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基于苯环利定的新型精神活性物质。

Phencyclidine-Based New Psychoactive Substances.

作者信息

Wallach Jason, Brandt Simon D

机构信息

Department of Pharmaceutical Sciences, Substance Use Disorder Institute, Philadelphia College of Pharmacy, University of the Sciences, Philadelphia, PA, USA.

School of Pharmacy & Biomolecular Sciences, Liverpool John Moores University, Liverpool, UK.

出版信息

Handb Exp Pharmacol. 2018;252:261-303. doi: 10.1007/164_2018_124.

Abstract

The serendipitous discovery of phencyclidine (PCP) in 1956 sets the stage for significant research efforts that resulted in a plethora of analogs and derivatives designed to explore the biological effects of this class. PCP soon became the prototypical dissociative agent that eventually sneaked through the doors of clinical laboratories and became an established street drug. Estimations suggest that around 14 PCP analogs were identified as "street drugs" in the period between the 1960s and 1990s. Fast forward to the 2000s, and largely facilitated by advancements in electronic forms of communication made possible through the Internet, a variety of new PCP analogs began to attract the attention of communities interested in the collaborative exploration of these substances. Traditionally, as was the case with the first-generation analogs identified in previous decades, the substances explored represented compounds already known in the scientific literature. As the decade of the noughties unfolded, a number of new PCP-derived substances appeared on the scene, which included some analogs that have not been previously recorded in the published literature. The aim of this chapter is to present a brief introductory overview of substances that have materialized as PCP-derived new psychoactive substances (NPS) in recent years and their known pharmacology. Since N-methyl-D-aspartate receptor (NMDAR) antagonism is implicated in mediating the subjective and mind-altering effects of many dissociative drugs, additional data are included from other analogs not presently identified as NPS.

摘要

1956年苯环利定(PCP)的意外发现为大量研究工作奠定了基础,这些研究产生了大量旨在探索此类药物生物学效应的类似物和衍生物。PCP很快成为典型的分离性药物,最终潜入临床实验室并成为一种既定的街头毒品。据估计,在20世纪60年代至90年代期间,约有14种PCP类似物被认定为“街头毒品”。快进到21世纪,在互联网实现的电子通信形式进步的极大推动下,各种新型PCP类似物开始吸引对协同探索这些物质感兴趣的群体的关注。传统上,就像前几十年发现的第一代类似物一样,所探索的物质代表科学文献中已为人知的化合物。随着21世纪第一个十年的展开,一些新的PCP衍生物质出现在人们视野中,其中包括一些以前在已发表文献中未记录的类似物。本章的目的是简要介绍近年来作为PCP衍生新精神活性物质(NPS)出现的物质及其已知药理学。由于N-甲基-D-天冬氨酸受体(NMDAR)拮抗作用与介导许多分离性药物的主观和改变意识的作用有关,因此还纳入了来自其他目前未被认定为NPS的类似物的额外数据。

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