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karuborin derivative

机译:卡尔博林·德里·阿希

摘要

PURPOSE: To provide the new compound having excellent cholecystokinin antagonistic activity and pancreatic juice secretion-inhibitory activity, useful as a preventive or medicine for digestive organ-related diseases such as pancreatic lesions or gastrointestinal diseases. ;CONSTITUTION: The compound of formula I (R1 is H, an alkyl, alkoxy or OH; R5 is H or combined with R1 into alkylenedioxy; R2 is H, a halogen, alkoxy or OH; R3 is H, an alkyl, carboxyalkyl, etc.; R4 is H, an alkyl, carboxyalkyl, aralkyl, formyl, etc.; n is 0-2) and a pharmacologically permissible salt thereof, e.g. 3-[9H-pirido(3,4-b)-indole-3-yl-carbonyl]amino-3-methyl-1-phenyl-2-indolinone. The compound of the formula I can be obtained by reaction between an amine compound of formula II or a salt thereof and a carboxylic acid compound of formula III, a reactive derivative therefrom or a salt thereof.;COPYRIGHT: (C)1994,JPO&Japio
机译:用途:提供具有优异的胆囊收缩素拮抗活性和胰液分泌抑制活性的新化合物,可用作预防或治疗消化器官相关疾病(如胰腺病变或胃肠道疾病)的药物。 ;组成:式I化合物(R 1 为H,烷基,烷氧基或OH; R 5 为H或与R 1 变成亚烷基二氧基; R 2 是H,卤素,烷氧基或OH; R 3 是H,烷基,羧基烷基等; R 4 为H,烷基,羧基烷基,芳烷基,甲酰基等; n为0-2)及其药理上允许的盐,例如3- [9H-吡啶基(3,4-b)-吲哚-3-基-羰基]氨基-3-甲基-1-苯基-2-吲哚满酮。式I化合物可以通过式II的胺化合物或其盐与式III的羧酸化合物,其反应性衍生物或其盐之间的反应获得。版权所有:(C)1994,JPO&Japio

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