Suppr超能文献

基于晶体结构的虚拟筛选发现新型选择性 κ 阿片受体激动剂。

Discovery of a novel selective kappa-opioid receptor agonist using crystal structure-based virtual screening.

机构信息

Department of Structural and Chemical Biology, Icahn School of Medicine at Mount Sinai , New York, New York 10029, United States.

出版信息

J Chem Inf Model. 2013 Mar 25;53(3):521-6. doi: 10.1021/ci400019t. Epub 2013 Mar 13.

Abstract

Kappa-opioid (KOP) receptor agonists exhibit analgesic effects without activating reward pathways. In the search for nonaddictive opioid therapeutics and novel chemical tools to study physiological functions regulated by the KOP receptor, we screened in silico its recently released inactive crystal structure. A selective novel KOP receptor agonist emerged as a notable result and is proposed as a new chemotype for the study of the KOP receptor in the etiology of drug addiction, depression, and/or pain.

摘要

κ 阿片受体(KOP)激动剂具有镇痛作用而不激活奖励途径。在寻找非成瘾性阿片类治疗药物和研究 KOP 受体调节的生理功能的新型化学工具的过程中,我们对其最近发布的无活性晶体结构进行了计算机筛选。一种新型选择性 KOP 受体激动剂脱颖而出,被提议作为研究阿片类药物成瘾、抑郁和/或疼痛中 KOP 受体的新化学类型。

相似文献

引用本文的文献

7
Molecular Basis of Opioid Action: From Structures to New Leads.阿片类药物作用的分子基础:从结构到新线索。
Biol Psychiatry. 2020 Jan 1;87(1):6-14. doi: 10.1016/j.biopsych.2019.08.028. Epub 2019 Sep 12.
9
Ultra-large library docking for discovering new chemotypes.超大库对接发现新化学型。
Nature. 2019 Feb;566(7743):224-229. doi: 10.1038/s41586-019-0917-9. Epub 2019 Feb 6.

本文引用的文献

1
Grand opening of structure-guided design for novel opioids.新型阿片类药物结构导向设计的盛大开业。
Trends Pharmacol Sci. 2013 Jan;34(1):6-12. doi: 10.1016/j.tips.2012.10.002. Epub 2012 Nov 3.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验