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Volumn 105, Issue 5, 2008, Pages 1448-1453
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Discovery of potent pteridine reductase inhibitors to guide antiparasite drug development
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Author keywords
Antifolates; Antitrypanosomatid agents; Drug discovery
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Indexed keywords
ANTIPARASITIC AGENT;
CELL PROTEIN;
DIHYDROFOLATE REDUCTASE;
ENZYME INHIBITOR;
FOLIC ACID ANTAGONIST;
PROTEIN PTR1;
PTERIDINE REDUCTASE INHIBITOR;
THYMIDYLATE SYNTHASE;
UNCLASSIFIED DRUG;
ANTIPROTOZOAL AGENT;
ANTITRYPANOSOMAL AGENT;
FOLIC ACID;
ISONIPECOTIC ACID;
METHYL 1 (4 ((2,4 DIAMINOPTERIDIN 6 YLMETHYL)METHYLAMINO)BENZOYL)PIPERIDINE 4 CARBOXYLATE;
METHYL 1 (4 (2,4 DIAMINOPTERIDIN 6 YLMETHYLAMINO)BENZOYL)PIPERIDINE 4 CARBOXYLATE;
METHYL 1-(4-((2,4-DIAMINOPTERIDIN-6-YLMETHYL)METHYLAMINO)BENZOYL)PIPERIDINE-4-CARBOXYLATE;
METHYL 1-(4-(2,4-DIAMINOPTERIDIN-6-YLMETHYLAMINO)BENZOYL)PIPERIDINE-4-CARBOXYLATE;
OXIDOREDUCTASE;
PROTOZOAL PROTEIN;
PTERIDINE DERIVATIVE;
PTERIDINE REDUCTASE;
ARTICLE;
BINDING AFFINITY;
COMPLEX FORMATION;
DRUG POTENCY;
DRUG SELECTIVITY;
DRUG SPECIFICITY;
ENZYME INHIBITION;
ENZYME SUBSTRATE;
LEISHMANIA MAJOR;
NONHUMAN;
PARASITOSIS;
PRIORITY JOURNAL;
SCREENING TEST;
TRYPANOSOMA CRUZI;
ANIMAL;
CHEMISTRY;
DRUG ANTAGONISM;
DRUG DESIGN;
DRUG EFFECT;
DRUG SCREENING;
DRUG SENSITIVITY;
ENZYMOLOGY;
X RAY CRYSTALLOGRAPHY;
LEISHMANIA MAJOR;
TRYPANOSOMA CRUZI;
TRYPANOSOMATIDAE;
ANIMALS;
ANTIPROTOZOAL AGENTS;
CRYSTALLOGRAPHY, X-RAY;
DRUG DESIGN;
DRUG EVALUATION, PRECLINICAL;
ENZYME INHIBITORS;
FOLIC ACID;
ISONIPECOTIC ACIDS;
LEISHMANIA MAJOR;
OXIDOREDUCTASES;
PARASITIC SENSITIVITY TESTS;
PROTOZOAN PROTEINS;
PTERIDINES;
TETRAHYDROFOLATE DEHYDROGENASE;
THYMIDYLATE SYNTHASE;
TRYPANOCIDAL AGENTS;
TRYPANOSOMA CRUZI;
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EID: 40349108458
PISSN: 00278424
EISSN: 10916490
Source Type: Journal
DOI: 10.1073/pnas.0704384105 Document Type: Article |
Times cited : (135)
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References (41)
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