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内地产缬草中的抗胆堿酯化合物。

Anticholinesterase Compounds from Endemic Prangos uechtritzii.

机构信息

Department of Pharmaceutical Botany, Faculty of Pharmacy, İzmir Katip Çelebi University, 35620, İzmir, Turkey.

Department of Pharmaceutical Botany, Faculty of Pharmacy, Ege University, 35040, İzmir, Turkey.

出版信息

Chem Biodivers. 2022 Nov;19(11):e202200557. doi: 10.1002/cbdv.202200557. Epub 2022 Oct 26.

Abstract

In this study, the anticholinesterase effects of the extracts and isolated compounds from the roots of endemic Prangos uechtritzii Boiss & Hausskn (Apiaceae) are reported. A novel polyacetylenic compound; (+)-8-O-methyloplopantriol A along with two known polyacetylenes; (-)-panaxynol, (+)-falcarindiol and fifteen known coumarin derivatives; umbelliferone, 6-formylumbelliferone, suberosin, 7-demethylsuberosin, (+)-ulopterol, tamarin, psoralen, imperatorin, (+)-oxypeucedanin, (+)-oxypeucedanin hydrate, (+)-oxypeucedanin methanolate, (+)-marmesin, (-)-prantschimgin, (+)-decursinol, and (-)-adicardin were isolated from the hexane (Pu-HE), chloroform (Pu-CE), and methanol (Pu-ME) extracts of P. uechtritzii roots. (-)-Panaxynol, (+)-falcarindiol, 6-formylumbelliferone, (+)-decursinol, and (-)-adicardin were obtained from the genus Prangos for the first time. (+)-8-O-Methyloplopantriol A inhibited both AChE (IC =194.5±5.8 μM) and BChE (IC =51.9±2.96 μM) enzymes. (+)-Falcarindiol, 6-formylumbelliferone, 7-demethylsuberosin, tamarin, and imperatorin also exhibited BChE-specific inhibitory activities (IC =27.88-93.86 μM). (+)-Falcarindiol (IC =27.88±0.91 μM) and imperatorin (IC =30.89±1.40 μM) as the most active components could be led compounds to develop new BChE inhibitors with further research against Alzheimer's disease.

摘要

本研究报道了来自特有植物新疆棱子芹(伞形科)根的提取物和分离化合物的抗胆碱酯酶作用。一种新的多炔化合物;(+)-8-O-甲基莪术醇 A 以及两种已知的多炔化合物;(-)-panaxynol、(+)-falcarindiol 和十五种已知的香豆素衍生物;茴芹素、6-甲酰茴芹素、菖蒲二烯、7-去甲基菖蒲二烯、(+)-ulopterol、tamarin、补骨脂素、花椒毒素、(+)-氧化前胡素、(+)-氧化前胡素水合物、(+)-氧化前胡素甲醇化物、(+)-marmesin、(-)-prantschimgin、(+)-decursinol 和(-)-adicardin 从新疆棱子芹根的正己烷(Pu-HE)、氯仿(Pu-CE)和甲醇(Pu-ME)提取物中分离得到。(-)-panaxynol、(+)-falcarindiol、6-甲酰茴芹素、(+)-decursinol 和(-)-adicardin 首次从棱子芹属植物中获得。(+)-8-O-甲基莪术醇 A 抑制 AChE(IC=194.5±5.8 μM)和 BChE(IC=51.9±2.96 μM)两种酶。(+)-falcarindiol、6-甲酰茴芹素、7-去甲基菖蒲二烯、tamarin 和花椒毒素也表现出对 BChE 的特异性抑制活性(IC=27.88-93.86 μM)。(+)-falcarindiol(IC=27.88±0.91 μM)和花椒毒素(IC=30.89±1.40 μM)作为最有效的成分,可以引导化合物进一步研究开发针对阿尔茨海默病的新型 BChE 抑制剂。

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