce significant temperature elevations when administered to a patient.

The term “pharmaceutically acceptable salt” refers to the relatively non-toxic, inorganic and organic acid addition salts of the inhibitor(s). These salts can be prepared in situ during the final isolation and purification of the inhibitor(s), or by separately reacting a purified inhibitor(s) in its free base form with a suitable organic or inorganic acid, and isolating the salt thus formed. Representative salts include the hydrobromide, hydrochloride, sulfate, bisulfate, phosphate, nitrate, acetate, valerate, oleate. palmitate, stearate, laurate, benzoate, lactate, phosphate, tosylate, citrate, maleate, fumarate, succinate, tartrate, naphthylate, mesylate, glucoheptonate, lactobionate, laurylsulphonate salts, and amino acid salts, and the like. (See, for example, Berge et al. (1977) “Pharmaceutical Salts”, J. Pharm. Sci. 66: 1-19.)

In other cases, the inhibitors useful in the methods of the present invention may contain one or more acidic functional groups and, thus, are capable of forming pharmaceutically acceptable salts with pharmaceutically acceptable bases. The term “pharmaceutically acceptable salts” in these instances refers to the relatively non-toxic inorganic and organic base addition salts of an inhibitor(s). These salts can likewise be prepared in situ during the final isolation and purification of the inhibitor(s), or by separately reacting the purified inhibitor(s) in its free acid form with a suitable base, such as the hydroxide, carbonate, or bicarbonate of a pharmaceutically acceptable metal cation, with ammonia, or with a pharmaceutically acceptable organic primary, secondary, or tertiary amine. Representative alkali or alkaline earth salts include the lithium, sodium, potassium, calcium, magnesium, and aluminum salts, and the like. Representative organic amines useful for the formation of base addition salts include ethylamine, diethylamine, ethylenediamine, ethanolamine, diethanolamine, piperazine, and the like (see, for example, Berge et al., supra).

Wetting agents, emulsifiers, and lubricants, such as sodium lauryl sulfate and magnesium stearate, as well as coloring agents, release agents, coating agents, sweetening, flavoring, and perfuming agents, preservatives and antioxidants can also be present in the compositions.

Examples of pharmaceutically acceptable antioxidants include: (1) water soluble antioxidants, such as ascorbic acid, cysteine hydrochloride, sodium bisulfate, sodium metabisulfite, sodium sulfite, and the like; (2) oil-soluble antioxidants, such as ascorbyl palmitate, butylated hydroxyanisole (BHA), butylated hydroxytoluene (BHT), lecithin, propyl gallate, alpha-tocopherol, and the like; and (3) metal chelating agents, such as citric acid, ethylenediamine tetraacetic acid (EDTA), sorbitol, tartaric acid, phosphoric acid, and the like.

Formulations suitable for oral administration may be in the fonn of capsules, cachets, pills, tablets, lozenges (using a flavored basis, usually sucrose and acacia or tragacanth), powders, granules, or as a solution or a suspension in an aqueous or non-aqueous liquid, or as an oil-in-water or water-in-oil liquid emulsion, or as an elixir or syrup, or as pastilles (using an inert matrix, such as gelatin and glycerin, or sucrose and acacia) and/or as mouthwashes, and the like, each containing a predetermined amount of an inhibitor(s) as an active ingredient. A composition may also be administered as a bolus, electuary, or paste.

In solid dosage forms for oral administration (capsules, tablets, pills, dragees, powders, granules, and the like), the active ingredient is mixed with one or more pharmaceutically acceptable carriers, such as sodium citrate or dicalcium phosphate, and/or any of the following: (1) fillers or extenders, such as starches, cyclodextrins, lactose, sucrose, glucose, mannitol, and/or silicic acid; (2) binders, such as, for example, carboxymethylcellulose, alginates, gelatin, polyvinyl pyrrolidone, sucrose, and/or acacia; (3) humectants, such as glycerol; (4) disintegrating agents, such as agar-agar, calcium carbonate, potato or tapioca starch, alginic acid, certain silicates, and sodium carbonate; (5) solution retarding agents, such as paraffin; (6) absorption accelerators, such as quaternary ammonium compounds; (7) wetting agents, such as, for example, acetyl alcohol and glycerol monostearate; (8) absorbents, such as kaolin and bentonite clay; (9) lubricants, such a talc, calcium stearate, magnesium stearate, solid polyethylene glycols, sodium iauryl sulfate, and mixtures thereof; and (10) coloring agents. In the case of capsules, tablets, and pills, the pharmaceutical compositions may also comprise buffering agents. Solid compositions of a similar type may also be employed as fillers in soft and hard-filled gelatin capsules using such excipients as lactose or milk sugars, as well as high molecular weight polyethylene glycols, and the like. A tablet may be made by compression or molding, optionally with one or more accessory ingredients. Compressed tablets may be prepared using binder (for example, gelatin or hydroxypropylmethyl cellulose), lubricant, inert diluent, preservative, disintegrant (for example, sodium starch glycolate or cross-linked sodium carboxymcthyl cellulose), surface-active or dispersing agent. Molded tablets may be made by molding in a suitable machine a mixture of the powdered inhibitor(s) moistened with an inert liquid diluent.

Tablets, and other solid dosage forms, such as dragees, capsules, pills, and granules, may optionally be scored or prepared with coatings and shells, such as enteric coatings and other coatings well known in the pharmaceutical-formulating art. They may also be formulated so as to provide slow or controlled release of the active ingredient therein using, for example, hydroxypropylmethyl cellulose in varying proportions to provide the desired release profile, other polymer matrices, liposomes, and/or microspheres. They may be sterilized by, for example, filtration through a bacteria-retaining filter, or by incorporating sterilizing agents in the form of sterile solid compositions which can be dissolved in sterile water, or some other sterile injectable medium immediately before use. These compositions may also optionally contain opacifying agents and may be of a composition that they release the active ingredient(s) only, or preferentially, in a certain portion of the gastrointestinal tract, optionally, in a delayed manner. Examples of embedding compositions which can be used include polymeric substances and waxes. The active ingredient can also be in micro-encapsulated form, if appropriate, with one or more of the above-described excipients.

Liquid dosage forms for oral administration include pharmaceutically acceptable emulsions, microemulsions, solutions, suspensions, syrups, and elixirs. In addition to the active ingredient, the liquid dosage forms may contain inert diluents commonly used in the art, such as, for example, water or other solvents, solubilizing agents, and emulsifiers such as ethyl alcohol, isopropyl alcohol, ethyl carbonate, ethyl acetate, benzyl alcohol, benzyl benzoate, propylene glycol, 1,3-butylene glycol, oils (in particular, cottonseed, groundnut, com, germ, olive, castor, and sesame oils), glycerol, tetrahydrofuryl alcohol, polyethylene glycols, and fatty acid esters of sorbitan, and mixtures thereof.

Besides inert diluents, the oral compositions can also include adjuvants such as wetting agents, emulsifying and suspending agents, sweetening, flavoring, coloring, perfuming, and preservative agents.

Suspensions, in addition to the active inhibitor(s) may contain suspending agents as, for example, ethoxylated isostearyl alcohols, polyoxyethylene sorbitol and sorbitan esters, microcrystalline cellulose, aluminum metahydroxide, bentonite, agar-agar and tragacanth, and mixtures thereof.

Formulations for rectal or vaginal administration may be presented as a suppository, which may be prepared by mixing one or more inhibitor(s) with one or more suitable nonirritating excipients or carriers comprising, for example, cocoa butter, polyethylene glycol, a suppository wax or a salicylate, which is solid at room temperature, but liquid at body temperature and, therefore, will melt in the rectum or vaginal cavity and release the active agent.

Formulations which are suitable for vaginal administration also include pessaries, tampons, creams, gels, pastes, foams, or spray formulations containing such carriers as are known in the art to be appropriate.

Dosage forms for the topical or transdermal administration of an inhibitor(s) include powders, sprays, ointments, pastes, creams, lotions, gels, solutions, patches, and inhalants. The active component may be mixed under sterile conditions with a pharmaceutically acceptable carrier, and with any preservatives, buffers, or propellants which may be required.

The ointments, pastes, creams, and gels may contain, in addition to inhibitor(s), excipients, such as animal and vegetable fats, oils, waxes, paraffins, starch, tragacanth, cellulose derivatives, polyethylene glycols, silicones, bentonites, silicic acid, talc, and zinc oxide, or mixtures thereof.

Powders and sprays can contain, in addition to an inhibitor(s), excipients such as lactose, talc, silicic acid, aluminum hydroxide, calcium silicates, and polyamide powder, or mixtures of these substances. Sprays can additionally contain customary propellants, such as chlorofluorohydrocarbons and volatile unsubstituted hydrocarbons, such as butane and propane.

The inhibitor(s) can be alternatively administered by aerosol. This is accomplished by preparing an aqueous aerosol, liposomal preparation, or solid particles containing the composition. A nonaqueous (e.g., fluorocarbon propellant) suspension could be used. Sonic nebulizers are preferred because they minimize exposing the agent to shear, which can result in degradation of the compound.

Ordinarily, an aqueous aerosol is made by formulating an aqueous solution or suspension of the agent together with conventional pharmaceutically acceptable carriers and stabilizers. The carriers and stabilizers vary with the requirements of the particular composition, but typically include nonionic surfactants (Tweens, Pluronics, sorbitan esters, lecithin, Cremophors), pharmaceutically acceptable co-solvents such as polyethylene glycol, innocuous proteins like serum albumin, oleic acid, amino acids such as glycine, buffers, salts, sugars, or sugar alcohols. Aerosols generally are prepared from isotonic solutions.

Transdermal patches have the added advantage of providing controlled delivery of an inhibitor(s) to the body. Such dosage forms can be made by dissolving or dispersing the agent in the proper medium. Absorption enhancers can also be used to increase the flux of the inhibitor(s) across the skin. The rate of such flux can be controlled by either providing a rate controlling membrane or dispersing the inhibitor(s) in a polymer matrix or gel.

Pharmaceutical compositions of this invention suitable for parenteral administration comprise one or more inhibitors(s) in combination with one or more pharmaceutically acceptable sterile aqueous or nonaqueous solutions, dispersions, suspensions or emulsions, or sterile powders which may be reconstituted into sterile injectable solutions or dispersions just prior to use, which may contain antioxidants, buffers, bacteriostats, solutes which render the formulation isotonic with the blood of the intended recipient or suspending or thickening agents.

Examples of suitable aqueous and nonaqueous carriers which may be employed in the pharmaceutical compositions of the invention include water, ethanol, polyols (such as glycerol, propylene glycol, polyethylene glycol, and the like), and suitable mixtures thereof, vegetable oils, such as olive oil, and injectable organic esters, such as ethyl oleate. Proper fluidity can be maintained, for example, by the use of coating materials, such as lecithin, by the maintenance of the required particle size in the case of dispersions, and by the use of surfactants.

These compositions may also contain adjuvants such as preservatives, wetting agents, emulsifying agents, and dispersing agents. Prevention of the action of microorganisms may be ensured by the inclusion of various antibacterial and antifungal agents, for example, paraben, chlorobutanol, phenol sorbic acid, and the like. It may also be desirable to include tonicity-adjusting agents, such as sugars, sodium chloride, and the like into the compositions. In addition, prolonged absorption of the injectable pharmaceutical form may be brought about by the inclusion of agents which delay absorption such as aluminum monostearate and gelatin.

In some cases, in order to prolong the effect of a drug, it is desirable to slow the absorption of the drug from subcutaneous or intramuscular injection. For example, delayed absorption of a parenterally administered drug form is accomplished by dissolving or suspending the drug in an oil vehicle.

Injectable depot forms are made by forming microcapsule matrices of inhibitor(s) in biodegradable polymers such as polylactide-polyglycolide. Depending on the ratio of drug to polymer, and the nature of the particular polymer employed, the rate of drug release can be controlled. Examples of other biodegradable polymers include poly(orthoesters) and poly(anhydrides). Depot injectable formulations are also prepared by entrapping the drug in liposomes or microemulsions which are compatible with body tissue.

The preparations of agents may be given orally, parenterally, topically, or rectally. They are, of course, given by forms suitable for each administration route. For example, they are administered in tablets or capsule form, by injection, inhalation, eye lotion, ointment, suppository, infusion; topically by lotion or ointment; and rectally by suppositories. Oral administration is preferred.

The phrases “parenteral administration” and “administered parenterally” as used herein means modes of administration other than enteral and topical administration, usually by injection, and includes, without limitation, intravenous, intramuscular, intraarterial, intrathecal, intracapsular, intraorbital, intracardiac, intradermal, intraperitoneal, transtracheal, subcutaneous, subcuticular, intraarticular, subcapsular, subarachnoid, intraspinal and intrastemal injection, and infusion.

The phrases “systemic administration,” “administered systemically,” “peripheral administration” and “administered peripherally” as used herein mean the administration of a ligand, drug, or other material other than directly into the central nervous system, such that it enters the patient’s system and thus, is subject to metabolism and other like processes, for example, subcutaneous administration.

These inhibitors(s) may be administered to humans and other animals for therapy by any suitable route of administration, including orally, nasally, as by, for example, a spray, rectally, intravaginally, parenterally, intracistemally, and topically, as by powders, ointments or drops, including buccally and sublingually.

Regardless of the route of administration selected, the inhibitor(s), which may be used in a suitable hydrated form, and/or the pharmaceutical compositions of the present invention, are formulated into pharmaceutically acceptable dosage forms by conventional methods known to those of skill in the art.

Actual dosage levels of the active ingredients in the pharmaceutical compositions of this invention may be varied so as to obtain an amount of the active ingredient which is effective to achieve the desired therapeutic response for a particular patient, composition, and mode of administration, without being toxic to the patient.

The concentration of a disclosed compound in a pharmaceutically acceptable mixture will vary depending on several factors, including the dosage of the compound to be administered, the pharmacokinetic characteristics of the compound(s) employed, and the route of administration. In general, the compositions of this invention may be provided in an aqueous solution containing about 0.1-10% w/v of a compound disclosed herein, among other substances, for parenteral administration. Typical dose ranges are from about 0.01 to about 50 mg/kg of body weight per day, given in 1-4 divided doses. Each divided dose may contain the same or different compounds of the invention. The dosage will be an effective amount depending on several factors including the overall health of a patient, and the formulation and route of administration of the selected compound(s).

The term “Cx.yalkyr refers to substituted or unsubstituted saturated hydrocarbon groups, including straight-chain alkyl and branched-chain alkyl groups that contain from x to y carbons in the chain, including haloalkyl groups such as trifluoromethyl and 2,2,2-trifluoroethyl, etc. Coalkyl indicates a hydrogen where the group is in a terminal position, a bond if internal. The terms “C2.yalkenyl” and uC2-yalkynyr refer to substituted or unsubstituted unsaturated aliphatic groups analogous in length and possible substitution to the alkyls described above, but that contain at least one double or triple bond respectively.

The term “alkoxy” refers to an alkyl group having an oxygen attached thereto. Representative alkoxy groups include methoxy, ethoxy, propoxy, tert-butoxy and the like. An "ether” is two hydrocarbons covalently linked by an oxygen. Accordingly, the substituent of an alkyl that renders that alkyl an ether is or resembles an alkoxy.

The term “Ci^alkoxyalkyl” refers to a C^alkyl group substituted with an alkoxy group, thereby forming an ether.

The term “Ci.saralkyl”, as used herein, refers to a Ci^alkyl group substituted with an aryl group.

The terms “amine” and “amino” are art-recognized and refer to both unsubstituted and substituted amines and salts thereof, e.g., a moiety that can be represented by the general formulae:

wherein RJ, R10 and Ri0 each independently represent a hydrogen, an alkyl, an alkenyl, -(CH2)m-RK, or R9 and R10 taken together with the N atom to which they are attached complete a heterocycle having from 4 to 8 atoms in the ring structure; R represents an aryl, a cycioalkyl, a cycloatkenyl, a heterocyclyl or a polycyclyl; and m is zero or an integer from ! to 8. In preferred embodiments, only one of R9 or R10 can be a carbonyl, e.g., R9, R10, and the nitrogen together do not form an imide. In even more preferred embodiments, R9 and R10 (and optionally R10 ) each independently represent a hydrogen, an alkyl, an alkenyl, or -(CHjjm-R8· In certain embodiments, the amino group is basic, meaning the protonated form has a pKa > 7.00.

The terms “amide” and “amido” are art-recognized as an amino-substituted carbonyl and includes a moiety that can be represented by the general formula:

wherein R9, R10 are as defined above. Preferred embodiments of the amide will not include imides which may be unstable.

The term “aryl” as used herein includes 5-, 6-, and 7-inembered substituted or unsubstituted single-ring aromatic groups in which each atom of the ring is carbon. The term “aryl” also includes polycyclic ring systems having two or more cyclic rings in which two or more carbons are common to two adjoining rings wherein at least one of the rings is aromatic, e.g., the other cyclic rings can be cycloalkyls, cycloalkenyls, cycloalkynyls, aryls, heteroaryls, and/or heterocyclyls. Ary! groups include benzene, naphthalene, phenanthrene, phenol, aniline, and the like.

The terms “carbocycle” and “carbocyclyl”, as used herein, refer to a non-aromatic substituted or unsubstituted ring in which each atom of the ring is carbon. The terms “carbocycle” and “carbocyclyl” also include polycyclic ring systems having two or more cyclic rings in which two or more carbons are common to two adjoining rings wherein at least one of the rings is carbocyclic, e.g., the other cyclic rings can be cycloalkyls, cycloalkenyls, cycloalkynyls, aryls, heteroaryls, and/or heterocyclyls.

The term “carbonyl” is art-recognized and includes such moieties as can be represented by the general formula:

wherein X is a bond or represents an oxygen or a sulfur, and R11 represents a hydrogen, an alkyl, an alkenyl, -(C^jm-R or a pharmaceutically acceptable salt, R represents a hydrogen, an alkyl, an alkenyl or -(CH2)m-Rs, where m and R8 are as defined above. Where X is an oxygen and R11 or R11 is not hydrogen, the formula represents an “ester”. Where X is an oxygen, and R11 is a hydrogen, the formula represents a “carboxylic acid”.

The terms “heteroaryl” includes substituted or unsubstituted aromatic 5- to 7-membered ring structures, more preferably 5- to 6-membered rings, whose ring structures include one to four heteroatoms. The term “heteroaryl” also includes polycyclic ring systems having two or more cyclic rings in which two or more carbons are common to two adjoining rings wherein at least one of the rings is heteroaromatic, e.g., the other cyclic rings can be cycloalkyls, cycloalkenyls, cycloalkynyls, aryls, heteroaryls, and/or heterocyclyls. Heteroaryl groups include, for example, pyrrole, furan, thiophene, imidazole, oxazole, thiazole, triazole, pyrazolc, pyridine, pyrazine, pyridazine and pyrimidine, and the like.

The term “heteroatom” as used herein means an atom of any element other than carbon or hydrogen. Preferred heteroatoms are nitrogen, oxygen, phosphorus, and sulfur.

The terms “heterocyclyl” or “heterocyclic group” refer to substituted or unsubstituted non-aromatic 3- to 10-membered ring structures, more preferably 3- to 7-membered rings, whose ring structures include one to four heteroatoms. The term terms “heterocyclyl” or “heterocyclic group” also include polycyclic ring systems having two or more cyclic rings in which two or more carbons are common to two adjoining rings wherein at least one of the rings is heterocyclic, e.g., the other cyclic rings can be cycloalkyls, cycloalkenyls, cycloalkynyls, aryls, heteroaryls, and/or heterocyclyls. Heterocyclyl groups include, for example, piperidine, piperazine, pyrrolidine, morpholine, lactones, lactams, and the like.

The term “C|-6hydroxyalkyl” refers to a C|.6alkyl group substituted with a hydroxy group.

The terms “polycyclyl” or “polycyclic" refer to two or more rings (e.g., cycloalkyls, cycloalkenyls, cycloalkynyls, aryls, heteroaryls, and/or heterocyclyls) in which two or more carbons are common to two adjoining rings, e.g., the rings are “fused rings”. Each of the rings of the polycycle can be substituted or unsubstituted.

The term “proteasome” as used herein is meant to include immuno- and constitutive proteasomes.

The term “substantially pure” as used herein, refers to a crystalline polymorph that is greater than 90% pure, meaning that contains less than 10% of any other compound, including the corresponding amorphous compound. Preferably, the crystalline polymorph is greater than 95% pure, or even greater than 98% pure.

The term “substituted” refers to moieties having substituents replacing a hydrogen on one or more carbons of the backbone. It will be understood that “substitution” or “substituted with” includes the implicit proviso that such substitution is in accordance with permitted valence of the substituted atom and the substituent, and that the substitution results in a stable compound, e.g., which does not spontaneously undergo transformation such as by rearrangement, cyclization, elimination, etc. As used herein, the term “substituted” is contemplated to include all permissible substituents of organic compounds. In a broad aspect, the permissible substituents include acyclic and cyclic, branched and unbranched, carbocyclic and heterocyclic, aromatic and non-aromatic substituents of organic compounds. The permissible substituents can be one or more and the same or different for appropriate organic compounds. For purposes of this invention, the heteroatoms such as nitrogen may have hydrogen substituents and/or any permissible substituents of organic compounds described herein which satisfy the valences of the heteroatoms. Substituents can include, for example, a halogen, a hydroxyl, a carbonyl (such as a carboxyl, an alkoxycarbonyl, a formyl, or an acyl), a thiocarbonyl (such as a thioester, a thioacetate, or a thioformate), an alkoxyl, a phosphoryl, a phosphate, a phosphonate, a phosphinate, an amino, an amido, an amidine, an imine, a cyano, a nitro, an azido, a sulfhydryl, an alkylthio, a sulfate, a sulfonate, a sulfamoyl, a sulfonamido, a sulfonyl, a heterocyclyl, an aralkyl, or an aromatic or heteroaromatic moiety. It will be understood by those skilled in the art that the moieties substituted on the hydrocarbon chain can themselves be substituted, if appropriate. A “therapeutically effective amount” of a compound with respect to the subject method of treatment, refers to an amount of the compound(s) in a preparation which, when administered as part of a desired dosage regimen (to a mammal, preferably a human) alleviates a symptom, ameliorates a condition, or slows the onset of disease conditions according to clinically acceptable standards for the disorder or condition to be treated or the cosmetic purpose, e.g., at a reasonable benefit/risk ratio applicable to any medical treatment.

The term “thioether” refers to an alkyl group, as defined above, having a sulfur moiety attached thereto. In preferred embodiments, the “thioether" is represented by -S-alkyl. Representative thioether groups include methylthio, ethylthio, and the like.

As used herein, the term “treating"' or “treatment"' includes reversing, reducing, or arresting the symptoms, clinical signs, and underlying pathology of a condition in manner to improve or stabilize a subject's condition.

Exemplification

Example I

Synthesis of Compound 1

Synthesis of(B)

Hydroxybenztriazole (HOBT) (10.81 g, 80.0 mmol) and DIEA (200.0 mmol, 25.85 g, 35 mL) was added to a solution of NBoc leucine (50.0 mmol, 1 1.56 g) and phenylalanine methyl ester (50.0 mmol, 10.78 g) in 500 mL of DMF. The mixture was cooled to 0 °C in an ice-water bath and benzotriazol-1 -yloxytris(dimethylamino)-phosphonium hexafluorophosphate (BOP) (80.0 mmol, 35.38 g) was added in several portions over five minutes. The reaction was placed under an atmosphere of argon and stirred overnight. The reaction was diluted with brine (1000 mL) and extracted with EtOAc (5 x 200 mL). The organic layers were combined and washed with water (10 x 100 mL) and brine (2 x 150 mL) and dried over MgS04. The MgS04 was removed by filtration and the volatiles removed under reduced pressure to give (A) (18.17 g). To a 50 mL 0 °C cooled solution of 80% TFA/DCM was added BocNHLeuPheOMe (45.86 mmol, 18.0 g). The solution was stirred and allowed to warm to room temperature over 2 hr. The volatiles were removed under reduced pressure to give an oil. BocNHhPhe (45.86 mmol, 12.81 g), DMF (500 mL), HOBT (73.37 mmol, 9.91 g) and DIEA (183.44 mmol, 23.70 g, 32.0 mL) were then added to the oil. The mixture was cooled to 0 °C in an ice-water bath and BOP (73.37 mmol, 32.45 g) was added in several portions over five minutes. The reaction was placed under argon and allowed to warm to room temperature overnight. The reaction was diluted with FLO (1500 mL) and extracted with DCM (5 x 300 mL). The organic layers were combined and washed with FLO (6 x 300 mL) and brine (1 x 300 mL) and dried over MgS04. The MgS04 was removed by filtration and the volatiles removed under reduced pressure to give a yellow solid. EtOH (200 mL, 95%) was then added to the yellow solid and the mixture was heated to 65 °C to dissolve all of the solids. The solution was then added to 1000 mL of chilled FLO and the resulting precipitate collected to give (B) (21.59 g).

Synthesis of (C) (B) (1.80 mmol, 1.0 g) was mixed with TFA/DCM (80%) and was stirred at room temperature for 1 hr, at which time the mixture was concentrated and placed under high vacuum for 2 hr giving the TFA salt of the tri-peptide amine. To a 0 °C solution of the TFA salt (1.80 mmol) in DMF (10 mL) was added DIEA (3.6 mmol, 0.7 mL) followed by chloroacetyl chloride (2.7 mmol, 0.215 mL). The reaction was allowed to warm to RT while stirring overnight under an atmosphere of nitrogen. The mixture was then diluted with brine (15 mL) and extracted with EtOAc (3x15 mL). The organic layers were combined, washed with FLO (2x15 mL) and brine (2 x 15 mL) and dried over Na2S04. The Na2S04 was removed by filtration and the volatiles removed under reduced pressure. The crude material was suspended in EtOAc and filtered to give (C) (0.640 g)

Synthesis of (D) K.I (0.019 mmol, 0.0032 g) and morpholine (0.110 mmol, 0.0096 g) were added to a solution of (C) (0.094 mmol, 0.050 g) in THF (10 mL) and the mixture was stirred overnight under an atmosphere of nitrogen. The volatiles were removed under reduced pressure and the crude material taken up in EtOAc (15 mL), washed with FLO (2x10 mL) and brine (2x10 mL) and dried over MgS04. The MgS04 was removed by filtration and the volatiles removed under reduced pressure to give (D).

Synthesis of (E)

LiOH (0.94 mmol, 0.023 g) was added to a slurry of (D) (0.094 mmol) in 4 mL of 3:1 MeOH/FLO cooled to 0 °C. After 12 hr at 5 °C the reaction was quenched with 20 mL sat. NH4C1 and diluted further with 10 mL H2O. The pH of the reaction mixture was adjusted to 3 with 1 N HC1, extracted with DCM (3x15 mL), and dried over MgS04.

The MgS04 was removed by filtration and the volatiles were removed under reduced pressure to give (E).

Synthesis of Compound 1 (E) (0.082 mmol, 0.046 g), DIEA (0.328 mmol, 0.057 mL) and HOBT (0.133 mmol, 0.018 g) were added to a stirred solution of (F) (0.082 mmol) in DMF (2 mL). The mixture was cooled to 0 °C in an ice bath and BOP (0.131 mmol, 0.058 g) was added in several portions. The mixture was stirred at 5 °C under an atmosphere of argon overnight. The reaction was then diluted with H2O (15 mL) and extracted with EtOAc. The organic layer was washed with water, sat. NaHCC>3, and brine and dried over anhydrous MgS04. The MgS04 was removed by filtration and the volatiles removed under reduced pressure to give compound 1 (0.034 g) (IC50 20S CT-L<100nM; IC50 Cell-Based CT-L<100nM).

Example 2

Compound 1 (1.0 g) was dissolved in methanol (16 mL) heated to 80 °C. Water (4 mL) was then slowly added and the clear solution was allowed to cool to ambient temperature and the solution was brought to supersaturation by evaporating off 10 mL of solvent with compressed air. The resulting crystals were filtered, washed with 8 mL 1:1 deionized water-methanol, and dried under vacuum for 12 hours to provide crystalline compound 1 (0.9 g) with a melting point of 212 °C.

The characteristic DSC curve of the sample is shown in Figure 1 as recorded on a TA Instruments Differential Scanning Calorimeter 2920 at a heating rate of 10 °C/minute.

Example 3

Compound 1 (1.0 g) was dissolved in acetonitrile (17 mL) heated to 80 °C. Water (8 mL) was then slowly added and the clear solution was allowed to cool to ambient temperature and the solution was brought to supersaturation by evaporating off 10 mL of solvent with compressed air. The resulting crystals were filtered, washed with 8 mL 1:1 deionized water-acetonitrile, and dried under vacuum for 12 hours to provide crystalline compound 1 (0.85 g) with a melting point of 212 °C.

Example 4

Compound 1 (1.0 g) was dissolved in ethanol (17 mL) heated to 80 °C. Water (5 mL) was then slowly added and the clear solution was allowed to cool to ambient temperature and the solution was brought to supersaturation by evaporating off 15 mL of solvent with compressed air. The resulting crystals were filtered, washed with 8 mL 1:1 deionized water-ethanol, and dried under vacuum for 12 hours to provide crystalline compound 1 (0.82 g) with a melting point of 212 °C.

Example 5

Compound 1 (1.0 g) was dissolved in ethyl acetate (30 mL) heated to 80 °C.

Water (5 mL) was then slowly added and the clear solution was allowed to cool to ambient temperature and the solution was brought to supersaturation by evaporating off 20 mL of solvent with compressed air. The resulting crystals were filtered, washed with 5 mL ethyl acetate, and dried under vacuum for 12 hours to provide crystalline compound 1 (0.60 g) with a melting point of 21 2 °C.

Example 6

Compound 1 (1.0 g) was dissolved in ethanol (15 mL) heated to 80 °C. Water (5 mL) was then slowly added and the clear solution was allowed to cool to ambient temperature and the solution was brought to supersaturation by evaporating off 10 mL of solvent with compressed air. The resulting crystals were filtered, washed with 10 mL 1:1 deionized water-ethanol, and dried under vacuum for 12 hours to provide crystalline compound 1 (0.54 g) with a melting point of 212 °C.

Example 7

Synthesis of (F)

Compound (G) (0.43 g) was prepared according to U.S. Pat. Application No. 2005-0256324 and was added to a flask along with Pd/C (10% wt, 0.10 g) followed by slow addition of TFA (35 mL). The flask was evacuated and back-flushed with hydrogen gas three times and then the reaction mixture was stirred under one atmosphere of hydrogen at room temperature for two hours. The reaction mixture was then filtered through Celite and the filtrate was concentrated under reduced pressure.

Dichloromethane (25 mL) was added and the volatiles removed under reduced pressure. The resultant thick yellow syrup was dried under high vacuum to a constant weight. The syrup was then transferred to 50 mL volumetric flask and rinsed with 8.5 mL diethyl ether to yield crystalline compound (F) (0.33g).

Synthesis of Compound 1 A 10 mL volumetric flask was charged with I-hydroxybenzotriazole (HOBT, 0.54 g) and N,N.N\N:-tetramethyi-0-(l H-benzotriazol-1 -yl)uronium hexafluorophosphate (HBTU, 1.54 g) and diluted to 50 mL with DMF. This stock solution of coupling reagents was 0.40 M for both HOBT and HBTU. (E) (0.61 g), (F) (0.33g), and the coupling reagent stock solution (2.7 mL), were added to a 10 mL volumetric flask and the mixture was cooled to 0 °C. D1EA (0.56 mL) was then added dropwise to the cooled solution. The mixture was allowed to stir at 0 °C for 60 minutes and was then quenched by the addition of saturated sodium bicarbonate (15 mL). The mixture was diluted with ethyl acetate (35 mL) and the layers separated.

The organic layer was washed saturated sodium bicarbonate (3x15 mL), brine (2x15 mL) and dried over sodium sulfate. The sodium sulfate was removed by filtration and the volatiles removed under reduced pressure to give a thick syrup which was further dried under high vacuum to give a crude compound 1 as a foam (0.59 g).

Example 8

Crude compound 1 (0.590 g) was completely dissolved in methanol (11 mL) by stirring and heating in an oil bath (80 °C) and deionized water (17 mL) was added dropwise. The mixture was seeded with crystalline compound 1, stirred and allowed to slowly evaporate for 12 hours to approximately 20 mL to precipitate compound 1. The suspension was filtered, washed with 1:1 deionized water-methanol (4 mL), and dried under vacuum for 12 hours at room temperature to yield compound 1 as a white solid (0.25 g). The crystallization was repeated two additional times to yield crystalline compound 1 (0.13 g).

Crystalline compound I (0.3 g) was dissolved in isopropanol (15 mL) by stirring and heating in an oil bath (80 °C). The solution was concentrated under reduced pressure to reduce volume to 5 mL. Deionized water (20 mL) was quickly added and the resultant suspension was rigorously stirred for ! hour. The glassy precipitate was filtered, rinsed with deionized water (25 mL) and dried to yield amorphous Compound 1 (0.3 g).

The characteristic DSC curve of the amorphous sample is shown in Figure 7 which was recorded on a TA Instruments Differential Scanning Calorimeter 2920 at a heating rate of 1 °C/minute for the amorphous form of Compound 1.

The characteristic X-ray diffraction pattern of the amorphous powder is shown in Figure 8 and was recorded on the Shimadzu XRD-6000 under Cu Ka radiation [voltage and current set at 40 kV and 40 mA; divergence and scattering slits set at Γ and receiving slit set at 0.15 mm; Nal scintillation detector used for diffracted radiation; a Θ-2Θ continuous scan at 3°/min (0.4 sec/0.02° step) from 2.5 to 40° 2Θ was used; samples were placed in an aluminum holder with silicon insert; and data collected and analyzed with XRD-6100/7000 v.5.0].

Example 9

Synthesis of (F) A flask was charged with (G) and ethyl acetate (400 ml) and the solution was cooled in an ice bath for 15 minutes with stirring. Trifluoroacetic acid (200 mL) was added dropwise, maintaining an internal temperature of less than 10 °C. Pd/C (3.6 g) was added in one portion and the flask was purged under high vacuum and refilled with hydrogen three times. After 2 hours, the reaction was filtered through Celite and the filtrate evaporated under reduced pressure to a thick orange oil which was swirled gently with 1 70 mL diethyl ether. As the flask was swirled, fine crystals formed. The flask was allowed to sit at room temperature, and rapid crystallization occurred. After 1 hour at ambient temperature, the flask was capped tightly and placed in the freezer overnight (< -5 °C). The resulting crystalline solid was filtered and washed with ice cold ethyl ether (50 mL) and dried under high vacuum. Fine white crystals (14.1 g; melting point: 137 °C) of (F) were obtained.

Synthesis of Compound 1 A flask was charged with (F) (10 g), (E) (15.3 g), HBTU (15.3 g), HOBt (5.5 g), and DMF (300mL). The mixture was stirred vigorously until dissolved and was placed in an NaCl/ice bath (-5 °C). After 15 minutes, DIEA (7.1 mL) was added dropwise over <10 minutes, maintaining an internal temperature of less than -3 °C. After addition was complete, the reaction mixture was stirred in the bath for one hour and was quenched by addition of saturated NaHCOi (aq.) (200 mL). The slurry was extracted with ethyl acetate (1.5 L) and the organic layer was washed with sat. NaHCC>3(aq.) (2 x 300 mL) and sat. NaCl (aq.) (200 mL), and then dried over MgSCL.

The organic layer was concentrated to ~50 mL under reduced pressure and methylethyl ketone (200 mL) was added, and (he solution was again concentrated to -50 mL. Methylethyl ketone (125 mL) was added again, and the solution was stirred in an oil bath (80 °C) until clear. The solution was then allowed to cool and was seeded with pure crystalline Compound 1. The mixture was stirred for 2 hours at 25 °C and then overnight at 0 °C. The white solid precipitate was filtered and washed with ice cold methylethyl ketone (300 mL) to give white solids. The solid was dried under high vacuum at ambient temperature to a constant weight to yield 13.5 g of pure compound 1.

Example 10

Synthesis of (F) A flask was charged with (H) (100 g) [see: Bioorg. Med. Chem. Letter 1999, 9, 2283-88], and dichloromethane (300 mL) under nitrogen and the solution was cooled in an ice bath to 0-5 °C. Trifluoroacetic acid (1 36.9 mL) was added dropwise with stirring at 0-10 °C, after which the reaction mixture was removed from the ice bath and stirred at room temperature for 2 hours. Methyl tert-butyl ether (300 mL) was then added and 400 mL of solvent was evaporated under reduced pressure. MTBE (200 mL) was then added via addition funnel and the solution stirred for 20 minutes at 20 °C, then heptanes (1000 mL) were added within 10 minutes and the reaction mixture cooled to 0-5 °C. The reaction mixture was stirred for 30 minutes and then the solids were filtered, rinsed with cold heptanes (0-5 °C, 3 x 100 mL) and dried under high vacuum to the constant weight to yield 90.69 g of (F) as a white solid.

Synthesis of Compound 1 A solution of (F) (137.53 g) in DMF (900 mL) was cooled in a NaCl/ice bath to -2 °C. HBTU (138.06 g), HOBT (55.90 g), (F) (90.00 g) and ice cold DMF (180 mL) were then added to the solution followed by addition of neat D1EA (67.19 g. 509.66 mmol) via a dropping funnel at a rate such that the internal temperature remained at -0 °C. After two hours, neat isopropylethylamine (24.0 g) was added via a dropping funnel. The mixture was stirred at 0 °C until conversion >99%. The reaction mixture was then transferred portionwise into a dropping funnel and slowly added to an ice cold half-saturated NaHCC>3 solution (3.6 L) (internal temperature maintained at 20 °C). The resulting slurry was stirred with a mechanical stirrer for 30 minutes and the solids were then filtered and the filter cake washed with ice cold water (2 x 1350 ml). The solids were then dissolved in dichloromethane (2.7 L) and the organic phase was extracted with water (portions of 2700 mL) until relative percent area for HOBt/HBTU was <15% by HFLC (200 pL solution for HPLC sample). The organic phase was filtered through a plug of sodium sulfate and subsequently inline filtered through a pad of active charcoal.

The organic phase was concentrated under reduced pressure and methylethyl ketone (1350 mL) was added and the solution concentrated again under reduced pressure. Methylethyl ketone (1350 mL) was then added and the solution concentrated again under reduced pressure. The resulting concentrated solution was cooled to 0 °C until solids were formed; then the mixture was heated to 75 °C as more methylethyl ketone was added (ca. 750 mL) until complete dissolution. The solution was cooled to 65 °C and seeded and the resulting solution/slurry was cooled at a rate of 0.5 °C/minute to 20 °C (stir rate of 60-70 rpm). The slurry was stirred for a minimum of 5 hours at 20 °C to allow for complete crystallization. The solids were filtered off and washed with ice cold methylethyl ketone (720 mL) and the filter cake was dried under a stream of nitrogen for 1 hour. The solids were transferred into a round bottom flask and dried under reduced pressure to constant weight to yield 1 16 g of crystalline compound 1.

Example 11

Methanol (200 mL) was added to crude Compound 1 and the mixture was concentrated to 100 mL. Additional methanol (275 mL) was added, along with deionized water (75 mL), and the mixture concentrated to 400 mL. The clear solution was then seeded with pure crystalline Compound 1, stirred and allowed to slowly evaporate under a stream of compressed air to 200 mL. The resulting yellowish solid was washed with deionized water (400 mL) and 1:1 deionized water-methanol (300 mL) until it turned white and filtrate turned clear. Compound 1 was then dried under vacuum for 12 hours.

The resulting compound 1 (17.3 g) was completely dissolved in methanol (275 mL) by stirring and heating in oil bath (bath set at 85 °C; mixture temperature less than 65 °C). Deionized water (75 mL) was added dropwise over 15 minutes, and the clear mixture was allowed to cool to room temperature. Seed crystals of compound 1 were added to the stirred solution, and the mixture was allowed to slowly concentrate under a stream of compressed air to approximately 250 mL over 9 hours. The crystals were then filtered and washed with 1:1 deionized water-methanol (300 mL). The white solid was dried under vacuum for 12 hours at 22 °C to yield crystalline compound 1 (14.0 g).

Example 12

Crude compound 1 (12.1 g) was completely dissolved in methanol (50 mL) by stirring and heating in oil bath (bath set at 85 °C; mixture temperature less than 65 °C). The clear solution was allowed to cool to room temperature and seed crystals of compound 1 were added to the solution. The mixture was allowed to crystallize over three hours at room temperature. The resulting solid was washed with 1:1 deionized water-methanol (500 mL), filtered, and dried under vacuum for 12 hours to yield crystalline compound 1 (9.4 g).

Example 13

Synthesis of (F) A flask was charged with (Η) (1 g) and ethyl acetate (20 mL) and the solution was cooled in an ice bath for 15 minutes with stirring. Trifluoroacetic acid (10 mL) was then added dropwise, while maintaining an internal temperature of less than 3 °C. After stirring at 0 °C for 2 hours, the reaction was allowed to warm to ambient temperature and was stirred for two additional hours. The solution was then evaporated under reduced pressure to a thick colorless oil. This crude mixture was swirled gently with 10 mL of diethyl ether and as the solution was swirled, fine crystals fonned. After 30 minutes at ambient temperature, the flask was capped tightly and placed in the freezer overnight.

The resulting crystalline solid was filtered and washed with ice cold diethyl ether, and then dried on high vacuum to a constant weight to give fine white crystals of (F) (670 mg)·

Example 14

Synthesis of Compound 1

Compound (E) (14.2 g), HBTU (14.3 g), HOBT (5.1 g) and DMF (300 mL), were added to (F) and the mixture was stirred at room temperature to complete dissolution.

The reaction was cooled in ice bath for 15 minutes, and DIEA (32 mL) was added over 15 minutes while maintaining an internal temperature of less than 10 °C. The reaction mixture was then stirred at 0 °C for one hour before it was quenched with saturated sodium bicarbonate (200 mL). The mixture was extracted with ethyl acetate (1.5 L), and the organic layer was washed with saturated sodium bicarbonate (2 x300 mL) and deionized water (1 x 200 mL). The combined aqueous wash was extracted with ethyl acetate (200 mL) and the organic layers were combined (1.7 L).

The combined organic layers (1.7 L) were concentrated under reduced pressure to 100 mL followed by addition of methanol (200 mL), and the mixture was again concentrated to 100 mL. Additional methanol ¢200 mL) was added, deionized water (75 mL) was slowly added with stirring, and the mixture concentrated to 300 mL. The clear solution was seeded with crystalline compound 1, stirred and allowed to slowly concentrate under a stream of compressed air to about 200 mL. The off-white solid was washed until solid turned white and filtrate turned clear with a 4:1 deionized water-methanol (2 L) and 1:1 deionized water-methanol (500 mL). The resulting solid was dried under vacuum for 12 hours at 22 °C to provide compound 1 (16.8 g).

Compound 1 was completely dissolved in ethanol (200 mL) by stirring and heating in oil bath (bath set at 85 °C; mixture temperature less than 65 °C). The clear solution was allowed to cool to room temperature and seed crystals of compound 1 were added to the stirred solution, and the mixture was flushed with air and allowed to crystallize. The mixture was then filtered, washed with 1:1 deionized water-ethanol (200 mL), and dried under vacuum for 12 hours at room temperature to yield 10.2 g of crystalline compound 1.

Example 15 Synthesis of (F) A 500 mL flask was equipped with a mechanical stirrer, thermocouple, cooling bath. (G) (12.5 g) was dissolved in ethyl acetate (125 mL) and the clear solution was cooled to 0-5 °C followed by slow addition of trifluoroacetic acid (375 mL) such that the internal temperature was maintained below 10 °C. After warming to room temperature, 5% Pd/C (1.25 g) was added and the reaction mixture under an atmosphere of hydrogen for 2 hours. The reaction mixture was filtered through a glass fiber and rinsed with ethyl acetate (50 mL). The filtrate was then concentrated under reduced pressure to yield a yellow oil. MTBE (50 mL) was added to the oil and co-evaporated to yellow oil at 25 °C. MTBE (60 mL) was again added and the mixture was cooled to -10 °C and stirred for 60 minutes. Heptanes (120 mL) were then slowly added to the stirred mixture and stirring was continued at -10 °C for an additional 15 minutes. The solids were collected by filtration and the crystals were rinsed with heptanes (2 x 40 mL) and dried under high vacuum at room temperature (22 °C) to a constant weight (10.1 g).

Synthesis of Compound 1 A flask equipped with a mechanical stirrer, thermocouple, cooling bath, nitrogen inlet and drying tube was charged with DMF, (F) (133.9 g), (E) (241.8 g), HBTU (242.8 g), and HOBT (86.5 g) and the mixture was stirred and cooled to 0-5 °C. DIEA (156 mL) was then added slowly over at least 30 minutes, while maintaining temperature between 0-5 °C. The reaction mixture was stirred at 0-5 °C for one hour and was then poured into a vigorously stirred saturated solution of sodium bicarbonate (3630 mL) and ethyl acetate (900 mL). Additional ethyl acetate (2000 mL) was added to extract the product and the organic layer was separated. The aqueous layer was then extracted with ethyl acetate (1930 mL). The organic phases were combined and washed with saturated solution of sodium bicarbonate (2420 mL) and brine (2420 mL), dried over magnesium sulfate (360 g), filtered through glass fiber filter and rinsed with ethyl acetate (2 x 360 mL).

The resulting solution was concentrated to a semisolid under reduced pressure and methanol (725 mL) was added and co-evaporated under reduced pressure to yield semisolid compound 1. The crude product was dissolved in methanol (5320 mL) and the solution was stirred while water (2130 mL) was added over twenty minutes. When addition of water was complete, approximately 0.3 g of pure crystalline seeds were added and the methanol/water solution was stirred for three hours. The resulting crystalline white solid was isolated by filtration and the fine white crystalline product was rinsed with a methanol/water solution (1:1, 1200 mL). The resulting solid was rinsed with methanol/water solution (1:1, 1200 mL) and the crystalline product was poured onto drying tray and dried to a constant weight under high vacuum at 27 °C under nitrogen bleed to yield crystalline compound 1 (230 g).

Example !6

Synthesis of (F) A 100 mL three-neck round bottom flask was charged with (G) (5 g) and dichloromethane (15 mL). The mixture was stirred until the solids had dissolved, and then placed in an ice bath. After 20 minutes, the internal temperature had reached 0.6 °C and trifluoroacetic acid was added dropwise over 5 min. After the addition was complete, the flask was allowed to warm to room temperature. After 2 hours, MTBE was added to the flask (35 mL) and the mixture was cooled in an ice bath, wherein (F) began to crystallize during cooling. Heptanes (65 mL) were then added to the flask dropwise over 15 min and the flask was placed in the freezer (-5 °C). After 1 hour, the solid white product was collected and washed with heptanes (10 mL) to provide 4.57 g of (F).

Example 17

Synthesis of Compound 1 Citrate Salt

Compound 1 (10 g) and citric acid (2.7 g) were dissolved in THF (75 mL) and acetonitrile (50 mL). The solution was then stirred for 2 hours at room temperature, at which time a white precipitate formed. The flask was then cooled to -10 °C and stirred overnight. The solids were filtered and washed with 100 mL acetonitrile to give 11.52 g of the citrate salt of compound 1.

Example 18

Synthesis of (H) and (Q)

Synthesis of (1) A suspension of dimethyl hydroxylamine hydrochloride {10.53 g, 108 mmol) in DCM (270 mL) under an atmosphere of argon was stirred vigorously for 0.5 hours followed by addition of TEA (10.92 g, 14.75 mL, 108 mmol) via addition funnel. A solution of Boc-Leucine-OH (25.0 g, 108 mmol) in DCM (270 mL) was cooled to 0 °C followed by dropwise addition of isobutylchlorofonnate (14.73 g, 13.98 mL, 108 mmol) via addition funnel. The mixture was further cooled to -20 °C and NMM (10.92 g, 11.87 mL, 108 mmol) was added via addition funnel at such a rate to maintain the internal temperature below -10 °C. After stirring for 5 minutes at -20 °C, the previously prepared dimethylhydroxylamine solution was added via a wide bore Teflon cannula. The reaction mixture was removed from the cooling bath and allowed to warm to room temperature overnight. The mixture was then diluted with water (100 mL) and stirred for 1 5 minutes.

The layers were separated and the aqueous layer extracted with DCM (2 x 50 mL). The organic layers were combined, washed with 1 N HC1 (4 x 150 mL), water (1 x 150 mL), sat. NaHCOi (2 x 100 mL), brine (1 x 250 mL) and dried over Na2SC>4. The Na2SC>4 was removed by filtration and the volatiles removed under reduced pressure to give (I) (28.05 g, 102 mmol).

Synthesis of (J)

To a 0 °C solution of (I) (10.0 g, 36.4 mmol,) in 100 mL of dry THF, under an atmosphere of argon was added isopropenyl magnesium bromide (364 mL, 182 mmol, 5.0 eq, 0.5 M solution in THF) dropwise using an addition funnel. The rate of addition was adjusted such that the internal reaction temperature was maintained below 5 °C.

After six hours the reaction mixture was poured into 250 mL of sat. NH4CI and 500 mL wet ice. After stirring for 30 minutes the mixture became clear and the volatiles were removed under reduced pressure and the crude material diluted with EtOAc (200 mL). The layers were separated and the aqueous layer extracted with EtOAc (3 x 150 mL), the organic layers were combined, washed with water (2 x 150 mL), brine (2 x 150 mL) and dried over MgS04. The MgS04 was removed by filtration and the volatiles removed under reduced pressure. Purification by flash chromatography (15:1 hexanes/ EtOAc) gave (J) as a solid (7.5 g, 29.37 mmol).

Synthesis of (K) and (L)

To a 0 °C solution of (J) (5.0 g, 19.58 mmol) in 200 mL of MeOH was added CeCl3-7H20 (8.75 g, 23.50 mmol). The solution was stirred under an atmosphere of argon until the CeCh-7H20 was completely dissolved. To this solution was added NaBH4 (0.88 g, 23.50 mmol) in 10 portions over 2 minutes. The reaction was then stirred under an atmosphere of argon at 0 °C for 6 hours. The reaction was quenched at 0 °C with approximately 2.5 mL of glacial HOAc and after 30 minutes of additional stirring at 0 °C the mixture become clear. The volatiles were removed under reduced pressure and the remaining oil taken up in EtOAc (200 niL). The organic layer was washed with water (2 x 100 mL), brine (2 x 100 mL) and dried over MgS04. The MgS04 was removed by filtration and the volatiles removed under reduced pressure giving (K.) and (L) as a waxy, white solid ¢4.75 g, 18.5 mmol). Ratio of diastereomers 4.5:1 as determined by HPLC.

Synthesis of (Μ), (N), (O) and (P)

To a solution of (K) and (L) (0.025 g, 0.097 mmol) in DCM (1 mL) was added amCPBA (0.018 g, 0.107 mmol). The mixture was stirred at room temperature for one hour at which time the mixture was diluted with sat. NaHCOi (5 mL). The layers were separated and the aqueous layer extracted with DCM (2x2 mL). The organic layers were combined and washed with water (2x5 mL), brine (2x5 mL) and dried over MgSCL. The MgSCL was removed by filtration and the volatiles removed under reduced pressure to give an oil.

Synthesis of (H) and (Q)

To a solution of Dess-Martin Periodinane (0.023 g, 0.055 mmol) in 1 mL MeCN at 5 °C was added a mixture of (Μ), (N), (O), and (P) (0.010 g, 0.037 mmol) as a solution in MeCN (1 mL). The mixture was placed under an atmosphere of argon and allowed to warm to room temperature while stirring overnight. When complete, a white precipitate had formed and the reaction was cooled in an ice-bath and diluted with 2 mL sat, NaHCC>3. The mixture was diluted with 10 mL of EtOAc and the solids removed by filtering through a plug of Celite. The mixture was transferred to a separatory funnel and the layers separated. The aqueous layer was extracted with EtOAc (2x5 mL) and the organic layers combined, washed with water (3x5 mL) and brine (1x10 mL) and then dried over Na2S04. The Na2S04 was removed by filtration and the volatiles removed under reduced pressure to give a mixture of (H) and (Q) as a light, yellow oil.

Example 19

Alternate Synthesis of (H) and (Q)

Alternate Synthesis of (H) and (0)

To a -5 °C solution of (R) (0.200 g, 0.78 mmol) in pyridine (3 mL) was added 10% aqueous NaOCl (1.5 mL) dropwise at a rate such that the internal reaction temperature remained below -4 °C. After the addition of NaOCl was complete, the reaction flask was placed in a 0 °C bath and stirred for two hours. The mixture was then diluted with EtOAc (10 mL), washed with water (2 x 10 mL), brine (2 x 10 mL) and dried over Na2SC>4. The Na2SC>4 was removed by filtration and the volatiles removed under reduced pressure to give the crude mixture of (H) and (Q). Purification by flash chromatography (20:1 hexanes/ EtOAc) gave (H) as an oil (0.059 g, 0.216 mmol) and (Q) as a solid (0.023 g, 0.085 mmol).

Example 20

Synthesis of Compound 1

Synthesis of (F)

To a 10 mL round bottomed flask was added (H) (0.050 g, 0.18 mmol) and DCM (0.80 mL). The mixture was cooled to 0 °C and neat TFA (0.20 mL) was added dropwise. After the addition of TFA was complete the flask was allowed to warm to room temperature while stirring for one hour. The volatiles were then removed under reduced pressure and the resulting oil was chased with DCM (2 mL x 2) and the volatiles removed under reduced pressure.

Synthesis of Compound 1

To a 10 mL round bottomed flask containing (F) was added (E) (0.085 g, 0.15 mmol), MeCN (2.0 mL), HOBT (0.031 g, 0.23 mmol), and HBTU (0.087 g, 0.23 mmol) and the mixture was cooled to 0 °C. To this mixture was slowly added DIEA (0.077 g, 0.104 mL, 0.6 mmol) and the mixture was allowed to stir at 0 °C for one hour before quenching with saturated NaHCOj (5 mL). The mixture was diluted with EtOAc (15 mL) and the layers were separated. The organic layer was washed with saturated NaHCCh (3 x 5 mL), brine (2x5 mL) and dried over Na2SC>4. The NaiSC^ was removed by filtration and the volatiles removed under reduced pressure to give a thick oil. To the flask containing the oil was added DCM (1 mL) and the placed under high vacuum while swirling giving Compound 1 (0.100 g, 0.14 mmol) as a foam.

Example 21

Synthesis of Compound 1

Alternate Synthesis of (S)

To a 10 mL round bottomed flask was added (G) (0.055g, 0.18 mmol), formic acid (2 mL), and Pd/C (5% wt, 0.05 g). Once the deprotection was deemed complete by TLC and LCMS, the volatiles were removed under reduced pressure. The oil was chased with DCM (2 mL x 2) and the volatiles removed under reduced pressure.

Synthesis of Compound 1

To a 10 mL round bottomed flask containing (S) was added (E) (0.085 g, 0.15 mmol), MeCN (2.0 mL), HOBT (0.031 g, 0.23 mmol), HBTU (0.087 g, 0.23 mmol) and the mixture was cooled to 0 °C. To this mixture was slowly added D1EA (0.077 g, 0.104 mL, 0.6 mmol). The mixture was then allowed to stir at 0 °C for 60 minutes and was quenched by the addition of saturated NaHCC>3 (5 mL). The mixture was diluted with EtOAc (15 mL) and the layers separated. The organic layer was washed with saturated NaHCC>3 (3x5 mL), brine (2x5 mL) and dried over NajSO,). The Na^SO^ was removed by filtration and the volatiles removed under reduced pressure to give a thick oil. To the flask containing the oil was added DCM (1 mL) and the mixture placed under high vacuum while swirling giving Compound 1 as a foam.

Example 22

Synthesis of (H)

Water (214 mL) was added to a three neck flask equipped with a mechanical stirrer, an addition funnel, and a thermocouple with display and cooled to an internal temperature of -5 to 0 °C. Solid calcium hypochlorite (107 g, 748 mmol) was then added over approximately 5 minutes, while the temperature of the mixture is maintained at approximately -5°C to 0°C. The mixture was then further cooled to -10°C to -5°C and stirred for 10 minutes followed by addition of NMP (1000 mL) via addition funnel at a rate to maintain internal temperature between -10 °C to -5 °C. The reaction slurry was then stirred at -10 °C for 15 minutes. (R) (47.8 g, 187 mmol) was dissolved in NMP (40 OmL) and added dropwise to the reaction mixture while maintaining the internal temperature between -15 °C and -10 °C. The reaction mixture was then stirred at -5 °C to 0 °C until the reaction was complete by TLC. Upon reaction completion, the mixture was quenched by slow addition of 1.0 M sodium thiosulfate solution (500 mL), maintaining an internal temperature of-10 °C to -5 °C. Ethyl Acetate (1000 mL) was then added, the layers were separated and the aqueous layer was extracted twice more. The combined organic layers were washed with water (500 mL) and brine (500 mL), dried over magnesium sulfate, filtered and concentrated under reduced pressure to a to yellow oil which was dissolved in hexanes (600 mL) and filtered through a plug of silica to provide (H) as a pale yellow oil (20.8 g).

Equivalents

Those skilled in the art will recognize, or be able to ascertain using no more than routine experimentation, numerous equivalents to the compounds and methods of use thereof described herein. Such equivalents are considered to be within the scope of this invention and are covered by the following claims.

All of the above-cited references and publications are hereby incorporated by reference.

Claims (11)

1. A crystalline compound having a structure of Formula (II)

(II) and having a melting point of about 211 to about 213 °C.

2. A crystalline compound having a structure of Formula (II)

(II) and having an XRPD pattern substantially as shown in Figure 2.

3. A crystalline compound having a structure of Formula (II)

(II) and having 2Θ values 6.10; 8.10; 9.32; 10.10; 11.00; 12.14; 12.50; 13.64; 13.94; 17.14; 17.52; 18.44; 20.38; 21.00; 22.26; 23.30; 24.66; 25.98; 26.02; 27.84; 28.00; 28.16; 29.98; 30.46; 32.98; 33.22; 34.52; 39.46.

4. A crystalline salt of a compound having a structure of Formula (II)

(II) and having a melting point of about 184 to about 188 °C, wherein the salt is a citrate salt.

5. A crystalline salt of a compound having a structure of Formula (II)

(II) and having an XRPD pattern substantially as shown in Figure 12, wherein the salt is a citrate salt.

6. A crystalline salt of a compound having a structure of Formula (II)

(N) and having 2Θ values 4.40; 7.22; 9.12; 12.36; 13.35; 14.34; 15.54; 16.14; 16.54; 17.00; 18.24; 18.58; 19.70; 19.90; 20.30; 20.42; 21.84; 22.02; 23.34; 23.84; 24.04; 24.08; 24.48; 24.76; 25.48; 26.18; 28.14; 28.20; 28.64; 29.64; 31.04; 31.84; 33.00; 33.20; 34.06; 34.30; 34.50; 35.18; 37.48; 37.90; 39.48, wherein the salt is a citrate salt.

7. A phamaceutical composition comprising a crystalline compound of any one of claims 1 to 3 and a pharmaceutically acceptable carrier.

8. A method for treating a disease or condition selected from cancer, autoimmune disease, graft or transplant-related condition, neurodegenerative disease, fibrotic-associated condition, ischemic-related conditions, infection (viral, parasitic or prokaryotic) and diseases associated with bone loss, comprising administering a crystalline compound of any one of claims 1 to 3 or a phamaceutical composition of claim 7.

9. The method of claim 8 wherein the disease or condition is cancer and the cancer is multiple myeloma.

10. Use of a crystalline compound of any one of claims 1 to 3 for the manufacture of a medicament for treating a disease or condition selected from cancer, autoimmune disease, graft or transplant-related condition, neurodegenerative disease, fibrotic-associated condition, ischemic-related conditions, infection (viral, parasitic or prokaryotic) and diseases associated with bone loss.

11. The crystalline compound of any one of claims 1 to 6; the phamaceutical composition of claim 7; the method of claim 8; or the use of claim 10, substantially as herein described with reference to any one or more of the examples but excluding comparative examples.