Spiroxatrine
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| MeSH | Spiroxatrine |
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Spiroxatrine (Spiroxamide, R5188) is a drug which acts as a selective antagonist at both the 5-HT1A receptor and the α2C adrenergic receptor.[1] It is an analog of spiperone and also has some dopamine antagonist effects and a relatively weak opioid action.[2][3]
References
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- ↑ Script error: No such module "Citation/CS1".
- ↑ NIEMEGEERS CJ, VERBRUGGEN FJ, VANNUETEN JM, JANSSEN PA. SPIROXAMIDE (R 5188): A NEW COMPOUND PRODUCING MORPHINE-LIKE AND CHLORPROMAZINE-LIKE EFFECTS IN ANIMALS. Int J Neuropharmacol. 1963 Dec;2:349-54. Script error: No such module "CS1 identifiers". Template:Catalog lookup link
- ↑ Leysen J, Tollenaere JP, Koch MHJ, Laduron P. Differentiation of opiate and neuroleptic receptor binding in rat brain. European Journal of Pharmacology 1977; 43(3):253-267. Script error: No such module "CS1 identifiers".
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