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European Journal of Medicinal Chemistry|June 18, 2015
Identification of a potent 5-phenyl-thiazol-2-ylamine-based inhibitor of FLT3 with activity against drug resistance-conferring point mutationsChiung-Tong Chen, John T-A Hsu, Wen-Hsing Lin, et al.Journal of Medicinal Chemistry|March 24, 2009
Design and structural analysis of novel pharmacophores for potent and selective peroxisome proliferator-activated receptor gamma agonistsChia-Hui Lin, Yi-Hui Peng, Mohane Selvaraj Coumar, et al.Bioorganic & Medicinal Chemistry|June 29, 2011
Discovery and evaluation of 3-phenyl-1H-5-pyrazolylamine-based derivatives as potent, selective and efficacious inhibitors of FMS-like tyrosine kinase-3 (FLT3)Wen-Hsing Lin, Shu-Yi Hsieh, Shih-Chieh Yen, et al.Bioorganic & Medicinal Chemistry|April 27, 2013
Discovery of 3-phenyl-1H-5-pyrazolylamine derivatives containing a urea pharmacophore as potent and efficacious inhibitors of FMS-like tyrosine kinase-3 (FLT3)Wen-Hsing Lin, John T-A Hsu, Shu-Yi Hsieh, et al.Journal of Medicinal Chemistry|July 2, 2013
Optimization of ligand and lipophilic efficiency to identify an in vivo active furano-pyrimidine Aurora kinase inhibitorHui-Yi Shiao, Mohane Selvaraj Coumar, Chun-Wei Chang, et al.Journal of Medicinal Chemistry|September 9, 2015
Identification of Substituted Naphthotriazolediones as Novel Tryptophan 2,3-Dioxygenase (TDO) Inhibitors through Structure-Based Virtual ScreeningJian-Sung Wu, Shu-Yu Lin, Fang-Yu Liao, et al.Proceedings of the National Academy of Sciences of the United States of America|April 24, 2013
Aurora kinase inhibitors reveal mechanisms of HURP in nucleation of centrosomal and kinetochore microtubulesJiun-Ming Wu, Chiung-Tong Chen, Mohane Selvaraj Coumar, et al.Journal of Medicinal Chemistry|June 17, 2010
Fast-forwarding hit to lead: aurora and epidermal growth factor receptor kinase inhibitor lead identificationMohane Selvaraj Coumar, Chang-Ying Chu, Cheng-Wei Lin, et al.Journal of Medicinal Chemistry|October 22, 2010
Design and synthesis of tetrahydropyridothieno[2,3-d]pyrimidine scaffold based epidermal growth factor receptor (EGFR) kinase inhibitors: the role of side chain chirality and Michael acceptor group for maximal potencyChia-Hsien Wu, Mohane Selvaraj Coumar, Chang-Ying Chu, et al.Oncotarget|November 19, 2016
Discovery of BPR1K871, a quinazoline based, multi-kinase inhibitor for the treatment of AML and solid tumors: Rational design, synthesis, in vitro and in vivo evaluationYung Chang Hsu, Mohane Selvaraj Coumar, Wen-Chieh Wang, et al.Pageof 8