CHEBI:42758 - aldehydo-D-glucose

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ChEBI Name aldehydo-D-glucose
ChEBI ID CHEBI:42758
ChEBI ASCII Name aldehydo-D-glucose
Definition The open chain form of D-glucose.
Stars This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs CHEBI:37625, CHEBI:42756
Supplier Information ChemicalBook:CB7399440, eMolecules:484241, ZINC000000084153
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Formaldehyde ( for-MAL-di-hide, US also fər-) (systematic name methanal) is an organic compound with the chemical formula CH2O and structure H−CHO, more precisely H2C=O. The compound is a pungent, colourless gas that polymerises spontaneously into paraformaldehyde. It is stored as aqueous solutions (formalin), which consists mainly of the hydrate CH2(OH)2. It is the simplest of the aldehydes (R−CHO). As a precursor to many other materials and chemical compounds, in 2006 the global production of formaldehyde was estimated at 12 million tons per year. It is mainly used in the production of industrial systematic names, e.g., for organic compound and chemical formulas. Formaldehyde also occurs naturally. It is derived from the degradation of polymerises, paraformaldehyde, and resins. particle boards act by converting N-methyl groups to formaldehyde. Formaldehyde is classified as a group 1 coating and can cause respiratory and skin serine upon exposure.
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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+/m0/s1
InChIKey GZCGUPFRVQAUEE-SLPGGIOYSA-N
SMILES [H]C(=O)[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO
Roles Classification
Biological Role(s): fundamental metabolite
Any metabolite produced by all living cells.
(via glucose )
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ChEBI Ontology
Outgoing aldehydo-D-glucose (CHEBI:42758) is a aldehydo-glucose (CHEBI:37663)
aldehydo-D-glucose (CHEBI:42758) is a D-glucose (CHEBI:17634)
aldehydo-D-glucose (CHEBI:42758) is enantiomer of aldehydo-L-glucose (CHEBI:37626)
Incoming 2-deoxy-2-fluoro-aldehydo-D-glucose (CHEBI:49135) has functional parent aldehydo-D-glucose (CHEBI:42758)
2-galloyl-D-glucose (CHEBI:136559) has functional parent aldehydo-D-glucose (CHEBI:42758)
3-O-methyl-D-glucose (CHEBI:73918) has functional parent aldehydo-D-glucose (CHEBI:42758)
6-O-methyl-D-glucose (CHEBI:20741) has functional parent aldehydo-D-glucose (CHEBI:42758)
aldehydo-D-glucosamine (CHEBI:20993) has functional parent aldehydo-D-glucose (CHEBI:42758)
aldehydo-D-glucuronic acid (CHEBI:47953) has functional parent aldehydo-D-glucose (CHEBI:42758)
aldehydo-D-kanosamine (CHEBI:31747) has functional parent aldehydo-D-glucose (CHEBI:42758)
aldehydo-L-glucose (CHEBI:37626) is enantiomer of aldehydo-D-glucose (CHEBI:42758)
IUPAC Names
aldehydo-D-gluco-hexose
aldehydo-D-glucose
Synonyms Sources
(2R,3S,4R,5R)-2,3,4,5,6-pentahydroxyhexanal IUPAC
aldehydo-D-glucose UniProt
D(+)-Glucose ChemIDplus
D-glucose PDBeChem
D-GLUCOSE IN LINEAR FORM PDBeChem
Dextrose ChemIDplus
Glucose ChemIDplus
WURCS=2.0/1,1,0/[o2122h]/1/ GlyTouCan
Manual Xrefs Databases
DB01914 DrugBank
G59743JO GlyTouCan
GLO PDBeChem
Glucose Wikipedia
View more database links
Registry Numbers Types Sources
1724615 Beilstein Registry Number Beilstein
306224 Gmelin Registry Number Gmelin
50-99-7 CAS Registry Number ChemIDplus
Last Modified
07 April 2021