Androgen induced oxidative stress inhibitors
AssigneeColby Pharmaceutical Company
InventorsHirak S. Basu, David A. Zarling, George Wilding, Farideh Mehraein-Ghomi, Dawn R. Church
Life of this patent
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Abstract
Described herein are pharmaceutical compositions and medicaments, and methods of using such pharmaceutical compositions and medicaments in the treatment of cancer.
Claims29
A compound having the structure of Formula (I):
- wherein:
- R1, R3 and R4 are each independently selected from H, D, F, Cl, Br, I, —CN, —NO2, —OH, —CF3, —OCF3, —OR4, —NR6R6, C1-C6alkyl, C3-C8cycloalkyl, C1-C6heteroalkyl, C1-C6haloalkyl, C2-C8heterocycloalkyl, optionally substituted aryl, optionally substituted O-aryl, optionally substituted heteroaryl, —N═N-aryl, —NHS(═O)2R5, —S(═O)2N(R6)2, —N(R6)S(═O)2N(R6)2, —C(═O)CF3, —C(═O)NHS(═O)2R5, —S(═O)2NHC(═O)R5, —N(R6)2, —N(R6)C(═O)R6, —N(R6)C(═O)N(R6)2, —N(R6)C(═O)OR5, —CO2R6, —C(═O)R6, —OC(═O)R5, —OC(═O)N(R6)2, —CON(R6)2, —SR6, —S(═O)R5, and —S(═O)2R5;
- each R5 is independently selected from C1-C6alkyl, C1-C6haloalkyl, C3-C8cycloalkyl, aryl, and benzyl;
- each R6 is independently selected from H, C1-C6alkyl, C1-C6haloalkyl, C3-C8cycloalkyl, aryl, and benzyl;
- R2 is selected from H, OH, OC(═O)C1-C6alkyl, or OC(═O)H;
- n is an integer selected from 0-4;
- m and o are each independently an integer selected from 0-5;
- or a pharmaceutically acceptable salt, solvate, prodrug or metabolite thereof.
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The compound of wherein R3 is S(═O)2OH.
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A compound selected from the group consisting of:
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A method of inhibiting the growth of human prostate cancer in a subject comprising administering to a subject in need thereof an inhibitor of the JunD-AR interaction.
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Dependencies are inferred from the claim text.