A new chemotype with promise against Trypanosoma cruzi
摘要:
Pyridyl benzamide 2 is a potent inhibitor of Trypanosoma cruzi, but not other protozoan parasites, and had a selectivity-index of >= 10. The initial structure-activity relationship (SAR) indicates that benzamide and sulfonamide functional groups, and N-methylpiperazine and sterically unhindered 3-pyridyl substructures are required for high activity against T. cruzi. Compound 2 and its active analogs had low to moderate metabolic stabilities in human and mouse liver microsomes.
[EN] HETEROARYL BENZAMIDES, COMPOSITIONS AND METHODS OF USE<br/>[FR] HÉTÉROARYL BENZAMIDES, COMPOSITIONS ET PROCÉDÉS D'UTILISATION
申请人:UNIV LELAND STANFORD JUNIOR
公开号:WO2011011514A1
公开(公告)日:2011-01-27
Provided are certain heteroaryl benzamides, compositions, and methods of their manufacture and use.
提供了某些杂环芳酰苯胺、组合物及其制备和使用方法。
HETEROARYL BENZAMIDES, COMPOSITIONS AND METHODS OF USE
申请人:Sutphin Patrick D.
公开号:US20120225862A1
公开(公告)日:2012-09-06
Provided are certain heteroaryl benzamides, compositions, and methods of their manufacture and use.
提供了某些杂环芳酰苯胺、组成物及其制造和使用方法。
JP5789603
申请人:——
公开号:——
公开(公告)日:——
A new chemotype with promise against Trypanosoma cruzi
作者:Xiaofang Wang、Monica Cal、Marcel Kaiser、Frederick S. Buckner、Galina I. Lepesheva、Austin G. Sanford、Alexander I. Wallick、Paul H. Davis、Jonathan L. Vennerstrom
DOI:10.1016/j.bmcl.2019.126778
日期:2020.1
Pyridyl benzamide 2 is a potent inhibitor of Trypanosoma cruzi, but not other protozoan parasites, and had a selectivity-index of >= 10. The initial structure-activity relationship (SAR) indicates that benzamide and sulfonamide functional groups, and N-methylpiperazine and sterically unhindered 3-pyridyl substructures are required for high activity against T. cruzi. Compound 2 and its active analogs had low to moderate metabolic stabilities in human and mouse liver microsomes.