beta-D-allose (CHEBI:40656)

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ChEBI Name	β-D-allose

ChEBI ID	CHEBI:40656

ChEBI ASCII Name	beta-D-allose

Definition	A D-allopyranose with a β-configuration at the anomeric position.

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

Secondary ChEBI IDs	CHEBI:40649, CHEBI:37685

Supplier Information	ChemicalBook:CB7125746, ChemicalBook:CB2752440, eMolecules:494705, eMolecules:29781161, Selleckchem:Levonorgestrel(Levonelle), ZINC000003814395

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Formula

C6H12O6

Net Charge

Average Mass

180.15588

Monoisotopic Mass

180.06339

InChI

InChI=1S/C6H12O6/c7-1-2-3(8)4(9)5(10)6(11)12-2/h2-11H,1H2/t2-,3-,4-,5-,6-/m1/s1

InChIKey

WQZGKKKJIJFFOK-QZABAPFNSA-N

SMILES

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

Roles Classification
Chemical Role(s):	antioxidant A substance that opposes oxidation or inhibits reactions brought about by dioxygen or peroxides. (via D-allopyranose )

Biological Role(s):	plant metabolite Any eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms. (via allose )

ChEBI Ontology
Outgoing	β-D-allose (CHEBI:40656) is a D-allopyranose (CHEBI:4093) β-D-allose (CHEBI:40656) is enantiomer of β-L-allose (CHEBI:37740)

Incoming	kaempferol 3-O-β-D-allopyranoside (CHEBI:75796) has functional parent β-D-allose (CHEBI:40656) quercetin 4'-O-α-L-rhamnopyranosyl-3-O-β-D-allopyranoside (CHEBI:66289) has functional parent β-D-allose (CHEBI:40656) β-L-allose (CHEBI:37740) is enantiomer of β-D-allose (CHEBI:40656)

IUPAC Name

β-D-allopyranose

Registry Number	Type	Source
1617535	Beilstein Registry Number	Beilstein

Last Modified

07 April 2021