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