CHEBI:4093 - D-allopyranose

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ChEBI Name D-allopyranose
ChEBI ID CHEBI:4093
ChEBI ASCII Name D-allopyranose
Definition The D-enantiomer of allopyranose.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
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Formula C6H12O6
Net Charge 0
Average Mass 180.15588
Monoisotopic Mass 180.063
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-IVMDWMLBSA-N
SMILES OC[C@H]1OC(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.
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 )
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ChEBI Ontology
Outgoing D-allopyranose (CHEBI:4093) has role antioxidant (CHEBI:22586)
D-allopyranose (CHEBI:4093) is a D-allose (CHEBI:17393)
D-allopyranose (CHEBI:4093) is a allopyranose (CHEBI:37742)
D-allopyranose (CHEBI:4093) is enantiomer of L-allopyranose (CHEBI:37741)
Incoming α-D-allose (CHEBI:37686) is a D-allopyranose (CHEBI:4093)
β-D-allose (CHEBI:40656) is a D-allopyranose (CHEBI:4093)
L-allopyranose (CHEBI:37741) is enantiomer of D-allopyranose (CHEBI:4093)
IUPAC Name
D-allopyranose
Synonym Source
D-Allose KEGG COMPOUND
Database Links Databases
C01487 KEGG COMPOUND
D-Allopyranose MetaCyc
DB03989 DrugBank
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Registry Numbers Types Sources
1907363 Reaxys Registry Number Reaxys
1907363 Beilstein Registry Number Beilstein
2595-97-3 CAS Registry Number KEGG COMPOUND
972272 Gmelin Registry Number Gmelin
Citations Waiting for Citations Types Sources
21717189 PubMed citation Europe PMC
21889400 PubMed citation Europe PMC
23064522 PubMed citation Europe PMC
23541813 PubMed citation Europe PMC
24014866 PubMed citation Europe PMC
4736394 PubMed citation Europe PMC
Last Modified
16 July 2015