CHEBI:102485 - 5-carboxy-2'-deoxyuridine

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ChEBI Name 5-carboxy-2'-deoxyuridine
ChEBI ID CHEBI:102485
Definition A nucleoside analogue that is 2'-deoxyuridine 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 C10H12N2O7
Net Charge 0
Average Mass 272.212
Monoisotopic Mass 272.06445
InChI InChI=1S/C10H12N2O7/c13-3-6-5(14)1-7(19-6)12-2-4(9(16)17)8(15)11-10(12)18/h2,5-7,13-14H,1,3H2,(H,16,17)(H,11,15,18)/t5-,6+,7+/m0/s1
InChIKey GAGYTXTVUMXAOC-RRKCRQDMSA-N
SMILES [C@@H]1(N2C(NC(=O)C(=C2)C(=O)O)=O)O[C@H](CO)[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.
drug metabolite

View more via ChEBI Ontology
ChEBI Ontology
Outgoing 5-carboxy-2'-deoxyuridine (CHEBI:102485) has functional parent uracil (CHEBI:17568)
5-carboxy-2'-deoxyuridine (CHEBI:102485) has role Mycoplasma genitalium metabolite (CHEBI:131604)
5-carboxy-2'-deoxyuridine (CHEBI:102485) has role drug metabolite (CHEBI:49103)
5-carboxy-2'-deoxyuridine (CHEBI:102485) is a aromatic carboxylic acid (CHEBI:33859)
5-carboxy-2'-deoxyuridine (CHEBI:102485) is a nucleoside analogue (CHEBI:60783)
5-carboxy-2'-deoxyuridine (CHEBI:102485) is a pyrimidine 2'-deoxyribonucleoside (CHEBI:19255)
IUPAC Name
5-carboxy-2'-deoxyuridine
Synonym Source
2'-Deoxy-5-carboxyuridine ChemIDplus
Manual Xref Database
HMDB0060774 HMDB
View more database links
Registry Numbers Types Sources
14599-46-3 CAS Registry Number ChemIDplus
433778 Reaxys Registry Number Reaxys
Citations Waiting for Citations Types Sources
110152 PubMed citation Europe PMC
14565347 PubMed citation Europe PMC
22817898 PubMed citation Europe PMC
28691 PubMed citation Europe PMC
6048518 PubMed citation Europe PMC
6116773 PubMed citation Europe PMC
Last Modified
04 April 2016