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D-glyceraldehyde (CHEBI:17378)

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ChEBI Name D-glyceraldehyde
ChEBI ID CHEBI:17378
ChEBI ASCII Name D-glyceraldehyde
Definition The D-enantiomer of glyceraldehyde.
Stars This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs CHEBI:21025, CHEBI:4186, CHEBI:12982, CHEBI:39973
Supplier Information
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Formula Source
C3H6O3 KEGG COMPOUND
Net Charge 0
Average Mass 90.07794
InChI
InChI=1S/C3H6O3/c4-1-3(6)2-5/h1,3,5-6H,2H2/t3-/m0/s1
InChIKey
MNQZXJOMYWMBOU-VKHMYHEASA-N
SMILES
[H]C(=O)[C@H](O)CO
Metabolite of Species Source
Isolated from Homo sapiens (NCBI:9606) DOI
Roles Classification
Biological Role(s): human metabolite
Any mammalian metabolite produced during a metabolic reaction in humans (Homo sapiens).
fundamental metabolite
Any metabolite produced by all living cells.
(via glyceraldehyde )
View more on the ChEBI Ontology
ChEBI Ontology
Outgoing D-glyceraldehyde (CHEBI:17378) has role human metabolite (CHEBI:77746)
D-glyceraldehyde (CHEBI:17378) is a glyceraldehyde (CHEBI:5445)
D-glyceraldehyde (CHEBI:17378) is enantiomer of L-glyceraldehyde (CHEBI:27975)
Incoming D-glyceraldehyde 3-phosphate (CHEBI:29052) has functional parent D-glyceraldehyde (CHEBI:17378)
L-glyceraldehyde (CHEBI:27975) is enantiomer of D-glyceraldehyde (CHEBI:17378)
IUPAC Name
(2R)-2,3-dihydroxypropanal
Synonyms Sources
D-(+)-glyceraldehyde ChemIDplus
D-2,3-dihydroxypropanal ChEBI
D-2,3-dihydroxypropionaldehyde ChEBI
D-aldotriose ChEBI
D-Glyceraldehyde KEGG COMPOUND
D-glycerose ChEBI
GLYCERALDEHYDE PDBeChem
Database Links Databases
3GR PDBeChem
C00577 KEGG COMPOUND
ECMDB01051 ECMDB
YMDB00575 YMDB
View more database links
Registry Numbers Types Sources
1720474 Reaxys Registry Number Reaxys
1720474 Beilstein Registry Number Beilstein
367-47-5 CAS Registry Number KEGG COMPOUND
453-17-8 CAS Registry Number KEGG COMPOUND
453-17-8 CAS Registry Number ChemIDplus
453-17-8 CAS Registry Number NIST Chemistry WebBook
5726453 Beilstein Registry Number Beilstein
Last Modified
21 July 2014

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