D-galactaro-1,5-lactone (CHEBI:84190)

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ChEBI Name	D-galactaro-1,5-lactone

ChEBI ID	CHEBI:84190

ChEBI ASCII Name	D-galactaro-1,5-lactone

Definition	An aldarolactone formed via intramolecular cyclocondensation of galactaric acid.

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

Supplier Information

Download	Molfile XML SDF

Formula

C6H8O7

Net Charge

Average Mass

192.12350

Monoisotopic Mass

192.02700

InChI

InChI=1S/C6H8O7/c7-1-2(8)4(5(10)11)13-6(12)3(1)9/h1-4,7-9H,(H,10,11)/t1-,2+,3+,4-/m0/s1

InChIKey

YLKFQNUGXOLRNI-KXMYSMCESA-N

SMILES

O[C@H]1[C@@H](O)[C@H](OC(=O)[C@@H]1O)C(O)=O

Metabolite of Species	Details
Agrobacterium tumefaciens (NCBI:txid358)	of strain C58 See: PubMed

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):	bacterial xenobiotic metabolite Any bacterial metabolite produced by metabolism of a xenobiotic compound in bacteria.

ChEBI Ontology
Outgoing	D-galactaro-1,5-lactone (CHEBI:84190) has functional parent galactaric acid (CHEBI:30852) D-galactaro-1,5-lactone (CHEBI:84190) has role bacterial xenobiotic metabolite (CHEBI:76976) D-galactaro-1,5-lactone (CHEBI:84190) is a aldarolactone (CHEBI:37426) D-galactaro-1,5-lactone (CHEBI:84190) is a carbohydrate acid (CHEBI:33720) D-galactaro-1,5-lactone (CHEBI:84190) is conjugate acid of D-galactaro-1,5-lactone(1−) (CHEBI:83383)

Incoming	D-galactaro-1,5-lactone(1−) (CHEBI:83383) is conjugate base of D-galactaro-1,5-lactone (CHEBI:84190)

Synonyms	Sources
(2S,3R,4S,5R)-3,4,5-trihydroxy-6-oxotetrahydro-2H-pyran-2-carboxylic acid	IUPAC
1,5-galactarolactone	MetaCyc
galactaro-1,5-lactone	MetaCyc
galactarolactone	MetaCyc

Registry Number	Type	Source
5270175	Reaxys Registry Number	Reaxys

Last Modified

07 January 2015