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CHEBI:10295 - α-L-sorbopyranose

ChEBI IDCHEBI:10295
ChEBI Nameα-L-sorbopyranose
Stars
ASCII Namealpha-L-sorbopyranose
Last Modified23 October 2015
DownloadsMolfile
FormulaC6H12O6
Net Charge0
Average Mass180.156
Monoisotopic Mass180.06339
SMILESOC[C@@]1(O)OC[C@H](O)[C@@H](O)[C@@H]1O
WURCSWURCS=2.0/1,1,0/[ha121h-2a_2-6]/1/
InChIInChI=1S/C6H12O6/c7-2-6(11)5(10)4(9)3(8)1-12-6/h3-5,7-11H,1-2H2/t3-,4+,5-,6+/m0/s1
InChIKeyLKDRXBCSQODPBY-BGPJRJDNSA-N
Roles Classification
Biological Roles:
human metabolite  Any mammalian metabolite produced during a metabolic reaction in humans (Homo sapiens).
Saccharomyces cerevisiae metabolite  Any fungal metabolite produced during a metabolic reaction in Baker's yeast (Saccharomyces cerevisiae ).
plant metabolite  Any eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms.
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)
α-L-sorbopyranose (CHEBI:10295) is a L-sorbopyranose (CHEBI:48649)
α-L-sorbopyranose (CHEBI:10295) is enantiomer of α-D-sorbopyranose (CHEBI:48677)
Incoming Relation(s)
α-D-sorbopyranose (CHEBI:48677) is enantiomer of α-L-sorbopyranose (CHEBI:10295)
IUPAC Name 
α-L-sorbopyranose
Synonym  Source
alpha-L-SorbopyranoseKEGG COMPOUND
Manual XrefsDatabases
C08356KEGG COMPOUND
Registry NumbersSources
Gmelin:1007083Gmelin
Beilstein:1423190Beilstein
CAS:470-15-5KEGG COMPOUND