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Bioorganic & Medicinal Chemistry Letters|April 6, 2010
Structure-based rational design, synthesis and antifungal activity of oxime-containing azole derivativesYulan Xu, Chunquan Sheng, Wenya Wang, et al.
European Journal of Medicinal Chemistry|October 23, 2012
Synthesis and preliminary bioevaluation of novel E-ring modified acetal analog of camptothecin as cytotoxic agentsLingjian Zhu, Chunlin Zhuang, Ning Lei, et al.
Journal of Molecular Modeling|July 14, 2009
Evolutionary trace analysis of CYP51 family: implication for site-directed mutagenesis and novel antifungal drug designChunquan Sheng, Shuanghong Chen, Haitao Ji, et al.
Chemistry & Biodiversity|October 17, 2013
Synthesis and biological assays of 9-(acylamino) homocamptothecins as DNA topoisomerase I inhibitorsWei Guo, Guoqiang Dong, Lingjian Zhu, et al.
Free Radical Biology & Medicine|February 12, 2018
Fragment-growing guided design of Keap1-Nrf2 protein-protein interaction inhibitors for targeting myocarditisNing Meng, Hua Tang, Hao Zhang, et al.
Chemical Communications (Cambridge, England)|August 21, 2015
The discovery of novel antifungal scaffolds by structural simplification of the natural product sampangineZhigan Jiang, Na Liu, Dandan Hu, et al.
European Journal of Medicinal Chemistry|July 10, 2010
Design, synthesis and antifungal activity of isosteric analogues of benzoheterocyclic N-myristoyltransferase inhibitorsChunquan Sheng, Hui Xu, Wenya Wang, et al.
Organic & Biomolecular Chemistry|April 5, 2016
Enantioselective organocatalytic Michael addition of isorhodanines to α,β-unsaturated aldehydesShanchao Wu, Yu Li, Yongqiang Zhang, et al.
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