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Biochemistry|June 1, 2000
Peroxidase activity in prostaglandin endoperoxide H synthase-1 occurs with a neutral histidine proximal heme ligandS A Seibold, J F Cerda, A M Mulichak, et al.The Journal of Biological Chemistry|December 31, 2000
Mutational and X-ray crystallographic analysis of the interaction of dihomo-gamma -linolenic acid with prostaglandin endoperoxide H synthasesE D Thuresson, M G Malkowski, K M Lakkides, et al.The Journal of Biological Chemistry|June 25, 1993
The crystallographic structure of the protease from human immunodeficiency virus type 2 with two synthetic peptidic transition state analog inhibitorsA M Mulichak, J O Hui, A G Tomasselli, et al.The Journal of Biological Chemistry|December 31, 2000
Prostaglandin endoperoxide H synthase-1: the functions of cyclooxygenase active site residues in the binding, positioning, and oxygenation of arachidonic acidE D Thuresson, K M Lakkides, C J Rieke, et al.Journal of Medicinal Chemistry|May 26, 1995
Use of medium-sized cycloalkyl rings to enhance secondary binding: discovery of a new class of human immunodeficiency virus (HIV) protease inhibitorsK R Romines, K D Watenpaugh, P K Tomich, et al.Bioorganic & Medicinal Chemistry Letters|January 5, 1999
Identification and SAR for a selective, nonpeptidyl thrombin inhibitorA M Naylor-Olsen, G S Ponticello, S D Lewis, et al.Journal of Medicinal Chemistry|November 26, 1997
Discovery of a novel, selective, and orally bioavailable class of thrombin inhibitors incorporating aminopyridyl moieties at the P1 positionD M Feng, S J Gardell, S D Lewis, et al.Pageof 2