Pharmaceutical compositions which inhibit FKBP52-mediated regulation of androgen receptor function and methods of using same

Patent metadata

Field	Value
Publication number	US-9233973-B2
Application number	US-201414336075-A
Country	US
Kind code	B2
Filing date	Jul 21, 2014
Priority date	Sep 15, 2009
Publication date	Jan 12, 2016
Grant date	Jan 12, 2016

Abstract

Pharmaceutical compositions that bind to a predicted FK506 Binding Protein 52 (FKBP52) interaction surface on the androgen receptor hormone binding domain, otherwise known as FKBP52 Targeting Agents (FTAs) are provided. These compositions of the present invention are found to specifically recognize the FKBP52 regulatory surface on the androgen receptor and inhibit FKBP52 from functionally interacting with the androgen receptor. Compositions comprising the pharmaceutical composition, as well as methods of use, treatment and screening are also provided.

First claim

The invention claimed is:

1. A method of inhibiting prostate cancer in a male mammal, the method comprising:
administering to the mammal a pharmaceutical composition comprising a compound selected from the group consisting of:

and pharmaceutically acceptable salts, solvates and stereoisomers thereof, wherein the composition comprises a pharmaceutically and physiologically acceptable carrier, in an amount effective to inhibit prostate cancer cell growth in the mammal.

2. The method of claim 1 , wherein the pharmaceutical composition further comprises one or more anti-androgenic compounds and/or one or more LH-RH agonists.

3. The method of claim 2 , wherein the one or more anti-androgenic compound(s) is/are selected from the group consisting of bicalutamide, nilutamide, and 5-alpha-reductase inhibitors.

4. The method of claim 3 , wherein the 5-alpha-reductase inhibitor(s) is/are selected from the group consisting of MK-906, 17-β-N,N-diethylcarbamoyl-4-methyl-4-aza-5-α-androstan-3-one, 4-azasteroid, 6-methylene-4-pregnene-3,20-dione, and 4-methyl-3-oxo-4-aza-5-α-pregnane-30(s) carboxylate.

5. The method of claim 1 , further comprising administering compound 1 or a pharmaceutically acceptable salt, solvate or stereoisomer thereof to the mammal, wherein compound 1 is

6. The method of claim 1 , wherein the compound is

or a pharmaceutically acceptable salt, solvate or stereoisomer thereof.

7. The method of claim 1 , wherein the compound is

or a pharmaceutically acceptable salt, solvate or stereoisomer thereof.

8. The method of claim 1 , further comprising administering compound 4 or a pharmaceutically acceptable salt, solvate or stereoisomer thereof to the mammal, wherein compound 4 is

9. The method of claim 1 , wherein the pharmaceutical composition further comprises one or more anti-androgenic compounds.

10. The method of claim 1 , wherein the pharmaceutical composition further comprises one or more LH-RH agonists.

11. The method of claim 9 , wherein the one or more anti-androgenic compound(s) is/are selected from the group consisting of bicalutamide, nilutamide, and 5-alpha-reductase inhibitors.

12. The method of claim 11 , wherein the 5-alpha-reductase inhibitor(s) is/are selected from the group consisting of MK-906, 17β-N,N-diethylcarbamoyl-4-methyl-4-aza-5-α-androstan-3-one, 4-azasteroid, 6-methylene-4-pregnene-3,20-dione, and 4-methyl-3-oxo-4-aza-5-α-pregnane-30(s) carboxylate.

13. The method of claim 6 , wherein the pharmaceutical composition further comprises one or more anti-androgenic compounds.

14. The method of claim 6 , wherein the pharmaceutical composition further comprises one or more LH-RH agonists.

15. The method of claim 13 , wherein the one or more anti-androgenic compound(s) is/are selected from the group consisting of bicalutamide, nilutamide, and 5-alpha-reductase inhibitors.

16. The method of claim 15 , wherein the 5-alpha-reductase inhibitor(s) is/are selected from the group consisting of MK-906, 17-β-N,N-diethylcarbamoyl-4-methyl-4-aza-5-α-androstan-3-one, 4-azasteroid, 6-methylene-4-pregnene-3,20-dione, and 4-methyl-3-oxo-4-aza-5-α-pregnane-30(s) carboxylate.

17. The method of claim 7 , wherein the pharmaceutical composition further comprises one or more anti-androgenic compounds.

18. The method of claim 7 , wherein the pharmaceutical composition further comprises one or more LH-RH agonists.

19. The method of claim 17 , wherein the one or more anti-androgenic compound(s) is/are selected from the group consisting of bicalutamide, nilutamide, and 5-alpha-reductase inhibitors.

20. The method of claim 19 , wherein the 5-alpha-reductase inhibitor(s) is/are selected from the group consisting of MK-906, 17-β-N,N-diethylcarbamoyl-4-methyl-4-aza-5-α-androstan-3-one, 4-azasteroid, 6-methylene-4-pregnene-3,20-dione, and 4-methyl-3-oxo-4-aza-5-α-pregnane-30(s) carboxylate.

Assignees

• Us Health
• Univ Texas
• Univ California Corp

Inventors

• Neckers Leonard M
• Cox Marc B
• Neckers Jane B
• Kim Yeong Sang
• Iwai Aki
• Ning Yangmin
• Kugelman-Tonos Johanny
• Balsiger Heather A
• Fletterick Robert

Classifications

• A61P3/10

  for hyperglycaemia, e.g. antidiabetics · CPC title

• A61P35/00

  Antineoplastic agents · CPC title

• A61P5/28

  Antiandrogens · CPC title

• A61K31/195

  having an amino group · CPC title

• A61K31/40

  having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil · CPC title