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CHEBI:102517 - 5-carboxy-2'-deoxyuridine 5'-monophosphate

ChEBI IDCHEBI:102517
ChEBI Name5-carboxy-2'-deoxyuridine 5'-monophosphate
Stars
DefinitionA nucleoside monophosphate analogue that is 2'-deoxyuridine-5'-monophosphate in which the hydrogen at position 5 on the uracil ring is replaced by a carboxy group.
Last Modified4 April 2016
DownloadsMolfile
FormulaC10H13N2O10P
Net Charge0
Average Mass352.192
Monoisotopic Mass352.03078
SMILESO=C(O)c1cn([C@H]2C[C@H](O)[C@@H](COP(=O)(O)O)O2)c(=O)nc1=O
InChIInChI=1S/C10H13N2O10P/c13-5-1-7(22-6(5)3-21-23(18,19)20)12-2-4(9(15)16)8(14)11-10(12)17/h2,5-7,13H,1,3H2,(H,15,16)(H,11,14,17)(H2,18,19,20)/t5-,6+,7+/m0/s1
InChIKeyYJPIHSPFORSHEC-RRKCRQDMSA-N
Species of MetaboliteComponentSourceComments
Mycoplasma genitalium (ncbitaxon:2097) - PubMed (22817898)
Roles Classification
Chemical Role:
Bronsted acid  A molecular entity capable of donating a hydron to an acceptor (Brønsted base).
Biological Role:
Mycoplasma genitalium metabolite  Any bacterial metabolite produced during a metabolic reaction in Mycoplasma genitalium.
ChEBI Ontology
Outgoing Relation(s)
5-carboxy-2'-deoxyuridine 5'-monophosphate (CHEBI:102517) has functional parent dUMP (CHEBI:17622)
5-carboxy-2'-deoxyuridine 5'-monophosphate (CHEBI:102517) has role Mycoplasma genitalium metabolite (CHEBI:131604)
5-carboxy-2'-deoxyuridine 5'-monophosphate (CHEBI:102517) is a aromatic carboxylic acid (CHEBI:33859)
5-carboxy-2'-deoxyuridine 5'-monophosphate (CHEBI:102517) is a nucleoside monophosphate analogue (CHEBI:48208)
5-carboxy-2'-deoxyuridine 5'-monophosphate (CHEBI:102517) is a pyrimidine 2'-deoxyribonucleoside 5'-monophosphate (CHEBI:36995)
IUPAC Name 
5-carboxy-2'-deoxyuridine 5'-(dihydrogen phosphate)
Synonyms  Source
5-carboxy-dUMPChEBI
5-carboxy-2'-deoxyuridine 5'-phosphateChEBI
Citations