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Results: 1-6 |
Results: 6
COMPARISON OF TERNARY CRYSTAL COMPLEXES OF F31 VARIANTS OF HUMAN DIHYDROFOLATE-REDUCTASE WITH NADPH AND A CLASSICAL ANTITUMOR FUROPYRIMIDINE
Authors: CODY V GALITSKY N LUFT JR PANGBORN W BLAKLEY RL GANGJEE A
Citation: V. Cody et al., COMPARISON OF TERNARY CRYSTAL COMPLEXES OF F31 VARIANTS OF HUMAN DIHYDROFOLATE-REDUCTASE WITH NADPH AND A CLASSICAL ANTITUMOR FUROPYRIMIDINE, Anti-cancer drug design, 13(4), 1998, pp. 307-315
SELECTIVE PNEUMOCYSTIS-CARINII DIHYDROFOLATE-REDUCTASE INHIBITORS - DESIGN, SYNTHESIS, AND BIOLOGICAL EVALUATION OF NEW 2,4-DIAMINO-5-SUBSTITUTED-FURO[2,3-D]PYRIMIDINES
Authors: GANGJEE A GUO X QUEENER SF CODY V GALITSKY N LUFT JR PANGBORN W
Citation: A. Gangjee et al., SELECTIVE PNEUMOCYSTIS-CARINII DIHYDROFOLATE-REDUCTASE INHIBITORS - DESIGN, SYNTHESIS, AND BIOLOGICAL EVALUATION OF NEW 2,4-DIAMINO-5-SUBSTITUTED-FURO[2,3-D]PYRIMIDINES, Journal of medicinal chemistry, 41(8), 1998, pp. 1263-1271
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
Authors: GANGJEE A VIDWANS AP VASUDEVAN A QUEENER SF KISLIUK RL CODY V LI RM GALITSKY N LUFT JR PANGBORN S
Citation: A. Gangjee et al., 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, Journal of medicinal chemistry, 41(18), 1998, pp. 3426-3434
COMPARISON OF TERNARY COMPLEXES OF PNEUMOCYSTIS-CARINII AND WILD-TYPEHUMAN DIHYDROFOLATE-REDUCTASE WITH COENZYME NADPH AND A NOVEL CLASSICAL ANTITUMOR FURO[2,3-D]PYRIMIDINE ANTIFOLATE
Authors: CODY V GALITSKY N LUFT JR PANGBORN W GANGJEE A DEVRAJ R QUEENER SF BLAKLEY RL
Citation: V. Cody et al., COMPARISON OF TERNARY COMPLEXES OF PNEUMOCYSTIS-CARINII AND WILD-TYPEHUMAN DIHYDROFOLATE-REDUCTASE WITH COENZYME NADPH AND A NOVEL CLASSICAL ANTITUMOR FURO[2,3-D]PYRIMIDINE ANTIFOLATE, Acta crystallographica. Section D, Biological crystallography, 53, 1997, pp. 638-649
COMPARISON OF 2 INDEPENDENT CRYSTAL-STRUCTURES OF HUMAN DIHYDROFOLATE-REDUCTASE TERNARY COMPLEXES REDUCED WITH NICOTINAMIDE ADENINE-DINUCLEOTIDE PHOSPHATE AND THE VERY TIGHT-BINDING INHIBITOR PT523
Authors: CODY V GALITSKY N LUFT JR PANGBORN W ROSOWSKY A BLAKLEY RL
Citation: V. Cody et al., COMPARISON OF 2 INDEPENDENT CRYSTAL-STRUCTURES OF HUMAN DIHYDROFOLATE-REDUCTASE TERNARY COMPLEXES REDUCED WITH NICOTINAMIDE ADENINE-DINUCLEOTIDE PHOSPHATE AND THE VERY TIGHT-BINDING INHIBITOR PT523, Biochemistry, 36(45), 1997, pp. 13897-13903
METHOTREXATE-RESISTANT VARIANTS OF HUMAN DIHYDROFOLATE-REDUCTASE WITHSUBSTITUTIONS OF LEUCINE-22 - KINETICS, CRYSTALLOGRAPHY, AND POTENTIAL AS SELECTABLE MARKERS
Authors: LEWIS WS CODY V GALITSKY N LUFT JR PANGBORN W CHUNDURU SK SPENCER HT APPLEMAN JR BLAKLEY RL
Citation: Ws. Lewis et al., METHOTREXATE-RESISTANT VARIANTS OF HUMAN DIHYDROFOLATE-REDUCTASE WITHSUBSTITUTIONS OF LEUCINE-22 - KINETICS, CRYSTALLOGRAPHY, AND POTENTIAL AS SELECTABLE MARKERS, The Journal of biological chemistry, 270(10), 1995, pp. 5057-5064
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