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British Journal of Pharmacology logoLink to British Journal of Pharmacology
. 1986 Jun;88(2):379–387. doi: 10.1111/j.1476-5381.1986.tb10214.x

Isothiouronium compounds as gamma-aminobutyric acid agonists.

R D Allan, H W Dickenson, B P Hiern, G A Johnston, R Kazlauskas
PMCID: PMC1916842  PMID: 3015310

Abstract

Analogues of gamma-aminobutyric acid (GABA) incorporating an isothiouronium salt as a replacement for a protonated amino functional group have been investigated for activity on: GABA receptors in the guinea-pig ileum; [3H]-GABA and [3H]-diazepam binding to rat brain membranes; and GABA uptake and transamination. For the homologous series of omega-isothiouronium alkanoic acids, maximum GABA-mimetic activity was found at 3-[(aminoiminomethyl)thio]propanoic acid. Introduction of unsaturation into this compound gave two isomeric conformationally restricted analogues. The trans isomer was inactive at GABA receptors while the cis compound ((Z)-3-[(aminoiminomethyl)thio]prop-2-enoic acid (ZAPA)) was more potent than muscimol and GABA as a GABA agonist with respect to low affinity GABA receptor sites. Both isomers were moderately potent at inhibiting the uptake of [3H]-GABA into rat brain slices. Comparison of possible conformations of the two unsaturated isomers by interactive computer graphics modelling and comparison with muscimol has led to a plausible active conformation of ZAPA, which may be a selective and potent agonist for low affinity GABA binding sites.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

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