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chemical compounds with beta blocker activity, method for their manufacture, compositions containing the relations and the application in the medicine

机译:具有β受体阻滞剂活性的化合物,其制备方法,包含该关系的组合物及其在医学中的应用

摘要

The invention relates to compounds of formula (I), physiologically acceptable salts thereof, formulations containing them, their preparation and their use in medicine. In formula (I) CHEM Q and Q1-Q8 are independently selected hydrogen and C1-4 alkyl; A is a group of formula -(CO)k-(NQ9)m-(CH2)n- where k and m are either both 0 or both 1, n is from 1 to 6, Q9 is selected from hydrogen and C1-4 alkyl and any of the -(CH2)n- groups independently are optionally substituted by one or two C1-4 alkyl groups; B is a C1-6 alkyl group; E and Z are independently selected from carboxy derivatives thereof; D is hydrogen or a C1-6 alkyl group which is optionally substituted by an amino group; (X) is a benzene ring or a naphthyl or indolyl ring system any of which is optionally substituted in any position by one or more substituents independently selected from C1-4 (itself optionally substituted by one or more halogen atoms (C1-4 alkoxy, halo, nitro, amino, carboxy, C1-4 alkoxycarbonyl and hydroxy; and -N Y is a pyrrolidinyl, oxazolidinyl or thiazolidinyl ring, or a ring system selected from indolinyl, quinolinyl and tetrahydroquinolinyl.
机译:本发明涉及式(I)的化合物,其生理上可接受的盐,包含它们的制剂,其制备及其在医学中的用途。式(I)中,CHEM Q和Q 1 -Q 8独立地选自氢和C 1-4烷基。 A是一组式-(CO)k-(NQ 9)m-(CH2)n-,其中k和m均为0或均为1,n为1至6,选择Q 9氢和C 1-4烷基和-(CH 2)n-中的任何一个独立地任选地被一个或两个C 1-4烷基取代; B为碳数1〜6的烷基。 E和Z独立地选自其羧基衍生物; D是氢或任选地被氨基取代的C 1-6烷基; (X)是苯环或萘基或吲哚基环系统,其任意位置在任何位置上任选地被一个或多个独立地选自C1-4的取代基取代(其本身任选地被一个或多个卤素原子(C1-4烷氧基,卤代,硝基,氨基,羧基,C 1-4烷氧基羰基和羟基;和-NY是吡咯烷基,恶唑烷基或噻唑烷基环,或选自吲哚基,喹啉基和四氢喹啉基的环系统。

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