Oenanthotoxin
| Names | |
|---|---|
| Preferred IUPAC name (2E,8E,10E,14R)-Heptadeca-2,8,10-triene-4,6-diyne-1,14-diol | |
| Other names Enanthotoxin | |
| Identifiers | |
| 3D model (JSmol) | |
| ChEBI | |
| ChEMBL | |
| ChemSpider | |
| KEGG | |
| PubChem CID | |
| UNII | |
| CompTox Dashboard (EPA) | |
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| Properties | |
| C17H22O2 | |
| Molar mass | 258.361 g·mol−1 | 
| Melting point | 86 °C (187 °F; 359 K) | 
| Hazards | |
| Lethal dose or concentration (LD, LC): | |
| LD50 (median dose) | 0.58 mg/kg for mice | 
| Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references | |
Oenanthotoxin is a toxin extracted from hemlock water-dropwort (Oenanthe crocata) and other plants of the genus Oenanthe. It is a central nervous system poison, and acts as a noncompetitive antagonist of the neurotransmitter gamma-aminobutyric acid. A case has been made for the presence of this toxin in local Oenanthe species playing a causative role in euthanasia in ancient Sardinia. It was crystallized in 1949 by Clarke and co-workers. It is structurally closely related to the toxins cicutoxin and carotatoxin. Oenanthotoxin is a C17 polyacetylene isomer of cicutoxin.