EMBL-EBI | Chemical Biology | ChEBI
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| Formula | C11H16O2 |
| Net Charge | 0 |
| Average Mass | 180.247 |
| Monoisotopic Mass | 180.11503 |
| SMILES | CCCCCc1cc(O)cc(O)c1 |
| InChI | InChI=1S/C11H16O2/c1-2-3-4-5-9-6-10(12)8-11(13)7-9/h6-8,12-13H,2-5H2,1H3 |
| InChIKey | IRMPFYJSHJGOPE-UHFFFAOYSA-N |
| Wikipedia |
|---|
| Roles Classification |
|---|
| Biological Role: | lichen metabolite Any metabolite that is produced during a metabolite reaction in lichens (composite organisms consisting of a fungus and a photosynthetic partner co-existing in a symbiotic relationship). |
| ChEBI Ontology |
|---|
| Outgoing Relation(s) |
| olivetol (CHEBI:66960) has role lichen metabolite (CHEBI:78361) |
| olivetol (CHEBI:66960) is a resorcinols (CHEBI:33572) |
| Incoming Relation(s) |
| olivetolic acid (CHEBI:66955) has functional parent olivetol (CHEBI:66960) |
| IUPAC Name |
|---|
| 5-pentylbenzene-1,3-diol |
| Synonyms | Source |
|---|---|
| 3,5-dihydroxyamylbenzene | ChemIDplus |
| 5-n-amylresorcinol | ChemIDplus |
| 5-pentyl-1,3-benzenediol | ChemIDplus |
| 5-n-pentylresorcinol | ChemIDplus |
| 5-pentylresorcinol | ChemIDplus |
| 5-(1-pentyl)resorcinol | ChEBI |
| UniProt Name | Source |
|---|---|
| olivetol | UniProt |
| Citations |
|---|