Department of Pharmacognosy and Pharmaceutical Botany, Faculty of Pharmaceutical Sciences, Chulalongkorn University, Bangkok 10330, Thailand.
Department of Pharmacognosy, University of Pharmacy, Yangon 11031, Myanmar.
Molecules. 2021 Jan 14;26(2):418. doi: 10.3390/molecules26020418.
Four new phenanthrene derivatives, gastrobellinols A-D (), were isolated from the methanolic extract of (Rchb.f.) Kuntze, along with eleven known phenolic compounds including agrostophyllin (), agrostophyllidin (), coniferyl aldehyde (), 4-hydroxybenzaldehyde (), agrostophyllone (), gigantol (), 4-(methoxylmethyl)phenol (), syringaldehyde (), 1-(4'-hydroxybenzyl)-imbricartin (), 6-methoxycoelonin (), and imbricatin (). Their structures were determined by spectroscopic methods. Each isolate was evaluated for α-glucosidase inhibitory activity. Compounds , , , , , , and showed higher activity than the drug acarbose. Gastrobellinol C () exhibited the strongest -glucosidase inhibition with an IC value of 45.92 μM. A kinetic study of showed competitive inhibition on the -glucosidase enzyme. This is the first report on the phytochemical constituents and -glucosidase inhibitory activity of
从(Rchb.f.)Kuntze 的甲醇提取物中分离得到了四种新的菲衍生物,即 gastrobellinols A-D(),以及包括 agrostophyllin()、agrostophyllidin()、coniferyl aldehyde()、4-hydroxybenzaldehyde()、agrostophyllone()、gigantol()、4-(methoxymethyl)phenol()、syringaldehyde()、1-(4'-羟基苄基)imbricartin()、6-methoxycoelonin()和 imbricatin()在内的 11 种已知酚类化合物。它们的结构通过光谱方法确定。对每个分离物进行了α-葡萄糖苷酶抑制活性评价。化合物、、、、、、和表现出比药物阿卡波糖更高的活性。Gastrobellinol C()对 -葡萄糖苷酶表现出最强的抑制活性,IC 值为 45.92 μM。对 gastrobellinol C 的动力学研究表明它对 -葡萄糖苷酶具有竞争性抑制作用。这是首次报道