CHEBI:37675 - aldehydo-D-mannose

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ChEBI Name aldehydo-D-mannose
ChEBI ID CHEBI:37675
ChEBI ASCII Name aldehydo-D-mannose
Definition The D-enantiomer of aldehydo-mannose.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
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Formula C6H12O6
Net Charge 0
Average Mass 180.15588
Monoisotopic Mass 180.06339
InChI InChI=1S/C6H12O6/c7-1-3(9)5(11)6(12)4(10)2-8/h1,3-6,8-12H,2H2/t3-,4-,5-,6-/m1/s1
InChIKey GZCGUPFRVQAUEE-KVTDHHQDSA-N
SMILES [H]C(=O)[C@@H](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 D-mannose )
fundamental metabolite
Any metabolite produced by all living cells.
(via mannose )
View more via ChEBI Ontology
ChEBI Ontology
Outgoing aldehydo-D-mannose (CHEBI:37675) is a aldehydo-mannose (CHEBI:37682)
aldehydo-D-mannose (CHEBI:37675) is a D-mannose (CHEBI:16024)
aldehydo-D-mannose (CHEBI:37675) is enantiomer of aldehydo-L-mannose (CHEBI:37681)
Incoming aldehydo-L-mannose (CHEBI:37681) is enantiomer of aldehydo-D-mannose (CHEBI:37675)
IUPAC Names
aldehydo-D-manno-hexose
aldehydo-D-mannose
Synonym Source
(2S,3S,4R,5R)-2,3,4,5,6-pentahydroxyhexanal IUPAC
Manual Xref Database
G95531HX GlyTouCan
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Registry Numbers Types Sources
1564373 Beilstein Registry Number Beilstein
1564373 Reaxys Registry Number Reaxys
328813 Gmelin Registry Number Gmelin
Last Modified
10 June 2014