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Volumn 12, Issue 13, 2004, Pages 3431-3441
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Synthesis and evaluation of 6-methylene-bridged uracil derivatives. Part 1: Discovery of novel orally active inhibitors of human thymidine phosphorylase
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Author keywords
2 Deoxy 5 (trifluoromethyl) uridine (F3dThd); 6 Methylene bridged uracil derivative; Thymidine phosphorylase inhibitor; TPI
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Indexed keywords
5 BROMO 6 (PYRROLIDINYLMETHYL)URACIL;
AMINE;
METHYL GROUP;
THYMIDINE PHOSPHORYLASE;
TRIFLURIDINE;
UNCLASSIFIED DRUG;
URACIL DERIVATIVE;
ANIMAL EXPERIMENT;
ANTINEOPLASTIC ACTIVITY;
ARTICLE;
CONTROLLED STUDY;
DRUG ABSORPTION;
DRUG MECHANISM;
DRUG POTENTIATION;
DRUG SCREENING;
DRUG SOLUBILITY;
DRUG SYNTHESIS;
ENZYME INHIBITION;
EXPERIMENTAL TEST;
FLUORINATION;
IN VIVO STUDY;
MOUSE;
NONHUMAN;
SUBSTITUTION REACTION;
ABSORPTION;
ADMINISTRATION, ORAL;
ANIMALS;
ANTINEOPLASTIC AGENTS;
ENZYME INHIBITORS;
FEMALE;
HUMANS;
HYDROCARBONS;
INHIBITORY CONCENTRATION 50;
MACACA FASCICULARIS;
MALE;
METHANE;
MICE;
MICE, NUDE;
MOLECULAR STRUCTURE;
STOMACH NEOPLASMS;
STRUCTURE-ACTIVITY RELATIONSHIP;
THYMIDINE PHOSPHORYLASE;
URACIL;
XENOGRAFT MODEL ANTITUMOR ASSAYS;
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EID: 2942553016
PISSN: 09680896
EISSN: None
Source Type: Journal
DOI: 10.1016/j.bmc.2004.04.036 Document Type: Article |
Times cited : (40)
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References (32)
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