CHEBI:132133 - cytosylglucuronic acid

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ChEBI Name cytosylglucuronic acid
ChEBI ID CHEBI:132133
Definition An N-glycosyl compound that is cytosine in which the proton at position 1 is replaced by a β-D-glucuronosyl residue.
Stars This entity has been manually annotated by the ChEBI Team.
Submitter Gemma Holliday
Supplier Information
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Formula C10H13N3O7
Net Charge 0
Average Mass 287.227
Monoisotopic Mass 287.07535
InChI InChI=1S/C10H13N3O7/c11-3-1-2-13(10(19)12-3)8-6(16)4(14)5(15)7(20-8)9(17)18/h1-2,4-8,14-16H,(H,17,18)(H2,11,12,19)/t4-,5-,6+,7-,8+/m0/s1
InChIKey CHKIQPXDGYGCHW-YOWKYNACSA-N
SMILES O1[C@H](C(O)=O)[C@H]([C@H](O)[C@H]([C@@H]1N2C=CC(=NC2=O)N)O)O
Metabolite of Species Details
Streptomyces griseochromogenes (NCBI:txid68214) See: PubMed
Roles Classification
Biological Role(s): bacterial metabolite
Any prokaryotic metabolite produced during a metabolic reaction in bacteria.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing cytosylglucuronic acid (CHEBI:132133) has functional parent β-D-glucuronic acid (CHEBI:28860)
cytosylglucuronic acid (CHEBI:132133) has functional parent cytosine (CHEBI:16040)
cytosylglucuronic acid (CHEBI:132133) has role bacterial metabolite (CHEBI:76969)
cytosylglucuronic acid (CHEBI:132133) is a N-glycosyl compound (CHEBI:21731)
cytosylglucuronic acid (CHEBI:132133) is a carbohydrate acid derivative (CHEBI:63436)
cytosylglucuronic acid (CHEBI:132133) is a monosaccharide derivative (CHEBI:63367)
cytosylglucuronic acid (CHEBI:132133) is a nucleobase-containing molecular entity (CHEBI:61120)
cytosylglucuronic acid (CHEBI:132133) is conjugate acid of cytosylglucuronate (CHEBI:132252)
Incoming cytosylglucuronate (CHEBI:132252) is conjugate base of cytosylglucuronic acid (CHEBI:132133)
IUPAC Name
4-amino-1-β-D-glucopyranuronosylpyrimidin-2(1H)-one
Synonyms Sources
1-(beta-D-Glucopyranosyluronic acid)cytosine ChemIDplus
1-(β-D-glucuronosyl)cytosine ChEBI
cytosyl-β-D-glucuronic acid ChEBI
Pentopyranic acid ChemIDplus
Manual Xref Database
CPD-17160 MetaCyc
View more database links
Registry Numbers Types Sources
59862-05-4 CAS Registry Number ChemIDplus
834916 Reaxys Registry Number Reaxys
Citations Waiting for Citations Types Sources
22753012 PubMed citation Europe PMC
23377931 PubMed citation Europe PMC
23874663 PubMed citation SUBMITTER
7649864 PubMed citation Europe PMC
8113166 PubMed citation Europe PMC
956050 PubMed citation Europe PMC
9711220 PubMed citation Europe PMC
Last Modified
18 October 2016