IP Library Granted Patent US 8,436,207
Granted Patent B2
US 8,436,207 · App. 13/238,910 · Granted May 7, 2013

Naphthalene-based inhibitors of anti-apoptotic proteins

Inventor: Maurizio Pellecchia (La Jolla, CA)
Assignee: Burnham Institute for Medical Research
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 8,436,207
App. No.
13/238,910
Granted
May 7, 2013
Kind
B2
Abstract

Methods of using apogossypol and its derivatives for treating inflammation is disclosed. Also, there is described a group of compounds having structure A, or a pharmaceutically acceptable salt, hydrate, N-oxide, or solvate thereof are provided: wherein each R is independently H, C(O)X, C(O)NHX, NH(CO)X, SO 2 NHX, or NHSO 2 X, wherein X is hydrogen, alkyl, substituted alkyl, aryl, substituted aryl, alkylaryl, substituted alkylaryl, heterocycle, or substituted heterocycle. Compounds of group A may be used for treating various diseases or disorders, such as cancer.

Claims (18)

1. A compound having structure A, or a pharmaceutically acceptable salt thereof:

wherein:

each R is independently C(O)NHX; and

X is alkylaryl, or substituted alkylaryl.

2. The compound of claim 1 , wherein X is (C 1 -C 6 )alkylaryl or substituted (C 1 -C 6 )alkylaryl, wherein each substituent is (C 1 -C 6 )alkyl, trifluoromethyl, halogen, phenyl or phenoxy.

3. The compound of claim 1 , wherein each R is independently C(O)NHCH 2 CH(CH 3 )C 6 H 5 .

4. A compound of claim 1 , or pharmaceutically acceptable salt thereof, having the structure:

5. A pharmaceutical composition comprising a compound of claim 1 , or pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier.

6. A pharmaceutical composition comprising a compound of claim 4 , or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier.

7. A method for treating breast cancer, colon cancer, lung cancer, ovarian cancer, prostate cancer, renal cancer, leukemia, lymphoma, or melanoma, the method comprising the step of administering to a subject in need thereof a therapeutically effective amount of a compound having structure A of claim 1 , or a combination thereof, or a pharmaceutically acceptable salt thereof, thereby treating the disease or the disorder.

8. A method of treating a cancer selected from breast cancer, colon cancer, lung cancer, ovarian cancer, prostate cancer, renal cancer, leukemia, lymphoma, and melanoma in a subject having at least one elevated BCL-2 family protein expression level, the method comprising the step of administering to the subject a therapeutically effective amount of a compound of claim 4 , or a pharmaceutically acceptable salt thereof.

9. The method of claim 8 , further comprising determining whether the subject is responsive to a therapy that utilizes the compound, comprising determining the level of at least one of the BCL-2 family protein in the subject and comparing to a normal control sample, wherein an elevated level is indicative of a subject responsive to the therapy that the compound, or a pharmaceutically acceptable salt thereof.

10. The method of claim 9 , wherein the determination is made based on a sample from the subject.

11. A method of determining whether a subject is responsive to a therapy that utilizes a compound of claim 4 , or a pharmaceutically acceptable salt thereof the method comprising the step of determining the level of at least one of the BCL-2 family protein in the subject and comparing to a normal control sample, wherein an elevated level is indicative of a subject responsive to the therapy that utilizes the compound, or a pharmaceutically acceptable salt thereof.

12. The method of claim 11 , wherein the determination is made based on a sample from the subject.

13. The method of claim 11 , wherein the sample is a biological fluid or tumor sample.

14. The method of claim 11 , wherein the BCL-2 family polynucleotide or polypeptide is selected from BCL-2, BCL-XL, BCL-W, MCL-1, and BCL-A1.

15. A method of inducing apoptosis in a cancer cell having a level of at least one of the BCL-2 family protein member greater than levels in a control cell, wherein the cancer cell is a breast cancer cell, colon cancer cell, lung cancer cell, ovarian cancer cell, prostate cancer cell, renal cancer cell, leukemia cell, lymphoma cell, or melanoma cell, the method comprising the step of administering to the cell an effective amount of a of claim 4 , or a pharmaceutically acceptable salt thereof, to reduce the level of BCL-2 family protein(s) and induce apoptosis in the cell.

Assignments (2)
CONFIRMATORY LICENSE Recorded Apr 2, 2024
From: SANFORD BURNHAM PREBYS MEDICAL DISCOVERY INSTITUTE
To: NATIONAL INSTITUTES OF HEALTH - DIRECTOR DEITR
Reel/Frame 066979/0262 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 19, 2011
From: PELLECCHIA, MAURIZIO
To: BURNHAM INSTITUTE FOR MEDICAL RESEARCH
Reel/Frame 027089/0659 →
Continuity (8)
Continuation 12760380 · Apr 14, 2010
Continuation In Part 12253918 · Oct 17, 2008
Provisional Application 61254172 · Oct 22, 2009
Provisional Application 61169686 · Apr 15, 2009
Provisional Application 61097171 · Sep 15, 2008
Provisional Application 61035969 · Mar 12, 2008
Provisional Application 60981400 · Oct 19, 2007
Related Publication 20120015992A1 · Jan 19, 2012