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Methods in Molecular Medicine|March 8, 2011
Synthesis of a versatile peptidomimetic scaffoldS Hanessian, G McNaughton-SmithBioorganic & Medicinal Chemistry Letters|January 5, 1999
Exploration of beta-turn scaffolding motifs as components of sialyl Le(X) mimetics and their relevance to P-selectinS Hanessian, H K Huynh, G V Reddy, et al.Current Pharmaceutical Design|May 16, 2009
Kv7 channels as targets for the treatment of painA D Wickenden, G McNaughton-SmithBioorganic & Medicinal Chemistry Letters|September 7, 1999
Synthesis of a phostone glycomimetic of the endothelin converting enzyme inhibitor phosphoramidonS Hanessian, O RogelBioorganic & Medicinal Chemistry Letters|April 1, 2000
Pyrrolidine as a cogwheel-like scaffold for the deployment of diverse functionality through cycloaddition reactions of metallo-1,3-dipoles in aqueous mediaS Hanessian, M BayrakdarianOrganic Letters|September 15, 2000
Catalytic asymmetric conjugate addition of nitroalkanes to cycloalkenonesS Hanessian, V PhamThe Japanese Journal of Antibiotics|December 1, 1979
Studies directed toward the total synthesis of antibiotics: (+)-spectinomycinS Hanessian, R RoyBioorganic & Medicinal Chemistry Letters|April 1, 2000
Design and synthesis of mimics of S-adenosyl-L-homocysteine as potential inhibitors of erythromycin methyltransferasesS Hanessian, P W SgarbiJournal of Computer-Aided Molecular Design|March 29, 2002
A comparative docking study and the design of potentially selective MMP inhibitorsS Hanessian, N Moitessier, E TherrienJournal of Medicinal Chemistry|September 7, 2001
Design and synthesis of matrix metalloproteinase inhibitors guided by molecular modeling. Picking the S(1) pocket using conformationally constrained inhibitorsS Hanessian, D B MacKay, N MoitessierPageof 3