๐ Synthesis, crystal structure, structure-activity relationships, and antiviral activity of a potent SARS coronavirus 3CL protease inhibitor
A potent SARS coronavirus (CoV) 3CL protease inhibitor (TG-0205221, K i = 53 nM) has been developed. TG-0205221 showed remarkable activity against SARS CoV and human coronavirus (HCoV) 229E replications by reducing the viral titer by 4.7 log (at 5 ฮผM) for SARS CoV and 5.2 log (at 1.25 ฮผM) for HCoV 229E. The crystal structure of TG-0205221 (resolution = 1.93 ร
) has revealed a unique binding mode comprising a covalent bond, hydrogen bonds, and numerous hydrophobic interactions. Structural comparisons between TG-0205221 and a natural peptide substrate were also discussed. This information may be applied toward the design of other 3CL protease inhibitors. ยฉ 2006 American Chemical Society.
author
๐ค Yang, Syaulan
๐ค Chen, Shu Jen
๐ค Hsu, Min Feng
๐ค Wu, Jen Dar
๐ค Tseng, Chien Te K.
๐ค Liu, Yu Fan
๐ค Chen, Hua Chien
๐ค Kuo, Chun Wei
๐ค Wu, Chi Shen
๐ค Chang, Li Wen
๐ค Chen, Wen Chang
๐ค Liao, Shao Ying
๐ค Chang, Teng Yuan
๐ค Hung, Hsin Hui
๐ค Shr, Hui Lin
๐ค Liu, Cheng Yuan
๐ค Huang, Yu An
๐ค Chang, Ling Yin
๐ค Hsu, Jen Chi
๐ค Peters, Clarence J.
๐ค Wang, Andrew H.J.
๐ค Hsu, Ming Chu
year
โฐ 2006
issn
๐ 00222623
volume
49
number
16
page
4971-4980
citedbycount
49
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