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从伊博加植物中生物合成一种抗成瘾药物。

Biosynthesis of an Anti-Addiction Agent from the Iboga Plant.

机构信息

Department of Natural Product Biosynthesis , Max Planck Institute of Chemical Ecology , Hans-Knöll-Straße 8 , 07745 Jena , Germany.

Department of Biological Chemistry , John Innes Centre , Norwich Research Park, Norwich NR4 7UH , United Kingdom.

出版信息

J Am Chem Soc. 2019 Aug 21;141(33):12979-12983. doi: 10.1021/jacs.9b05999. Epub 2019 Aug 6.

Abstract

(-)-Ibogaine and (-)-voacangine are plant derived psychoactives that show promise as treatments for opioid addiction. However, these compounds are produced by hard to source plants, making these chemicals difficult for broad-scale use. Here we report the complete biosynthesis of (-)-voacangine, and de-esterified voacangine, which is converted to (-)-ibogaine by heating, enabling biocatalytic production of these compounds. Notably, (-)-ibogaine and (-)-voacangine are of the opposite enantiomeric configuration compared to the other major alkaloids found in this natural product class. Therefore, this discovery provides insight into enantioselective enzymatic formal Diels-Alder reactions.

摘要

(-)-伊博加因和(-)-沃卡辛因是源自植物的精神活性物质,它们在治疗阿片类药物成瘾方面显示出了潜力。然而,这些化合物是由难以获得的植物产生的,这使得这些化学物质难以广泛使用。在这里,我们报告了(-)-沃卡辛因和(-)-去酯化沃卡辛因的完全生物合成,(-)-去酯化沃卡辛因通过加热转化为(-)-伊博加因,从而能够生物催化这些化合物的生产。值得注意的是,(-)-伊博加因和(-)-沃卡辛因的对映异构体构型与该天然产物类中发现的其他主要生物碱相反。因此,这一发现为对映选择性酶促形式的 Diels-Alder 反应提供了新的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/106e/6706869/616d9575ad7b/ja9b05999_0001.jpg

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