IP Library Granted Patent US 6,995,187
Granted Patent B1
US 6,995,187 · App. 10/110,830 · Granted Feb 7, 2006

Peripheral cannabinoid receptor (CB2) selective ligands

Assignee: University of Connecticut
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Quick Facts
Patent No.
US 6,995,187
App. No.
10/110,830
Granted
Feb 7, 2006
Kind
B1
Abstract

Novel polycyclic cannabinoid analogs are presented which have preferentially high affinities for the cannabinoid CB2 receptor sites. The improved receptor affinity makes these analogs therapeutically useful as medications in individuals and animals for treatment of pain, glaucoma, epilepsy, nausea associated with chemotherapy.

Claims (45)

1. A compound of the formula:

and physiologically acceptable salts thereof, wherein

R 1 is selected from H; OH; OCH 3 ; N 3 ; and NH 2 ;

R 2 is selected from (CH 2 ) n CH 3 , where n is an integer from 4–6; C(CH 3 ) 2 (CH 2 ) n CH 3 , where n is an integer from 3–5; (CH 2 ) n C≡CH where n is an integer from 3–5; and C≡C(CH 2 ) n CH 3 where n is an integer from 2–4; and

R 3 is selected from H; CH 3 ; C 2 H 5 ; C 3 H 7 ; and C 4 H 9 .

2. The compound of claim 1 wherein R 1 is OH and R 2 is 1,1-dimethylheptyl and R 3 is CH 3 .

3. The compound of claim 1 wherein R 1 and R 3 are each OH and R 2 is 1,1-dimethylheptyl.

4. A method of preferentially stimulating the CB2 receptors in an individual or animal for the treatment of at least one of pain an peripheral pain comprising administering to the individual or animal a therapeutically effective amount of a compound having the formula:

and physiologically acceptable salts thereof, wherein

R 1 is selected from H; OH; OCH 3 ; N 3 ; and NH 2 ;

R 2 is selected from (CH 2 ) n CH 3 , where n is an integer from 4–6; C(CH 3 ) 2 (CH 2 ) n CH 3 , where n is an integer from 3–5; (CH 2 ) n C≡CH where n is an integer from 3–5; and C≡C(CH 2 ) n CH 3 where n is an integer from 2–4; and

R 3 is selected from H; CH 3 ; C 2 H 6 ; C 3 H 7 ; and C 4 H 9 .

5. A pharmaceutical composition containing a therapeutically effective amount of a compound having the formula:

and physiologically acceptable salts thereof, wherein

R 1 is selected from H; OH; OCH 3 ; N 3 ; and NH 2 ;

R 2 is selected from (CH 2 ) n CH 3 , where n is an integer from 4–6; C(CH 3 ) 2 (CH 2 ) n CH 3 , where n is an integer from 3–5; (CH 2 ) n C≡CH where n is an integer from 3–5; and C≡C(CH 2 ) n CH 3 where n is an integer from 2–4; and

R 3 is selected from H; CH 3 ; C 2 H 5 ; C 3 H 7 ; and C 4 H 9 .

6. The compound of claim 1 wherein:

R 1 is selected from OH and NH 2 ;

R 2 is C(CH 3 ) 2 (CH 2 ) n CH 3 , where n is an integer from 3–5; and

R 3 is selected from H and CH 3 .

7. The compound of claim 1 wherein:

R 1 is selected from H; OH and OCH 3 ;

R 2 is selected from (CH 2 ) n CH 3 , where n is an integer from 4–6; C(CH 3 ) 2 (CH 2 ) n CH 3 , where n is an integer from 3–5; (CH 2 ) n C≡CH where n is an integer from 3–5; and C≡C(CH 2 ) n CH 3 where n is an integer from 2–4; and

R 3 is selected from H; CH 3 ; C 2 H 5 ; C 3 H 7 ; and C 4 H 9 .

8. The compound of claim 1 wherein:

R 1 is selected from H; N 3 ; and NH 2 ;

R 2 is selected from (CH 2 ) n CH 3 , where n is an integer from 4–6; C(CH 3 ) 2 (CH 2 ) n CH 3 , where n is an integer from 3–5; (CH 2 ) n C≡CH where n is an integer from 3–5; and C≡C(CH 2 ) n CH 3 where n is an integer from 2–4; and

R 3 is selected from H; CH 3 ; C 2 H 5 ; C 3 H 7 ; and C 4 H 9 .

9. The method of claim 4 wherein:

R 1 is selected from H; OH and OCH 3 ;

R 2 is selected from (CH 2 ) n CH 3 , where n is an integer from 4–6; C(CH 3 ) 2 (CH 2 ) n CH 3 , where n is an integer from 3–5; (CH 2 ) n C≡CH where n is an integer from 3–5; and C≡C(CH 2 ) n CH 3 where n is an integer from 2–4; and

R 3 is selected from H; CH 3 ; C 2 H 5 ; C 3 H 7 ; and C 4 H 9 .

10. The method of claim 4 wherein:

R 1 is selected from H; N 3 ; and NH 2 ;

R 2 is selected from (CH 2 ) n CH 3 , where n is an integer from 4–6; C(CH 3 ) 2 (CH 2 ) n CH 3 , where n is an integer from 3–5; (CH 2 ) n C≡CH where n is an integer from 3–5; and C≡C(CH 2 ) n CH 3 where n is an integer from 2–4; and

R 3 is selected from H; CH 3 ; C 2 H 5 ; C 3 H 7 ; and C 4 H 9 .

11. The pharmaceutical composition of claim 5 wherein:

R 1 is selected from H; OH and OCH 3 ;

R 2 is selected from (CH 2 ) n CH 3 , where n is an integer from 4–6; C(CH 3 ) 2 (CH 2 ) n CH 3 , where n is an integer from 3–5; (CH 2 ) n C≡CH where n is an integer from 3–5; and C≡C(CH 2 ) n CH 3 where n is an integer from 2–4; and

R 3 is selected from H; CH 3 : C 2 H 5 ; C 3 H 7 ; and C 4 H 9 .

12. The pharmaceutical composition of claim 5 wherein:

R 1 is selected from H; N 3 ; and NH 2 H;

R 2 is selected from (CH 2 ) n CH 3 , where n is an integer from 4–6; C(CH 3 ) 2 (CH 2 ) n CH 3 , where n is an integer from 3–5; (CH 2 )C≡CH where n is an integer from 3–5; and C≡C(CH 2 ) n CH 3 where n is an integer from 2–4; and

R 3 is selected from H; CH 3 ; C 2 H 5 ; C 3 H 7 ; and C 4 H 9 .

Assignments (2)
CONFIRMATORY LICENSE Recorded Sep 29, 2016
From: UNIVERSITY OF CONNECTICUT
To: NATIONAL INSTITUTES OF HEALTH - DIRECTOR DEITR
Reel/Frame 040181/0838 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 17, 2003
From: MAKRIYANNIS, ALEXANDROS; KHANOLKAR, ATMARAM D.
To: UNIVERSITY OF CONNECTICUT
Reel/Frame 013839/0760 →
Continuity (1)
Provisional Application 6016014600 · Oct 18, 1999