IP Library Granted Patent US 8,524,763
Granted Patent B2
US 8,524,763 · App. 12/564,819 · Granted Sep 3, 2013

Inhibitors of store operated calcium release

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Quick Facts
Patent No.
US 8,524,763
App. No.
12/564,819
Granted
Sep 3, 2013
Kind
B2
Abstract

Described herein are compounds and pharmaceutical compositions containing such compounds, which modulate the activity of store-operated calcium (SOC) channels. Also described herein are methods of using such SOC channel modulators, alone and in combination with other compounds, for treating diseases, disorders or conditions that would benefit from inhibition of SOC channel activity.

Claims (35)

1. A pharmaceutical composition comprising a pharmaceutically acceptable diluent, excipient or binder, and a compound of Formula (I):

wherein:

L is a bond;

R is hydrogen, CO 2 R 1 , an optionally substituted heteroaryl, or an optionally substituted heterocycloalkyl;

R 1 is hydrogen, C 1 -C 6 alkyl, C 1 -C 6 cycloalkyl, C 1 -C 6 haloalkyl, phenyl or benzyl;

R 2 is cycloalkyl, aryl, arylalkyl, heteroaryl, heteroarylalkyl, or heteroarylalkenyl, wherein cycloalkyl, aryl, arylalkyl, heteroaryl, heteroarylalkyl, or heteroarylalkenyl is optionally substituted with at least one R 5 ;

R 3 and R 6 are each independently hydrogen, C 1 -C 6 alkyl, —C(O)—C 1 -C 6 alkyl, or —C(O)NR 1 —C 1 -C 6 alkyl, wherein C 1 -C 6 alkyl is optionally substituted with at least one R 5 ;

R 4 is aryl or heteroaryl; wherein aryl or heteroaryl is optionally substituted with at least one R 5 ;

each R 5 is independently selected from F, Cl, Br, I, —CN, alkyne, C 1 -C 6 alkylalkyne, —NO 2 , —OH, —CF 3 , —OCF 3 , —OR 8 , C 1 -C 6 alkyl, C 3 -C 8 cycloalkyl, C 1 -C 6 heteroalkyl, C 1 -C 6 haloalkyl, tetrazolyl, C 2 -C 8 heterocycloalkyl, optionally substituted aryl, optionally substituted heteroaryl, —NHS(═O) 2 R 8 , —S(═O) 2 N(R 9 ) 2 , —N(R 9 )S(═O) 2 N(R 9 ) 2 , —C(═O)CF 3 , —C(═O)NHS(═O) 2 R 8 , —S(═O) 2 NHC(═O)R 8 , —N(R 9 ) 2 , —N(R 9 )C(═O)R 8 , —N(R 9 )C(═O)N(R 9 ) 2 , —N(R 9 )C(═O)OR 8 , —CO 2 R 9 , —C(═O)R 8 , —OC(═O)R 8 , —OC(═O)N(R 9 ) 2 , —CON(R 9 ) 2 , —SR 8 , —S(═O)R 8 , and —S(═O) 2 R 8 ;

each R 8 is independently selected from C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 3 -C 8 cycloalkyl, phenyl, and benzyl; and

each R 9 is independently selected from H, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 3 -C 8 cycloalkyl, phenyl, and benzyl; or pharmaceutically acceptable salt thereof.

2. A pharmaceutical composition comprising a pharmaceutically acceptable diluent, excipient or binder, and a compound selected from:

or pharmaceutically acceptable salt, pharmaceutically acceptable solvate, or pharmaceutically acceptable prodrug thereof.

3. A compound of Formula (I):

wherein:

L is a bond;

R is hydrogen, CO 2 R 1 , an optionally substituted heteroaryl, or an optionally substituted heterocycloalkyl;

R 1 is hydrogen, C 1 -C 6 alkyl, C 1 -C 6 cycloalkyl, C 1 -C 6 haloalkyl, phenyl or benzyl;

R 2 is cycloalkyl, aryl, arylalkyl, heteroaryl, heteroarylalkyl, or heteroarylalkenyl, wherein cycloalkyl, aryl, arylalkyl, heteroaryl, heteroarylalkyl, or heteroarylalkenyl is optionally substituted with at least one R 5 ;

R 3 and R 6 are each independently hydrogen, C 1 -C 6 alkyl, —C(O)—C 1 -C 6 alkyl, or —C(O)NR 1 —C 1 -C 6 alkyl, wherein C 1 -C 6 alkyl is optionally substituted with at least one R 5 ;

R 4 is aryl or heteroaryl; wherein aryl or heteroaryl is optionally substituted with at least one R 5 ;

each R 5 is independently selected from F, Cl, Br, I, —CN, alkyne, C 1 -C 6 alkylalkyne, —NO 2 , —OH, —CF 3 , —OCF 3 , —OR 8 , C 1 -C 6 alkyl, C 3 -C 8 cycloalkyl, C 1 -C 6 heteroalkyl, C 1 -C 6 haloalkyl, tetrazolyl, C 2 -C 8 heterocycloalkyl, optionally substituted aryl, optionally substituted heteroaryl, —NHS(═O) 2 R 8 , —S(═O) 2 N(R 9 ) 2 , —N(R 9 )S(═O) 2 N(R 9 ) 2 , —C(═O)CF 3 , —C(═O)NHS(═O) 2 R 8 , —S(═O) 2 NHC(═O)R 8 , —N(R 9 ) 2 , —N(R 9 )C(═O)R 8 , —N(R 9 )C(═O)N(R 9 ) 2 , —N(R 9 )C(═O)OR 8 , —CO 2 R 9 , —C(═O)R 8 , —OC(═O)R 8 , —OC(═O)N(R 9 ) 2 , —CON(R 9 ) 2 , —SR 8 , —S(═O)R 8 , and —S(═O) 2 R 8 ;

each R 8 is independently selected from C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 3 -C 8 cycloalkyl, phenyl, and benzyl; and

each R 9 is independently selected from H, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 3 -C 8 cycloalkyl, phenyl, and benzyl; or

a pharmaceutically acceptable salt thereof.

4. The compound of claim 3 wherein R is CO 2 H.

5. The compound of claim 3 wherein R is H.

6. The compound of claim 3 wherein R 3 and R 6 are each independently C 1 -C 6 alkyl.

7. The compound of claim 3 wherein R 2 is aryl.

8. The compound of claim 3 wherein R 4 is aryl.

9. The compound of claim 7 wherein aryl is phenyl.

10. The compound of claim 7 wherein phenyl is substituted with F, Cl, Br, or I.

11. The compound of claim 7 wherein phenyl is substituted with —OR 8 .

12. The compound of claim 11 wherein R 8 is phenyl.

13. The compound of claim 8 wherein aryl is phenyl.

Assignments (2)
SECURITY INTEREST Recorded Mar 4, 2025
From: CALCIMEDICA, INC.
To: AVENUE CAPITAL MANAGEMENT II, L.P.
Reel/Frame 070394/0314 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 17, 2010
From: WHITTEN, JEFFREY P.
To: CALCIMEDICA, INC.
Reel/Frame 023951/0042 →