Suppr超能文献

直接凝血酶抑制剂的杂环核心类似物。

Heterocyclic core analogs of a direct thrombin inhibitor.

机构信息

Merck Research Laboratories, Rahway, NJ, USA.

Albany Molecular Research, Singapore Research Center, Singapore.

出版信息

Bioorg Med Chem Lett. 2014 Feb 15;24(4):1111-5. doi: 10.1016/j.bmcl.2014.01.002. Epub 2014 Jan 10.

Abstract

Thrombin is a serine protease that plays a key role in blood clotting. Pyrrolidine 1 is a potent thrombin inhibitor discovered at Merck several years ago. Seven analogs (2-8) of 1 in which the pyrrolidine core was replaced with various heterocycles were prepared and evaluated for activity against thrombin, clotting factors VIIa, IXa, Xa, and XIIa, and trypsin. The thiomorpholine analog 6 was the most active, essentially matching the thrombin inhibitory activity of 1 with slightly improved selectivity over trypsin.

摘要

凝血酶是一种丝氨酸蛋白酶,在血液凝固中起着关键作用。几年前,默克公司发现了吡咯烷 1,这是一种强效的凝血酶抑制剂。为了评估其对凝血酶、VIIa、IXa、Xa 和 XIIa 因子以及胰蛋白酶的活性,我们制备并研究了吡咯烷核心被各种杂环取代的 1 的七种类似物(2-8)。硫代吗啉类似物 6 的活性最高,其对凝血酶的抑制活性与 1 基本相当,对胰蛋白酶的选择性略有提高。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验