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 No supplier information found for this compound.
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Formula C6H12O6
Net Charge 0
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-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
Synonyms Sources
D-Allose KEGG COMPOUND
WURCS=2.0/1,1,0/[a2222h-1x_1-5]/1/ GlyTouCan
Manual Xrefs Databases
C01487 KEGG COMPOUND
D-allopyranose MetaCyc
DB03989 DrugBank
G74407MX GlyTouCan
View more database links
Registry Numbers Types Sources
1907363 Reaxys Registry Number Reaxys
2595-97-3 CAS Registry Number KEGG COMPOUND
972272 Gmelin Registry Number Gmelin
Citations Waiting for Citations
Last Modified
10 March 2021