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Volumn 44, Issue 2, 2009, Pages 678-688
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Design, synthesis and evaluation of novel uracil acetamide derivatives as potential inhibitors of Plasmodium falciparum dUTP nucleotidohydrolase
e
MEDIVIR AB
(Sweden)
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Author keywords
Anti malarial; Anti plasmodial; dUTP nucleotidohydrolase; Uracil acetamide
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Indexed keywords
1 [N (2 TRIPHENYLMETHYLAMINOETHYL)ACETAMIDE URACIL;
1 [N (3 TRIPHENYLMETHYLAMINOBUTYL)ACETAMIDE]URACIL;
1 [N (3 TRIPHENYLMETHYLAMINOPROPYL)ACETAMIDE]URACIL;
1 [N (TRIPHENYLMETHYL)DIAMINODI(N PROPYL)ACETAMIDE]URACIL;
1 [N (TRIPHENYLMETHYLAMINOETHYL) N (AMINOETHYL)ACETAMIDE]URACIL;
1 [N HYDROXYETHYL N (TRIPHENYLMETHYLAMINO)ETHYLACETAMIDE]URACIL;
ACETAMIDE DERIVATIVE;
ANTIMALARIAL AGENT;
DEOXYURIDINE TRIPHOSPHATE PYROPHOSPHATASE;
N [3 (TERT BUTYL DIPHENYL SILANYLOXY)PROPYL 2 URACIL ACETAMIDE;
N [4 (TERT BUTYL DIPHENYL SILANYLOXY)BUTYL 2 URACIL ACETAMIDE;
UNCLASSIFIED DRUG;
URACIL ACETAMIDE DERIVATIVE;
URACIL DERIVATIVE;
ANIMAL CELL;
ARTICLE;
BIOASSAY;
BIOLOGICAL ACTIVITY;
CELL DEATH;
CELL LINE;
CELL STRAIN L6;
CONTROLLED STUDY;
DNA FRAGMENTATION;
DRUG CYTOTOXICITY;
DRUG DESIGN;
DRUG STRUCTURE;
DRUG SYNTHESIS;
ENZYME INHIBITION;
HYDROGENATION;
IC 50;
IN VITRO STUDY;
MOLECULAR MODEL;
NONHUMAN;
PLASMODIUM FALCIPARUM;
RAT;
SILYLATION;
ACETAMIDES;
ANIMALS;
DRUG DESIGN;
ENZYME INHIBITORS;
PLASMODIUM FALCIPARUM;
PYROPHOSPHATASES;
STRUCTURE-ACTIVITY RELATIONSHIP;
URACIL;
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EID: 60149107206
PISSN: 02235234
EISSN: 17683254
Source Type: Journal
DOI: 10.1016/j.ejmech.2008.05.018 Document Type: Article |
Times cited : (47)
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References (13)
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