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Bioorganic & Medicinal Chemistry|July 17, 2019
Optimization and biological evaluation of nicotinamide derivatives as Aurora kinase inhibitorsBaohui Qi, Xingwei Xu, Ying Yang, et al.
Bioorganic & Medicinal Chemistry|November 12, 2023
Design, synthesis and biological evaluation of EGFR kinase inhibitors that spans the orthosteric and allosteric sitesMengmeng Fan, Liping Hu, Shengmin Shi, et al.
European Journal of Medicinal Chemistry|July 31, 2020
Identification of novel quinoline analogues bearing thiazolidinones as potent kinase inhibitors for the treatment of colorectal cancerYuting Zhou, Xingwei Xu, Fei Wang, et al.
European Journal of Medicinal Chemistry|November 8, 2021
Dual target inhibitors based on EGFR: Promising anticancer agents for the treatment of cancers (2017-)Liping Hu, Mengmeng Fan, Shengmin Shi, et al.
Journal of Enzyme Inhibition and Medicinal Chemistry|August 31, 2022
Discovery of novel conjugates of quinoline and thiazolidinone urea as potential anti-colorectal cancer agentLi Xiong, Huan He, Mengmeng Fan, et al.
Journal of Ethnopharmacology|December 30, 2019
The effect of methanol extract from Saussurea involucrata in the lipopolysaccharide-stimulated inflammation in cultured RAW 264.7 cellsGuowei Gong, Feng Xie, Yuzhong Zheng, et al.
European Journal of Medicinal Chemistry|February 7, 2018
Identification of novel N1-(2-aryl-1, 3-thiazolidin-4-one)-N3-aryl ureas showing potent multi-tyrosine kinase inhibitory activitiesBaohui Qi, Ying Yang, Huan He, et al.
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