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Bioorganic & Medicinal Chemistry Letters|March 10, 2004
Highly potent and long-acting trimeric and tetrameric inhibitors of influenza virus neuraminidaseKeith G Watson, Rachel Cameron, Rob J Fenton, et al.Journal of Medicinal Chemistry|October 17, 2024
Core Modifications of GSK3335103 toward Orally Bioavailable αvβ6 Inhibitors with Improved Synthetic TractabilityHeather F Hryczanek, John Barrett, Tim N Barrett, et al.Journal of Medicinal Chemistry|December 17, 2016
Structure-Activity Relationships of Small Molecule Autotaxin Inhibitors with a Discrete Binding ModeLisa M Miller, Willem-Jan Keune, Diana Castagna, et al.Journal of Medicinal Chemistry|September 10, 2019
Discovery of an Orally Bioavailable Pan αv Integrin Inhibitor for Idiopathic Pulmonary FibrosisNiall A Anderson, Sebastien Campos, Sharon Butler, et al.Journal of Medicinal Chemistry|July 8, 2005
Design and synthesis of new nonsteroidal glucocorticoid modulators through application of an "agreement docking" methodMike Barker, Margaret Clackers, Derek A Demaine, et al.ACS Medicinal Chemistry Letters|June 6, 2014
Cyclopropyl Carboxamides: A New Oral Antimalarial Series Derived from the Tres Cantos Anti-Malarial Set (TCAMS)Lourdes Rueda, Isabel Castellote, Julia Castro-Pichel, et al.Bioorganic & Medicinal Chemistry Letters|July 10, 2007
Non-steroidal glucocorticoid agonists: the discovery of aryl pyrazoles as A-ring mimeticsMargaret Clackers, Diane M Coe, Derek A Demaine, et al.Proceedings of the National Academy of Sciences of the United States of America|October 14, 2009
Design and x-ray crystal structures of high-potency nonsteroidal glucocorticoid agonists exploiting a novel binding site on the receptorKeith Biggadike, Randy K Bledsoe, Diane M Coe, et al.Journal of Medicinal Chemistry|September 13, 2024
Discovery and Development of Highly Potent and Orally Bioavailable Nonpeptidic αvβ6 Integrin InhibitorsPanayiotis A Procopiou, John Barrett, Matthew H J Crawford, et al.Bioorganic & Medicinal Chemistry Letters|January 25, 2011
Discovery of a potent series of non-steroidal non α-trifluoromethyl carbinol glucocorticoid receptor agonists with reduced lipophilicityHawa Diallo, Davina C Angell, Heather A Barnett, et al.Pageof 19