L-gulonic acid (CHEBI:16154)

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ChEBI Name	L-gulonic acid

ChEBI ID	CHEBI:16154

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	eMolecules:30151951, ZINC000003869787

Download	Molfile XML SDF

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Formula

C6H12O7

Net Charge

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

InChIKey

RGHNJXZEOKUKBD-QTBDOELSSA-N

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 )

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)

IUPAC Name

L-gulonic acid

Registry Number	Type	Source
526-97-6	CAS Registry Number	KEGG COMPOUND

Citation

Last Modified

23 October 2015