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

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ChEBI Name 5-dehydro-4-deoxy-D-glucuronic acid
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
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Formula C6H8O6
Net Charge 0
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
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 )
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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)
4-deoxy-L-threo-hex-5-ulosuronic acid
Synonym Source
4-deoxy-L-threo-5-hexulosuronic acid ChEBI
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Citations Waiting for Citations Types Sources
10441389 PubMed citation Europe PMC
15148314 PubMed citation Europe PMC
16630576 PubMed citation Europe PMC
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21147778 PubMed citation Europe PMC
Last Modified
25 November 2011