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一种制备氘代Salvinorin A的简便方法:[2,2,2-2H3]-Salvinorin A的合成。

A facile method for the preparation of deuterium labeled salvinorin A: synthesis of [2,2,2-2H3]-salvinorin A.

作者信息

Tidgewell Kevin, Harding Wayne W, Schmidt Mark, Holden Kenneth G, Murry Daryl J, Prisinzano Thomas E

机构信息

Division of Medicinal and Natural Products Chemistry, College of Pharmacy, The University of Iowa, Iowa City, IA 52242, USA.

出版信息

Bioorg Med Chem Lett. 2004 Oct 18;14(20):5099-102. doi: 10.1016/j.bmcl.2004.07.081.

DOI:10.1016/j.bmcl.2004.07.081
PMID:15380207
Abstract

Salvinorin A is a novel hallucinogen isolated from the widely available leaves of Salvia divinorum. Based on its mechanism of action, salvinorin A has shown potential as a stimulant abuse therapeutic. However, there are no methods for the detection of salvinorin A or its metabolites in biological fluids. In order to begin developing salvinorin A as a potential therapeutic, an understanding of its metabolism is needed. Here, a straightforward synthesis of a deuterium labeled analog of salvinorin A and its utility as an internal standard for the detection of salvinorin A and its metabolites in biological fluids by LC-MS is described.

摘要

萨尔维诺林A是一种从广泛可得的鼠尾草叶中分离出的新型致幻剂。基于其作用机制,萨尔维诺林A已显示出作为兴奋剂滥用治疗药物的潜力。然而,目前尚无检测生物体液中萨尔维诺林A或其代谢物的方法。为了开始将萨尔维诺林A开发为一种潜在的治疗药物,需要了解其代谢情况。在此,描述了一种萨尔维诺林A氘代类似物的直接合成方法及其作为通过液相色谱-质谱法检测生物体液中萨尔维诺林A及其代谢物的内标的用途。

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Bioorg Med Chem Lett. 2004 Oct 18;14(20):5099-102. doi: 10.1016/j.bmcl.2004.07.081.
2
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