Protease Inhibitors (chemical synthesis) < Protease Inhibitors (chemistry) < Protease Inhibitors (classification)

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List of bibliographic references

Number of relevant bibliographic references: 62.
[0-20] [0 - 20][0 - 50][20-40]

Ident.	Authors (with country if any)	Title
000A67 (2004)	John T-A Hsu [République populaire de Chine] ; Chih-Jung Kuo ; Hsing-Pang Hsieh ; Yeau-Ching Wang ; Kuo-Kuei Huang ; Coney P-C Lin ; Ping-Fang Huang ; Xin Chen ; Po-Huang Liang	Evaluation of metal-conjugated compounds as inhibitors of 3CL protease of SARS-CoV.
000B25 (2004)	Jan E. Blanchard [Canada] ; Nadine H. Elowe ; Carly Huitema ; Pascal D. Fortin ; Jonathan D. Cechetto ; Lindsay D. Eltis ; Eric D. Brown	High-throughput screening identifies inhibitors of the SARS coronavirus main proteinase.
000D65 (2005)	Bing Liu [République populaire de Chine] ; Jiaju Zhou	SARS-CoV protease inhibitors design using virtual screening method from natural products libraries.
000F44 (2005)	Lili Chen ; Chunshan Gui ; Xiaomin Luo ; Qingang Yang ; Stephan Günther ; Elke Scandella ; Christian Drosten ; Donglu Bai ; Xichang He ; Burkhard Ludewig ; Jing Chen ; Haibin Luo ; Yiming Yang ; Yifu Yang ; Jianping Zou ; Volker Thiel ; Kaixian Chen ; Jianhua Shen ; Xu Shen ; Hualiang Jiang	Cinanserin Is an Inhibitor of the 3C-Like Proteinase of Severe Acute Respiratory Syndrome Coronavirus and Strongly Reduces Virus Replication In Vitro†
000F53 (2005)	Li-Rung Chen [République populaire de Chine] ; Yu-Chin Wang ; Yi Wen Lin ; Shan-Yen Chou ; Shyh-Fong Chen ; Lee Tai Liu ; Ying-Ta Wu ; Chih-Jung Kuo ; Tom Shieh-Shung Chen ; Shin-Hun Juang	Synthesis and evaluation of isatin derivatives as effective SARS coronavirus 3CL protease inhibitors.
000F87 (2005)	Li Ding [République populaire de Chine] ; Xin-Xiang Zhang ; Ping Wei ; Keqiang Fan ; Luhua Lai	The interaction between severe acute respiratory syndrome coronavirus 3C-like proteinase and a dimeric inhibitor by capillary electrophoresis.
001021 (2005)	Jiun-Jie Shie [Taïwan] ; Jim-Min Fang ; Chih-Jung Kuo ; Tun-Hsun Kuo ; Po-Huang Liang ; Hung-Jyun Huang ; Wen-Bin Yang ; Chun-Hung Lin ; Jiun-Ling Chen ; Yin-Ta Wu ; Chi-Huey Wong	Discovery of potent anilide inhibitors against the severe acute respiratory syndrome 3CL protease.
001201 (2005)	Ting-Wai Lee [Canada] ; Maia M. Cherney ; Carly Huitema ; Jie Liu ; Karen Ellis James ; James C. Powers ; Lindsay D. Eltis ; Michael N G. James	Crystal structures of the main peptidase from the SARS coronavirus inhibited by a substrate-like aza-peptide epoxide.
001230 (2005)	Ulrich Kaeppler [Allemagne] ; Nikolaus Stiefl ; Markus Schiller ; Radim Vicik ; Alexander Breuning ; Werner Schmitz ; Daniel Rupprecht ; Carsten Schmuck ; Knut Baumann ; John Ziebuhr ; Tanja Schirmeister	A new lead for nonpeptidic active-site-directed inhibitors of the severe acute respiratory syndrome coronavirus main protease discovered by a combination of screening and docking methods.
001414 (2005)	Nicholas A. Meanwell [États-Unis] ; Makonen Belema ; David J. Carini ; Stanley V. D'Andrea ; John F. Kadow ; Mark Krystal ; B Narasimhulu Naidu ; Alicia Regueiro-Ren ; Paul M. Scola ; Sing-Yuen Sit ; Michael A. Walker ; Tao Wang ; Kap-Sun Yeung	Developments in antiviral drug design, discovery and development in 2004.
001473 (2006)	Rolf Hilgenfeld [Allemagne] ; Ksenia Pumpor	Sometimes intermediates. Do the job!
001525 (2006)	Keng-Chang Tsai [République populaire de Chine] ; Shih-Yuan Chen ; Po-Huang Liang ; I-Lin Lu ; Neeraj Mahindroo ; Hsing-Pang Hsieh ; Yu-Sheng Chao ; Lincoln Liu ; Donald Liu ; Wei Lien ; Thy-Hou Lin ; Su-Ying Wu	Discovery of a novel family of SARS-CoV protease inhibitors by virtual screening and 3D-QSAR studies.
001586 (2006)	Jiang Yin [Canada] ; Maia M. Cherney ; Ernst M. Bergmann ; Jianmin Zhang ; Carly Huitema ; Hanna Pettersson ; Lindsay D. Eltis ; John C. Vederas ; Michael N G. James	An episulfide cation (thiiranium ring) trapped in the active site of HAV 3C proteinase inactivated by peptide-based ketone inhibitors.
001614 (2006)	Pamela Hamill [Canada] ; Derek Hudson ; Richard Y. Kao ; Polly Chow ; Meera Raj ; Hongyan Xu ; Martin J. Richer ; François Jean	Development of a red-shifted fluorescence-based assay for SARS-coronavirus 3CL protease: identification of a novel class of anti-SARS agents from the tropical marine sponge Axinella corrugata.
001623 (2006)	I-Lin Lu [République populaire de Chine] ; Neeraj Mahindroo ; Po-Huang Liang ; Yi-Hui Peng ; Chih-Jung Kuo ; Keng-Chang Tsai ; Hsing-Pang Hsieh ; Yu-Sheng Chao ; Su-Ying Wu	Structure-based drug design and structural biology study of novel nonpeptide inhibitors of severe acute respiratory syndrome coronavirus main protease.
001669 (2007)	S-Q Wang [République populaire de Chine] ; Q-S Du ; K. Zhao ; A-X Li ; D-Q Wei ; K-C Chou	Virtual screening for finding natural inhibitor against cathepsin-L for SARS therapy.
001761 (2006)	Lili Chen [République populaire de Chine] ; Shuai Chen ; Chunshan Gui ; Jianhua Shen ; Xu Shen ; Hualiang Jiang	Discovering severe acute respiratory syndrome coronavirus 3CL protease inhibitors: virtual screening, surface plasmon resonance, and fluorescence resonance energy transfer assays.
001803 (2006)	Luhua Lai [République populaire de Chine] ; Xiaofeng Han ; Hao Chen ; Ping Wei ; Changkang Huang ; Shiyong Liu ; Keqiang Fan ; Lu Zhou ; Zhenming Liu ; Jianfeng Pei ; Ying Liu	Quaternary structure, substrate selectivity and inhibitor design for SARS 3C-like proteinase.
001805 (2006)	Haitao Yang [République populaire de Chine] ; Mark Bartlam ; Zihe Rao	Drug design targeting the main protease, the Achilles' heel of coronaviruses.
001859 (2007)	Qi-Shi Du [République populaire de Chine] ; Hao Sun ; Kuo-Chen Chou	Inhibitor design for SARS coronavirus main protease based on "distorted key theory".
001941 (2007)	Dariusz Plewczynski [Pologne] ; Marcin Hoffmann ; Marcin Von Grotthuss ; Krzysztof Ginalski ; Leszek Rychewski	In silico prediction of SARS protease inhibitors by virtual high throughput screening.

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