CHEBI:17925 - α-D-glucose

ChEBI IDCHEBI:17925
ChEBI Nameα-D-glucose
Stars
ASCII Namealpha-D-glucose
DefinitionD-Glucopyranose having α-configuration at the anomeric centre.
Secondary ChEBI IDsCHEBI:10242, CHEBI:12318, CHEBI:22386, CHEBI:40557, CHEBI:42802
Last Modified18 April 2024
DownloadsMolfile
FormulaC6H12O6
Net Charge0
Average Mass180.156
Monoisotopic Mass180.06339
SMILESOC[C@H]1O[C@H](O)[C@H](O)[C@@H](O)[C@@H]1O
WURCSWURCS=2.0/1,1,0/[a2122h-1a_1-5]/1/
InChIInChI=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
InChIKeyWQZGKKKJIJFFOK-DVKNGEFBSA-N
Species of MetaboliteComponentSourceComments
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).
Escherichia coli metabolite  Any bacterial metabolite produced during a metabolic reaction in Escherichia coli.
Saccharomyces cerevisiae metabolite  Any fungal metabolite produced during a metabolic reaction in Baker's yeast (Saccharomyces cerevisiae ).
antiviral agent  A substance that destroys or inhibits replication of viruses.
mouse metabolite  Any mammalian metabolite produced during a metabolic reaction in a mouse (Mus musculus).
antimicrobial agent  A substance that kills or slows the growth of microorganisms, including bacteria, viruses, fungi and protozoans.
anti-obesity agent  Any substance which is used to reduce or control weight.
anti-HIV agent  An antiviral agent that destroys or inhibits the replication of the human immunodeficiency virus.
human metabolite  Any mammalian metabolite produced during a metabolic reaction in humans (Homo sapiens).
antibacterial agent  A substance (or active part thereof) that kills or slows the growth of bacteria.
antifungal agent  An antimicrobial agent that destroys fungi by suppressing their ability to grow or reproduce.
immunosuppressive agent  An agent that suppresses immune function by one of several mechanisms of action. Classical cytotoxic immunosuppressants act by inhibiting DNA synthesis. Others may act through activation of T-cells or by inhibiting the activation of helper cells. In addition, an immunosuppressive agent is a role played by a compound which is exhibited by a capability to diminish the extent and/or voracity of an immune response.
analgesic  An agent capable of relieving pain without the loss of consciousness or without producing anaesthesia. In addition, analgesic is a role played by a compound which is exhibited by a capability to cause a reduction of pain symptoms.
fundamental metabolite  Any metabolite produced by all living cells.
fundamental metabolite  Any metabolite produced by all living cells.
Applications:
hypoglycemic agent  A drug which lowers the blood glucose level.
anticonvulsant  A drug used to prevent seizures or reduce their severity.
neuroprotective agent  Any compound that can be used for the treatment of neurodegenerative disorders.
renoprotective agent  Any compound that is able to prevent damage to the kidneys.
antineoplastic agent  A substance that inhibits or prevents the proliferation of neoplasms.
gastrointestinal drug  A drug used for its effects on the gastrointestinal system, e.g. controlling gastric acidity, regulating gastrointestinal motility and water flow, and improving digestion.
antipsychotic agent  Antipsychotic drugs are agents that control agitated psychotic behaviour, alleviate acute psychotic states, reduce psychotic symptoms, and exert a quieting effect.
antihypertensive agent  Any drug used in the treatment of acute or chronic vascular hypertension regardless of pharmacological mechanism.
hyperglycemic agent  A drug which increases the blood glucose level.
antiinfective agent  A substance used in the prophylaxis or therapy of infectious diseases.
anti-inflammatory agent  Any compound that has anti-inflammatory effects.
anticholesteremic drug  A substance used to lower plasma cholesterol levels.
immunosuppressive agent  An agent that suppresses immune function by one of several mechanisms of action. Classical cytotoxic immunosuppressants act by inhibiting DNA synthesis. Others may act through activation of T-cells or by inhibiting the activation of helper cells. In addition, an immunosuppressive agent is a role played by a compound which is exhibited by a capability to diminish the extent and/or voracity of an immune response.
cardiovascular drug  A drug that affects the rate or intensity of cardiac contraction, blood vessel diameter or blood volume.
analgesic  An agent capable of relieving pain without the loss of consciousness or without producing anaesthesia. In addition, analgesic is a role played by a compound which is exhibited by a capability to cause a reduction of pain symptoms.
ChEBI Ontology
Outgoing Relation(s)
α-D-glucose (CHEBI:17925) has role mouse metabolite (CHEBI:75771)
α-D-glucose (CHEBI:17925) is a D-glucopyranose (CHEBI:4167)
α-D-glucose (CHEBI:17925) is enantiomer of α-L-glucose (CHEBI:37630)
Incoming Relation(s)
(2ξ)-6-O-α-D-glucopyranosyl-D-arabino-hexitol (CHEBI:192266) has functional parent α-D-glucose (CHEBI:17925)
1-O-(α-D-glucopyranosyl)-N-icosa-11,14-dienoylphytosphingosine (CHEBI:63000) has functional parent α-D-glucose (CHEBI:17925)
1-O-(α-D-glucopyranosyl)-N-tetracosanylphytosphingosine (CHEBI:63012) has functional parent α-D-glucose (CHEBI:17925)
2,6-diamino-2,3,6-trideoxy-α-D-glucose (CHEBI:72336) has functional parent α-D-glucose (CHEBI:17925)
2,6-diamino-2,6-dideoxy-α-D-glucose (CHEBI:41105) has functional parent α-D-glucose (CHEBI:17925)
2'-N-acetylparomamine (CHEBI:65018) has functional parent α-D-glucose (CHEBI:17925)
4-O-α-D-glucopyranosylmoranoline (CHEBI:70736) has functional parent α-D-glucose (CHEBI:17925)
6-O-(trans-4-coumaroyl)-α-D-glucopyranose (CHEBI:76092) has functional parent α-D-glucose (CHEBI:17925)
galloyl α-D-glucose (CHEBI:49215) has functional parent α-D-glucose (CHEBI:17925)
maltitol (CHEBI:68428) has functional parent α-D-glucose (CHEBI:17925)
myricetin 3-O-α-D-glucopyranoside (CHEBI:75823) has functional parent α-D-glucose (CHEBI:17925)
myricetin 3'-O-α-D-glucopyranoside (CHEBI:75826) has functional parent α-D-glucose (CHEBI:17925)
myricetin 4'-O-α-D-glucopyranoside (CHEBI:75827) has functional parent α-D-glucose (CHEBI:17925)
paromamine (CHEBI:7933) has functional parent α-D-glucose (CHEBI:17925)
α-D-Galp-(1→2)-α-D-Glcp (CHEBI:155057) has functional parent α-D-glucose (CHEBI:17925)
α-D-Galp-(1→4)-α-D-Glcp (CHEBI:151923) has functional parent α-D-glucose (CHEBI:17925)
α-D-Galp-(1→6)-α-D-Glcp (CHEBI:151217) has functional parent α-D-glucose (CHEBI:17925)
α-D-Glcp-(1→2)-D-Galf (CHEBI:155379) has functional parent α-D-glucose (CHEBI:17925)
α-D-Glcp-(1→2)-D-Galp (CHEBI:154973) has functional parent α-D-glucose (CHEBI:17925)
α-D-Glcp-(1→2)-L-Fucp (CHEBI:154730) has functional parent α-D-glucose (CHEBI:17925)
α-D-Glcp-(1→2)-β-D-Galf (CHEBI:156705) has functional parent α-D-glucose (CHEBI:17925)
α-D-Glcp-(1→3)-D-Arap (CHEBI:148938) has functional parent α-D-glucose (CHEBI:17925)
α-D-Glcp-(1→3)-α-D-GalpNAc (CHEBI:148178) has functional parent α-D-glucose (CHEBI:17925)
α-D-Glcp-(1→4)-D-Galp (CHEBI:150544) has functional parent α-D-glucose (CHEBI:17925)
α-D-Glcp-(1→4)-D-GlcpNAc (CHEBI:152766) has functional parent α-D-glucose (CHEBI:17925)
α-D-Glcp-(1→4)-D-Xylp (CHEBI:153794) has functional parent α-D-glucose (CHEBI:17925)
α-D-Glcp-(1→4)-α-D-AllpNAc (CHEBI:151160) has functional parent α-D-glucose (CHEBI:17925)
α-D-Glcp-(1→4)-α-L-Fucp (CHEBI:155105) has functional parent α-D-glucose (CHEBI:17925)
α-D-Glcp-(1→4)-β-D-Galp (CHEBI:150654) has functional parent α-D-glucose (CHEBI:17925)
α-D-Glcp-(1→6)-D-GlcpNAc (CHEBI:151906) has functional parent α-D-glucose (CHEBI:17925)
α-D-Glcp-(1→6)-β-D-Galp (CHEBI:150328) has functional parent α-D-glucose (CHEBI:17925)
α-D-Glcp-(1↔1)-α-D-Xylp (CHEBI:156688) has functional parent α-D-glucose (CHEBI:17925)
α-D-GlcpNAc-(1→1)-α-D-Glcp (CHEBI:152022) has functional parent α-D-glucose (CHEBI:17925)
α-D-glucosamine (CHEBI:44678) has functional parent α-D-glucose (CHEBI:17925)
α-D-glucose 1-phosphate (CHEBI:29042) has functional parent α-D-glucose (CHEBI:17925)
α-D-glucose 1,6-bisphosphate (CHEBI:18148) has functional parent α-D-glucose (CHEBI:17925)
α-D-glucose 3-phosphate (CHEBI:27818) has functional parent α-D-glucose (CHEBI:17925)
α-D-glucose 6-phosphate (CHEBI:17665) has functional parent α-D-glucose (CHEBI:17925)
α-D-glucoside (CHEBI:22390) has functional parent α-D-glucose (CHEBI:17925)
α-D-kanosamine (CHEBI:72343) has functional parent α-D-glucose (CHEBI:17925)
α-L-Fucp-(1→2)-α-D-Glcp (CHEBI:155103) has functional parent α-D-glucose (CHEBI:17925)
α-L-Fucp-(1→3)-α-D-Glcp (CHEBI:152009) has functional parent α-D-glucose (CHEBI:17925)
α-L-Fucp-(1→4)-α-D-Glcp (CHEBI:146668) has functional parent α-D-glucose (CHEBI:17925)
α-L-Fucp-(1→6)-α-D-Glcp (CHEBI:154224) has functional parent α-D-glucose (CHEBI:17925)
β-D-Galp-(1→2)-α-D-Glcp (CHEBI:153828) has functional parent α-D-glucose (CHEBI:17925)
β-D-Galp-(1→3)-α-D-Glcp (CHEBI:147758) has functional parent α-D-glucose (CHEBI:17925)
β-D-GlcpNAc-(1→3)-α-D-Glcp (CHEBI:150053) has functional parent α-D-glucose (CHEBI:17925)
β-D-Xylp-(1→6)-α-D-Glcp (CHEBI:156784) has functional parent α-D-glucose (CHEBI:17925)
β-L-Fucp-(1→2)-α-D-Glcp (CHEBI:151754) has functional parent α-D-glucose (CHEBI:17925)
β-L-Fucp-(1→3)-α-D-Glcp (CHEBI:152771) has functional parent α-D-glucose (CHEBI:17925)
β-L-Fucp-(1→4)-α-D-Glcp (CHEBI:152122) has functional parent α-D-glucose (CHEBI:17925)
β-L-Fucp-(1→6)-α-D-Glcp (CHEBI:154924) has functional parent α-D-glucose (CHEBI:17925)
2-deoxy-2-fluoro-α-D-glucose (CHEBI:49132) has parent hydride α-D-glucose (CHEBI:17925)
α-L-glucose (CHEBI:37630) is enantiomer of α-D-glucose (CHEBI:17925)
α-D-glucosyl group (CHEBI:30684) is substituent group from α-D-glucose (CHEBI:17925)
IUPAC Name 
α-D-glucopyranose
Synonyms  Source
alpha-D-GlucoseKEGG COMPOUND
ALPHA-D-GLUCOSEPDBeChem
α-dextroseChemIDplus
α-D-GlcChEBI
UniProt Name  Source
α-D-glucoseUniProt
Manual XrefsDatabases
C00001122KNApSAcK
C00267KEGG COMPOUND
G58161NSGlyTouCan
G58161NSGlyGen
GLCPDBeChem
Registry NumbersSources
Beilstein:1281608Beilstein
Gmelin:329225Gmelin
Beilstein:5730158Beilstein
CAS:492-62-6NIST Chemistry WebBook
CAS:492-62-6ChemIDplus
CAS:492-62-6KEGG COMPOUND
Citations