Sethy_1991_J.Pharm.Pharmacol_43_670

Reference

Title : alpha-Methyl analogues of acetylenic amines as striatal muscarinic antagonists - Sethy_1991_J.Pharm.Pharmacol_43_670
Author(s) : Sethy VH , Heier RF , Moon MW
Ref : J Pharm Pharmacol , 43 :670 , 1991
Abstract :

The effect of acetylenic amines, with or without alpha-methyl substitution, on striatal acetylcholine (ACh) concentration in rats was investigated. Oxotremorine, oxotremorine-1, and U-77053 (trimethyl (4-(1-pyrrolidinyl)-2 butynyl)-urea), the unsubstituted amines, increased striatal ACh concentration. On the other hand, the corresponding alpha-methyl substituted analogues, alpha-methyl-oxotremorine, BM-5, and alpha-methyl U-77053, decreased the concentration of ACh in the striatum. The results indicate that substitution of alpha-methyl in acetylenic amines converts compounds from agonists to antagonists for striatal muscarinic receptors.

PubMedSearch : Sethy_1991_J.Pharm.Pharmacol_43_670
PubMedID: 1685530

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Citations formats

Sethy VH, Heier RF, Moon MW (1991)
alpha-Methyl analogues of acetylenic amines as striatal muscarinic antagonists
J Pharm Pharmacol 43 :670

Sethy VH, Heier RF, Moon MW (1991)
J Pharm Pharmacol 43 :670