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Journal of Medicinal Chemistry|May 9, 1998
Selective Pneumocystis carinii dihydrofolate reductase inhibitors: design, synthesis, and biological evaluation of new 2,4-diamino-5-substituted-furo[2,3-d]pyrimidinesA Gangjee, X Guo, S F Queener, et al.Journal of Research of the National Institute of Standards and Technology|August 9, 2016
Standard Reference Material (SRM 1990) For Single Crystal Diffractometer AlignmentW Wong-Ng, T Siegrist, G T DeTitta, et al.Acta Crystallographica. Section D, Biological Crystallography|August 10, 2004
Comparison of ternary complexes of Pneumocystis carinii and wild-type human dihydrofolate reductase with coenzyme NADPH and a novel classical antitumor furo[2,3-d]pyrimidine antifolateV Cody, N Galitsky, J R Luft, et al.Biochemistry|March 29, 2000
Structural studies on bioactive compounds. 30. Crystal structure and molecular modeling studies on the Pneumocystis carinii dihydrofolate reductase cofactor complex with TAB, a highly selective antifolateV Cody, D Chan, N Galitsky, et al.The Journal of Biological Chemistry|March 10, 1995
Methotrexate-resistant variants of human dihydrofolate reductase with substitutions of leucine 22. Kinetics, crystallography, and potential as selectable markersW S Lewis, V Cody, N Galitsky, et al.Journal of Medicinal Chemistry|August 28, 1998
Structure-based design and synthesis of lipophilic 2,4-diamino-6-substituted quinazolines and their evaluation as inhibitors of dihydrofolate reductases and potential antitumor agentsA Gangjee, A P Vidwans, A Vasudevan, et al.Pageof 4