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Anticancer Research|January 4, 2012
A high-throughput cell-based screening for L858R/T790M mutant epidermal growth factor receptor inhibitorsWen-Hsing Lin, Jen-Shin Song, Tzu-Wen Lien, et al.Plos One|January 14, 2014
Evaluation of the antitumor effects of BPR1J-340, a potent and selective FLT3 inhibitor, alone or in combination with an HDAC inhibitor, vorinostat, in AML cancerWen-Hsing Lin, Teng-Kuang Yeh, Weir-Torn Jiaang, et al.Bioorganic & Medicinal Chemistry Letters|June 26, 2012
3-Phenyl-1H-5-pyrazolylamine-based derivatives as potent and efficacious inhibitors of FMS-like tyrosine kinase-3 (FLT3)John T-A Hsu, Teng-Kuang Yeh, Shih-Chieh Yen, et al.Chemmedchem|December 30, 2009
Identification, SAR studies, and X-ray co-crystallographic analysis of a novel furanopyrimidine aurora kinase A inhibitorMohane Selvaraj Coumar, Ming-Tsung Tsai, Chang-Ying Chu, et al.Chemmedchem|July 24, 2012
Anti-influenza drug discovery: identification of an orally bioavailable quinoline derivative through activity- and property-guided lead optimizationJiann-Yih Yeh, Mohane Selvaraj Coumar, Hui-Yi Shiao, et al.Journal of Medicinal Chemistry|January 23, 2010
Anti-influenza drug discovery: structure-activity relationship and mechanistic insight into novel angelicin derivativesJiann-Yih Yeh, Mohane Selvaraj Coumar, Jim-Tong Horng, et al.Journal of Medicinal Chemistry|February 3, 2006
Indol-1-yl acetic acids as peroxisome proliferator-activated receptor agonists: design, synthesis, structural biology, and molecular docking studiesNeeraj Mahindroo, Chiung-Chiu Wang, Chun-Chen Liao, et al.Analytical Biochemistry|March 25, 2008
A cell-based high-throughput screen for epidermal growth factor receptor pathway inhibitorsWen-Hsing Lin, Jen-Shin Song, Teng-Yuan Chang, et al.Journal of Medicinal Chemistry|April 28, 2006
Structure-based drug design of a novel family of PPARgamma partial agonists: virtual screening, X-ray crystallography, and in vitro/in vivo biological activitiesI-Lin Lu, Chien-Fu Huang, Yi-Hui Peng, et al.Bioorganic Chemistry|March 16, 2020
Drug-like property optimization: Discovery of orally bioavailable quinazoline-based multi-targeted kinase inhibitorsShu-Yu Lin, Chun-Feng Chang, Mohane Selvaraj Coumar, et al.Pageof 8