CHEBI:17167 - (R)-lactaldehyde

ChEBI IDCHEBI:17167
ChEBI Name(R)-lactaldehyde
Stars
ASCII Name(R)-lactaldehyde
DefinitionThe (R)-stereoisomer of lactaldehyde.
Secondary ChEBI IDsCHEBI:340, CHEBI:11000, CHEBI:18683
Last Modified28 May 2024
DownloadsMolfile
FormulaC3H6O2
Net Charge0
Average Mass74.079
Monoisotopic Mass74.03678
SMILES[H]C(=O)[C@@H](C)O
InChIInChI=1S/C3H6O2/c1-3(5)2-4/h2-3,5H,1H3/t3-/m1/s1
InChIKeyBSABBBMNWQWLLU-GSVOUGTGSA-N
Species of MetaboliteComponentSourceComments
Homo sapiens (ncbitaxon:9606) - DOI (10.1038/nbt.2488)
Escherichia coli (ncbitaxon:562) - PubMed (21988831)
Mus musculus (ncbitaxon:10090) - PubMed (19425150) Source: BioModels - MODEL1507180067
Roles Classification
Biological Roles:
mouse metabolite  Any mammalian metabolite produced during a metabolic reaction in a mouse (Mus musculus).
human metabolite  Any mammalian metabolite produced during a metabolic reaction in humans (Homo sapiens).
Escherichia coli metabolite  Any bacterial metabolite produced during a metabolic reaction in Escherichia coli.
mouse metabolite  Any mammalian metabolite produced during a metabolic reaction in a mouse (Mus musculus).
ChEBI Ontology
Outgoing Relation(s)
(R)-lactaldehyde (CHEBI:17167) has role Escherichia coli metabolite (CHEBI:76971)
(R)-lactaldehyde (CHEBI:17167) has role human metabolite (CHEBI:77746)
(R)-lactaldehyde (CHEBI:17167) has role mouse metabolite (CHEBI:75771)
(R)-lactaldehyde (CHEBI:17167) is a lactaldehyde (CHEBI:18419)
(R)-lactaldehyde (CHEBI:17167) is enantiomer of (S)-lactaldehyde (CHEBI:18041)
Incoming Relation(s)
(S)-lactaldehyde (CHEBI:18041) is enantiomer of (R)-lactaldehyde (CHEBI:17167)
IUPAC Name 
(2R)-2-hydroxypropanal
Synonyms  Source
(R)-LactaldehydeKEGG COMPOUND
D-LactaldehydeKEGG COMPOUND
D-2-HydroxypropionaldehydeKEGG COMPOUND
(R)-lactaldehydeChEBI
D-2-hydroxypropionaldehydeChEBI
D-lactaldehydeChEBI
UniProt Name  Source
(R)-lactaldehydeUniProt
Manual XrefsDatabases
C00937KEGG COMPOUND
C00937KEGG COMPOUND
Registry NumbersSources
Reaxys:1719826Reaxys
Citations