Division of Organic Chemistry, National Chemical Laboratory (CSIR-NCL), Dr. Homi Bhabha Road, Pune 411 008, India.
Bioorg Med Chem. 2011 Dec 1;19(23):7129-35. doi: 10.1016/j.bmc.2011.09.058. Epub 2011 Oct 5.
We report herein, design and synthesis of vinylaminophosphonates, a novel class of compounds as possible cysteine protease inhibitors. The synthesis of vinylaminophosphonates has been accomplished employing Tsuji-Trost reaction as a key step. The synthesized compounds were assayed against papain, a model cysteine protease and some of our synthesized compounds showed IC(50) values in the range of 30-54 μM thereby suggesting that these chemical entities thus could constitute an interesting template for the design of potential novel protease inhibitors.
我们在此报告,设计和合成乙烯基氨膦酸酯,作为可能的半胱氨酸蛋白酶抑制剂的一类新化合物。乙烯基氨膦酸酯的合成采用了作为关键步骤的 Tsuji-Trost 反应。对合成的化合物进行了木瓜蛋白酶的测定,作为模型半胱氨酸蛋白酶,我们的一些合成化合物的 IC 50 值在 30-54 μM 范围内,这表明这些化学实体可以作为设计潜在新型蛋白酶抑制剂的有趣模板。