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Current Opinion in Drug Discovery & Development|December 1, 2001
Combinatorial synthesis of aminoglycoside librariesS J Sucheck, Y K ShueAntimicrobial Agents and Chemotherapy|March 24, 2010
Effects of inoculum, pH, and cations on the in vitro activity of fidaxomicin (OPT-80, PAR-101) against Clostridium difficileF Babakhani, J Seddon, N Robert, et al.Antimicrobial Agents and Chemotherapy|February 13, 2008
Safety, tolerance, and pharmacokinetic studies of OPT-80 in healthy volunteers following single and multiple oral dosesY K Shue, P S Sears, S Shangle, et al.Anaerobe|September 17, 2009
Typing and susceptibility of bacterial isolates from the fidaxomicin (OPT-80) phase II study for C. difficile infectionD M Citron, F Babakhani, E J C Goldstein, et al.Journal of Medicinal Chemistry|May 1, 1992
Synthesis and in vitro characterization of novel amino terminally modified oxotremorine derivatives for brain muscarinic receptorsD S Garvey, J T Wasicak, J Y Chung, et al.Journal of Medicinal Chemistry|January 21, 1994
Tetrapeptide CCK agonists: structure-activity studies on modifications at the N-terminusR L Elliott, H Kopecka, M J Bennett, et al.Bioorganic & Medicinal Chemistry|September 1, 1993
Double bond isosteres of the peptide bond: synthesis and biological activity of cholecystokinin (CCK) C-terminal hexapeptide analogsY K Shue, M D Tufano, G M Carrera, et al.Journal of Medicinal Chemistry|May 27, 1994
Novel Asp32-replacement tetrapeptide analogues as potent and selective CCK-A agonistsR L Elliott, H Kopecka, M D Tufano, et al.Pageof 1