A compound represented by formula (1) (in the formula: ring-D represents a three- to eight-membered hydrocarbon ring; R
a
represents an optionally substituted amino C
1-6
alkyl group or the like; R
b1
and R
b2
each independently represent a hydrogen atom, a halogen atom, or the like; R
c
represents an optionally substituted C
6-10
aryl group or the like; R
d
represents a hydrogen atom or the like; and ring-Q represents a (hetero)aryl group or the like which may be substituted with a carboxyl group or the like) or a pharmaceutically acceptable salt thereof exhibits an excellent FXIa inhibitory activity, and is useful as a therapeutic agent against thrombosis or the like.
FUSED RING COMPOUNDS AS PARTIAL AGONISTS OF PPAR-GAMMA
申请人:Tawaraishi Taisuke
公开号:US20110009384A1
公开(公告)日:2011-01-13
The present invention provides an agent for the prophylaxis or treatment of diabetes, which has a superior hypoglycemic action, and is associated with a fewer side effects such as body weight gain and the like.
The resent invention relates an agent for the prophylaxis or treatment of diabetes, which comprises a compound represented by
wherein each symbol is as defined in the description, or a salt thereof or a prodrug thereof.
The present invention provides an agent for the prophylaxis or treatment of diabetes, which has a superior hypoglycemic action, and is associated with a fewer side effects such as body weight gain and the like.
The present invention relates an agent for the prophylaxis or treatment of diabetes, which comprises a compound represented by
wherein each symbol is as defined in the description, or a salt thereof or a prodrug thereof.