IP Library Granted Patent US 8,168,800
Granted Patent B2
US 8,168,800 · App. 12/740,329 · Granted May 1, 2012

Aβ-binding small molecules

Assignee: The Regents of the University of California
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Quick Facts
Patent No.
US 8,168,800
App. No.
12/740,329
Granted
May 1, 2012
Kind
B2
Abstract

In one aspect, the present invention provides for compounds and labeled compounds of Formula I, and pharmaceutical compositions thereof. In another aspect, the present invention provides for methods of using compounds or labeled compounds of Formula I for various therapeutic and imaging purposes, including, but not limited to, treating Alzheimer's disease in patient and imaging Aβ peptide aggregates in a patient.

Claims (28)

1. A compound of Formula I:

or a pharmaceutically acceptable salt thereof, wherein in Formula I:

L is C 1-6 alkylene;

X is phenyl substituted with fluorine, bromine or iodine;

Ar is phenyl substituted at the 4-position with one substituent selected from the group consisting of perfluoro(C 1 -C 4 )alkoxy and —OR c ;

wherein R c is C 1-4 alkyl;

R 1 is a member selected from the group consisting of hydrogen, C 1-6 alkyl and C 1-6 haloalkyl;

R 2 is a member selected from the group consisting of hydrogen, halogen, C 1-6 alkoxy, C 1-6 alkylamino, C 1-6 dialkylamino, C 1-6 alkyl and C 1-6 haloalkyl;

R 3a and R 3b are each a member independently selected from the group consisting of hydrogen, C 1-6 alkyl, C 1-6 haloalkyl, and C 1-6 alkoxy, and wherein R 3a and R 3b and the nitrogen atom to which each is attached are optionally combined to form a 5- to 6-membered ring; and

the subscript m is 1.

2. The compound of claim 1 , wherein L is selected from the group consisting of —CH 2 —, —CH 2 CH 2 —, —CH 2 CH 2 CH 2 —, and —CH 2 CH 2 CH 2 CH 2 —.

3. The compound of claim 1 , wherein L is selected from the group consisting of —CH 2 —, —CH 2 CH 2 —, and —CH 2 CH 2 CH 2 —.

4. The compound of claim 1 , wherein Ar is selected from the group consisting of:

5. The compound of claim 1 , wherein said compound is of Formula Ia

6. The compound of claim 1 , wherein said compound is selected from the group consisting of

3-(3-iodo-benzyl)-2-(4-methoxy-phenylamino)-8-methyl-6-oxo-3,6-dihydrochromeno [6,7-d]imidazole-7-carboxylic acid amide;

3-(3-bromobenzyl)-2-(4-methoxyphenylamino)-8-methyl-6-oxo-3,6-dihydrochromeno [7,6-d]imidazole-7-carboxylic acid amide;

3-(3-fluorobenzyl)-2-(4-methoxyphenylamino)-8-methyl-6-oxo-3,6-dihydrochromeno [7,6-d]imidazole-7-carboxylic acid amide;

3-(4-bromobenzyl)-2-(4-methoxyphenylamino)-8-methyl-6-oxo-3,6-dihydrochromeno [7,6-d]imidazole-7-carboxylic acid amide;

3-(4-iodobenzyl)-2-(4-methoxyphenylamino)-8-methyl-6-oxo-3,6-dihydrochromeno [7,6-d]imidazole-7-carboxylic acid amide;

3-(4-bromophenethyl)-2-(4-methoxyphenylamino)-8-methyl-6-oxo-3,6-dihydrochromeno [7,6-d]imidazole-7-carboxylic acid amide;

3-(3-bromobenzyl)-8-methyl-6-oxo-2-(4-(trifluoromethoxy)phenylamino)-3,6-dihydrochromeno [7,6-d]imidazole-7-carboxylic acid amide;

3-(3-iodobenzyl)-8-methyl-6-oxo-2-(4-(trifluoromethoxy)phenylamino)-3,6-dihydrochromeno [7,6-d]imidazole-7-carboxylic acid amide; and

3-(4-bromobenzyl)-8-methyl-6-oxo-2-(4-(trifluoromethoxy)phenylamino)-3,6-dihydrochromeno [7,6-d]imidazole-7-carboxylic acid amide.

7. The compound of claim 1 , wherein said compound is selected from the group consisting of:

8. The compound of claim 1 , wherein said compound is:

9. The compound of claim 1 , wherein said compound is selected from the group consisting of:

10. The compound of claim 1 , wherein said compound is:

Assignments (2)
CONFIRMATORY LICENSE Recorded Mar 15, 2011
From: UNIVERSITY OF CALIFORNIA
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 025954/0274 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 24, 2010
From: JIN, LEE-WAY; LAM, KIT S.; LIU, RUIWU; HONG, HYUN-SEOK; MAEZAWA, IZUMI
To: THE REGENTS OF THE UNIVERSITY OF CALIFORNIA
Reel/Frame 025421/0478 →
Continuity (2)
Provisional Application 60985138 · Nov 2, 2007
Related Publication 20110071301A1 · Mar 24, 2011