CHEBI:15903 - β-D-glucose

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
ChEBI Name β-D-glucose
ChEBI ID CHEBI:15903
ChEBI ASCII Name beta-D-glucose
Definition D-Glucopyranose with β configuration at the anomeric centre.
Stars This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs CHEBI:41140, CHEBI:12373, CHEBI:22795, CHEBI:10397
Supplier Information
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Formula C6H12O6
Net Charge 0
Average Mass 180.15588
Monoisotopic Mass 180.063
InChI InChI=1S/C6H12O6/c7-1-2-3(8)4(9)5(10)6(11)12-2/h2-11H,1H2/t2-,3-,4+,5-,6-/m1/s1
InChIKey WQZGKKKJIJFFOK-VFUOTHLCSA-N
SMILES OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O
Metabolite of Species Details
Mus musculus (NCBI:10090) Source: BioModels - MODEL1507180067 See: PubMed
Daphnia magna (NCBI:35525) See: Mixtures of similarly acting compounds in Daphnia magna: From gene to metabolite and beyondTine Vandenbrouck, Oliver A.H. Jones, Nathalie Dom, Julian L. Griffin, Wim De CoenEnvironment International 36 (2010) 254-268
Roles Classification
Biological Role(s): epitope
The biological role played by a material entity when bound by a receptor of the adaptive immune system. Specific site on an antigen to which an antibody binds.
mouse metabolite
Any mammalian metabolite produced during a metabolic reaction in a mouse (Mus musculus).
(via D-glucopyranose )
Escherichia coli metabolite
Any bacterial metabolite produced during a metabolic reaction in Escherichia coli.
(via D-glucopyranose )
Saccharomyces cerevisiae metabolite
Any fungal metabolite produced during a metabolic reaction in Baker's yeast (Saccharomyces cerevisiae ).
(via D-glucopyranose )
human metabolite
Any mammalian metabolite produced during a metabolic reaction in humans (Homo sapiens).
(via D-glucopyranose )
fundamental metabolite
Any metabolite produced by all living cells.
(via glucose )
View more via ChEBI Ontology
ChEBI Ontology
Outgoing β-D-glucose (CHEBI:15903) has role epitope (CHEBI:53000)
β-D-glucose (CHEBI:15903) has role mouse metabolite (CHEBI:75771)
β-D-glucose (CHEBI:15903) is a D-glucopyranose (CHEBI:4167)
β-D-glucose (CHEBI:15903) is enantiomer of β-L-glucose (CHEBI:37631)
Incoming β-D-glucosamine (CHEBI:28393) has functional parent β-D-glucose (CHEBI:15903)
β-D-glucose 1-phosphate (CHEBI:16218) has functional parent β-D-glucose (CHEBI:15903)
β-D-glucose 6-phosphate (CHEBI:17719) has functional parent β-D-glucose (CHEBI:15903)
β-D-glucoside (CHEBI:22798) has functional parent β-D-glucose (CHEBI:15903)
β-D-glucosyl crocetin (CHEBI:62765) has functional parent β-D-glucose (CHEBI:15903)
(+)-abscisic acid β-D-glucopyranosyl ester (CHEBI:22151) has functional parent β-D-glucose (CHEBI:15903)
(S)-2-trans-abscisic acid β-D-glucopyranosyl ester (CHEBI:62437) has functional parent β-D-glucose (CHEBI:15903)
1,2,6-tris-O-galloyl-β-D-glucose (CHEBI:27395) has functional parent β-D-glucose (CHEBI:15903)
1,2-di-O-sinapoyl-β-D-glucose (CHEBI:27993) has functional parent β-D-glucose (CHEBI:15903)
1-O-(indol-3-ylacetyl)-β-D-glucose (CHEBI:17990) has functional parent β-D-glucose (CHEBI:15903)
1-O-trans-cinnamoyl-β-D-glucopyranose (CHEBI:16279) has functional parent β-D-glucose (CHEBI:15903)
1-O-sinapoyl-β-D-glucose (CHEBI:16546) has functional parent β-D-glucose (CHEBI:15903)
1-thio-β-D-glucopyranose (CHEBI:42896) has functional parent β-D-glucose (CHEBI:15903)
2-deoxy-2-fluoro-β-D-glucose (CHEBI:49128) has functional parent β-D-glucose (CHEBI:15903)
3,6-di-O-methyl-β-D-glucose (CHEBI:59473) has functional parent β-D-glucose (CHEBI:15903)
3-O-(cis-4-coumaroyl)-β-D-glucopyranose (CHEBI:76093) has functional parent β-D-glucose (CHEBI:15903)
3-O-(trans-4-coumaroyl)-β-D-glucopyranose (CHEBI:76094) has functional parent β-D-glucose (CHEBI:15903)
4,6-(1'-carboxyethylidene)-3-O-methyl-β-D-glucopyranose (CHEBI:59362) has functional parent β-D-glucose (CHEBI:15903)
6-O-(trans-4-coumaroyl)-β-D-glucopyranose (CHEBI:76089) has functional parent β-D-glucose (CHEBI:15903)
6-O-(indole-3-acetyl)-β-D-glucose (CHEBI:20685) has functional parent β-D-glucose (CHEBI:15903)
7-(β-D-glucosyloxy)indole-3-acetic acid (CHEBI:20774) has functional parent β-D-glucose (CHEBI:15903)
abacopterin B (CHEBI:65355) has functional parent β-D-glucose (CHEBI:15903)
abacopterin C (CHEBI:65356) has functional parent β-D-glucose (CHEBI:15903)
abacopterin D (CHEBI:65357) has functional parent β-D-glucose (CHEBI:15903)
bis(β-D-glucosyl) crocetin (CHEBI:62768) has functional parent β-D-glucose (CHEBI:15903)
FR207944 (CHEBI:65913) has functional parent β-D-glucose (CHEBI:15903)
galloyl β-D-glucose (CHEBI:24183) has functional parent β-D-glucose (CHEBI:15903)
isorhamnetin 3-O-β-D-glucopyranoside (CHEBI:75750) has functional parent β-D-glucose (CHEBI:15903)
isorhamnetin 7-O-β-D-glucopyranoside (CHEBI:75752) has functional parent β-D-glucose (CHEBI:15903)
kaempferol 5-O-β-D-glucopyranoside (CHEBI:75802) has functional parent β-D-glucose (CHEBI:15903)
kaempferol 7-O-β-D-glucopyranoside (CHEBI:75790) has functional parent β-D-glucose (CHEBI:15903)
miserotoxin (CHEBI:6951) has functional parent β-D-glucose (CHEBI:15903)
myricetin 3'-O-β-D-glucopyranoside (CHEBI:75816) has functional parent β-D-glucose (CHEBI:15903)
myricetin 3-O-β-D-glucopyranoside (CHEBI:75813) has functional parent β-D-glucose (CHEBI:15903)
myricetin 7-O-β-D-glucopyranoside (CHEBI:75820) has functional parent β-D-glucose (CHEBI:15903)
quercetin 3-O-β-D-glucopyranoside (CHEBI:68352) has functional parent β-D-glucose (CHEBI:15903)
quercetin 4ʼ-O-β-D-glucopyranoside (CHEBI:75839) has functional parent β-D-glucose (CHEBI:15903)
staphyloxanthin (CHEBI:71690) has functional parent β-D-glucose (CHEBI:15903)
tryptophan N-glucoside (CHEBI:76121) has functional parent β-D-glucose (CHEBI:15903)
β-L-glucose (CHEBI:37631) is enantiomer of β-D-glucose (CHEBI:15903)
β-D-glucosyl group (CHEBI:30697) is substituent group from β-D-glucose (CHEBI:15903)
IUPAC Name
β-D-glucopyranose
Synonyms Sources
beta-D-Glucose KEGG COMPOUND
BETA-D-GLUCOSE PDBeChem
β-D-glucose UniProt
Database Links Databases
845 DrugCentral
BGC PDBeChem
C00221 KEGG COMPOUND
DB02379 DrugBank
View more database links
Registry Numbers Types Sources
1281607 Reaxys Registry Number Reaxys
1281607 Beilstein Registry Number Beilstein
492-61-5 CAS Registry Number ChemIDplus
492-61-5 CAS Registry Number NIST Chemistry WebBook
648637 Gmelin Registry Number Gmelin
Citations Waiting for Citations Types Sources
19443021 PubMed citation Europe PMC
25568069 PubMed citation Europe PMC
Last Modified
22 February 2017