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the new oximes derivees acid, 3 - (azidomethyl 7 - amino acetamido cephalosporanique, their method of preparation.their application as medicines and pharmaceutical compositions containing them

机译:这种新的肟衍生了3-(叠氮基甲基7-氨基乙酰氨基头孢菌素)酸及其制备方法。它们作为药物和含有它们的药物组合物的应用

摘要

3-Azidomethyl-7- 2-(2-amino-4-thiazolyl)-2-oximino-acetamido -3-c- ephem-4-carboxylic acid derivs. (syn isomers) of formula (I) and their acid-addn. salts are claimed: (where R is H, opt. unsatd. 1-4C alkyl, (CH2)nR1 or benzoly; R1 is COOA' or NH2; n = 1-4; A and A' are H, an equiv. of an alkali(ne earth) metal, Mg, NH4 or organic ammonium cation, or a readily cleavable ester residue). Also claimed are new intermediates for the prepn. of (I). (I) are active against Gram-positive and -negative Lacteria, e.g. with MIC values of =0.5 mu g/ml against Staph. aureus, E. coli, K. pneumoniae, Proteus mirabilis and Salm. typhimurium, including antibiotic-resistant strains of these spp. They can be used as antibacterial medicaments and disinfectants.
机译:3-叠氮基甲基-7-(2-(2-氨基-4-噻唑基)-2-氧亚氨基-乙酰胺基-3-c-ephem-4-羧酸衍生。式(I)的(顺式异构体)及其酸加成基。要求保护的盐:(其中R是H,不饱和的1-4C烷基,(CH 2)n R 1或苯甲酰基; R 1是COOA'或NH 2; n = 1-4; A和A'是H,等价于(碱土金属),Mg,NH4或有机铵阳离子,或易于裂解的酯残基)。还要求保护该新的中间体。 (I)。 (I)对革兰氏阳性和阴性Lacteria具有活性,例如对葡萄球菌的MIC值为= 0.5μg / ml。金黄色葡萄球菌,大肠杆菌,肺炎克雷伯菌,奇异变形杆菌和Salm。鼠伤寒沙门氏菌,包括这些菌的抗药性菌株。它们可用作抗菌药物和消毒剂。

著录项

  • 公开/公告号BE875560A

    专利类型

  • 公开/公告日1979-10-15

    原文格式PDF

  • 申请/专利权人 ROUSSEL-UCLAF;

    申请/专利号BE19790194585

  • 发明设计人

    申请日1979-04-13

  • 分类号C07D;A61K;

  • 国家 BE

  • 入库时间 2022-08-22 20:52:22

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