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PDBe Entry: 1boz 
STRUCTURE-BASED DESIGN AND SYNTHESIS OF LIPOPHILIC 2,4-DIAMINO-6-SUBSTITUTED QUINAZOLINES AND THEIR EVALUATION AS INHIBITORS OF DIHYDROFOLATE REDUCTASE AND POTENTIAL ANTITUMOR AGENTS
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OXIDOREDUCTASE
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X-RAY DIFFRACTION
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Resolution: 2.1 Å, R-factor: 20.2%, Spacegroup: H 3
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12/08/1998, deposition: 06/08/1998, last revision: 24/02/2009
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Gangjee, A. ; Vidwans, A.P. ; Vasudevan, A. ; Queener, S.F. ; Kisliuk, R.L. ; Cody, V. ; Li, R. ; Galitsky, N. ; Luft, J.R. ; Pangborn, W.
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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. J.MED.CHEM. vol:41, pag:3426-3434 (1998) [PubMed ID 9719595 ]
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OXIDOREDUCTASE
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1.5.1.3 ExPASy BRENDA (A)
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Homo sapiens(human) 9606 (A)
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Dihydrofolate reductase (EC 1.5.1.3) P00374 (A)
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A
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| A |
PROTEIN (DIHYDROFOLATE REDUCTASE) |
Protein |
P00374 (DYR_HUMAN)
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186 |
100% |
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| A |
NADPH DIHYDRO-NICOTINAMIDE-ADENINE-DINUCLEOTIDE PHOSPHATE |
NDP
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| A |
N6-(2,5-DIMETHOXY-BENZYL)-N6-METHYL-PYRIDO[2,3-D]PYRIMIDINE-2,4,6-TRIAMINE |
PRD
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