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Salazinic Acid-Derived Depsidones and Diphenylethers with α-Glucosidase Inhibitory Activity from the Lichen Parmotrema dilatatum.

Salazinic Acid-Derived Depsidones and Diphenylethers with α-Glucosidase Inhibitory Activity from the Lichen Parmotrema dilatatum.

机构信息

Center of Excellence in Natural Products Chemistry, Department of Chemistry, Faculty of Science, Chulalongkorn University, Pathumwan, Bangkok, Thailand.

Program in Biotechnology, Faculty of Science, Chulalongkorn University, Pathumwan, Bangkok, Thailand.

出版信息

Planta Med. 2020 Nov;86(16):1216-1224. doi: 10.1055/a-1203-0623. Epub 2020 Aug 20.

Abstract

Three new depsidones, parmosidones F - G (1 - 2), and 8'-O-methylsalazinic acid (3), and 3 new diphenylethers, parmetherines A - C (4 - 6), together with 2 known congeners were isolated from the whole thalli of , a foliose chlorolichen. Their structures were unambiguously determined by extensive spectroscopic analyses and comparison with literature data. The isolated polyphenolics were assayed for their α-glucosidase inhibitory activities. Newly reported benzylated depsidones 1: and 2: in particular inhibited α-glucosidase with IC values of 2.2 and 4.3 µM, respectively, and are thus more potent than the positive control, acarbose.

摘要

从叶状绿藻全株中分离得到三种新的去甲二萜类化合物, Parmosidones F-G(1-2)和 8'-O-甲基水杨酸(3),以及三种新的二苯醚类化合物 Parmetherines A-C(4-6),此外还分离得到两种已知的同系物。通过广泛的光谱分析和与文献数据的比较,明确了它们的结构。对分离得到的多酚进行了α-葡萄糖苷酶抑制活性测试。新报道的苄基去甲二萜类化合物 1:和 2:对α-葡萄糖苷酶的抑制活性分别为 2.2 和 4.3 μM,明显优于阳性对照阿卡波糖。

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