首页> 外文会议>1996 Chinese Peptide Symposium July 21-25, 1996, Chengdu, China >Phosphonamidate based inhibitors of angiotensin - Converting enzyme (ACE)
【24h】

Phosphonamidate based inhibitors of angiotensin - Converting enzyme (ACE)

机译:基于磷酰胺盐的血管紧张素抑制剂-转化酶(ACE)

获取原文
获取原文并翻译 | 示例

摘要

The development of the first clinically available orally active ACE (angiotensin - converting enzyme) inhibitor, captopri [1,2] by Squibb group in 1977 started a new appraoch to antihypertension therapy. Reviewing the history of the captopril development, one of the key ideas in this process was a hypothesis that ACE is related structurally and mechanistically to carboxypeptidase A. This allowed the Squibb group to develop a hypothetical model of the ACE active site which led to the design of the first non-peptide inhibitor [3].
机译:1977年,Squibb组开发了第一种临床上可用的口服活性ACE(血管紧张素转换酶)抑制剂卡托普利[1,2],这为抗高血压治疗开辟了新的道路。回顾卡托普利的发展历史,在这一过程中的主要思想之一是关于ACE与羧肽酶A在结构上和机理上相关的假设。这使Squibb组能够开发出ACE活性位点的假想模型,从而进行了设计。第一非肽抑制剂[3]。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

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