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| Formula | C6H12O6 |
| Net Charge | 0 |
| Average Mass | 180.156 |
| Monoisotopic Mass | 180.06339 |
| SMILES | OC[C@H]1O[C@H](O)[C@H](O)[C@@H](O)[C@@H]1O |
| WURCS | WURCS=2.0/1,1,0/[a2122h-1a_1-5]/1/ |
| 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-DVKNGEFBSA-N |
| Species of Metabolite | Component | Source | Comments |
|---|---|---|---|
| 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). 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. antiviral agent A substance that destroys or inhibits replication of viruses. 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. anti-HIV agent An antiviral agent that destroys or inhibits the replication of the human immunodeficiency virus. anti-obesity agent Any substance which is used to reduce or control weight. Escherichia coli metabolite Any bacterial metabolite produced during a metabolic reaction in Escherichia coli. 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. human metabolite Any mammalian metabolite produced during a metabolic reaction in humans (Homo sapiens). Saccharomyces cerevisiae metabolite Any fungal metabolite produced during a metabolic reaction in Baker's yeast (Saccharomyces cerevisiae ). 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: | hyperglycemic agent A drug which increases the blood glucose level. anticonvulsant A drug used to prevent seizures or reduce their severity. renoprotective agent Any compound that is able to prevent damage to the kidneys. antiinfective agent A substance used in the prophylaxis or therapy of infectious diseases. anticholesteremic drug A substance used to lower plasma cholesterol levels. cardiovascular drug A drug that affects the rate or intensity of cardiac contraction, blood vessel diameter or blood volume. 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. antipsychotic agent Antipsychotic drugs are agents that control agitated psychotic behaviour, alleviate acute psychotic states, reduce psychotic symptoms, and exert a quieting effect. neuroprotective agent Any compound that can be used for the treatment of neurodegenerative disorders. hypoglycemic agent A drug which lowers the blood glucose level. anti-inflammatory agent Any compound that has anti-inflammatory effects. antihypertensive agent Any drug used in the treatment of acute or chronic vascular hypertension regardless of pharmacological mechanism. 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. 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. antineoplastic agent A substance that inhibits or prevents the proliferation of neoplasms. |
| 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-Glucose | KEGG COMPOUND |
| ALPHA-D-GLUCOSE | PDBeChem |
| α-dextrose | ChemIDplus |
| α-D-Glc | ChEBI |
| UniProt Name | Source |
|---|---|
| α-D-glucose | UniProt |
| Citations |
|---|