Hydrogen (chemistry) < Hydrogen Bonding < Hydrogen Bonding (drug effects)

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List of bibliographic references

Number of relevant bibliographic references: 27.
[0-20] [0 - 20][0 - 27][20-26][20-40]

Ident.	Authors (with country if any)	Title
000262 (2003)	Kuo-Chen Chou [États-Unis] ; Dong-Qing Wei ; Wei-Zhu Zhong	Binding mechanism of coronavirus main proteinase with ligands and its implication to drug design against SARS.
000483 (2003)	Xiang Xu [République populaire de Chine] ; Yunqing Liu ; Susan Weiss ; Eddy Arnold ; Stefan G. Sarafianos ; Jianping Ding	Molecular model of SARS coronavirus polymerase: implications for biochemical functions and drug design.
000608 (2004)	Geoff Sutton [Royaume-Uni] ; Elizabeth Fry ; Lester Carter ; Sarah Sainsbury ; Tom Walter ; Joanne Nettleship ; Nick Berrow ; Ray Owens ; Robert Gilbert ; Andrew Davidson ; Stuart Siddell ; Leo L M. Poon ; Jonathan Diprose ; David Alderton ; Martin Walsh ; Jonathan M. Grimes ; David I. Stuart	The nsp9 replicase protein of SARS-coronavirus, structure and functional insights.
000B51 (2004)	Qi-Shi Du [République populaire de Chine] ; Shu-Qing Wang ; Yu Zhu ; Dong-Qing Wei ; Hong Guo ; Suzanne Sirois ; Kuo-Chen Chou	Polyprotein cleavage mechanism of SARS CoV Mpro and chemical modification of the octapeptide.
000C21 (2004)	Chi-Yuan Chou [Taïwan] ; Hui-Chuan Chang ; Wen-Chi Hsu ; Tien-Zheng Lin ; Chao-Hsiung Lin ; Gu-Gang Chang	Quaternary structure of the severe acute respiratory syndrome (SARS) coronavirus main protease.
001194 (2005)	Chung-Ke Chang [République populaire de Chine] ; Shih-Che Sue ; Tsan-Hung Yu ; Chiu-Min Hsieh ; Cheng-Kun Tsai ; Yen-Chieh Chiang ; Shin-Jye Lee ; Hsin-Hao Hsiao ; Wen-Jin Wu ; Chi-Fon Chang ; Tai-Huang Huang	The dimer interface of the SARS coronavirus nucleocapsid protein adapts a porcine respiratory and reproductive syndrome virus-like structure.
001433 (2006)	Hao Chen [République populaire de Chine] ; Ping Wei ; Changkang Huang ; Lei Tan ; Ying Liu ; Luhua Lai	Only one protomer is active in the dimer of SARS 3C-like proteinase.
001507 (2006)	D-Q Wei [République populaire de Chine] ; R. Zhang ; Q-S Du ; W-N Gao ; Y. Li ; H. Gao ; S-Q Wang ; X. Zhang ; A-X Li ; S. Sirois ; K-C Chou	Anti-SARS drug screening by molecular docking.
001599 (2006)	Syaulan Yang [République populaire de Chine] ; Shu-Jen Chen ; Min-Feng Hsu ; Jen-Dar Wu ; Chien-Te K. Tseng ; Yu-Fan Liu ; Hua-Chien Chen ; Chun-Wei Kuo ; Chi-Shen Wu ; Li-Wen Chang ; Wen-Chang Chen ; Shao-Ying Liao ; Teng-Yuan Chang ; Hsin-Hui Hung ; Hui-Lin Shr ; Cheng-Yuan Liu ; Yu-An Huang ; Ling-Yin Chang ; Jen-Chi Hsu ; Clarence J. Peters ; Andrew H-J Wang ; Ming-Chu Hsu	Synthesis, crystal structure, structure-activity relationships, and antiviral activity of a potent SARS coronavirus 3CL protease inhibitor.
001757 (2007)	Kewen Zheng [République populaire de Chine] ; Guozheng Ma ; Jinming Zhou ; Min Zen ; Wenna Zhao ; Yongjun Jiang ; Qingsen Yu ; Jialiang Feng	Insight into the activity of SARS main protease: Molecular dynamics study of dimeric and monomeric form of enzyme.
001A09 (2007)	Jiang Yin [Canada] ; Chunying Niu [Canada] ; Maia M. Cherney [Canada] ; Jianmin Zhang [Canada] ; Carly Huitema [Canada] ; Lindsay D. Eltis [Canada] ; John C. Vederas [Canada] ; Michael N. G. James [Canada]	A Mechanistic View of Enzyme Inhibition and Peptide Hydrolysis in the Active Site of the SARS-CoV 3C-like Peptidase
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 Wong	Structure-based design and synthesis of highly potent SARS-CoV 3CL protease inhibitors.
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
001C75 (2008)	Gustav R Der [Danemark] ; Ole Kristensen ; Jette S. Kastrup ; S Ren Buus ; Michael Gajhede	Structure of a SARS coronavirus-derived peptide bound to the human major histocompatibility complex class I molecule HLA-B*1501.
001C84 (2008)	Alex G. Taranto [Brésil] ; Paulo Carvalho ; Mitchell A. Avery	QM/QM studies for Michael reaction in coronavirus main protease (3CL Pro).
001D18 (2008)	Veena Nukoolkarn [Thaïlande] ; Vannajan Sanghiran Lee ; Maturos Malaisree ; Ornjira Aruksakulwong ; Supot Hannongbua	Molecular dynamic simulations analysis of ritonavir and lopinavir as SARS-CoV 3CL(pro) inhibitors.
001E45 (2009)	Krongsakda Phakthanakanok [Thaïlande] ; Khanok Ratanakhanokchai ; Khin Lay Kyu ; Pornthep Sompornpisut ; Aaron Watts ; Surapong Pinitglang	A computational analysis of SARS cysteine proteinase-octapeptide substrate interaction: implication for structure and active site binding mechanism.
002059 (2010)	Yantao Chen [République populaire de Chine] ; Mingliang Wang ; Qianling Zhang ; Jianhong Liu	Construction of an implicit membrane environment for the lattice Monte Carlo simulation of transmembrane protein.
002213 (2010)	Jun Liu ; Peng Wu ; Feng Gao ; Jianxun Qi ; Ai Kawana-Tachikawa ; Jing Xie ; Christopher J. Vavricka ; Aikichi Iwamoto ; Taisheng Li ; George F. Gao	Novel Immunodominant Peptide Presentation Strategy: a Featured HLA-A*2402-Restricted Cytotoxic T-Lymphocyte Epitope Stabilized by Intrachain Hydrogen Bonds from Severe Acute Respiratory Syndrome Coronavirus Nucleocapsid Protein▿ †
002264 (2010)	Zai Wang ; Jian-Dong Huang ; Kin-Ling Wong ; Pei-Gang Wang ; Hao-Jie Zhang ; Julian A. Tanner ; Ottavia Spiga ; Andrea Bernini ; Bo-Jian Zheng ; Neri Niccolai	On the mechanisms of bananin activity against severe acute respiratory syndrome coronavirus
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 Hayashi	Design and synthesis of new tripeptide-type SARS-CoV 3CL protease inhibitors containing an electrophilic arylketone moiety.

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