EMBL-EBI | Chemical Biology | ChEBI
Example searches: iron*, InChI=1S/CH4O/c1-2/h2H,1H3, caffeine | Advanced Search
| Formula | C20H32O3 |
| Net Charge | 0 |
| Average Mass | 320.473 |
| Monoisotopic Mass | 320.23514 |
| SMILES | CCCCC/C=C\C/C=C\C(O)/C=C\C/C=C\CCCC(=O)O |
| InChI | InChI=1S/C20H32O3/c1-2-3-4-5-6-7-10-13-16-19(21)17-14-11-8-9-12-15-18-20(22)23/h6-9,13-14,16-17,19,21H,2-5,10-12,15,18H2,1H3,(H,22,23)/b7-6-,9-8-,16-13-,17-14- |
| InChIKey | ZUOCVLADVGGUGH-OVMCANAPSA-N |
| Species of Metabolite | Component | Source | Comments |
|---|---|---|---|
| Rattus norvegicus (ncbitaxon:10116) | - | PubMed (9435160) | |
| Homo Sapiens (ncbitaxon:9606) | - | PubMed (9435160) |
| Roles Classification |
|---|
| Chemical Role: | Bronsted acid A molecular entity capable of donating a hydron to an acceptor (Brønsted base). |
| Biological Roles: | rat metabolite Any mammalian metabolite produced during a metabolic reaction in rat (Rattus norvegicus). human xenobiotic metabolite Any human metabolite produced by metabolism of a xenobiotic compound in humans. |
| ChEBI Ontology |
|---|
| Outgoing Relation(s) |
| 10-HETE (CHEBI:134453) has functional parent arachidonic acid (CHEBI:15843) |
| 10-HETE (CHEBI:134453) has role human xenobiotic metabolite (CHEBI:76967) |
| 10-HETE (CHEBI:134453) has role rat metabolite (CHEBI:86264) |
| 10-HETE (CHEBI:134453) is a HETE (CHEBI:36275) |
| 10-HETE (CHEBI:134453) is a secondary allylic alcohol (CHEBI:134396) |
| 10-HETE (CHEBI:134453) is conjugate acid of 10-HETE(1−) (CHEBI:133345) |
| Incoming Relation(s) |
| 10-HETE(1−) (CHEBI:133345) is conjugate base of 10-HETE (CHEBI:134453) |
| IUPAC Name |
|---|
| (5Z,8Z,11Z,14Z)-10-hydroxyicosa-5,8,11,14-tetraenoic acid |
| Synonyms | Source |
|---|---|
| (5Z,8Z,11Z,14Z)-10-hydroxyicosatetraenoic acid | ChEBI |
| 10-hydroxy-(5Z,8Z,11Z,14Z)-eicosatetraenoate | ChEBI |
| 10-hydroxyarachidonic acid | ChEBI |
| 10-hydroxy-(5Z,8Z,11Z,14Z)-icosatetraenoate | ChEBI |
| Manual Xrefs | Databases |
|---|---|
| HMDB0012508 | HMDB |
| Registry Numbers | Sources |
|---|---|
| Reaxys:24193913 | Reaxys |
| Citations |
|---|