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新型抗焦虑药SQ 65,396对3H-地西泮结合的增强作用

Enhancement of 3H-diazepam binding by SQ 65,396: a novel anti-anxiety agent.

作者信息

Beer B, Klepner C A, Lippa A S, Squires R F

出版信息

Pharmacol Biochem Behav. 1978 Dec;9(6):849-51. doi: 10.1016/0091-3057(78)90367-2.

Abstract

SQ 65,396, a clinically active anti-anxiety agent, enhanced the binding of 3H-diazepam at 1.5 nM. This effect was due to an increase in the affinity for the ligand, without a change in the number of 3H-diazepam binding sites. This action of SQ 65,396 may mediate its anti-anxiety effects by affecting the action of an endogenous modulator of the "benzodiazepine receptor." Several other substances and treatments increase the affinity of 3H-diazepam for its receptors by mechanisms which may be related to the effect produced by SQ 65,396.

摘要

SQ 65,396是一种具有临床活性的抗焦虑药物,它在1.5纳摩尔浓度时增强了3H-地西泮的结合。这种效应是由于对配体的亲和力增加,而3H-地西泮结合位点的数量没有变化。SQ 65,396的这一作用可能通过影响“苯二氮䓬受体”内源性调节剂的作用来介导其抗焦虑作用。其他几种物质和处理通过可能与SQ 65,396产生的效应相关的机制增加了3H-地西泮对其受体的亲和力。

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