首页> 外国专利> compound or a pharmaceutically acceptable salt or prodrug thereof, method for producing an antibacterial effect on a warm-blooded animal, use of a pharmaceutically acceptable salt or compound, or an in vivo hydrolysable ester thereof, pharmaceutical composition, and, a process for preparing a pharmaceutically acceptable salt or compound or an in vivo hydrolysable ester thereof.

compound or a pharmaceutically acceptable salt or prodrug thereof, method for producing an antibacterial effect on a warm-blooded animal, use of a pharmaceutically acceptable salt or compound, or an in vivo hydrolysable ester thereof, pharmaceutical composition, and, a process for preparing a pharmaceutically acceptable salt or compound or an in vivo hydrolysable ester thereof.

机译:化合物或其药学上可接受的盐或前药,对温血动物产生抗菌作用的方法,药学上可接受的盐或化合物或其体内可水解酯的用途,药物组合物以及制备其的方法药学上可接受的盐或化合物或其体内可水解的酯。

摘要

COMPOUND OR A PHARMACEUTICALLY ACCEPTABLE SALT OR PRODUCT OF THE SAME, A METHOD FOR PROVIDING AN ANTIBACTERIAL EFFECT ON A HOT BLOOD ANIMAL, USE OF A PHARMACEUTICALLY ACCEPTABLE COMPOSITE, OR HYDROATIC HYDROATIC SALT A process for the preparation of a pharmaceutically acceptable compound or salt or an in vivo hydrolyzable ester thereof. wherein R¬ 1¬ is selected from hydrogen, halogen, cyano, optionally substituted methyl; R¬2¬ and R¬3¬ are independently selected from hydrogen, fluorine, chlorine and trifluoromethyl; and R¬5¬ are independently selected from, for example, optionally substituted hydrogen, methyl, (2-4C) alkyl, C (O) R¬6¬ or R¬4¬ and R¬5¬ together with nitrogen at the same time. which they are attached, form an optionally substituted 4- or 5- membered saturated or partially unsaturated heterocyclyl ring or an optionally substituted imidazole ring. Methods for manufacturing the compounds of formula (I), compositions containing them and their use as antibacterial agents are also described.
机译:化合物或药学上可接受的盐或类似产品,提供对热血动物的抗菌作用的方法,使用药学上可接受的复合物或水解性盐制备药学上可接受的化合物或盐的方法其体内可水解的酯。其中R 1-选自氢,卤素,氰基,任选取代的甲基; R 2和R 3独立地选自氢,氟,氯和三氟甲基; R 5和R 5彼此独立地选自例如任选取代的氢,甲基,(2-4C)烷基,C(O)R 6或R 4和R 5以及相同的氮。时间。它们连接的基团形成任选取代的4或5元饱和或部分不饱和杂环基环或任选取代的咪唑环。还描述了制备式(I)化合物的方法,包含它们的组合物以及它们作为抗菌剂的用途。

著录项

  • 公开/公告号BRPI0511554A

    专利类型

  • 公开/公告日2008-01-02

    原文格式PDF

  • 申请/专利权人 ASTRAZENECA AB;

    申请/专利号BR2005PI11554

  • 申请日2005-05-24

  • 分类号C07D413/14;A61K31/4192;A61K31/422;A61K31/4427;A61P31/04;

  • 国家 BR

  • 入库时间 2022-08-21 20:08:48

相似文献

  • 专利
  • 外文文献
  • 中文文献
获取专利

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号