Indirubin derivatives, and uses thereof

Patent metadata

Field	Value
Publication number	US-10435367-B2
Application number	US-201313826204-A
Country	US
Kind code	B2
Filing date	Mar 14, 2013
Priority date	Mar 14, 2013
Publication date	Oct 8, 2019
Grant date	Oct 8, 2019

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.

First claim

The invention claimed is:

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.

Assignees

• Hope City
• The National And Kapodistrian Univ Of Athens

Inventors

• Nam Sangkil
• Jove Richard
• Skaltsounis Leandros

Classifications

• C07D401/14

  containing three or more hetero rings · CPC title

• C07D209/40 Primary

  Nitrogen atoms, not forming part of a nitro radical, e.g. isatin semicarbazone · CPC title