拮抗剂和嘌呤能神经假说:P2Y受体的变构调节剂2,2 ' -pyridylisatogen tosylate (PIT)。回顾四分之一个世纪的进步

M Spedding , K Menton , A Markham , D.F Weetman
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引用次数: 10

摘要

2,2 ' -Pyridylisatogen tosylate (PIT)是平滑肌P2Y反应的选择性拮抗剂,不拮抗腺苷的作用。对嘌呤能神经刺激的反应对PIT有抵抗性。PIT是非洲爪蟾卵母细胞中表达的重组P2Y1受体对ATP响应的变构调节剂,在低浓度(0.1-10 μM)下ATP增强,在高浓度(10 μM)下ATP拮抗。放射配体结合谱显示,PIT不与任何其他受体相互作用,除了对腺苷A1受体的亲和力较低(pKi, 5.3)。该化合物识别嘌呤位点,然后在长时间孵育或高浓度后可能引起与巯基的不可逆结合。PIT是一个强有力的自旋诱捕器。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Antagonists and the purinergic nerve hypothesis: 2,2′-pyridylisatogen tosylate (PIT), an allosteric modulator of P2Y receptors. A retrospective on a quarter century of progress

2,2′-Pyridylisatogen tosylate (PIT) is a selective antagonist of P2Y responses in smooth muscle and does not antagonise the effects of adenosine. Responses to purinergic nerve stimulation are resistant to PIT. PIT is an allosteric modulator of responses to ATP in recombinant P2Y1 receptors expressed in Xenopus oocytes with potentiation of ATP at low concentrations (0.1–10 μM) and antagonism at higher ones (>10 μM). A radioligand binding profile showed that PIT did not interact with any other receptors, with the exception of low affinity for the adenosine A1 receptor (pKi, 5.3). The compound recognises purine sites and then may cause irreversible binding to sulfhydryl groups following prolonged incubation or high concentrations. PIT is a potent spin trapper.

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