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Bioorganic Chemistry|December 13, 2024
Design, synthesis, and biological evaluation of novel 3-naphthylthiophene derivatives as potent SIRT2 inhibitors for the treatment of myocardial fibrosisZhuo Zhang, Chao Ma, Xiong Gao, et al.
European Journal of Medicinal Chemistry|April 10, 2023
Discovery of novel tryptamine derivatives as GluN2B subunit-containing NMDA receptor antagonists via pharmacophore-merging strategy with orally available therapeutic effect of cerebral ischemiaJishun Quan, Huali Yang, Fengyun Qin, et al.
Chemical Biology & Drug Design|March 28, 2009
Chalcone derivatives inhibit glutathione S-transferase P1-1 activity: insights into the interaction mode of alpha, beta-unsaturated carbonyl compoundsJian Wang, Shaojie Wang, Dandan Song, et al.
Molecular Diversity|February 4, 2026
Interpretable machine learning-driven identification of novel DENV NS2B-NS3 protease inhibitors through multi-stage virtual screening and experimental validationShengjie Hu, Yan Xiao, Hailun Jiang, et al.
RSC Medicinal Chemistry|March 31, 2025
Discovery of new imidazole[1,2-a] pyridine derivatives as CDK9 inhibitors: design, synthesis and biological evaluationZihan Sun, Shijun Sun, Xiayu Li, et al.
European Journal of Medicinal Chemistry|July 4, 2026
Discovery of highly selective and potent CYP1B1 inhibitors for overcoming paclitaxel resistance in A549/Taxol cellsTing Wang, Yujiang Fu, Bohou Song, et al.
Chemical & Pharmaceutical Bulletin|October 6, 2005
Compounds structurally related to tamoxifen as openers of large-conductance calcium-activated K+ channelYu Sha, Toshihiko Tashima, Yumi Mochizuki, et al.
Bioorganic & Medicinal Chemistry|March 20, 2016
Discovery of novel N,N-3-phenyl-3-benzylaminopropionanilides as potent inhibitors of cholesteryl ester transfer protein in vivoHonglei Xie, Yiqun Li, Changlin Bai, et al.
European Journal of Medicinal Chemistry|December 29, 2024
Design, synthesis and biological evaluation of galantamine analogues for cognitive improvement in Alzheimer's diseaseMengzhen Li, Chao Ma, Yao Li, et al.
European Journal of Medicinal Chemistry|April 2, 2020
Design, synthesis and biological evaluation of tetrahydroquinoline-based reversible LSD1 inhibitorsXinran Wang, Cai Zhang, Xiangyu Zhang, et al.
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