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CHEBI:4093 - D-allopyranose

ChEBI IDCHEBI:4093
ChEBI NameD-allopyranose
Stars
ASCII NameD-allopyranose
DefinitionThe D-enantiomer of allopyranose.
Last Modified10 March 2021
DownloadsMolfile
FormulaC6H12O6
Net Charge0
Average Mass180.156
Monoisotopic Mass180.06339
SMILESOC[C@H]1OC(O)[C@H](O)[C@H](O)[C@@H]1O
WURCSWURCS=2.0/1,1,0/[a2222h-1x_1-5]/1/
InChIInChI=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
InChIKeyWQZGKKKJIJFFOK-IVMDWMLBSA-N
Roles Classification
Chemical Role:
antioxidant  A substance that opposes oxidation or inhibits reactions brought about by dioxygen or peroxides.
Biological Role:
plant metabolite  Any eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms.
ChEBI Ontology
Outgoing Relation(s)
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 Relation(s)
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-AlloseKEGG COMPOUND
Manual XrefsDatabases
C01487KEGG COMPOUND
DB03989DrugBank
D-allopyranoseMetaCyc
G74407MXGlyTouCan
Registry NumbersSources
Gmelin:972272Gmelin
Reaxys:1907363Reaxys
CAS:2595-97-3KEGG COMPOUND
Citations