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

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ChEBI Name 5-carboxy-2'-deoxyuridine 5'-monophosphate
Definition A 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.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
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Formula C10H13N2O10P
Net Charge 0
Average Mass 352.192
Monoisotopic Mass 352.03078
InChI InChI=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
SMILES [C@@H]1(N2C(NC(=O)C(=C2)C(=O)O)=O)O[C@H](COP(O)(=O)O)[C@H](C1)O
Metabolite of Species Details
Mycoplasma genitalium (NCBI:txid2097) See: PubMed
Roles Classification
Chemical Role(s): Bronsted acid
A molecular entity capable of donating a hydron to an acceptor (Bronsted base).
(via oxoacid )
Biological Role(s): Mycoplasma genitalium metabolite
Any bacterial metabolite produced during a metabolic reaction in Mycoplasma genitalium.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing 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)
5-carboxy-2'-deoxyuridine 5'-(dihydrogen phosphate)
Synonyms Sources
5-carboxy-2'-deoxyuridine 5'-phosphate ChEBI
5-carboxy-dUMP ChEBI
Citation Waiting for Citations Type Source
22817898 PubMed citation Europe PMC
Last Modified
04 April 2016