IP Library Patent Application 10600116
Patent Application
App. No. 10/600,116

Enhancing treatment of MDR cancer with adenosine A3 antagonists

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Patent No.
US None
App. No.
10/600,116
Abstract

The present invention discloses the use of high affinity adenosine A 3 receptor antagonists for enhancing chemotherapeutic treatment of cancers expressing adenosine A 3 receptors and cancers expressing P-glycoprotein or MRP. In preferred embodiments, adenosine A 3 receptor antagonists are administered before or during administration of a taxane family, vinca alkaloid, camptothecin or antibiotic chemotherapeutic agent.

Claims (53)

1 . A method of synergistically enhancing the chemotherapeutic treatment of cancer expressing adenosine A 3 receptors comprising administering to a mammal in need thereof an effective amount of a high affinity adenosine A 3 receptor antagonists either prior to or during administration of a chemotherapeutic cancer agent.

2 . The method of claim 1 wherein the chemotherapeutic cancer agent is a taxane family compound.

3 . The method of claim 1 wherein the chemotherapeutic cancer agent is a vinca alkaloid compound.

4 . The method of claim 1 wherein the chemotherapeutic cancer agent is a camptothecin compound.

5 . The method of claim 1 wherein the chemotherapeutic cancer agent is an antibiotic compound.

6 . The method of claim 1 wherein the high affinity adenosine A 3 receptor antagonist is a compound of formula:

wherein:

A is imidazole, pyrazole, or triazole;

R is —C(X)R 1 , —C(X)—N(R 1 ) 2 , —C(X)OR 1 , —C(X)SR 1 , —SO n R 1 , —SO n SR 1 , or —SO n —N(R 1 ) 2 ;

R 1 is hydrogen, alkyl, substituted alkyl, alkenyl, substituted alkenyl, alkynyl, substituted alkynyl, aryl, substituted aryl, heteroaryl, heterocyclic, lower alkenyl, lower alkanoyl, or, if linked to a nitrogen atom, then taken together with the nitrogen atom, forms an azetidine ring or a 5-6 membered heterocyclic ring containing one or more heteroatoms;

R 2 is hydrogen, alkyl, substituted alkyl, alkenyl, aralkyl, substituted aralkyl, heteroaryl, substituted heteroaryl or aryl;

R 3 is furan, pyrrole, thiophene, benzofuran, benzypyrrole, benzothiophene, optionally substituted with one or more substituents selected from the group consisting of hydroxy, acyl, alkyl, alkoxy, alkenyl, alkynyl, substituted alkyl, substituted alkoxy, substituted alkenyl, substituted alkynyl, amino, substituted amino, aminoacyl, acyloxy, acylamino, alkaryl, aryl, substituted aryl, aryloxy, azido, carboxyl, carboxylalkyl, cyano, halo, nitro, heteroaryl, heteroaryloxy, heterocyclic, heterocyclooxy, aminoacyloxy, thioalkoxy, substituted thioalkoxy, —SO-alkyl, —SO-substituted alkyl, —SO-aryl, —SO-heteroaryl, —SO 2 -alkyl, —SO 2 -substituted alkyl, —SO 2 -aryl, —SO 2 -heteroaryl, and trihalomethyl;

X is O, S, or NR 1 ; and

pharmaceutically acceptable salts thereof.

7 . The method of claim 1 wherein the high affinity adenosine A 3 receptor antagonist is a compound of formula:

wherein:

A is imidazole, pyrazole, or triazole;

R 2 is hydrogen, alkyl, substituted alkyl, alkenyl, aralkyl, substituted aralkyl, heteroaryl, substituted heteroaryl or aryl; R 3 is furan; and

R 6 is aryl, substituted aryl, heteroaryl, substituted heteroaryl, heterocycle or substituted heterocycle; and

pharmaceutically acceptable salts thereof.

8 . The method of claim 6 wherein R 2 is selected from the group consisting of hydrogen, alky, alkenyl and aryl.

9 . The method of claim 6 wherein A is a triazolo ring.

10 . The method of claim 6 wherein A is a pyrazolo ring.

11 . The method of claim 1 wherein the cancer is selected from the group consisting of human leukemia, melanoma, pancreatic carcinoma, breast carcinoma, prostrate carcinoma, colon carcinoma, ovarian carcinoma, lung carcinoma, histiocytic lymphoma, astrocytoma and keratinocytoma.

12 . A method of synergistically enhancing the chemotherapeutic treatment of cancer expressing adenosine A 3 receptors comprising administering to a mammal in need thereof an effective amount of a high affinity adenosine A 3 receptor antagonists either prior to or during administration of a chemotherapeutic cancer agent wherein the cancer has multi-drug resistance that is P-glycoprotein dependent.

13 . The method of claim 11 wherein the chemotherapeutic cancer agent is a taxane family compound.

14 . The method of claim 11 wherein the chemotherapeutic cancer agent is a vinca alkaloid compound.

15 . The method of claim 11 wherein the chemotherapeutic cancer agent is a camptothecin compound.

16 . The method of claim 11 wherein the chemotherapeutic cancer agent is an antibiotic compound.

17 . The method of claim 11 wherein the high affinity adenosine A 3 receptor antagonist is a compound of formula:

wherein:

A is imidazole, pyrazole, or triazole;

R is —C(X)R 1 , —C(X)—N(R 1 ) 2 , —C(X)OR 1 , —C(X)SR 1 , —SO n R 1 , —SO n SR 1 , or —SO n —N(R 1 ) 2 ;

R 1 is hydrogen, alkyl, substituted alkyl, alkenyl, substituted alkenyl, alkynyl, substituted alkynyl, aryl, substituted aryl, heteroaryl, heterocyclic, lower alkenyl, lower alkanoyl, or, if linked to a nitrogen atom, then taken together with the nitrogen atom, forms an azetidine ring or a 5-6 membered heterocyclic ring containing one or more heteroatoms;

R 2 is hydrogen, alkyl, substituted alkyl, alkenyl, aralkyl, substituted aralkyl, heteroaryl, substituted heteroaryl or aryl;

R 3 is furan, pyrrole, thiophene, benzofuran, benzypyrrole, benzothiophene, optionally substituted with one or more substituents selected from the group consisting of hydroxy, acyl, alkyl, alkoxy, alkenyl, alkynyl, substituted alkyl, substituted alkoxy, substituted alkenyl, substituted alkynyl, amino, substituted amino, aminoacyl, acyloxy, acylamino, alkaryl, aryl, substituted aryl, aryloxy, azido, carboxyl, carboxylalkyl, cyano, halo, nitro, heteroaryl, heteroaryloxy, heterocyclic, heterocyclooxy, aminoacyloxy, thioalkoxy, substituted thioalkoxy, —SO-alkyl, —SO-substituted alkyl, —SO-aryl, —SO-heteroaryl, —SO2-alkyl, —SO2-substituted alkyl, —SO2-aryl, —SO2-heteroaryl, and trihalomethyl;

X is O, S, or NR 1 ; and

pharmaceutically acceptable salts thereof.

18 . The method of claim 11 wherein the high affinity adenosine A 3 receptor antagonist is a compound of formula:

wherein:

A is imidazole, pyrazole, or triazole;

R 2 is hydrogen, alkyl, substituted alkyl, alkenyl, aralkyl, substituted aralkyl, heteroaryl, substituted heteroaryl or aryl; R 3 is furan; and

R 6 is heteroaryl or substituted heteroaryl; and

pharmaceutically acceptable salts thereof.

19 . The method of claim 16 wherein R2 is selected from the group consisting of hydrogen, alkyl, alkenyl and aryl.

20 . The method of claim 16 wherein A is a triazolo ring.

21 . The method of claim 16 wherein A is a pyrazolo ring.

22 . The method of claim 11 wherein the cancer is selected from the group consisting of human leukemia, melanoma, pancreatic carcinoma, breast carcinoma, prostrate carcinoma, colon carcinoma, ovarian carcinoma, lung carcinoma, histiocytic lymphoma, astrocytoma and keratinocytoma.

23 . A method of synergistically enhancing the chemotherapeutic treatment of cancer expressing adenosine A 3 receptors comprising administering to a mammal in need thereof an effective amount of a high affinity adenosine A 3 receptor antagonist and a adenosine-5′-triphosphate depleting agent either prior to or during administration of a chemotherapeutic cancer agent wherein the cancer has multi-drug resistance that is P-glycoprotein dependent.

24 . The method of claim 21 wherein the adenosine-5′-triphosphate depleting agent consists of a compound selected from the group consisting of L-alanosine and adenosine kinase inhibitors.

25 . The method of claim 21 wherein the adenosine-5′-triphosphate depleting agent consists of a compound or a salt of a compound selected from the group consisting of 2-deoxyglucose, cyanine, oligomycin, valinomycin, and azide.

26 . A method of treating skin carcinoma comprising administering to a human patient in need thereof an effective amount of a high affinity adenosine A 3 receptor antagonist either prior to or during administration of a chemotherapeutic cancer agent wherein the chemotherapeutic cancer agent is a taxane family compound.

27 . The method of claim 24 wherein the high affinity adenosine A 3 receptor antagonist is administered in a topical application.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 22, 2005
From: BOREA, PIER ANDREA; BARALDI, PIER GIOVANNI; CHEN, SHIH-FONG; LEUNG, EDWARD
To: KING PHARMACEUTICALS RESEARCH & DEVELOPMENT, INC.
Reel/Frame 016211/0119 →