Chemistry:Oxotremorine
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Short description: Chemical compound
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| Routes of administration | Oral, intravenous |
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| Formula | C12H18N2O |
| Molar mass | 206.28 g·mol−1 |
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Oxotremorine is a drug that acts as a selective muscarinic acetylcholine receptor agonist.[1]
Oxotremorine produces ataxia, tremor and spasticity, similar to those symptoms seen in Parkinsonism, and has thus become a research tool in experimental studies aimed at determining more effective anti-Parkinsonian drugs.[2]
Oxotremorine also produces antipsychotic effects.[3]
References
- ↑ "Effects of the muscarinic agonist oxotremorine on membrane fluidity in rat lymphocytes". Biochemistry and Molecular Biology International 29 (6): 1047–54. April 1993. INIST:4025194. PMID 8330013.
- ↑ Modern Pharmacology with Clinical Applications. Lippincott Williams & Wilkins. 2004. ISBN 978-0-7817-3762-3.[page needed]
- ↑ "Antipsychotic property of a muscarinic receptor agonist in animal models for schizophrenia". Pharmacology, Biochemistry, and Behavior 91 (1): 140–9. November 2008. doi:10.1016/j.pbb.2008.06.023. INIST:20678587. PMID 18651995.
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