复旦大学：《药物设计学》课程教学资源（教学研究）基于配体结构的药物设计_Rational design of 2-pyrrolinones as inhibitors of HIV-1 integrase
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复旦大学：《药物设计学》课程教学资源（教学研究）基于配体结构的药物设计_Discovery of flavonoid derivatives as anti-HCV agents via pharmacophore search combining molecular docking strategy
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Antitumor agents 294. Novel E-ring-modified camptothecin–4b-anilino-40- O-demethyl-epipodophyllotoxin conjugates as DNA topoisomerase I inhibitors and cytotoxic agents
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复旦大学：《药物设计学》课程教学资源（教学研究）基于靶点结构的药物设计_Molecular Insights on the Cyclic Peptide Nanotube-Mediated Transportation of Antitumor Drug
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复旦大学：《药物设计学》课程教学资源（教学研究）基于靶点结构的药物设计_Discovery of a Novel 5-HT2A Inhibitor by Pharmacophore-based Virtual Screening
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复旦大学：《药物设计学》课程教学资源（教学研究）基于靶点结构的药物设计_新型多巴胺D3受体抑制剂的发现
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Dopamine D1 Receptor Agonist and D2 Receptor Antagonist Effects of the Natural Product (2)–Stepholidine_Molecular Modeling
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Bis(9)-(−)-nor-meptazinol as a novel dual-binding AChEI potently ameliorates scopolamine-induced cognitive deficits in mice
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Molecular Insights into the D1R Agonist and D2R-D3R Antagonist Effects of the Natural Product (−)-Stepholidine_Molecular Modeling and Dynamics Simulations
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复旦大学：《药物设计学》课程教学资源（教学研究）基于靶点结构的药物设计_Micelle-Based Brain-Targeted Drug Delivery Enabled by a Nicotine Acetylcholine Receptor Ligand
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