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TargetThymidine phosphorylase
LigandBDBM20033
Substrate/CompetitorBDBM1
Meas. Tech.Enzyme Inhibition Assay
IC50 2000±n/a nM
Citation Nencka, RVotruba, IHrebabecký, HTloust'ová, EHorská, KMasojídková, MHolý, A Design and synthesis of novel 5,6-disubstituted uracil derivatives as potent inhibitors of thymidine phosphorylase. Bioorg Med Chem Lett16:1335-7 (2006) [PubMed]  Article
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Thymidine phosphorylase
Name:Thymidine phosphorylase
Synonyms:TYPH_ECOLI | TdRPase | Thymidine Phosphorylase (TP) | deoA | tpp | ttg
Type:Enzyme
Mol. Mass.:47198.54
Organism:Escherichia coli
Description:n/a
Residue:440
Sequence:
MFLAQEIIRKKRDGHALSDEEIRFFINGIRDNTISEGQIAALAMTIFFHDMTMPERVSLT
MAMRDSGTVLDWKSLHLNGPIVDKHSTGGVGDVTSLMLGPMVAACGGYIPMISGRGLGHT
GGTLDKLESIPGFDIFPDDNRFREIIKDVGVAIIGQTSSLAPADKRFYATRDITATVDSI
PLITASILAKKLAEGLDALVMDVKVGSGAFMPTYELSEALAEAIVGVANGAGVRTTALLT
DMNQVLASSAGNAVEVREAVQFLTGEYRNPRLFDVTMALCVEMLISGKLAKDDAEARAKL
QAVLDNGKAAEVFGRMVAAQKGPTDFVENYAKYLPTAMLTKAVYADTEGFVSEMDTRALG
MAVVAMGGGRRQASDTIDYSVGFTDMARLGDQVDGQRPLAVIHAKDENNWQEAAKAVKAA
IKLADKAPESTPTVYRRISE
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  Blast E-value cutoff:
BDBM20033
BDBM1
NameBDBM20033
Synonyms:6-(azetidin-1-yl)-5-bromo-1,3-diazinane-2,4-dione | uracil, 3
TypeSmall organic molecule
Emp. Form.C7H8BrN3O2
Mol. Mass.246.061
SMILESBrc1c([nH]c(=O)[nH]c1=O)N1CCC1
Structure
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