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萨尔维诺林A:从天然产物到人类治疗药物

Salvinorin A: from natural product to human therapeutics.

作者信息

Vortherms Timothy A, Roth Bryan L

机构信息

Department of Pharmacology, School of Medicine, University of North Carolina, Chapel Hill, NC 27599, USA.

出版信息

Mol Interv. 2006 Oct;6(5):257-65. doi: 10.1124/mi.6.5.7.

DOI:10.1124/mi.6.5.7
PMID:17035666
Abstract

The hallucinogenic plant Salvia divinorum (i.e., "magic mint") is a member of the Sage family that has been used for divination and shamanism by the Mazatecs. Over the past decade or so, S. divinorum has been increasingly used recreationally. The neoclerodane diterpene salvinorin A is the active component of S. divinorum, and recently, the kappa opioid receptor (KOR) has been identified, in vitro and in vivo, as its molecular target. The discovery of KOR as the molecular target of salvinorin A has opened up many opportunities for drug discovery and drug development for a number of psychiatric and non-psychiatric disorders.

摘要

致幻植物鼠尾草(即“魔法薄荷”)是唇形科植物的一种,马萨特克人曾用它来进行占卜和萨满仪式。在过去十年左右的时间里,鼠尾草越来越多地被用于娱乐目的。新克罗烷二萜类化合物Salvinorin A是鼠尾草的活性成分,最近,κ阿片受体(KOR)在体外和体内均被确定为其分子靶点。KOR作为Salvinorin A分子靶点的发现,为多种精神疾病和非精神疾病的药物发现和药物开发带来了诸多机遇。

相似文献

1
Salvinorin A: from natural product to human therapeutics.萨尔维诺林A:从天然产物到人类治疗药物
Mol Interv. 2006 Oct;6(5):257-65. doi: 10.1124/mi.6.5.7.
2
Salvinorin A: a potent naturally occurring nonnitrogenous kappa opioid selective agonist.Salvinorin A:一种强效的天然非含氮κ阿片受体选择性激动剂。
Proc Natl Acad Sci U S A. 2002 Sep 3;99(18):11934-9. doi: 10.1073/pnas.182234399. Epub 2002 Aug 21.
3
Salvinorin A, an active component of the hallucinogenic sage salvia divinorum is a highly efficacious kappa-opioid receptor agonist: structural and functional considerations.Salvinorin A是致幻鼠尾草(Salvia divinorum)的一种活性成分,是一种高效的κ-阿片受体激动剂:结构与功能方面的考量。
J Pharmacol Exp Ther. 2004 Mar;308(3):1197-203. doi: 10.1124/jpet.103.059394. Epub 2004 Jan 8.
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Pharmacological activity of salvinorin A, the major component of Salvia divinorum.紫蝶莎罗中的主要成分——紫堇醇灵 A 的药理学活性。
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A unique natural selective kappa-opioid receptor agonist, salvinorin A, and its roles in human therapeutics.一种独特的天然选择性κ-阿片受体激动剂——Salvinorin A及其在人类治疗中的作用。
Phytochemistry. 2017 May;137:9-14. doi: 10.1016/j.phytochem.2017.02.001. Epub 2017 Feb 10.
6
[Salvinorin A and related diterpenes--biological activity and potential therapeutic uses].[萨尔维诺林A及相关二萜类化合物——生物活性与潜在治疗用途]
Postepy Biochem. 2012;58(4):485-91.
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The hallucinogenic herb Salvia divinorum and its active ingredient salvinorin A reduce inflammation-induced hypermotility in mice.致幻草药鼠尾草及其活性成分二萜内酯A可减轻小鼠炎症诱导的运动亢进。
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Synthetic studies of neoclerodane diterpenes from Salvia divinorum: semisynthesis of salvinicins A and B and other chemical transformations of salvinorin A.来自鼠尾草叶马先蒿中新克罗烷二萜的合成研究:萨尔维菌素A和B的半合成以及萨尔维诺灵A的其他化学转化
J Nat Prod. 2006 Jan;69(1):107-12. doi: 10.1021/np050398i.
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New neoclerodane diterpenoids isolated from the leaves of Salvia divinorum and their binding affinities for human kappa opioid receptors.从鼠尾草叶中分离出的新型新克罗烷二萜类化合物及其与人κ阿片受体的结合亲和力。
Bioorg Med Chem. 2005 Oct 1;13(19):5635-9. doi: 10.1016/j.bmc.2005.05.054.
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Neuropharmacology of the naturally occurring kappa-opioid hallucinogen salvinorin A.天然 κ-阿片样物质致幻剂藜芦醛甲醚的神经药理学。
Pharmacol Rev. 2011 Jun;63(2):316-47. doi: 10.1124/pr.110.003244. Epub 2011 Mar 28.

引用本文的文献

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Discovery of Novel, Selective, and Nonbasic Agonists for the Kappa-Opioid Receptor Determined by Salvinorin A-Based Virtual Screening.基于沙林醇 A 的虚拟筛选发现新型、选择性、非碱性 κ-阿片受体激动剂。
J Med Chem. 2024 Aug 22;67(16):13788-13801. doi: 10.1021/acs.jmedchem.4c00590. Epub 2024 Aug 1.
2
Solving an Old Puzzle: Elucidation and Evaluation of the Binding Mode of Salvinorin A at the Kappa Opioid Receptor.解决一个老难题:阐明并评估沙芹内酯 A 在κ 阿片受体上的结合模式。
Molecules. 2023 Jan 11;28(2):718. doi: 10.3390/molecules28020718.
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Pharmacokinetics and Pharmacodynamics of Salvinorin A and : Clinical and Forensic Aspects.
鼠尾草叶大麻酚A的药代动力学与药效学:临床与法医学方面
Pharmaceuticals (Basel). 2021 Feb 3;14(2):116. doi: 10.3390/ph14020116.
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Salvinorin A preserves cerebral pial artery autoregulation after forebrain ischemia via the PI3K/AKT/cGMP pathway.Salvinorin A通过PI3K/AKT/cGMP途径在前脑缺血后维持软脑膜动脉的自身调节。
Braz J Med Biol Res. 2018 Mar 15;51(5):e6714. doi: 10.1590/1414-431X20176714.
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Quantitative determination of salvinorin A, a natural hallucinogen with abuse liability, in Internet-available Salvia divinorum and endemic species of Salvia in Taiwan.对具有滥用倾向的天然致幻剂——萨尔维诺林A在网络上可获取的鼠尾草属植物以及台湾鼠尾草属本地物种中的定量测定。
J Food Drug Anal. 2014 Sep;22(3):370-378. doi: 10.1016/j.jfda.2014.01.017. Epub 2014 Feb 16.
6
Salvinorin A Inhibits Airway Hyperreactivity Induced by Ovalbumin Sensitization.Salvinorin A抑制卵清蛋白致敏诱导的气道高反应性。
Front Pharmacol. 2017 Jan 13;7:525. doi: 10.3389/fphar.2016.00525. eCollection 2016.
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Kappa Opioids, Salvinorin A and Major Depressive Disorder.κ阿片类物质、Salvinorin A与重度抑郁症
Curr Neuropharmacol. 2016;14(2):165-76. doi: 10.2174/1570159x13666150727220944.
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Kappa Opioid Receptor-Induced Aversion Requires p38 MAPK Activation in VTA Dopamine Neurons.κ阿片受体诱导的厌恶反应需要腹侧被盖区多巴胺能神经元中的p38丝裂原活化蛋白激酶激活。
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Kappa Opioid Receptor Agonist and Brain Ischemia.κ阿片受体激动剂与脑缺血
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Salvinorin A decreases mortality and improves neurological outcome in a neonatal mouse hypoxia model.Salvinorin A可降低新生小鼠缺氧模型的死亡率并改善神经学转归。
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