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化学生物学经典系列:依他唑嗪和相关苯并咪唑类。

DARK Classics in Chemical Neuroscience: Etonitazene and Related Benzimidazoles.

机构信息

iKem BT, H-1033 Budapest, Hungary.

European Monitoring Centre for Drugs and Drug Addiction, 1249-289 Lisbon, Portugal.

出版信息

ACS Chem Neurosci. 2021 Apr 7;12(7):1072-1092. doi: 10.1021/acschemneuro.1c00037. Epub 2021 Mar 24.

Abstract

Etonitazene and related 2-benzylbenzimidazoles are potent analgetics invented in the research laboratories of the Swiss pharmaceutical giant CIBA in the late 1950s. Though the unprecedented structure distinguishes this class of compounds from poppy-derived and other synthetic analgetics, a range of studies indicate that these drugs are selective μ opioid receptor agonists possessing morphine-like pharmacotoxicological properties in animals as well as humans. Several unscheduled members of this synthetically readily accessible class of opioids that are not controlled under the international and national drug control systems have recently emerged on the illicit drug market. Among them, isotonitazene has been implicated in at least 200 fatalities in Europe and North America. None of the 2-benzylbenzimidazole derivatives have been developed into medicines, but etonitazene and some of its derivatives have been used as receptor probes and in addiction behavior studies in animals. The unique structure has inspired research on such benzimidazoles and related benzimidazolones of which "brorphine" made its debut as one of the newest psychoactive substance to emerge on the illicit opioid drug market in mid-2019. This in-depth review provides a historical introduction, an overview on the chemistry, pharmacological profiles, adverse effects, addiction liability, regulatory status, and the impact on chemical neuroscience of the 2-benzylbenzimidazoles. Structurally related benzimidazoles with opioid and/or analgesic properties are also discussed briefly.

摘要

依他佐辛和相关的 2-苄基苯并咪唑类是上世纪 50 年代末瑞士制药巨头汽巴公司研发实验室发明的强效镇痛药。尽管这种前所未有的结构使这类化合物有别于罂粟衍生和其他合成镇痛药,但一系列研究表明,这些药物是选择性μ阿片受体激动剂,在动物和人类中具有类似吗啡的药理毒理学特性。最近,一些未列入管制的、在国际和国家药物控制系统下不受管制的此类合成阿片类药物在非法毒品市场上出现。其中,异依他佐辛至少在欧洲和北美导致了 200 人死亡。2-苄基苯并咪唑类衍生物中没有一种被开发成药物,但依他佐辛和其一些衍生物已被用作受体探针,并用于动物成瘾行为研究。独特的结构激发了对这类苯并咪唑类和相关苯并咪唑酮类的研究,其中“布罗啡”作为 2019 年中期出现在非法阿片类药物市场上的最新精神活性物质之一首次亮相。这篇深入的综述提供了一个历史介绍,概述了 2-苄基苯并咪唑类的化学、药理学特征、不良反应、成瘾性、监管状况以及对化学神经科学的影响。本文还简要讨论了具有阿片类和/或镇痛特性的结构相关苯并咪唑类。

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