Luqing Shang - Publications

Affiliations: 
2018 Georgia State University, Atlanta, GA, United States 

29 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2019 Ma Y, Li L, He S, Shang C, Sun Y, Liu N, Meek TD, Wang Y, Shang L. Application of Dually Activated Michael Acceptor to the Rational Design of Reversible Covalent Inhibitor for Enterovirus 71 3C Protease. Journal of Medicinal Chemistry. PMID 31184893 DOI: 10.1021/acs.jmedchem.9b00387  0.56
2018 Qiao D, Shen T, Zhu M, Liang X, Zhang L, Yin Z, Wang B, Shang L. A highly selective and sensitive fluorescent probe for simultaneously distinguishing and sequentially detecting HS and various thiol species in solution and in live cells. Chemical Communications (Cambridge, England). PMID 30411108 DOI: 10.1039/c8cc07761d  0.64
2018 Ma Y, Shang C, Yang P, Li L, Zhai Y, Yin Z, Wang B, Shang L. 4-Iminooxazolidin-2-one as a bioisostere of the cyanohydrin moiety: inhibitors of enterovirus 71 3C protease. Journal of Medicinal Chemistry. PMID 30365311 DOI: 10.1021/acs.jmedchem.8b01335  0.64
2018 Nie Q, Xu X, Zhang Q, Ma Y, Yin Z, Shang L. 3D-quantitative structure-activity relationship study for the design of novel enterovirus A71 3C protease inhibitors. Chemical Biology & Drug Design. PMID 29877617 DOI: 10.1111/cbdd.13344  0.64
2018 Fu S, Nie Q, Ma Y, Song P, Ren X, Luo C, Shang L, Yin Z. Target-guided screening of fragments (TGSOF) in the discovery of inhibitors against EV-A71 3C protease. Chemical Communications (Cambridge, England). PMID 29497732 DOI: 10.1039/c8cc00469b  0.64
2017 Liang X, Xu X, Qiao D, Yin Z, Shang L. The dual mechanism ICT-FRET-based fluorescent probe for the selective detection of hydrogen peroxide. Chemistry, An Asian Journal. PMID 29063729 DOI: 10.1002/asia.201701382  0.64
2017 Wang Y, Cao L, Zhai Y, Yin Z, Sun Y, Shang L. Structure of EV71 3C(pro) in complex with NK-1.8k: Indications for the development of anti-enterovirus protease inhibitor. Antimicrobial Agents and Chemotherapy. PMID 28461310 DOI: 10.1128/AAC.00298-17  0.64
2017 Wang Y, Cao L, Zhai Y, Ma J, Nie Q, Li T, Yin Z, Sun Y, Shang L. Inhibition of enterovirus 71 replication by an α-hydroxy-nitrile derivative NK-1.9k. Antiviral Research. PMID 28063993 DOI: 10.1016/j.antiviral.2017.01.002  0.64
2016 Zeng D, Zhang R, Nie Q, Cao L, Shang L, Yin Z. Discovery of 2'-α-C-Methyl-2'-β-C-fluorouridine Phosphoramidate Prodrugs as Inhibitors of Hepatitis C Virus. Acs Medicinal Chemistry Letters. 7: 1197-1201. PMID 27994763 DOI: 10.1021/acsmedchemlett.6b00270  0.64
2016 Zhai Y, Ma Y, Ma F, Nie Q, Ren X, Wang Y, Shang L, Yin Z. Structure-activity relationship study of peptidomimetic aldehydes as enterovirus 71 3C protease inhibitors. European Journal of Medicinal Chemistry. 124: 559-573. PMID 27614190 DOI: 10.1016/j.ejmech.2016.08.064  0.64
2016 Han Z, Liang X, Wang Y, Qing J, Cao L, Shang L, Yin Z. The discovery of indole derivatives as novel hepatitis C virus inhibitors. European Journal of Medicinal Chemistry. 116: 147-155. PMID 27061978 DOI: 10.1016/j.ejmech.2016.03.062  0.64
2016 Zeng D, Ma Y, Zhang R, Nie Q, Cui Z, Wang Y, Shang L, Yin Z. Synthesis and structure-activity relationship of α-keto amides as enterovirus 71 3C protease inhibitors. Bioorganic & Medicinal Chemistry Letters. PMID 26916437 DOI: 10.1016/j.bmcl.2016.02.039  0.64
2016 Han Z, Liang X, Ren X, Shang L, Yin Z. A novel 3, 7-dihydroxyphenoxazine-based fluorescent probe for selective detection of intracellular hydrogen peroxide. Chemistry, An Asian Journal. PMID 26807851 DOI: 10.1002/asia.201501304  0.64
2015 Guo Y, Wang Y, Cao L, Wang P, Qing J, Zheng Q, Shang L, Yin Z, Sun Y. A conserved inhibitory mechanism of a lycorine derivative against enterovirus and hepatitis C virus. Antimicrobial Agents and Chemotherapy. PMID 26596952 DOI: 10.1128/AAC.02274-15  0.52
2015 Zhai Y, Zhao X, Cui Z, Wang M, Wang Y, Li L, Sun Q, Yang X, Zeng D, Liu Y, Sun Y, Lou Z, Shang L, Yin Z. Cyanohydrin as an Anchoring Group for Potent and Selective Inhibitors of Enterovirus 71 3C Protease. Journal of Medicinal Chemistry. PMID 26571192 DOI: 10.1021/acs.jmedchem.5b01013  0.64
2015 Wang P, Zhang S, Meng Q, Liu Y, Shang L, Yin Z. Site-specific chemical modification of peptide and protein by thiazolidinediones. Organic Letters. 17: 1361-4. PMID 25738512 DOI: 10.1021/acs.orglett.5b00005  0.64
2015 Shang L, Zhang S, Yang X, Sun J, Li L, Cui Z, He Q, Guo Y, Sun Y, Yin Z. Biochemical characterization of recombinant Enterovirus 71 3C protease with fluorogenic model peptide substrates and development of a biochemical assay. Antimicrobial Agents and Chemotherapy. 59: 1827-36. PMID 25421478 DOI: 10.1128/AAC.04698-14  0.64
2014 Li L, Basavannacharya C, Chan KW, Shang L, Vasudevan SG, Yin Z. Structure-guided Discovery of a Novel Non-peptide Inhibitor of Dengue Virus NS2B-NS3 Protease. Chemical Biology & Drug Design. PMID 25533891 DOI: 10.1111/cbdd.12500  0.52
2014 Shang L, Wang Y, Qing J, Shu B, Cao L, Lou Z, Gong P, Sun Y, Yin Z. An adenosine nucleoside analogue NITD008 inhibits EV71 proliferation. Antiviral Research. 112: 47-58. PMID 25446894 DOI: 10.1016/j.antiviral.2014.10.009  0.64
2014 Shang L, Lin K, Yin Z. Resistance mutations against HCV protease inhibitors and antiviral drug design. Current Pharmaceutical Design. 20: 694-703. PMID 23688081  0.64
2013 Shang L, Xu M, Yin Z. Antiviral drug discovery for the treatment of enterovirus 71 infections. Antiviral Research. 97: 183-94. PMID 23261847 DOI: 10.1016/j.antiviral.2012.12.005  0.64
2011 Schüller A, Yin Z, Brian Chia CS, Doan DN, Kim HK, Shang L, Loh TP, Hill J, Vasudevan SG. Tripeptide inhibitors of dengue and West Nile virus NS2B-NS3 protease. Antiviral Research. 92: 96-101. PMID 21763725 DOI: 10.1016/j.antiviral.2011.07.002  0.64
2010 Wang Q, Xu F, Mou J, Zhang J, Shang L, Luan Y, Yuan Y, Liu Y, Li M, Fang H, Wang B, Xu W. Design, synthesis and preliminary activity evaluation of novel L-lysine derivatives as aminopeptidase N/CD13 inhibitors. Protein and Peptide Letters. 17: 847-53. PMID 20156182 DOI: 10.2174/092986610791306661  0.64
2010 Mou J, Fang H, Liu Y, Shang L, Wang Q, Zhang L, Xu W. Design, synthesis and primary activity assay of bi- or tri-peptide analogues with the scaffold l-arginine as amino-peptidase N/CD13 inhibitors. Bioorganic & Medicinal Chemistry. 18: 887-95. PMID 19969464 DOI: 10.1016/j.bmc.2009.11.036  0.72
2009 Liu Y, Shang L, Fang H, Zhu H, Mu J, Wang Q, Wang X, Yuan Y, Xu W. Design, synthesis, and preliminary studies of the activity of novel derivatives of N-cinnamoyl-L-aspartic acid as inhibitors of aminopeptidase N/CD13. Bioorganic & Medicinal Chemistry. 17: 7398-404. PMID 19782572 DOI: 10.1016/j.bmc.2009.07.014  0.72
2009 Mou J, Fang H, Jing F, Wang Q, Liu Y, Zhu H, Shang L, Wang X, Xu W. Design, synthesis and primary activity evaluation of L-arginine derivatives as amino-peptidase N/CD13 inhibitors. Bioorganic & Medicinal Chemistry. 17: 4666-73. PMID 19454370 DOI: 10.1016/j.bmc.2009.04.056  0.72
2009 Shang L, Fang H, Zhu H, Wang X, Wang Q, Mu J, Wang B, Kishioka S, Xu W. Design, synthesis and SAR studies of tripeptide analogs with the scaffold 3-phenylpropane-1,2-diamine as aminopeptidase N/CD13 inhibitors. Bioorganic & Medicinal Chemistry. 17: 2775-84. PMID 19299146 DOI: 10.1016/j.bmc.2009.02.034  0.72
2008 Shang L, Wang Q, Fang H, Mu J, Wang X, Yuan Y, Wang B, Xu W. Novel 3-phenylpropane-1,2-diamine derivates as inhibitors of aminopeptidase N (APN). Bioorganic & Medicinal Chemistry. 16: 9984-90. PMID 18996018 DOI: 10.1016/j.bmc.2008.10.025  0.72
2008 Shang L, Maeda T, Xu W, Kishioka S. Evaluation of a novel aminopeptidase N inhibitor, in vitro, using two assay systems. Journal of Enzyme Inhibition and Medicinal Chemistry. 23: 198-205. PMID 18343904 DOI: 10.1080/14756360701515541  0.72
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