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Molecular Chaperones < Molecular Conformation < Molecular Diagnostic Techniques  Facettes :

List of bibliographic references

Number of relevant bibliographic references: 24.
[0-20] [0 - 20][0 - 24][20-23][20-40]
Ident.Authors (with country if any)Title
000A12 (2018) Min-Han Lin [Taïwan] ; David C. Moses [Taïwan] ; Chih-Hua Hsieh [Taïwan] ; Shu-Chun Cheng [Taïwan] ; Yau-Hung Chen [Taïwan] ; Chiao-Yin Sun [Taïwan] ; Chi-Yuan Chou [Taïwan]Disulfiram can inhibit MERS and SARS coronavirus papain-like proteases via different modes.
000B91 (2016) Bo Su [République populaire de Chine] ; Chunlong Cai [République populaire de Chine] ; Meng Deng [République populaire de Chine] ; Qingmin Wang [République populaire de Chine]Spatial Configuration and Three-Dimensional Conformation Directed Design, Synthesis, Antiviral Activity, and Structure-Activity Relationships of Phenanthroindolizidine Analogues.
000D81 (2015) Jun-Li Yang [Corée du Sud] ; Thi-Kim-Quy Ha ; Basanta Dhodary ; Euisun Pyo ; Ngoc Hieu Nguyen ; Hyomoon Cho ; Eunhee Kim ; Won Keun OhOleanane triterpenes from the flowers of Camellia japonica inhibit porcine epidemic diarrhea virus (PEDV) replication.
000E88 (2014) Yahira M. Báez-Santos [États-Unis] ; Scott J. Barraza ; Michael W. Wilson ; Michael P. Agius ; Anna M. Mielech ; Nicole M. Davis ; Susan C. Baker ; Scott D. Larsen ; Andrew D. MesecarX-ray structural and biological evaluation of a series of potent and highly selective inhibitors of human coronavirus papain-like proteases.
001046 (2014) Dustin B. Ritchie [Canada] ; Jingchyuan Soong ; William K A. Sikkema ; Michael T. WoodsideAnti-frameshifting ligand reduces the conformational plasticity of the SARS virus pseudoknot.
001144 (2013) Sivakoteswara Rao Mandadapu [États-Unis] ; Pathum M. Weerawarna ; Allan M. Prior ; Roxanne Adeline Z. Uy ; Sridhar Aravapalli ; Kevin R. Alliston ; Gerald H. Lushington ; Yunjeong Kim ; Duy H. Hua ; Kyeong-Ok Chang ; William C. GroutasMacrocyclic inhibitors of 3C and 3C-like proteases of picornavirus, norovirus, and coronavirus.
001199 (2013) Pillaiyar Thanigaimalai [Japon] ; Sho Konno ; Takehito Yamamoto ; Yuji Koiwai ; Akihiro Taguchi ; Kentaro Takayama ; Fumika Yakushiji ; Kenichi Akaji ; Yoshiaki Kiso ; Yuko Kawasaki ; Shen-En Chen ; Aurash Naser-Tavakolian ; Arne Schön ; Ernesto Freire ; Yoshio HayashiDesign, synthesis, and biological evaluation of novel dipeptide-type SARS-CoV 3CL protease inhibitors: structure-activity relationship study.
001582 (2010) Iou-Jiun Kang [République populaire de Chine] ; Li-Wen Wang ; Teng-Kuang Yeh ; Chung-Chi Lee ; Yen-Chun Lee ; Sheng-Ju Hsu ; Yen-Shian Wu ; Jing-Chyi Wang ; Yu-Sheng Chao ; Andrew Yueh ; Jyh-Haur ChernSynthesis, activity, and pharmacokinetic properties of a series of conformationally-restricted thiourea analogs as novel hepatitis C virus inhibitors.
001845 (2009) Fumiaki N. Ishikawa [États-Unis] ; Hsiao-Kang Chang ; Marco Curreli ; Hsiang-I Liao ; C Anders Olson ; Po-Chiang Chen ; Rui Zhang ; Richard W. Roberts ; Ren Sun ; Richard J. Cote ; Mark E. Thompson ; Chongwu ZhouLabel-free, electrical detection of the SARS virus N-protein with nanowire biosensors utilizing antibody mimics as capture probes.
001B59 (2008) Arun K. Ghosh [États-Unis] ; Gangli Gong ; Valerie Grum-Tokars ; Debbie C. Mulhearn ; Susan C. Baker ; Melissa Coughlin ; Bellur S. Prabhakar ; Katrina Sleeman ; Michael E. Johnson ; Andrew D. MesecarDesign, synthesis and antiviral efficacy of a series of potent chloropyridyl ester-derived SARS-CoV 3CLpro inhibitors.
001C36 (2007) S-Q Wang [République populaire de Chine] ; Q-S Du ; K. Zhao ; A-X Li ; D-Q Wei ; K-C ChouVirtual screening for finding natural inhibitor against cathepsin-L for SARS therapy.
001C75 (2007) Masahiro Ikejiri [Japon] ; Masayuki Saijo ; Shigeru Morikawa ; Shuetsu Fukushi ; Tetsuya Mizutani ; Ichiro Kurane ; Tokumi MaruyamaSynthesis and biological evaluation of nucleoside analogues having 6-chloropurine as anti-SARS-CoV agents.
001C78 (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.
001D50 (2007) Pedro Serrano [États-Unis] ; Margaret A. Johnson ; Marcius S. Almeida ; Reto Horst ; Torsten Herrmann ; Jeremiah S. Joseph ; Benjamin W. Neuman ; Vanitha Subramanian ; Kumar S. Saikatendu ; Michael J. Buchmeier ; Raymond C. Stevens ; Peter Kuhn ; Kurt WüthrichNuclear magnetic resonance structure of the N-terminal domain of nonstructural protein 3 from the severe acute respiratory syndrome coronavirus.
001D73 (2007) Qi-Shi Du [République populaire de Chine] ; Hao Sun ; Kuo-Chen ChouInhibitor design for SARS coronavirus main protease based on "distorted key theory".
001D83 (2007) Dariusz Plewczynski [Pologne] ; Marcin Hoffmann ; Marcin Von Grotthuss ; Krzysztof Ginalski ; Leszek RychewskiIn silico prediction of SARS protease inhibitors by virtual high throughput screening.
001E39 (2007) Jeremiah S. Joseph [États-Unis] ; Kumar Singh Saikatendu ; Vanitha Subramanian ; Benjamin W. Neuman ; Michael J. Buchmeier ; Raymond C. Stevens ; Peter KuhnCrystal structure of a monomeric form of severe acute respiratory syndrome coronavirus endonuclease nsp15 suggests a role for hexamerization as an allosteric switch.
001E44 (2007) Daniel R. Beniac [Canada] ; Shauna L. Devarennes ; Anton Andonov ; Runtao He ; Tim F. BoothConformational reorganization of the SARS coronavirus spike following receptor binding: implications for membrane fusion.
001E91 (2007) Masahiro Ikejiri [Japon] ; Takayuki Ohshima ; Keizo Kato ; Masaaki Toyama ; Takayuki Murata ; Kunitada Shimotohno ; Tokumi Maruyama5'-O-masked 2'-deoxyadenosine analogues as lead compounds for hepatitis C virus (HCV) therapeutic agents.
001F83 (2006) Rolf Hilgenfeld [Allemagne] ; Kanchan Anand ; Jeroen R. Mesters ; Zihe Rao ; Xu Shen ; Hualiang Jiang ; Jinzhi Tan ; Koen H G. VerschuerenStructure and dynamics of SARS coronavirus main proteinase (Mpro).
002222 (2006) Eric Assen B. Kantchev [République populaire de Chine] ; Chung-Chieh Chang ; Ding-Kwo ChangDirect Fmoc/tert-Bu solid phase synthesis of octamannosyl polylysine dendrimer-peptide conjugates.

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