CHEBI:40886 - β-L-arabinopyranose

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
ChEBI Name β-L-arabinopyranose
ChEBI ID CHEBI:40886
ChEBI ASCII Name beta-L-arabinopyranose
Definition A L-arabinopyranose with a β-configuration at the anomeric position.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
Download Molfile XML SDF
more structures >>
Formula C5H10O5
Net Charge 0
Average Mass 150.12990
Monoisotopic Mass 150.05282
InChI InChI=1S/C5H10O5/c6-2-1-10-5(9)4(8)3(2)7/h2-9H,1H2/t2-,3-,4+,5-/m0/s1
InChIKey SRBFZHDQGSBBOR-KLVWXMOXSA-N
SMILES O[C@H]1CO[C@H](O)[C@H](O)[C@H]1O
Roles Classification
Biological Role(s): Escherichia coli metabolite
Any bacterial metabolite produced during a metabolic reaction in Escherichia coli.
(via L-arabinopyranose )
mouse metabolite
Any mammalian metabolite produced during a metabolic reaction in a mouse (Mus musculus).
(via L-arabinopyranose )
Saccharomyces cerevisiae metabolite
Any fungal metabolite produced during a metabolic reaction in Baker's yeast (Saccharomyces cerevisiae ).
(via L-arabinose )
human metabolite
Any mammalian metabolite produced during a metabolic reaction in humans (Homo sapiens).
(via L-arabinose )
algal metabolite
Any eukaryotic metabolite produced during a metabolic reaction in algae including unicellular organisms like chlorella and diatoms to multicellular organisms like giant kelps and brown algae.
(via L-arabinose )
fundamental metabolite
Any metabolite produced by all living cells.
(via arabinose )
View more via ChEBI Ontology
ChEBI Ontology
Outgoing β-L-arabinopyranose (CHEBI:40886) is a L-arabinopyranose (CHEBI:17535)
β-L-arabinopyranose (CHEBI:40886) is enantiomer of β-D-arabinopyranose (CHEBI:46996)
Incoming 4-amino-4-deoxy-β-L-arabinopyranose (CHEBI:46993) has functional parent β-L-arabinopyranose (CHEBI:40886)
β-D-arabinopyranose (CHEBI:46996) is enantiomer of β-L-arabinopyranose (CHEBI:40886)
IUPAC Name
β-L-arabinopyranose
Synonyms Sources
β-L-arabinopyranose UniProt
BETA-L-ARABINOSE PDBeChem
WURCS=2.0/1,1,0/[a211h-1b_1-5]/1/ GlyTouCan
Manual Xrefs Databases
ARB PDBeChem
C00001113 KNApSAcK
C02479 KEGG COMPOUND
C11476 KEGG COMPOUND
G86614XL GlyTouCan
G86614XL GlyGen
View more database links
Registry Numbers Types Sources
1722190 Beilstein Registry Number Beilstein
1732761 Gmelin Registry Number Gmelin
5328-37-0 CAS Registry Number KEGG COMPOUND
Last Modified
27 January 2022