Effect of hydroxyl group configuration in hydroxyethylamine dipeptide isosteres on HIV protease inhibition. Evidence for multiple binding modes

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Veröffentlicht in:	Journal of medicinal chemistry 1991-03, Vol.34 (3), p.1222-1225
Hauptverfasser:	Rich, Daniel H, Sun, Chong Qing, Prasad, J. V. N. Vara, Pathiasseril, Ahammadunny, Toth, Mihaly V, Marshall, Garland R, Clare, Michael, Mueller, Richard A, Houseman, Kathryn
Format:	Artikel
Sprache:	eng
Schlagworte:	AIDS/HIV Amino Acid Sequence aspartic proteinase Chemical Phenomena Chemistry Dipeptides - chemistry Dipeptides - metabolism Ethanolamines - chemistry Ethanolamines - metabolism Exact sciences and technology HIV Protease - metabolism HIV Protease Inhibitors Hydrogen Bonding hydroxyethylamine dipeptide Molecular Conformation Molecular Sequence Data Molecular Structure Organic chemistry Peptides Preparations and properties Stereoisomerism Structure-Activity Relationship
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