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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.

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Showing results (21-30 of 24) with videos related to

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You have reached the last page of results.This site can display upto 24 results.

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.

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