The present invention provides a compound of Formula I or a pharmaceutically acceptable salt thereof, wherein R
1
, R
2
, R
3
, A
1
, A
2
, A
3
, B
1
, B
2
, B
3
and B
4
are as defined herein. The compounds of Formula I have been found to act as glucagon antagonists or inverse agonists. Consequently, the compounds of Formula I and the pharmaceutical compositions thereof are useful for the treatment of diseases, disorders, or conditions mediated by glucagon.
The present invention provides a compound of Formula I or a pharmaceutically acceptable salt thereof, wherein R1, R2, R3, A1, A2, A3, B1, B2, B3 and B4 are as defined herein. The compounds of Formula I have been found to act as glucagon antagonists or inverse agonists. Consequently, the compounds of Formula I and the pharmaceutical compositions thereof are useful for the treatment of diseases, disorders, or conditions mediated by glucagon.
[EN] QUINOLINYL GLUCAGON RECEPTOR MODULATORS<br/>[FR] MODULATEURS DES RÉCEPTEURS DE QUINOLINYLGLUCAGON
申请人:PFIZER
公开号:WO2013014569A1
公开(公告)日:2013-01-31
The present invention provides a compound of Formula I or a pharmaceutically acceptable salt thereof, wherein R1, R2, R3, A1, A2, A3, B1, B2, B3 and B4 are as defined herein. The compounds of Formula I have been found to act as glucagon antagonists or inverse agonists. Consequently, the compounds of Formula I and the pharmaceutical compositions thereof are useful for the treatment of diseases, disorders, or conditions mediated by glucagon.