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Bioorganic & Medicinal Chemistry|March 6, 2009
Novel trans-2-aryl-cyclopropylamine analogues as potent and selective dipeptidyl peptidase IV inhibitorsTing-Yueh Tsai, Tsu Hsu, Chiung-Tong Chen, et al.
Journal of Medicinal Chemistry|February 7, 2023
Development of Furanopyrimidine-Based Orally Active Third-Generation EGFR Inhibitors for the Treatment of Non-Small Cell Lung CancerMu-Chun Li, Mohane Selvaraj Coumar, Shu-Yu Lin, et al.
Journal of Medicinal Chemistry|July 10, 2009
Synthesis and evaluation of 3-aroylindoles as anticancer agents: metabolite approachYu-Shan Wu, Mohane Selvaraj Coumar, Jang-Yang Chang, et al.
Pharmacogenomics|July 18, 2013
CYP1A2 genetic polymorphisms are associated with early antidepressant escitalopram metabolism and adverse reactionsHsiang-Wei Kuo, Shu Chih Liu, Hsiao-Hui Tsou, et al.
Cell Chemical Biology|July 18, 2024
Discovery of a mu-opioid receptor modulator that in combination with morphinan antagonists induces analgesiaYi-Han Huang, Shu-Yu Lin, Li-Chin Ou, et al.
Cancer Science|November 3, 2010
BPR0C261 is a novel orally active antitumor agent with antimitotic and anti-angiogenic activitiesChih-Bo Hu, Ching-Ping Chen, Teng-Kuang Yeh, et al.
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