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Journal of Medicinal Chemistry|November 1, 1987
Optimization and in vivo evaluations of a series of small, potent, and specific renin inhibitors containing a novel Leu-Val replacementJ F Dellaria, R G Maki, B A Bopp, et al.Science (New York, N.Y.)|August 3, 1990
Design, activity, and 2.8 A crystal structure of a C2 symmetric inhibitor complexed to HIV-1 proteaseJ Erickson, D J Neidhart, J VanDrie, et al.Journal of Medicinal Chemistry|November 1, 1981
N-(Methanesulfonyl)-16-phenoxyprostaglandincarboxamides: tissue-selective, uterine stimulantsT K Schaaf, J S Bindra, J F Eggler, et al.Journal of Medicinal Chemistry|December 1, 1984
[(Aminomethyl)aryloxy]acetic acid esters. A new class of high-ceiling diuretics. 2. Modifications of the oxyacetic side chainJ J Plattner, A K Fung, J R Smital, et al.Journal of Medicinal Chemistry|December 1, 1984
[(Aminomethyl)aryloxy]acetic acid esters. A new class of high-ceiling diuretics. 1. Effects of nitrogen and aromatic nuclear substitutionC M Lee, J J Plattner, C W Ours, et al.Journal of Medicinal Chemistry|December 1, 1988
Renin inhibitors. Dipeptide analogues of angiotensinogen utilizing a structurally modified phenylalanine residue to impart proteolytic stabilityJ J Plattner, P A Marcotte, H D Kleinert, et al.Journal of Medicinal Chemistry|May 15, 1992
Nonpeptide renin inhibitors employing a novel 3-aza(or oxa)-2,4-dialkyl glutaric acid moiety as a P2/P3 amide bond replacementW R Baker, A K Fung, H D Kleinert, et al.Journal of Medicinal Chemistry|January 1, 1985
[(Aminomethyl)arloxy]acetic acid esters. A new class of high-ceiling diuretics. 3. Variation in the bridge between the aromatic rings to complete mapping of the receptorJ J Plattner, Y C Martin, J R Smital, et al.Virology|October 30, 1998
Human serum attenuates the activity of protease inhibitors toward wild-type and mutant human immunodeficiency virusA Molla, S Vasavanonda, G Kumar, et al.Journal of Medicinal Chemistry|May 30, 1998
Anhydrolide macrolides. 2. Synthesis and antibacterial activity of 2,3-anhydro-6-O-methyl 11,12-carbazate erythromycin A analoguesG Griesgraber, M J Kramer, R L Elliott, et al.Pageof 7