5-dehydro-4-deoxy-D-glucuronic acid (CHEBI:17782)

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ChEBI Name	5-dehydro-4-deoxy-D-glucuronic acid

ChEBI ID	CHEBI:17782

ChEBI ASCII Name	5-dehydro-4-deoxy-D-glucuronic acid

Definition	A hexuronic acid that results from hydrolytic ring cleavage of the hemiacetal group of 4-deoxy-α-L-threo-hex-4-enopyranuronic acid with subsequent tautomerisation of the resulting enol to the corresponding ketone.

Stars	This entity has been manually annotated by the ChEBI Team.

Secondary ChEBI IDs	CHEBI:1821, CHEBI:20357

Supplier Information

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Formula

C6H8O6

Net Charge

Average Mass

176.12410

Monoisotopic Mass

176.03209

InChI

InChI=1S/C6H8O6/c7-2-5(10)3(8)1-4(9)6(11)12/h2-3,5,8,10H,1H2,(H,11,12)/t3-,5-/m0/s1

InChIKey

IMUGYKFHMJLTOU-UCORVYFPSA-N

SMILES

[H]C(=O)[C@H](O)[C@@H](O)CC(=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 )

ChEBI Ontology
Outgoing	5-dehydro-4-deoxy-D-glucuronic acid (CHEBI:17782) is a aldehyde (CHEBI:17478) 5-dehydro-4-deoxy-D-glucuronic acid (CHEBI:17782) is a hexuronic acid (CHEBI:24592) 5-dehydro-4-deoxy-D-glucuronic acid (CHEBI:17782) is conjugate acid of 5-dehydro-4-deoxy-D-glucuronate (CHEBI:17117)

Incoming	5-dehydro-4-deoxy-2-O-sulfo-D-glucuronic acid (CHEBI:63275) has functional parent 5-dehydro-4-deoxy-D-glucuronic acid (CHEBI:17782) 5-dehydro-4-deoxy-D-glucuronate (CHEBI:17117) is conjugate base of 5-dehydro-4-deoxy-D-glucuronic acid (CHEBI:17782)

IUPAC Name

4-deoxy-L-threo-hex-5-ulosuronic acid

Synonym	Source
4-deoxy-L-threo-5-hexulosuronic acid	ChEBI

Last Modified

25 November 2011