EMBL-EBI | Chemical Biology Resources | ChEBI
Example searches: iron*, InChI=1S/CH4O/c1-2/h2H,1H3, caffeine | Advanced Search
| Formula | C6H6O |
| Net Charge | 0 |
| Average Mass | 94.113 |
| Monoisotopic Mass | 94.04186 |
| SMILES | Oc1ccccc1 |
| InChI | InChI=1S/C6H6O/c7-6-4-2-1-3-5-6/h1-5,7H |
| InChIKey | ISWSIDIOOBJBQZ-UHFFFAOYSA-N |
| Wikipedia |
|---|
| Species of Metabolite | Component | Source | Comments |
|---|---|---|---|
| Mus musculus (ncbitaxon:10090) | - | PubMed (19425150) | Source: BioModels - MODEL1507180067 |
| Roles Classification |
|---|
| Biological Roles: | anti-HSV agent An antiviral agent that destroys or inhibits the replication of the herpes simplex virus (also known as the human herpes virus). mouse metabolite Any mammalian metabolite produced during a metabolic reaction in a mouse (Mus musculus). disinfectant An antimicrobial agent that is applied to non-living objects to destroy harmful microorganisms or to inhibit their activity. human xenobiotic metabolite Any human metabolite produced by metabolism of a xenobiotic compound in humans. 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. antiviral agent A substance that destroys or inhibits replication of viruses. |
| Applications: | 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. antiseptic drug A substance used locally on humans and other animals to destroy harmful microorganisms or to inhibit their activity (cf. disinfectants, which destroy microorganisms found on non-living objects, and antibiotics, which can be transported through the lymphatic system to destroy bacteria within the body). |
| ChEBI Ontology |
|---|
| Outgoing Relation(s) |
| phenol (CHEBI:15882) has role analgesic (CHEBI:35480) |
| phenol (CHEBI:15882) has role anti-HSV agent (CHEBI:64952) |
| phenol (CHEBI:15882) has role antiseptic drug (CHEBI:48218) |
| phenol (CHEBI:15882) has role antiviral agent (CHEBI:22587) |
| phenol (CHEBI:15882) has role disinfectant (CHEBI:48219) |
| phenol (CHEBI:15882) has role human xenobiotic metabolite (CHEBI:76967) |
| phenol (CHEBI:15882) has role mouse metabolite (CHEBI:75771) |
| phenol (CHEBI:15882) is a phenols (CHEBI:33853) |
| phenol (CHEBI:15882) is conjugate acid of phenolate (CHEBI:50526) |
| Incoming Relation(s) |
| (2-hydroxyphenyl)acetic acid (CHEBI:28478) has functional parent phenol (CHEBI:15882) |
| p-nitrophenyl phenyl phosphonate (CHEBI:91050) has functional parent phenol (CHEBI:15882) |
| trans-anol (CHEBI:73343) has functional parent phenol (CHEBI:15882) |
| 2-hydroxybenzenesulfonic acid (CHEBI:71049) has functional parent phenol (CHEBI:15882) |
| 2-phenoxyethanol (CHEBI:64275) has functional parent phenol (CHEBI:15882) |
| 2,3,6-trinitrophenol (CHEBI:59049) has functional parent phenol (CHEBI:15882) |
| 2,6-di-tert-butyl-4-methylphenol (CHEBI:34247) has functional parent phenol (CHEBI:15882) |
| 3-hydroxybenzenesulfonic acid (CHEBI:71047) has functional parent phenol (CHEBI:15882) |
| 4-hydroxybenzenesulfonic acid (CHEBI:32354) has functional parent phenol (CHEBI:15882) |
| 5-sulfosalicylic acid (CHEBI:68555) has functional parent phenol (CHEBI:15882) |
| phenol O-(β-D-glucuronide) (CHEBI:64681) has functional parent phenol (CHEBI:15882) |
| phenoxenium (CHEBI:52245) has functional parent phenol (CHEBI:15882) |
| phenoxy radical (CHEBI:137811) has functional parent phenol (CHEBI:15882) |
| phenyl acetate (CHEBI:8082) has functional parent phenol (CHEBI:15882) |
| phenyl hydrogen phosphonate (CHEBI:91048) has functional parent phenol (CHEBI:15882) |
| phenyl hydrogen sulfate (CHEBI:27905) has functional parent phenol (CHEBI:15882) |
| picric acid (CHEBI:46149) has functional parent phenol (CHEBI:15882) |
| salicyl alcohol (CHEBI:16464) has functional parent phenol (CHEBI:15882) |
| triphenyl phosphate (CHEBI:35033) has functional parent phenol (CHEBI:15882) |
| phenolate (CHEBI:50526) is conjugate base of phenol (CHEBI:15882) |
| IUPAC Name |
|---|
| phenol |
| Synonyms | Source |
|---|---|
| 2-allphenol | ChEMBL |
| acide carbolique | NIST Chemistry WebBook |
| acide phénique | ChEBI |
| Benzenol | KEGG COMPOUND |
| carbolic acid | NIST Chemistry WebBook |
| Carbolsäure | ChEBI |
| Brand Names | Source |
|---|---|
| Chloraseptic | ChEMBL |
| S.b. ward | ChEMBL |
| UniProt Name | Source |
|---|---|
| phenol | UniProt |
| Citations |
|---|