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刘新泳
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[31] 康东伟. Discovery and Characterization of Fluorine-Substituted Diarylpyrimidine Derivatives as Novel HIV-.... 《Journal of Medicinal Chemistry》, 63, 1298, 2020.
[32] 康东伟. Structure-Based Bioisosterism Yields HIV-1 NNRTIs with Improved Drug-Resistance Profiles and Favo.... 《Journal of Medicinal Chemistry》, 63, 4837, 2020.
[33] 康东伟. In situ click chemistry-based rapid discovery of novel HIV-1 NNRTIs by exploiting the hydrophobic.... EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 193, 2020.
[34] 康东伟. Exploring the hydrophobic channel of NNIBP leads to the discovery of novel piperidine-substituted.... ACTA PHARMACEUTICA SINICA B, 10, 878, 2020.
[35] 杨斐. Chiral Metal Nanoparticle Superlattices Enabled by Porphyrin-Based Supramolecular Structures. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2021.
[36] 康东伟. 2,4,5-Trisubstituted Pyrimidines as Potent HIV-1 NNRTIs: Rational Design, Synthesis, Activity Eva.... 《Journal of Medicinal Chemistry》, 64, 4239, 2021.
[37] 封达. Design, synthesis, and evaluation of "dual-site"-binding diarylpyrimidines targeting both NNIBP a.... EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 211, 2021.
[38] 汪昭. Targeting dual tolerant regions of binding pocket: Discovery of novel morpholine-substituted diar.... EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 206, 2020.
[39] 康东伟. Structure-Activity Relationship Exploration of NNIBP Tolerant Region I Leads to Potent HIV-1 NNRT.... ACS INFECTIOUS DISEASES, 6, 2225, 2020.
[40] 康东伟. Further Exploring Solvent-Exposed Tolerant Regions of Allosteric Binding Pocket for Novel HIV-1 N.... ACS Medicinal Chemistry Letters, 9, 370, 2018.
total557 4/56
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