![]() |
Volumn 10, Issue 3, 2002, Pages 525-530
|
Synthesis and enzymatic evaluation of pyridinium-substituted uracil derivatives as novel inhibitors of thymidine phosphorylase
|
Author keywords
[No Author keywords available]
|
Indexed keywords
1 (2,4 DIHYDROXYPYRIMIDIN 6 YL)PYRIDINIUM CHLORIDE;
1 (5 BROMO 2,4 DIHYDROXYPYRIMIDIN 6 YL)PYRIDINIUM CHLORIDE;
1 (5 CHLORO 2,4 DIHYDROXYPYRIMIDIN 6 YL)PYRIDINIUM CHLORIDE;
1 [(2,4 DIHYDROXY 5 METHYLPYRIMIDIN 1 YL)METHYL]PYRIDINIUM CHLORIDE;
1 [(2,4 DIHYDROXY 5 METHYLPYRIMIDIN 6 YL)METHYL]PYRIDINIUM CHLORIDE;
1 [(2,4 DIHYDROXYPYRIMIDIN 6 YL)METHYL]PYRIDINIUM CHLORIDE;
1 [(5 BROMO 2,4 DIHYDROXYPYRIMIDIN 6 YL)METHYL]PYRIDINIUM CHLORIDE;
1 [(5 CHLORO 2,4 DIHYDROXYPYRIMIDIN 6 YL)METHYL]PYRIDINIUM CHLORIDE;
1 [2 (2,4 DIHYDROXY 5 METHYLPYRIMIDIN 1 YL)ETHYL]PYRIDINIUM BROMIDE;
2 AMINO 1 [(5 CHLORO 2,4 DIHYDROXYPYRIMIDIN 6 YL)METHYL]PYRIDINIUM CHLORIDE;
3 AMINO 1 [(5 CHLORO 2,4 DIHYDROXYPYRIMIDIN 6 YL)METHYL]PYRIDINIUM CHLORIDE;
6 AMINO 5 BROMOURACIL;
PYRIDINIUM DERIVATIVE;
THYMIDINE PHOSPHORYLASE;
UNCLASSIFIED DRUG;
URACIL DERIVATIVE;
ANTINEOPLASTIC AGENT;
DRUG DERIVATIVE;
ENZYME INHIBITOR;
URACIL;
AMINO ACID SEQUENCE;
ARTICLE;
CONTROLLED STUDY;
DRUG ACTIVITY;
DRUG POTENCY;
DRUG SCREENING;
DRUG SYNTHESIS;
ENZYME INHIBITION;
ESCHERICHIA COLI;
IC 50;
NONHUMAN;
SEQUENCE HOMOLOGY;
STRUCTURE ACTIVITY RELATION;
DRUG ANTAGONISM;
ENZYMOLOGY;
NEOVASCULARIZATION (PATHOLOGY);
SOLUBILITY;
SYNTHESIS;
ANTINEOPLASTIC AGENTS;
ENZYME INHIBITORS;
ESCHERICHIA COLI;
INHIBITORY CONCENTRATION 50;
NEOVASCULARIZATION, PATHOLOGIC;
PYRIDINIUM COMPOUNDS;
SOLUBILITY;
STRUCTURE-ACTIVITY RELATIONSHIP;
THYMIDINE PHOSPHORYLASE;
URACIL;
|
EID: 0036152769
PISSN: 09680896
EISSN: None
Source Type: Journal
DOI: 10.1016/S0968-0896(01)00309-1 Document Type: Article |
Times cited : (31)
|
References (44)
|