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化学生物神经科学经典:芬太尼。

DARK Classics in Chemical Neuroscience: Fentanyl.

机构信息

Department of Pharmaceutical Sciences , Lipscomb University College of Pharmacy , Nashville , Tennessee 37204 , United States.

Department of Pharmaceutical Sciences , Concordia University Wisconsin School of Pharmacy , Mequon , Wisconsin 53097 , United States.

出版信息

ACS Chem Neurosci. 2018 Oct 17;9(10):2428-2437. doi: 10.1021/acschemneuro.8b00174. Epub 2018 Jun 12.

Abstract

Fentanyl rose to prominence as an alternative analgesic to morphine nearly 50 years ago; today, fentanyl has re-emerged as a dangerous recreational substance. The increased potency and analgesic effect of fentanyl are advantageous in the treatment of pain but are also responsible for the rise in unintentional opioid overdose deaths. In response to this crisis, fentanyl, its analogues, and even precursors are under heightened regulatory scrutiny. Despite this controversial history, derivatization of fentanyl has resulted in numerous synthetic analogues that provide valuable insights into opioid receptor binding and signaling events. In this review, the impact of fentanyl on chemical neuroscience is shown through its synthesis and properties, manufacturing, metabolism, pharmacology, approved and off-label indications, adverse effects, and the responsibility it has in the opioid epidemic.

摘要

芬太尼作为一种替代吗啡的止痛药物,在近 50 年前崭露头角;如今,芬太尼又重新成为一种危险的消遣性药物。芬太尼的效力和止痛效果增强,这在治疗疼痛方面是有利的,但也导致了非故意阿片类药物过量死亡的增加。为了应对这一危机,芬太尼、其类似物甚至前体都受到了更严格的监管审查。尽管存在这种有争议的历史,但芬太尼的衍生化已产生了许多合成类似物,为阿片受体结合和信号事件提供了有价值的见解。在这篇综述中,通过芬太尼的合成和性质、制造、代谢、药理学、批准和非批准的适应症、副作用以及它在阿片类药物流行中的责任,展示了芬太尼对化学生物学的影响。

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