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lilly, their process of preparaderivati acid 6 - amino - spiro tion and application pharmaceutical penam - 2.4 - piperidino - 3 - carboxy

机译:礼来公司,其制备前皮前酸6-氨基的分散及应用药物[penam-2.4-piperidino]-3-羧基

摘要

6-Amino-spiro[penam-2,4'-piperidine]-3-carboxylic acid derivatives having the formula IMAGE wherein R is a methyl, phenyl or benzyl radical, Z1 is a hydrogen atom and Z2 is a radical selected from those known from penicillin chemistry and is preferably a 2-phenylacetyl, 2-amino-2-phenylacetyl, 5-methyl-3-phenyl-4-isoxazolecarbonyl or 2,6-dimethoxybenzoyl radical, or Z1 and Z2 together represent a bivalent radical Z3 and preferably a (hexahydro-1H-azepin-1-yl)methylene radical, as well as the pharmaceutically acceptable non-toxic salts thereof and process for preparing the same. These compounds have valuable antibacterial properties and are useful as therapeutic agents in the treatment of infectious diseases caused by Gram-positive and Gram-negative bacteria.
机译:具有式的6-氨基-螺[penam-2,4'-哌啶] -3-羧酸衍生物,其中R为甲基,苯基或苄基,Z1为氢原子,Z2为选自以下的基团从青霉素化学已知的那些,优选为2-苯基乙酰基,2-氨基-2-苯基乙酰基,5-甲基-3-苯基-4-异唑基羰基或2,6-二甲氧基苯甲酰基,或Z1和Z2一起代表二价基团Z3优选的是(六氢-1H-氮杂-1-基)亚甲基基团及其药学上可接受的无毒盐及其制备方法。这些化合物具有有价值的抗菌性能,可用作治疗由革兰氏阳性和革兰氏阴性细菌引起的传染病的治疗剂。

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