(Q27683531)

6

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author name string

Chi-Pang Chuck

1

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Chao Chen

2

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Zhihai Ke

3

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David Chi-Cheong Wan

European Journal of Medicinal Chemistry

4

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publication date

January 2013

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published in

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volume

59

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page(s)

1-6

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cites work

Coronavirus diversity, phylogeny and interspecies jumping

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Unique and conserved features of genome and proteome of SARS-coronavirus, an early split-off from the coronavirus group 2 lineage

13 September 2020

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Detection of four human coronaviruses in respiratory infections in children: a one-year study in Colorado

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Epidemiology and clinical presentations of the four human coronaviruses 229E, HKU1, NL63, and OC43 detected over 3 years using a novel multiplex real-time PCR method.

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Characterization of a novel coronavirus associated with severe acute respiratory syndrome

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The Genome sequence of the SARS-associated coronavirus

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Design of wide-spectrum inhibitors targeting coronavirus main proteases

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Synthesis, crystal structure, structure-activity relationships, and antiviral activity of a potent SARS coronavirus 3CL protease inhibitor

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Structure-based design, synthesis, and evaluation of peptide-mimetic SARS 3CL protease inhibitors

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Design and synthesis of peptidomimetic severe acute respiratory syndrome chymotrypsin-like protease inhibitors

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Inhibition of the severe acute respiratory syndrome 3CL protease by peptidomimetic alpha,beta-unsaturated esters

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Design, synthesis, and evaluation of trifluoromethyl ketones as inhibitors of SARS-CoV 3CL protease

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Crystal structures of the main peptidase from the SARS coronavirus inhibited by a substrate-like aza-peptide epoxide.

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Profiling of substrate specificity of SARS-CoV 3CL

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Profiling of substrate specificities of 3C-like proteases from group 1, 2a, 2b, and 3 coronaviruses

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3C-like proteinase from SARS coronavirus catalyzes substrate hydrolysis by a general base mechanism

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Peptide aldehydes and nitriles as transition state analog inhibitors of cysteine proteases

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Odanacatib in the treatment of postmenopausal women with low bone mineral density: Three-year continued therapy and resolution of effect

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1-[[(3-hydroxy-1-adamantyl)amino]acetyl]-2-cyano-(S)-pyrrolidine: a potent, selective, and orally bioavailable dipeptidyl peptidase IV inhibitor with antihyperglycemic properties

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