CHEBI:76793 - 5-carboxycytosine

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ChEBI Name 5-carboxycytosine
Definition A nucleobase analogue that is cytosine in which the hydrogen at position 5 is replaced by a carboxy group.
Stars This entity has been manually annotated by the ChEBI Team.
Submitter Bruce May
Supplier Information
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Formula C5H5N3O3
Net Charge 0
Average Mass 155.11150
Monoisotopic Mass 155.03309
InChI InChI=1S/C5H5N3O3/c6-3-2(4(9)10)1-7-5(11)8-3/h1H,(H,9,10)(H3,6,7,8,11)
SMILES Nc1nc(=O)[nH]cc1C(O)=O
Roles Classification
Chemical Role(s): Bronsted base
A molecular entity capable of accepting a hydron from a donor (Bronsted acid).
(via organic amino compound )
Bronsted acid
A molecular entity capable of donating a hydron to an acceptor (Bronsted base).
(via oxoacid )
Biological Role(s): metabolite
Any intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing 5-carboxycytosine (CHEBI:76793) has functional parent cytosine (CHEBI:16040)
5-carboxycytosine (CHEBI:76793) has role metabolite (CHEBI:25212)
5-carboxycytosine (CHEBI:76793) is a aminopyrimidine (CHEBI:38338)
5-carboxycytosine (CHEBI:76793) is a aromatic carboxylic acid (CHEBI:33859)
5-carboxycytosine (CHEBI:76793) is a nucleobase analogue (CHEBI:67142)
5-carboxycytosine (CHEBI:76793) is a pyrimidone (CHEBI:38337)
4-amino-2-oxo-1,2-dihydropyrimidine-5-carboxylic acid
Synonyms Sources
4-amino-2-oxopyrimidine-5-carboxylic acid ChEBI
5-carboxylcytosine ChEBI
Cytosine-5-carboxylic acid ChemIDplus
Registry Numbers Types Sources
141857 Reaxys Registry Number Reaxys
3650-93-9 CAS Registry Number ChemIDplus
Citations Waiting for Citations Types Sources
21778364 PubMed citation SUBMITTER
23602152 PubMed citation SUBMITTER
24063363 PubMed citation SUBMITTER
Last Modified
16 January 2014