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Protease Inhibitors (blood) < Protease Inhibitors (chemical synthesis) < Protease Inhibitors (chemistry)  Facettes :

List of bibliographic references

Number of relevant bibliographic references: 28.
[0-20] [0 - 20][0 - 28][20-27][20-40]
Ident.Authors (with country if any)Title
000420 (2003) Ekachai Jenwitheesuk [États-Unis] ; Ram SamudralaIdentifying inhibitors of the SARS coronavirus proteinase.
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 JuangSynthesis and evaluation of isatin derivatives as effective SARS coronavirus 3CL protease inhibitors.
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 WongDiscovery of potent anilide inhibitors against the severe acute respiratory syndrome 3CL protease.
001230 (2005) Ulrich Kaeppler [Allemagne] ; Nikolaus Stiefl ; Markus Schiller ; Radim Vicik ; Alexander Breuning ; Werner Schmitz ; Daniel Rupprecht ; Carsten Schmuck ; Knut Baumann ; John Ziebuhr ; Tanja SchirmeisterA 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.
001497 (2006) Samer I. Al-Gharabli [Allemagne] ; Syed T Ali Shah ; Steffen Weik ; Marco F. Schmidt ; Jeroen R. Mesters ; Daniel Kuhn ; Gerhard Klebe ; Rolf Hilgenfeld ; Jörg RademannAn efficient method for the synthesis of peptide aldehyde libraries employed in the discovery of reversible SARS coronavirus main protease (SARS-CoV Mpro) inhibitors.
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 WuStructure-based drug design and structural biology study of novel nonpeptide inhibitors of severe acute respiratory syndrome coronavirus main protease.
001859 (2007) Qi-Shi Du [République populaire de Chine] ; Hao Sun ; Kuo-Chen ChouInhibitor design for SARS coronavirus main protease based on "distorted key theory".
001A48 (2007) Yi-Ming Shao [République populaire de Chine] ; Wen-Bin Yang ; Hung-Pin Peng ; Min-Feng Hsu ; Keng-Chang Tsai ; Tun-Hsun Kuo ; Andrew H-J Wang ; Po-Huang Liang ; Chun-Hung Lin ; An-Suei Yang ; Chi-Huey WongStructure-based design and synthesis of highly potent SARS-CoV 3CL protease inhibitors.
001B84 (2008) Jianmin Zhang [Canada] ; Carly Huitema ; Chunying Niu ; Jiang Yin ; Michael N G. James ; Lindsay D. Eltis ; John C. VederasAryl methylene ketones and fluorinated methylene ketones as reversible inhibitors for severe acute respiratory syndrome (SARS) 3C-like proteinase.
001B98 (2008) Yi-Ming Shao [Taïwan] ; Wen-Bin Yang [Taïwan] ; Tun-Hsun Kuo [Taïwan] ; Keng-Chang Tsai [Taïwan] ; Chun-Hung Lin [Taïwan] ; An-Suei Yang [Taïwan] ; Po-Huang Liang [Taïwan] ; Chi-Huey Wong [Taïwan, États-Unis]Design, synthesis, and evaluation of trifluoromethyl ketones as inhibitors of SARS-CoV 3CL protease
001C26 (2008) Carly Huitema [Canada] ; Jianmin Zhang ; Jiang Yin ; Michael N G. James ; John C. Vederas ; Lindsay D. EltisHeteroaromatic ester inhibitors of hepatitis A virus 3C proteinase: Evaluation of mode of action.
001C95 (2008) Usman Bacha [États-Unis] ; Jennifer Barrila ; Sandra B. Gabelli ; Yoshiaki Kiso ; L. Mario Amzel ; Ernesto FreireDevelopment of broad-spectrum halomethyl ketone inhibitors against coronavirus main protease 3CL(pro).
001D60 (2008) Qingang Yang [République populaire de Chine] ; Lili Chen ; Xuchang He ; Zhenting Gao ; Xu Shen ; Donglu BaiDesign and synthesis of cinanserin analogs as severe acute respiratory syndrome coronavirus 3CL protease inhibitors.
001D64 (2008) Kenichi Akaji [Japon] ; Hiroyuki Konno [Japon] ; Mari Onozuka [Japon] ; Ayumi Makino [Japon] ; Hiroyuki Saito [Japon] ; Kazuto Nosaka [Japon]Evaluation of peptide-aldehyde inhibitors using R188I mutant of SARS 3CL protease as a proteolysis-resistant mutant
001E87 (2009) Thomas Regnier [Japon] ; Diganta Sarma ; Koushi Hidaka ; Usman Bacha ; Ernesto Freire ; Yoshio Hayashi ; Yoshiaki KisoNew developments for the design, synthesis and biological evaluation of potent SARS-CoV 3CL(pro) inhibitors.
001F75 (2009) Arun K. Ghosh [États-Unis] ; Jun Takayama [États-Unis] ; Yoann Aubin [États-Unis] ; Kiira Ratia [États-Unis] ; Rima Chaudhuri [États-Unis] ; Yahira Baez [États-Unis] ; Katrina Sleeman [États-Unis] ; Melissa Coughlin [États-Unis] ; Daniel B. Nichols [États-Unis] ; Debbie C. Mulhearn [États-Unis] ; Bellur S. Prabhakar [États-Unis] ; Susan C. Baker [États-Unis] ; Michael E. Johnson [États-Unis] ; Andrew D. Mesecar [États-Unis]Structure-Based Design, Synthesis, and Biological Evaluation of a Series of Novel and Reversible Inhibitors for the Severe Acute Respiratory Syndrome-Coronavirus Papain-Like Protease
002081 (2010) Holger Steuber [Allemagne] ; Rolf HilgenfeldRecent advances in targeting viral proteases for the discovery of novel antivirals.
002144 (2010) R. Ramajayam [Taïwan] ; Kian-Pin Tan ; Hun-Ge Liu ; Po-Huang LiangSynthesis, docking studies, and evaluation of pyrimidines as inhibitors of SARS-CoV 3CL protease.
002232 (2010) R. Ramajayam [Taïwan] ; Kian-Pin Tan ; Hun-Ge Liu ; Po-Huang LiangSynthesis and evaluation of pyrazolone compounds as SARS-coronavirus 3C-like protease inhibitors.
002596 (2013) Jon Jacobs [États-Unis] ; Valerie Grum-Tokars ; Ya Zhou ; Mark Turlington ; S Adrian Saldanha ; Peter Chase ; Aimee Eggler ; Eric S. Dawson ; Yahira M. Baez-Santos ; Sakshi Tomar ; Anna M. Mielech ; Susan C. Baker ; Craig W. Lindsley ; Peter Hodder ; Andrew Mesecar ; Shaun R. StaufferDiscovery, synthesis, and structure-based optimization of a series of N-(tert-butyl)-2-(N-arylamido)-2-(pyridin-3-yl) acetamides (ML188) as potent noncovalent small molecule inhibitors of the severe acute respiratory syndrome coronavirus (SARS-CoV) 3CL protease.
002600 (2013) Sho Konno [Japon] ; Pillaiyar Thanigaimalai ; Takehito Yamamoto ; Kiyohiko Nakada ; Rie Kakiuchi ; Kentaro Takayama ; Yuri Yamazaki ; Fumika Yakushiji ; Kenichi Akaji ; Yoshiaki Kiso ; Yuko Kawasaki ; Shen-En Chen ; Ernesto Freire ; Yoshio HayashiDesign and synthesis of new tripeptide-type SARS-CoV 3CL protease inhibitors containing an electrophilic arylketone moiety.

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