Shuli Mao, Ph.D.
Affiliations: | Emory University, Atlanta, GA |
Area:
Medicinal, Bioorganic, Synthetic Organic, ComputationalGoogle:
"Shuli Mao"Mean distance: 9.82 | S | N | B | C | P |
Parents
Sign in to add mentorDennis C. Liotta | grad student | 2006 | Emory | |
(Part I: Synthesis and anti-HIV activity of novel cyclobutyl nucleoside and nucleotide analogs. Part II: Synthesis of enantiomerically pure D-FDOC ((+)-2',3'-dideoxy-5-fluoro-oxacytidine).) |
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Publications
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Bluemling GR, Mao S, Natchus MG, et al. (2022) The prophylactic and therapeutic efficacy of the broadly active antiviral ribonucleoside N-Hydroxycytidine (EIDD-1931) in a mouse model of lethal Ebola virus infection. Antiviral Research. 209: 105453 |
Lu G, Bluemling GR, Mao S, et al. (2017) A simple in vitro assay to evaluate the incorporation efficiency of ribonucleotide analog 5' -triphosphates into RNA by human mitochondrial DNA-dependent RNA polymerase. Antimicrobial Agents and Chemotherapy |
Jimenez-Somarribas A, Mao S, Yoon JJ, et al. (2017) Identification of Non-Nucleoside Inhibitors of the Respiratory Syncytial Virus Polymerase Complex. Journal of Medicinal Chemistry |
Hu H, Mao S, Bugrysheva JV, et al. (2014) Group A streptococcus inhibitors by high-throughput virtual screening. European Journal of Medicinal Chemistry. 82: 120-6 |
Li Y, Mao S, Hager MW, et al. (2007) Synthesis and evaluation of 2′-substituted cyclobutyl nucleosides and nucleotides as potential anti-HIV agents Bioorganic and Medicinal Chemistry Letters. 17: 3398-3401 |
Hernandez-Santiago BI, Chen H, Asif G, et al. (2005) Pharmacology and pharmacokinetics of the antiviral agent β-D-2′,3′-dideoxy-3′-oxa-5-fluorocytidine in cells and rhesus monkeys Antimicrobial Agents and Chemotherapy. 49: 2589-2597 |
Mao S, Bouygues M, Welch C, et al. (2004) Synthesis of enantiomerically pure D-FDOC, an anti-HIV agent Bioorganic and Medicinal Chemistry Letters. 14: 4991-4994 |
Painter GR, Almond MR, Mao S, et al. (2004) Biochemical and mechanistic basis for the activity of nucleoside analogue inhibitors of HIV reverse transcriptase Current Topics in Medicinal Chemistry. 4: 1035-1044 |