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Journal of Combinatorial Chemistry|May 13, 2003
The solid-phase synthesis and use of N-monosubstituted piperazines in chemical library synthesisJoseph M Salvino, Baudouin Gerard, Hai Fen Ye, et al.Bioorganic & Medicinal Chemistry|October 23, 2004
Photo-caged agonists of the nuclear receptors RARgamma and TRbeta provide unique time-dependent gene expression profiles for light-activated gene patterningKristian H Link, Federico G Cruz, Hai-Fen Ye, et al.Bioorganic & Medicinal Chemistry Letters|November 22, 2005
Synthesis and structure-activity relationships of a new series of 2alpha-substituted trans-4,5-dimethyl-4-(3-hydroxyphenyl)piperidine as mu-selective opioid antagonistsBertrand Le Bourdonnec, Allan J Goodman, Mathieu Michaut, et al.Journal of Medicinal Chemistry|December 8, 2006
Elucidation of the bioactive conformation of the N-substituted trans-3,4-dimethyl-4-(3-hydroxyphenyl)piperidine class of mu-opioid receptor antagonistsBertrand Le Bourdonnec, Allan J Goodman, Mathieu Michaut, et al.ACS Medicinal Chemistry Letters|January 19, 2023
Discovery of Pyrazolopyridine Derivatives as HPK1 InhibitorsQinda Ye, Kai Liu, Hai-Fen Ye, et al.ACS Medicinal Chemistry Letters|January 19, 2023
Potent and Selective Biaryl Amide Inhibitors of Hematopoietic Progenitor Kinase 1 (HPK1)Alexander Sokolsky, Oleg Vechorkin, Joshua R Hummel, et al.ACS Medicinal Chemistry Letters|March 16, 2023
Discovery of Orally Bioavailable FGFR2/FGFR3 Dual Inhibitors via Structure-Guided Scaffold Repurposing ApproachMinh H Nguyen, Hai-Fen Ye, Yao Xu, et al.ACS Medicinal Chemistry Letters|June 18, 2025
Discovery of INCB126503 as a Potent and Selective FGFR2/3 InhibitorMinh H Nguyen, Anlai Wang, Lisa Truong, et al.Pageof 1