首页> 外国专利> ANTHRANYL DERIVATIVES HAVING AN ANTICHOLECYSTOKININ ACTIVITY(ANTI-CCK-1), A PROCESS FOR THEIR PREPARATION, AND PHARMACEUTICAL USE THEREOF

ANTHRANYL DERIVATIVES HAVING AN ANTICHOLECYSTOKININ ACTIVITY(ANTI-CCK-1), A PROCESS FOR THEIR PREPARATION, AND PHARMACEUTICAL USE THEREOF

机译:具有抗胆囊收缩素活性(ANTI-CCK-1)的蒽基衍生物及其制备方法和其医药用途

摘要

Anthranylic compounds having anti-CCK activity of general formula (I) in which, n is a whole number lying between 0 and 7; R1 is chosen independently from the groups (II), in which X1 is chosen independently from, S, O, NR2 an d X2 is a group chosen from: H, C1-C4 alkyl, F, Cl, CF3, OCH3, OC2H5, CN; R2 i s chosen from H or CH3; R3 is chosen from H, CH3, F, Cl, CF3, OCH3; R4 is chos en from the groups: H, -S-(CH2)m-R5, -SO2- (CH2)m-R5 (n different from 0), a branched alkyl group, a cyclo alkyl, a cyclo alkenyl, the group 1 or 2 adamantile, a phenyl group optionally substituted; R5 is chosen from the groups: H, linear or branched alkyl, cyclo alkyl, the group 1 or 2 adamantil e, a suitably substituted phenyl group.
机译:具有通式(I)的抗CCK活性的邻氨基苯甲酸酯化合物,其中,n为0至7之间的整数; R1独立地选自基团(II),其中X1独立地选自S,O,NR2和d X2是选自以下基团:H,C1-C4烷基,F,Cl,CF3,OCH3,OC2H5, CN; R2选自H或CH3; R3选自H,CH3,F,Cl,CF3,OCH3; R4选自以下基团:H,-S-(CH 2)m -R 5,-SO 2-(CH 2)m -R 5(n不同于0),支链烷基,环烷基,环烯基, 1或2族金刚烷基,任选取代的苯基; R 5选自:H,直链或支链烷基,环烷基,基团1或2的金刚烷基,适当取代的苯基。

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