Muscimol
| Names | |
|---|---|
| IUPAC name
5-(Aminomethyl)-1,2-oxazol-3(2H)-one | |
| Other names
Agarin, Pantherine, Agarine, Pantherin | |
| Identifiers | |
3D model (JSmol) |
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| 774694 | |
| ChEBI | |
| ChEMBL | |
| ChemSpider | |
| ECHA InfoCard | 100.018.574 |
| EC Number |
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| KEGG | |
PubChem CID |
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| UNII | |
| UN number | 2811 3077 |
CompTox Dashboard (EPA) |
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| Properties | |
| C4H6N2O2 | |
| Molar mass | 114.104 g·mol−1 |
| Melting point | 184 to 185 °C (363 to 365 °F; 457 to 458 K) |
| very soluble | |
| Solubility in ethanol | slightly soluble |
| Solubility in methanol | very soluble |
| Pharmacology | |
| Legal status |
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| Hazards | |
| GHS labelling: | |
| H300 | |
| P264, P270, P301+P316, P321, P330, P405, P501 | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references | |
Muscimol, also known as agarin or pantherine, as well as 5-(aminomethyl)-1,2-oxazol-3-ol, is the principal psychoactive constituent of Amanita muscaria and Amanita pantherina. Muscimol is an isoxazole alkaloid and a potent and selective orthosteric agonist for the GABAA receptor It displays sedative–hypnotic, depressant, and hallucinogenic psychoactivity. It is widely used to study GABAergic function in the brain.
Muscimol is under investigation for its potential to treat anxiety, insomnia, and neurological disorders, though its psychoactive nature requires careful regulation. A systematic review and meta-analysis of 22 studies found that muscimol reduces neuropathic pain symptoms, with effects beginning within 15 minutes and lasting up to three hours. Muscimol was tested in small clinical trials between 1977 and 1982 for conditions like schizophrenia, Huntington’s disease, and tardive dyskinesia, but showed limited efficacy and was eventually supplanted by the related compound gaboxadol. A later phase I trial for epilepsy in 2012 was also discontinued.
It was first isolated from Amanita pantherina in 1964, has a semi-rigid isoxazole structure and can be extracted from mushrooms or synthesized through various chemical routes, with modern methods improving upon earlier low-yield syntheses.
In vivo, muscimol exhibits dose-dependent effects with reversible central nervous system symptoms at higher doses and is rapidly metabolized in the brain without evidence of long-term toxicity. In Australia, muscimol is classified as a Schedule 9 prohibited substance, meaning its use is highly restricted and only allowed for approved scientific or medical purposes. In the United States, it is not federally controlled, but the FDA has deemed A. muscaria and muscimol unapproved for use in foods and is currently reviewing their use in dietary supplements. Louisiana banned the consumption of A. muscaria in 2005.