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BJU International|July 31, 2026
Oncologic outcomes of radical radiotherapy in frail patients with upper tract urothelial carcinomaWilly Po-Yuan Chen, Wing-Keen Yap, Hao-Lun Luo, et al.Journal of Medicinal Chemistry|April 30, 2014
Discovery of 4-aryl-N-arylcarbonyl-2-aminothiazoles as Hec1/Nek2 inhibitors. Part I: optimization of in vitro potencies and pharmacokinetic propertiesYing-Shuan E Lee, Shih-Hsien Chuang, Lynn Y L Huang, et al.Journal of Medicinal Chemistry|August 5, 2010
Discovery of pyrrole-indoline-2-ones as Aurora kinase inhibitors with a different inhibition profileChao-Cheng Chiang, Yu-Hsiang Lin, Shu Fu Lin, et al.European Journal of Medicinal Chemistry|November 4, 2010
Synthesis and structure-activity relationship of 3-O-acylated (-)-epigallocatechins as 5α-reductase inhibitorsShu Fu Lin, Yu-Hsiang Lin, Mengju Lin, et al.European Journal of Medicinal Chemistry|March 1, 2020
Discovery of T-1101 tosylate as a first-in-class clinical candidate for Hec1/Nek2 inhibition in cancer therapyShih-Hsien Chuang, Ying-Shuan E Lee, Lynn Y L Huang, et al.Journal of Medicinal Chemistry|January 25, 2021
Copper(I)-Catalyzed Nitrile-Addition/N-Arylation Ring-Closure Cascade: Synthesis of 5,11-Dihydro-6H-indolo[3,2-c]quinolin-6-ones as Potent Topoisomerase-I InhibitorsWen-Yun Hsueh, Ying-Shuan E Lee, Min-Sian Huang, et al.Pageof 14