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The Journal of Biological Chemistry|December 31, 1997
X-ray crystallographic studies of Candida albicans dihydrofolate reductase. High resolution structures of the holoenzyme and an inhibited ternary complexM Whitlow, A J Howard, D Stewart, et al.Journal of Medicinal Chemistry|September 1, 1995
Selective inhibitors of Candida albicans dihydrofolate reductase: activity and selectivity of 5-(arylthio)-2,4-diaminoquinazolinesJ H Chan, J S Hong, L F Kuyper, et al.Journal of Medicinal Chemistry|August 25, 2001
X-Ray crystal structures of Candida albicans dihydrofolate reductase: high resolution ternary complexes in which the dihydronicotinamide moiety of NADPH is displaced by an inhibitorM Whitlow, A J Howard, D Stewart, et al.Journal of Medicinal Chemistry|March 1, 1985
Receptor-based design of dihydrofolate reductase inhibitors: comparison of crystallographically determined enzyme binding with enzyme affinity in a series of carboxy-substituted trimethoprim analoguesL F Kuyper, B Roth, D P Baccanari, et al.Journal of Medicinal Chemistry|February 16, 1996
High-affinity inhibitors of dihydrofolate reductase: antimicrobial and anticancer activities of 7,8-dialkyl-1,3-diaminopyrrolo[3,2-f]quinazolines with small molecular sizeL F Kuyper, D P Baccanari, M L Jones, et al.Science (New York, N.Y.)|June 13, 1997
Peptide agonist of the thrombopoietin receptor as potent as the natural cytokineS E Cwirla, P Balasubramanian, D J Duffin, et al.Pageof 4