IP Library Granted Patent US 9,320,722
Granted Patent B2
US 9,320,722 · App. 14/498,618 · Granted Apr 26, 2016

Regulators of aldehyde dehydrogenase ALDH3A1 and related therapeutic methods

Inventor: Thomas D. Hurley (Indianapolis, IN)
Assignee: Indiana University Research and Technology Corporation
A61K31/145A61K31/136A61K31/167A61K31/381A61K31/4184A61K31/426A61K31/4436A61K31/4439A61K31/4468A61K31/5377A61K31/5386A61K31/553A61K31/63A61K31/635A61K45/06
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Quick Facts
Patent No.
US 9,320,722
App. No.
14/498,618
Granted
Apr 26, 2016
Kind
B2
Abstract

Described herein are compositions and methods for the treatment of cancer, and in particular cancers characterized by a high level of ALD3H1 activity, which is associated with chemoresistance to cancer chemotherapeutic agents that are degraded by ALD3H1. The compositions described herein act as competitive inhibitors of ALD3H1 and thereby reduce breakdown of chemotherapeutics by this enzyme, and increase their efficacy for cancer treatment.

Claims (51)

1. A pharmaceutical composition for cancer treatment comprising a pharmaceutically acceptable excipient and a therapeutically effective amount of a compound having a structure selected from the group consisting of:

(a) Formula (I):

wherein:

R1 is selected from the group consisting of —CH 3 , —CF 3 , —NHCH 3 , and —NHCH(CH 3 ) 2 ;

R3 is selected from the group consisting of —NO 2 , —F, Cl, —OH, and —OCH 3 ;

R4 is —H;

R5 is selected from the group consisting of —H, —F, and —NH-cyclopropyl;

R6 is selected from the group consisting of —NHCOCH 3 , —N(CH 3 ) 2 , —CH 3 , —OCH 3 , and —OCHF 2 ;

R7 is —H; and

R8 is —H.

2. The pharmaceutical composition of claim 1 , wherein the compound has the structure of Formula (I):

wherein:

R1 is selected from the group consisting of —CH 3 , —CF 3 , —NHCH 3 , and —NHCH(CH 3 ) 2 ;

R3 is selected from the group consisting of —NO 2 , —F, —Cl, —OH, and —OCH 3 ;

R4 is —H;

R5 is selected from the group consisting of —H, —F, and —NH-cyclopropyl;

R6 is selected from the group consisting of —NHCOCH 3 , —N(CH 3 ) 2 , —CH 3 , —OCH 3 , and —OCHF 2 ;

R7 is —H; and

R8 is —H.

3. The pharmaceutical composition of claim 2 , wherein the compound has the structure of Formula (Ia) (Compound CB29):

4. The pharmaceutical composition of claim 1 , further comprising one or more chemotherapeutic agents that are substrates for ALDH3A1.

5. The pharmaceutical composition of claim 4 , wherein the one or more chemotherapeutic agent comprise paclitaxel, doxorubicin, or 4-hydroxycyclophosphamide.

6. A method for treating cancer comprising administering to a subject in need thereof a pharmaceutical composition comprising a therapeutically effective amount of a compound having a structure selected from the group consisting of:

(a) Formula (I):

wherein:

R1 is selected from the group consisting of —CH 3 , —CF 3 , —NHCH 3 , and —NHCH(CH 3 ) 2 ;

R3 is selected from the group consisting of —NO 2 , —F, —Cl, —OH, and —OCH 3 ;

R4 is —H;

R5 is selected from the group consisting of —H, —F, and —NH-cyclopropyl;

R6 is selected from the group consisting of —NHCOCH 3 , —N(CH 3 ) 2 , —CH 3 , —OCH 3 , and —OCHF 2 ;

R7 is —H; and

R8 is —H;

and wherein the subject is treated with one or more chemotherapeutic agents that are substrates for ALDH3A1.

7. The method of claim 6 , wherein the compound has the structure of Formula (I):

wherein:

R1 is selected from the group consisting of —CH 3 , —CF 3 , —NHCH 3 , and —NHCH(CH 3 ) 2 ;

R3 is selected from the group consisting of —NO 2 , —F, —Cl, —OH, and —OCH 3 ;

R4 is —H;

R5 is selected from the group consisting of —H, —F, and —NH-cyclopropyl;

R6 is selected from the group consisting of —NHCOCH 3 , —N(CH 3 ) 2 , — CH 3 , —OCH 3 , and —OCHF 2 ;

R7 is —H; and

R8 is —H.

8. The method of claim 7 , wherein the compound has the structure of Formula (Ia) (Compound CB29):

9. The method of claim 6 , wherein the one or more chemotherapeutic agents comprise paclitaxel, doxorubicin, or 4-hydroxycyclophosphamide.

10. The method of claim 6 , wherein the one or more chemotherapeutic agents are administered to the subject before the administration of the pharmaceutical composition.

11. The method of claim 6 , wherein the one or more chemotherapeutic agents are administered to the subject after the administration of the pharmaceutical composition.

12. The method of claim 6 , wherein the one or more chemotherapeutic agents are co-administered with the pharmaceutical composition.

13. The method of claim 12 , wherein the pharmaceutical composition comprises in combination the therapeutically effective amount of the compound and the one or more chemotherapeutic agents.

14. The method of claim 6 , wherein the subject to be treated is suffering from a cancer characterized by overexpression of ALDH3A1.

15. The method of claim 14 , wherein the subject is suffering from hepatoma, lung adenocarcinoma, myeloma, breast cancer, colon cancer, or glioblastoma.

16. The method of claim 6 , further comprising obtaining from the subject a biological sample comprising cancer cells, and determining an ALDH3A1 mRNA, protein expression, or enzymatic activity level before, during, or after treatment with the pharmaceutical composition.

Assignments (2)
CONFIRMATORY LICENSE Recorded Jan 5, 2015
From: INDIANA UNIVERSITY RESEARCH AND TECHNOLOGY CORPORATION
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 034719/0976 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 6, 2014
From: HURLEY, THOMAS D.
To: INDIANA UNIVERSITY RESEARCH & TECHNOLOGY CORPORATION
Reel/Frame 034118/0242 →
Continuity (2)
Provisional Application 61883393 · Sep 27, 2013
Related Publication 20150202169A1 · Jul 23, 2015