IP Library Granted Patent US 7,094,774
Granted Patent B2
US 7,094,774 · App. 10/780,103 · Granted Aug 22, 2006

26,27-homologated-20-epi-2-alkylidene-19-nor-vitamin D compounds

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Quick Facts
Patent No.
US 7,094,774
App. No.
10/780,103
Granted
Aug 22, 2006
Kind
B2
Abstract

This invention provides a novel class of vitamin D related compounds, namely, the 2-alkylidene-19-nor-vitamin D derivatives, as well as a general method for their chemical synthesis. The compounds have the formula: where Y 1 and Y 2 , which may be the same or different, are each selected from the group consisting of hydrogen and a hydroxy-protecting group, R 6 and R 8 , which may be the same or different, are each selected from hydrogen, alkyl, hydroxyalkyl and fluoroalkyl, or when taken together represent the group —(CH 2 ) x — where x is an integer from 2 to 5, and where the group R represents any of the typical side chains known for vitamin D type compounds. These 2-substituted compounds are characterized by relatively high intestinal calcium transport activity and relatively high bone calcium mobilization activity resulting in novel therapeutic agents for the treatment of diseases where bone formation is desired, particularly low bone turnover osteoporosis. These compounds also exhibit pronounced activity in arresting the proliferation of undifferentiated cells and inducing their differentiation to the monocyte thus evidencing use as anti-cancer agents and for the treatment of diseases such as psoriasis.

Claims (24)

1. A method of treating a cancerous disease selected from the group consisting of leukemia, colon cancer, breast cancer and prostate cancer comprising administering to a patient with said disease an effective amount of 20(S)-1α,25-dihydroxy-2-methylene26,27-dihomo- 19-norvitainin D 3 having the structure

2. The method of claim 1 wherein the compound is administered orally.

3. The method of claim 1 wherein the compound is administered parenterally.

4. The method of claim 1 wherein the compound is administered transdermally.

5. The method of claim 1 wherein said effective amount comprises about 0.01 μg/day to about 100 μg/day of 20(S)-1α,25-dihydroxy-2-methylene-26,27-dihomo- 19-norvitamin D 3 .

6. The method of claim 1 wherein said effective amount comprises about 0.1 μg/day to about 50 μg/day of 20(S)-1α,25-dihydroxy-2-methylene-26,27-dihomo-19-norvitamin D 3 .

7. A method of treating a cancerous disease selected from the group consisting of leukemia, colon cancer, breast cancer and prostate cancer comprising administering to a patient with said disease an effective amount of 20(S)-26,27-dimethylene-25-methoxy-2-methylene-19-norvitamin D 3 having the structure

8. The method of claim 7 wherein the compound is administered orally.

9. The method of claim 7 wherein the compound is administered parenterally.

10. The method of claim 7 wherein the compound is administered transdermally.

11. The method of claim 7 wherein said effective amount comprises about 0.1 μg/day to about 100 μg/day of 20(S)-26,27-dimethylene-25-methoxy-2-methylene-19-norvitamin D 3 .

12. The method of claim 7 wherein said effective amount comprises about 0.1 μg/day to about 50 μg/day of 20(S)-26,27-dimethylene-25-methoxy-2-methylene-19-norvitamin D 3 .

13. A method of treating a cancerous disease selected from the group consisting of leukemia, colon cancer, breast cancer and prostate cancer comprising administering to a patient with said disease an effective amount of 20(S-1α,25-dihydroxy-26,27-dimethylene-2-methylene-19-norvitamin D 3 having the structure

14. The method of claim 13 wherein the compound is administered orally.

15. The method of claim 13 wherein the compound is administered parenterally.

16. The method of claim 13 wherein the compound is administered transdermally.

17. The method of claim 13 wherein said effective amount comprises about 0.01 μg/day to about 100 μg/day of 20(S)-1α,25-dihydroxy-26,27-dimethylene-2-methylene-19-norvitamin D 3 .

18. The method of claim 13 wherein said effective amount comprises about 0.1 μg/day to about 50 μg/day of 20(S)-1α,25-dihydroxy-26,27-dimethylene-2-methylene-19-norvitamin D 3 .

19. A method of treating a cancerous disease selected from the group consisting of leukemia, colon cancer, breast cancer and prostate cancer comprising administering to a patient with said disease an effective amount of 20(S)-26,27-dimethylene-1α-hydroxy-2-methylene-24-dehydro-19-norvitamin D 3 having the structure

20. The method of claim 19 wherein the compound is administered orally.

21. The method of claim 19 wherein the compound is administered parenterally.

22. The method of claim 19 wherein the compound is administered transdermally.

23. The method of claim 19 wherein said effective amount comprises about 0.01 μg/day to about 100 μg/day of 20(S)-26,27-dimethylene-1α-hydroxy-2-methylene-24-dehydro-19-norvitamin D 3 .

24. The method of claim 19 wherein said effective amount comprises about 0.1 μg/day to about 50 μg/day of20(S)-26,27-dimetyyl-1α-hydroxy-2-methylene-24-dehydro-19-norvitamin D 3 .

Assignments (3)
CONFIRMATORY LICENSE Recorded May 8, 2018
From: WISCONSIN ALUMNI RESEARCH FOUNDATION
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 046101/0160 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 31, 2014
From: DELUCA, HECTOR F.; SICINSKI, RAFAL R.
To: WISCONSIN ALUMNI RESEARCH FOUNDATION
Reel/Frame 032106/0763 →
SECURITY AGREEMENT Recorded Apr 24, 2009
From: QUATRX PHARMACEUTICALS COMPANY
To: HERCULES TECHNOLOGY GROWTH CAPITAL, INC.
Reel/Frame 022584/0669 →