N Galitsky

Ligand-induced conformational changes in the crystal structures of Pneumocystis carinii dihydrofolate reductase complexes with folate and NADP+.

W Pangborn, V. Cody, J. Luft, 2000, Biochemistry.

Structure-based design and synthesis of lipophilic 2,4-diamino-6-substituted quinazolines and their evaluation as inhibitors of dihydrofolate reductases and potential antitumor agents.

W Pangborn, A. Vasudevan, V. Cody, 1998, Journal of medicinal chemistry.

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 antifolate.

W Pangborn, S F Queener, V Cody, 1997, Acta crystallographica. Section D, Biological crystallography.

Comparison of two independent crystal structures of human dihydrofolate reductase ternary complexes reduced with nicotinamide adenine dinucleotide phosphate and the very tight-binding inhibitor PT523.

W Pangborn, V. Cody, J. Luft, 1997, Biochemistry.

Design, synthesis, and X-ray crystal structure of a potent dual inhibitor of thymidylate synthase and dihydrofolate reductase as an antitumor agent.

V. Cody, S F Queener, V Cody, 2000, Journal of medicinal chemistry.

Structure-based design of selective inhibitors of dihydrofolate reductase: synthesis and antiparasitic activity of 2, 4-diaminopteridine analogues with a bridged diarylamine side chain.

V. Cody, S F Queener, A Rosowsky, 1999, Journal of medicinal chemistry.