4.5 Article

New developments for the design, synthesis and biological evaluation of potent SARS-CoV 3CLpro inhibitors

期刊

BIOORGANIC & MEDICINAL CHEMISTRY LETTERS
卷 19, 期 10, 页码 2722-2727

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.bmcl.2009.03.118

关键词

SARS-CoV; Protease inhibitors; Drug design; Synthesis

资金

  1. Frontier Research Program
  2. Ministry of Education, Culture, Sports, Science and Technology, Japan
  3. Japan Society for the Promotion of Science's Post-Doctoral Fellowship
  4. National Institutes of Health [GM 57144]

向作者/读者索取更多资源

A series of trifluoromethyl, benzothiazolyl or thiazolyl ketone-containing peptidic compounds as SARS-CoV 3CL protease inhibitors were developed and their potency was evaluated by in vitro protease inhibitory assays. Three candidates had encouraging results for the development of new anti-SARS compounds. (C) 2009 Elsevier Ltd. All rights reserved.

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