CHEBI:6182 - aldehydo-L-arabinose

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
ChEBI Name aldehydo-L-arabinose
ChEBI ID CHEBI:6182
ChEBI ASCII Name aldehydo-L-arabinose
Definition The open-chain aldehyhde form of L-arabinose.
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/c6-1-3(8)5(10)4(9)2-7/h1,3-5,7-10H,2H2/t3-,4-,5+/m0/s1
InChIKey PYMYPHUHKUWMLA-VAYJURFESA-N
SMILES [H]C(=O)[C@H](O)[C@@H](O)[C@@H](O)CO
Roles Classification
Biological Role(s): 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 aldehydo-L-arabinose (CHEBI:6182) is a aldehydo-arabinose (CHEBI:46982)
aldehydo-L-arabinose (CHEBI:6182) is a L-arabinose (CHEBI:30849)
aldehydo-L-arabinose (CHEBI:6182) is enantiomer of aldehydo-D-arabinose (CHEBI:46983)
Incoming aldehydo-D-arabinose (CHEBI:46983) is enantiomer of aldehydo-L-arabinose (CHEBI:6182)
IUPAC Names
aldehydo-L-arabino-pentose
aldehydo-L-arabinose
Synonyms Sources
(2R,3S,4S)-2,3,4,5-tetrahydroxypentanal IUPAC
L-Arabinose KEGG COMPOUND
WURCS=2.0/1,1,0/[o211h]/1/ GlyTouCan
Manual Xrefs Databases
C11476 KEGG COMPOUND
G47203JO GlyGen
G47203JO GlyTouCan
View more database links
Registry Numbers Types Sources
1723085 Reaxys Registry Number Reaxys
1723085 Beilstein Registry Number Beilstein
5244985 Beilstein Registry Number Beilstein
5328-37-0 CAS Registry Number ChemIDplus
Citation Waiting for Citations Type Source
17336832 PubMed citation Europe PMC
Last Modified
07 April 2021