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罂粟碱的生物转化及代谢产物与人磷酸二酯酶 10a 的计算机对接研究。

Biotransformation of papaverine and in silico docking studies of the metabolites on human phosphodiesterase 10a.

机构信息

National Center for Natural Products Research, School of Pharmacy, The University of Mississippi, MS, 38677, USA; Department of Pharmacognosy, Faculty of Pharmacy, Tanta University, Tanta, 31527, Egypt.

National Center for Natural Products Research, School of Pharmacy, The University of Mississippi, MS, 38677, USA.

出版信息

Phytochemistry. 2021 Mar;183:112598. doi: 10.1016/j.phytochem.2020.112598. Epub 2020 Dec 25.

Abstract

The metabolism of papaverine, the opium benzylisoquinoline alkaloid, with Aspergillus niger NRRL 322, Beauveria bassiana NRRL 22864, Cunninghamella echinulate ATCC 18968 and Cunninghamella echinulate ATCC 1382 has resulted in O-demethylation, O-methylglucosylation and N-oxidation products. Two new metabolites (4″-O-methyl-β-D-glucopyranosyl) 4'-demethyl papaverine and (4″-O-methyl-β-D-glucopyranosyl) 6-demethyl papaverine, (Metabolites 5 and 6) together with 4'-O-demethylated papaverine (Metabolite 1), 3'-O-demethylated papaverine (Metabolite 2), 6-O-demethylated papaverine (Metabolite 3) and papaverine N-oxide (Metabolite 4) were isolated. The structure elucidation of the metabolites was based primarily on 1D, 2D-NMR analyses and HRMS. These metabolism results were consistent with the previous plant cell transformation studies on papaverine and isopapaverine and the microbial metabolism of papaveraldine. In silico docking studies of the metabolites using crystals of human phosphodiesterase 10a (hPDE10a) revealed that compounds 4, 1, 6, 3, and 5 possess better docking scores and binding poses with favorable interactions than the native ligand papaverine.

摘要

阿魏酰苯乙胺(罂粟碱,鸦片苄基异喹啉生物碱)与黑曲霉 NRRL 322、球孢白僵菌 NRRL 22864、卷枝毛霉 ATCC 18968 和卷枝毛霉 ATCC 1382 的代谢物为 O-去甲基化、O-甲基葡萄糖苷化和 N-氧化产物。两种新的代谢产物(4″-O-甲基-β-D-吡喃葡萄糖基)4'-去甲基罂粟碱和(4″-O-甲基-β-D-吡喃葡萄糖基)6-去甲基罂粟碱(代谢物 5 和 6)以及 4'-去甲基罂粟碱(代谢物 1)、3'-去甲基罂粟碱(代谢物 2)、6-O-去甲基罂粟碱(代谢物 3)和罂粟碱 N-氧化物(代谢物 4)被分离出来。代谢物的结构阐明主要基于 1D、2D-NMR 分析和 HRMS。这些代谢结果与之前对罂粟碱和异罂粟碱的植物细胞转化研究以及罂粟啡林的微生物代谢结果一致。使用人磷酸二酯酶 10a(hPDE10a)的晶体对代谢物进行计算机对接研究表明,与天然配体罂粟碱相比,化合物 4、1、6、3 和 5 具有更好的对接评分和结合构象,并具有有利的相互作用。

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