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Journal of Pharmaceutical Sciences|January 1, 1980
Antiradiation compounds XVII: binding ability of radiation-protective N-heterocyclic aminoethyl disulfides and thiosulfates to DNAW O Foye, M M Karkaria, W H ParsonsBiochemistry International|April 1, 1991
A new class of potent, slowly reversible dehydropeptidase inhibitorsW H Parsons, R Hajdu, W R Schoen, et al.Journal of Medicinal Chemistry|July 30, 1999
32-Indolyl ether derivatives of ascomycin: three-dimensional structures of complexes with FK506-binding proteinJ W Becker, J Rotonda, J G Cryan, et al.Journal of Medicinal Chemistry|August 1, 1989
Cholecystokinin antagonists. Synthesis and biological evaluation of 3-substituted benzolactamsW H Parsons, A A Patchett, M K Holloway, et al.Journal of Medicinal Chemistry|August 1, 1989
(3-Amino-2-oxoalkyl)phosphonic acids and their analogues as novel inhibitors of D-alanine:D-alanine ligaseP K Chakravarty, W J Greenlee, W H Parsons, et al.Biochemical and Biophysical Research Communications|November 30, 1983
Benzolactams. A new class of converting enzyme inhibitorsW H Parsons, J L Davidson, D Taub, et al.Journal of Medicinal Chemistry|September 1, 1991
Design and synthesis of P2-P1'-linked macrocyclic human renin inhibitorsA E Weber, T A Halgren, J J Doyle, et al.Journal of Medicinal Chemistry|September 1, 1988
Phosphinic acid inhibitors of D-alanyl-D-alanine ligaseW H Parsons, A A Patchett, H G Bull, et al.Bioorganic & Medicinal Chemistry Letters|August 18, 1999
C32-O-phenalkyl ether derivatives of the immunosuppressant ascomycin: a tether length studyM T Goulet, P J Sinclair, F Wong, et al.Journal of Medicinal Chemistry|February 4, 1994
Selective protection and relative importance of the carboxylic acid groups of zaragozic acid A for squalene synthase inhibitionT Biftu, J J Acton, G D Berger, et al.Pageof 2