Wermuth C G, Chambon J P, Heaulme M, Melikian A, Schlewer G, Leyris R, Biziére K
Department de Pharmacochimie Moléculaire, Centre de Neurochimie du CNRS, Université Louis Pasteur, Strasbourg, France.
Eur J Pharmacol. 1987 Dec 15;144(3):375-8. doi: 10.1016/0014-2999(87)90391-8.
Pyridazinyl derivatives of gamma-aminobutyric acid (GABA) have recently been shown to be selective, reversible and competitive GABAA antagonists. Unlike what is observed with all other GABAA antagonists, the affinity of these compounds for the GABAA receptor is not modified by thiocyanate. The chemical structure of these pyridazinyl-GABA derivatives differs from that of other GABAA antagonists by the presence of a free carboxylic group in their structure. We speculated that this could explain their lack of sensitivity to thiocyanate. Consequently, we synthesized three structural analogues of these pyridazinyl-GABA derivatives in which we replaced the free carboxyl group by a cyano group. These compounds displaced [3H]GABA from rat brain membranes and reversed the GABA-induced enhancement of [3H]diazepam binding. However their affinity for the GABAA receptor increased 10- to 20-fold in the presence of thiocyanate. Thus, sensitivity to thiocyanate appears to be related more to the absence of an anionic functional group than to the agonist or antagonist nature of the GABAA ligand.
γ-氨基丁酸(GABA)的哒嗪基衍生物最近已被证明是选择性、可逆且竞争性的GABAA拮抗剂。与所有其他GABAA拮抗剂不同的是,这些化合物对GABAA受体的亲和力不会因硫氰酸盐而改变。这些哒嗪基-GABA衍生物的化学结构与其他GABAA拮抗剂的不同之处在于其结构中存在一个游离羧基。我们推测这可以解释它们对硫氰酸盐不敏感的原因。因此,我们合成了这些哒嗪基-GABA衍生物的三种结构类似物,其中我们用氰基取代了游离羧基。这些化合物从大鼠脑膜上置换了[3H]GABA,并逆转了GABA诱导的[3H]地西泮结合增强。然而,在硫氰酸盐存在的情况下,它们对GABAA受体的亲和力增加了10至20倍。因此,对硫氰酸盐的敏感性似乎更多地与缺乏阴离子官能团有关,而不是与GABAA配体的激动剂或拮抗剂性质有关。