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method of inhibiting class d enzymes in the treatment of bacterial infection in a patient in need

机译:有需要的患者中抑制d类酶治疗细菌感染的方法

摘要

This invention relates to certain bicyclic 6-alkylidene penems acting as inhibitors of class-D enzymes. 225 -lactamases hydrolyze 225 -lactam antibiotics and as such serve as a primary cause of bacterial resistance. The compounds of the present invention when combined with? -Lactam antibiotics will provide effective treatment against life-threatening bacterial infections. In accordance with the present invention, compounds of formula 1 or a pharmaceutically acceptable salt or in vivo hydrolysable R5 ester thereof are provided: Formula (1) wherein: one of A and B denotes hydrogen and the other a fused bicyclic heteroaryl group optionally substituted; and X = O or S.
机译:本发明涉及某些用作D类酶抑制剂的双环6-亚烷基青霉烯。 <225>-内酰胺酶水解<225>-内酰胺抗生素,因此是细菌耐药性的主要原因。当与结合本发明的化合物? -内酰胺抗生素将为威胁生命的细菌感染提供有效的治疗。根据本发明,提供了式1化合物或其药学上可接受的盐或体内可水解的R5酯:式(1)其中:A和B之一表示氢,另一个表示任选取代的稠合双环杂芳基; X = O或S。

著录项

  • 公开/公告号BRPI0610957A2

    专利类型

  • 公开/公告日2010-08-03

    原文格式PDF

  • 申请/专利权人 WYETH;

    申请/专利号BR2006PI10957

  • 申请日2006-05-26

  • 分类号A61K31/424;A61K31/429;A61K31/43;A61P31/04;

  • 国家 BR

  • 入库时间 2022-08-21 18:47:21

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