CHEBI:16154 - L-gulonic acid

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
ChEBI Name L-gulonic acid
ChEBI ASCII Name L-gulonic acid
Definition A gulonic acid formed by oxidising the aldehyde group of L-gulose to a carboxylic acid group.
Stars This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs CHEBI:6235, CHEBI:21319, CHEBI:21318
Supplier Information
Download Molfile XML SDF
more structures >>
Formula C6H12O7
Net Charge 0
Average Mass 196.15530
Monoisotopic Mass 196.05830
InChI InChI=1S/C6H12O7/c7-1-2(8)3(9)4(10)5(11)6(12)13/h2-5,7-11H,1H2,(H,12,13)/t2-,3+,4-,5-/m0/s1
SMILES OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)C(O)=O
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): mammalian metabolite
Any animal metabolite produced during a metabolic reaction in mammals.
(via gulonic acid )
View more via ChEBI Ontology
ChEBI Ontology
Outgoing L-gulonic acid (CHEBI:16154) is a gulonic acid (CHEBI:24462)
L-gulonic acid (CHEBI:16154) is conjugate acid of L-gulonate (CHEBI:13115)
L-gulonic acid (CHEBI:16154) is enantiomer of D-gulonic acid (CHEBI:87753)
Incoming 2-dehydro-L-idonic acid (CHEBI:19543) has functional parent L-gulonic acid (CHEBI:16154)
3-dehydro-L-gulonic acid (CHEBI:16142) has functional parent L-gulonic acid (CHEBI:16154)
6-deoxy-6-[(2R,3R,4R)-3,4-dihydroxy-2-(hydroxymethyl)pyrrolidin-1-yl]-L-gulonic acid (CHEBI:46440) has functional parent L-gulonic acid (CHEBI:16154)
L-gulono-1,4-lactone (CHEBI:17587) has functional parent L-gulonic acid (CHEBI:16154)
L-gulonate (CHEBI:13115) is conjugate base of L-gulonic acid (CHEBI:16154)
D-gulonic acid (CHEBI:87753) is enantiomer of L-gulonic acid (CHEBI:16154)
L-gulonic acid
Synonyms Sources
Gulonic acid KEGG COMPOUND
L-Gulonic acid KEGG COMPOUND
Manual Xrefs Databases
HMDB0003290 HMDB
View more database links
Registry Number Type Source
526-97-6 CAS Registry Number KEGG COMPOUND
Citation Waiting for Citations Type Source
23970495 PubMed citation Europe PMC
Last Modified
23 October 2015