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European Journal of Medicinal Chemistry|June 27, 2025
Molecular hybridization-driven FAK inhibitors: N-2,4-diarylaminopyrimidine-3-sulfamoyl-benzamide derivatives with improved antitumor potencyLidong Gong, Zichao Liang, Xianling Ning, et al.
Bioorganic & Medicinal Chemistry|June 22, 2017
Synthesis and biological activity of peptide proline-boronic acids as proteasome inhibitorsLiqiang Han, Yanzhao Wen, Ridong Li, et al.
European Journal of Medicinal Chemistry|April 9, 2019
Discovery and optimization of thienopyridine derivatives as novel urea transporter inhibitorsYan Zhao, Min Li, Bowen Li, et al.
Bioorganic & Medicinal Chemistry Letters|June 11, 2018
Synthesis and biological evaluation of curcumin derivatives modified with α-amino boronic acid as proteasome inhibitorsWenjie Zhang, Heyuan Bai, Liqiang Han, et al.
The Journal of Organic Chemistry|January 5, 2019
Transition Metal-Free Intermolecular C(sp<sup>2</sup>)-H Direct Amination of Furanones via a Redox PathwayQiang Wei, Junfeng Wang, Eman A Akam, et al.
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