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Journal of Medicinal Chemistry|March 21, 2013
De novo fragment design: a medicinal chemistry approach to fragment-based lead generationFrancisco X Talamas, Gloria Ao-Ieong, Ken A Brameld, et al.
Journal of Medicinal Chemistry|September 28, 2013
Discovery of a novel series of potent non-nucleoside inhibitors of hepatitis C virus NS5BRyan C Schoenfeld, David L Bourdet, Ken A Brameld, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 12, 2025
Impairment of DET1 causes neurological defects and lethality in mice and humansOzge Karayel, Allison Soung, Hem Gurung, et al.
Journal of Medicinal Chemistry|March 29, 2014
Discovery of selective 4-Amino-pyridopyrimidine inhibitors of MAP4K4 using fragment-based lead identification and optimizationTerry D Crawford, Chudi O Ndubaku, Huifen Chen, et al.
ACS Medicinal Chemistry Letters|August 20, 2015
Structure-Based Design of GNE-495, a Potent and Selective MAP4K4 Inhibitor with Efficacy in Retinal AngiogenesisChudi O Ndubaku, Terry D Crawford, Huifen Chen, et al.
Bioorganic & Medicinal Chemistry Letters|July 18, 2008
Discovery and optimization of pyridazinone non-nucleoside inhibitors of HIV-1 reverse transcriptaseZachary K Sweeney, James P Dunn, Yu Li, et al.
ACS Medicinal Chemistry Letters|April 16, 2020
Implementation of the CYP Index for the Design of Selective Tryptophan-2,3-dioxygenase InhibitorsBrendan T Parr, Richard Pastor, Benjamin D Sellers, et al.
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