IP Library Granted Patent US 10,435,367
Granted Patent B2
US 10,435,367 · App. 13/826,204 · Granted Oct 8, 2019

Indirubin derivatives, and uses thereof

Inventors: Sangkil Nam (Duarte, CA); Richard Jove (Duarte, CA); Leandros Skaltsounis (Athens, GR)
Assignees: City of Hope; The National and Kapodistrian University of Athens
C07D209/40C07D401/14
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Quick Facts
Patent No.
US 10,435,367
App. No.
13/826,204
Granted
Oct 8, 2019
Kind
B2
Abstract

Indirubin is the major active anti-tumor component of a traditional Chinese herbal medicine used for treatment of chronic myelogenous leukemia (CML). Indirubin derivatives (IRDs) potently reduce the viabilities of various cancer cells and affect kinase activities. IRDs disclosed herein provide new therapeutics for cancer and conditions regulated by the kinase activities.

Claims (16)

1. A compound of the structure of IRD No. 176:

IRD No. 176.

2. A pharmaceutical composition comprising a therapeutically effective amount of the compound according to claim 1 and a pharmaceutically acceptable carrier.

3. A method of treating a cancer or tumor in a subject comprising administering to the subject a therapeutically effective amount of compound IRD No. 176, wherein the cancer or tumor is selected from the group consisting of leukemia, prostate cancer, melanoma, pancreatic cancer, and ovarian cancer.

4. The method according to claim 3 , wherein the leukemia treated is CML.

5. The method according to claim 4 , wherein the cancer is leukemia, and the indirubin derivative is IRD No.

6. A method of treating a condition in a subject regulated by a protein kinase selected from the group consisting of ABL1, ABL1 (T315I mutant), Aurora A, c-Src, FGR, FLT3, HCK, LYN, JAK2, and TYK2 comprising administering to the subject a therapeutically effective amount of compound IRD No. 176.

7. The method according to claim 6 , wherein the protein kinase is ABL1.

8. The method according to claim 6 , wherein the protein kinase is ABL1 (T315I mutant).

9. The method according to claim 6 , wherein the protein kinase is Aurora A.

10. The method according to claim 6 , wherein the protein kinase is c-Src.

11. The method according to claim 6 , wherein the protein kinase is FGR, FLT3, HCK, LYN, or TYK2.

12. The method according to claim 6 , wherein the protein kinase is JAK2.

13. A method of preparing the IRD according to claim 1 , the method comprises the following steps:

A1) provide a compound having Structure A, wherein R Y is —OR N —W (IRD-W), wherein W is Br, Cl or I; and

A2) coupling IRD-W of Step A1) with R N ′—H in the presence of microwave until the conversion to IRD-N is substantially complete.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 17, 2016
From: JOVE, RICHARD; NAM, SANGKIL
To: CITY OF HOPE
Reel/Frame 039469/0974 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 17, 2016
From: SKALTSOUNIS, ALEXIOS-LEANDROS
To: NATIONAL AND KAPODISTRIAN UNIVERSITY OF ATHENS
Reel/Frame 039717/0832 →
CONFIRMATORY LICENSE Recorded Oct 29, 2015
From: CITY OF HOPE/BECKMAN RESEARCH INSTITUTE
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 037007/0151 →
Continuity (1)
Related Publication 20140275168A1 · Sep 18, 2014
Cited By (1)
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