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Bioorganic & Medicinal Chemistry Letters|January 20, 2024
Discovery of novel oridonin sulfamide derivatives as potent NLRP3 inhibitors by a visible-light photocatalysis-enabled peripheral editingMochenxuan Li, Chuanhao Wang, Shuang Ye, et al.European Journal of Medicinal Chemistry|March 14, 2007
3D-QSAR and molecular docking studies on benzothiazole derivatives as Candida albicans N-myristoyltransferase inhibitorsChunquan Sheng, Jie Zhu, Wannian Zhang, et al.Oncotarget|October 29, 2014
A novel drug discovery strategy: mechanistic investigation of an enantiomeric antitumor agent targeting dual p53 and NF-κB pathwaysChunlin Zhuang, Chunquan Sheng, Woo Shik Shin, et al.European Journal of Medicinal Chemistry|October 15, 2011
Synthesis and biological evaluation of thio-benzodiazepines as novel small molecule inhibitors of the p53-MDM2 protein-protein interactionChunlin Zhuang, Zhenyuan Miao, Lingjian Zhu, et al.European Journal of Medicinal Chemistry|April 6, 2011
Synthesis and biological evaluation of novel 7-acyl homocamptothecins as Topoisomerase I inhibitorsWenfeng Liu, Lingjian Zhu, Wei Guo, et al.European Journal of Medicinal Chemistry|June 18, 2014
Design, synthesis and antifungal activity of novel triazole derivatives containing substituted 1,2,3-triazole-piperdine side chainsZhigan Jiang, Julin Gu, Chen Wang, et al.Chemical Biology & Drug Design|April 11, 2016
Discovery of 7-Methyl-10-Hydroxyhomocamptothecins with 1,2,3-Triazole Moiety as Potent Topoisomerase I InhibitorsXiguo Xu, Yuelin Wu, Wenfeng Liu, et al.Journal of Medicinal Chemistry|April 14, 2006
Structure-based optimization of azole antifungal agents by CoMFA, CoMSIA, and molecular dockingChunquan Sheng, Wannian Zhang, Haitao Ji, et al.Chemistry & Biodiversity|April 21, 2026
Synthesis and In Vitro Antibacterial Activities of Novel Cyclopeptide Macolacin DerivativesZheng Yao, Anhua Huang, Keli Yang, et al.Archiv Der Pharmazie|September 30, 2011
Synthesis and biological evaluation of novel homocamptothecins conjugating with dihydropyrimidine derivatives as potent topoisomerase I inhibitorsLingjian Zhu, Pengfei Cheng, Ning Lei, et al.Pageof 10