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a lateral channel cephalosporines alpha acylaminoacetique main decisions and measures taken

机译:侧通道头孢菌素α酰基氨基乙酸主要决定和采取的措施

摘要

Compounds of the formula IMAGE wherein R1 denotes optionally substituted phenyl, thienyl, furyl or 1,4-cyclohexadienyl, R2 represents a free carboxyl group or an esterified carboxyl group which can be split physiologically, R3 represents hydrogen, lower alkoxy or an optionally substituted methyl group and B represents an optionally substitued six-membered ring with 1 to 3 ring nitrogen atoms, which is bonded to the carbonyl group -C(=O)- by one of its carbon atoms, the nitrogen atoms of a monocyclic six-membered ring having 2 nitrogen atoms being either adjacent or separated by two ring carbon atoms, and the salts of such compounds which have a salt-forming group, including the inner salts, for example the 7 beta -[D(-)- alpha -(3,5-Dioxo-2,3,4,5-tetrahydro-1,2,4-triazine-6-carboxamido)-phenylace tamido]-cephalosporanic acid, have antibiotic activity.
机译:的化合物,其中R1代表任选取代的苯基,噻吩基,呋喃基或1,4-环己二烯基,R2代表可以进行生理学拆分的游离羧基或酯化羧基,R3代表氢,低级烷氧基或任选地取代的甲基,B代表一个可被1至3个环氮原子取代的六元环,该环通过其碳原子之一(单环六-碳原子的氮原子)与羰基-C(= O)-键合具有与两个环碳原子相邻或隔开的两个氮原子的单环,以及具有成盐基团的此类化合物的盐,包括内盐,例如7β-[D(-)-α- (3,5-二氧代-2,3,4,5-四氢-1,2,4-三嗪-6-羧酰胺基)-苯乙酰胺基]-头孢烷酸,具有抗生素活性。

著录项

  • 公开/公告号BE828933A

    专利类型

  • 公开/公告日1975-11-12

    原文格式PDF

  • 申请/专利权人

    申请/专利号BE19750156230

  • 发明设计人

    申请日1975-05-12

  • 分类号C07D;

  • 国家 BE

  • 入库时间 2022-08-23 03:00:58

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