摘要 |
A benzodiazepine derivative of the formula (I): <CHEM> wherein R1 is a bond, -CH2-, -CH2O-, -OCH2-, -SCH2- or a group of the formula: <CHEM> R2 is a lower alkyl, -COOR5, -CONH(CH2)nCOOR5, -CONHSO2R5, -SO2NHCOR5, or an optionally substituted heterocyclic group (R5 is a hydrogen atom, lower alkyl or benzyl and n is an integer of 1 to 5); R3 is a bond, -CO- or -CONH-; and R4 is an optionally substituted heterocyclic group, optionally substituted lower alkyl, optionally substituted lower cycloalkyl, optionally substituted aryl, or lower alkoxycarbonyl group, or a pharmaceutically acceptable salt thereof, which has a high affinity for gastrin receptors and/or CCK-B receptors but not for CCK-A receptors, and is useful for treating diseases associated with gastrin receptors and/or CCK-B receptors without inducing the side effects associated with CCK-A receptors. |