发明授权
US4585860A 7-acylamino-3-vinylcephalosporanic acid derivatives useful for treatment
of infectious diseases in human beings and animals
失效
用于治疗人类和动物感染性疾病的7-酰基氨基-3-乙烯基头孢烷酸衍生物
- 专利标题: 7-acylamino-3-vinylcephalosporanic acid derivatives useful for treatment of infectious diseases in human beings and animals
- 专利标题(中): 用于治疗人类和动物感染性疾病的7-酰基氨基-3-乙烯基头孢烷酸衍生物
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申请号: US493051申请日: 1983-05-09
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公开(公告)号: US4585860A公开(公告)日: 1986-04-29
- 发明人: Takao Takaya , Hisashi Takasugi , Takashi Masugi , Hideaki Yamanaka , Kohji Kawabata
- 申请人: Takao Takaya , Hisashi Takasugi , Takashi Masugi , Hideaki Yamanaka , Kohji Kawabata
- 申请人地址: JPX Osaka
- 专利权人: Fujisawa Pharmaceutical Co., Ltd.
- 当前专利权人: Fujisawa Pharmaceutical Co., Ltd.
- 当前专利权人地址: JPX Osaka
- 优先权: GBX7939985 19791119; GBX8004335 19800208; GBX8012991 19800421; GBX8022920 19800714
- 主分类号: A61K31/545
- IPC分类号: A61K31/545 ; A61K31/546 ; A61P31/04 ; C07D209/48 ; C07D213/75 ; C07D239/42 ; C07D257/06 ; C07D271/06 ; C07D271/07 ; C07D277/20 ; C07D277/46 ; C07D277/48 ; C07D277/56 ; C07D285/08 ; C07D417/12 ; C07D501/06 ; C07D501/18 ; C07D501/20 ; C07D501/22 ; C07D501/24 ; C07D501/36 ; C07F9/6561 ; A01N43/84
摘要:
The invention relates to novel compounds of high antimicrobial activity of the formula: ##STR1## in which R.sup.1 is amino-substituted-heterocyclic group which may have halogen, protected amino-substituted-heterocyclic group which may have halogen, or a group of the formula: ##STR2## wherein R.sup.3 is lower alkyl,R.sup.2 is carboxy or a protected carboxy group, andA is lower alkylene which may have a substituent selected from the group consisting of amino, a protected amino group, hydroxy, oxo and a group of the formula: .dbd.N.about.OR.sup.4, wherein R.sup.4 is hydrogen, cyclo(lower)alkenyl, lower alkynyl, lower alkenyl, lower alkenyl substituted by carboxy or a protected carboxy group, lower alkyl, or lower alkyl substituted by one or more substituents selected from carboxy, a protected carboxy group, amino, a protected amino group, cyano, phosphono, a protected phosphono group and a heterocyclic group which may have suitable substituents.
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