IP Library › Granted Patent US 8,609,716
Granted Patent B2
US 8,609,716 · App. 13/632,293 · Granted Dec 17, 2013

Chondropsin-class antitumor V-ATPase inhibitor compounds, compositions and methods of use thereof

Inventors: Michael R. Boyd (Mobile, AL); Kirk R. Gustafson (Frederick, MD)
Assignee: The United States of America, as represented by the Secretary, Department of Health and Human Services
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 8,609,716
App. No.
13/632,293
Granted
Dec 17, 2013
Kind
B2
Abstract

A composition comprising a substantially purified compound of the formula: in combination with at least one additional therapeutic agent, and methods of preventing or treating cancer and a condition treatable by the inhibition of vacuolar-type (H+)-ATPase.

Claims (20)

1. A method of killing or selectively inhibiting the growth of cancer cells, of a cancer selected from the group consisting of leukemias, lymphomas, melanomas and solid tumors, in a patient in need thereof, which method comprises administering to the patient an effective amount of at least one compound of the formula:

wherein:

R 1 is H, a straight-chain or branched C 1-30 saturated alkyl, a straight-chain or branched C 2-30 unsaturated alkyl, or an aryl comprising 6-10 carbon atoms in the ring skeleton thereof, wherein R 1 is unsubstituted or substituted with one or more substituents, which are the same or different, selected from the group consisting of a halogen, an oxo, OR 1a , CO 2 R 1a , and OC(O)R 1a , wherein R 1a is H, a straight-chain or branched C 1-30 saturated alkyl, a straight-chain or branched C 2-30 unsaturated alkyl, or an aryl comprising 6-10 carbon atoms in the ring skeleton thereof;

R 2 -R 8 are the same or different and each is R 10 , C(O)R 10 , SO 3 R 10 , or SO 2 R 10 , wherein R 10 is H, a straight-chain or branched C 1-30 saturated alkyl, a straight-chain or branched C 2-30 unsaturated alkyl, or an aryl comprising 6-10 carbon atoms in the ring skeleton thereof, wherein R 10 is unsubstituted or substituted with one or more substituents, which are the same or different, selected from the group consisting of a halogen, an oxo, OR 10a , CO 2 R 10a and OC(O)R 10a , wherein R 10a is H, a straight-chain or branched C 1-30 saturated alkyl, a straight-chain or branched C 2-30 unsaturated alkyl, or an aryl comprising 6-10 carbon atoms in the ring skeleton thereof; and

R 9 is a substituent of the formula:

wherein the R 9a substituents are the same or different and each is R 11 , C(O)R 11 , or SO 2 R 11 , wherein R 11 is H, a straight-chain or branched C 1-30 saturated alkyl, a straight-chain or branched C 2-30 unsaturated alkyl, or an aryl comprising 6-10 carbon atoms in the ring skeleton thereof, wherein R 11 is unsubstituted or substituted with one or more substituents, which are the same or different, selected from the group consisting of a halogen, an oxo, OR 11a , CO 2 R 11a and OC(O)R 11a , wherein R 11a is H, a straight-chain or branched C 1 -C 30 saturated alkyl, a straight-chain or branched C 2-30 unsaturated alkyl, or an aryl comprising 6-10 carbon atoms in the ring skeleton thereof;

wherein R 1a , R 10a and R 11a are unsubstituted or substituted with one or more substituents selected from the group consisting of a halogen, an oxo, and a hydroxyl;

or a pharmaceutically acceptable salt thereof,

whereupon the cancer cells are killed or their growth is selectively inhibited.

2. The method of claim 1 , wherein the method further comprises administering an anticancer effective amount of at least one additional compound other than a compound of formula (I), which is an anti-cancer compound.

3. The method of claim 1 , wherein the at least one additional compound is a salicylihalamide.

4. The method of claim 1 , wherein the solid tumor is selected from the group consisting of lung cancer, colon cancer, CNS cancer, melanoma, ovarian cancer, renal cancer, prostate cancer, head and neck cancer, testicular cancer, germ-line cancers, endocrine tumors, uterine cancer, breast cancer, sarcomas, gastric cancer, hepatic cancer, esophageal cancer and pancreatic cancer.

5. The method of claim 1 , wherein the solid tumor is selected from the group consisting of colon cancer, melanoma, breast cancer, ovarian cancer and non-small lung cancer.

6. The method of claim 1 , wherein:

R 1 , R 2 , R 4 , R 5 , R 6 , R 7 , R 8 , and each R 9a are H; and

R 3 is methyl.

7. The method of claim 6 , wherein the solid tumor is selected from the group consisting of lung cancer, colon cancer, CNS cancer, melanoma, ovarian cancer, renal cancer, prostate cancer, head and neck cancer, testicular cancer, germ-line cancers, endocrine tumors, uterine cancer, breast cancer, sarcomas, gastric cancer, hepatic cancer, esophageal cancer and pancreatic cancer.

8. The method of claim 6 , wherein the solid tumor is selected from the group consisting of colon cancer, melanoma, breast cancer, ovarian cancer and non-small lung cancer.

9. The method of claim 6 , wherein the method further comprises administering an anticancer effective amount of at least one additional compound other than a compound of formula (I), which is an anti-cancer compound.

10. The method of claim 9 , wherein the at least one additional compound is a salicylihalamide.

Continuity (6)
Continuation 12909979 · Oct 22, 2010
Continuation 12402560 · Mar 12, 2009
Division 11674245 · Feb 13, 2007
Division 10521930
Provisional Application 60398092 · Jul 24, 2002
Related Publication 20130023500A1 · Jan 24, 2013