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Sesquiterpenoids and 2-(2-phenylethyl)chromones respectively acting as α-glucosidase and tyrosinase inhibitors from agarwood of an Aquilaria plant

机译:倍半萜和2-(2-苯基乙基)色酮分别作为沉香植物沉香中的α-葡萄糖苷酶和酪氨酸酶抑制剂

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摘要

The ethyl ether extract of agarwood from an Aquilaria plant afforded six new sesquiterpenoids, Agarozizanol A − F (>1−>6), together with four known sesquiterpenoids and six known 2-(2-phenylethyl)chromones. Their structures were elucidated via detailed spectroscopic analysis, X-ray diffraction, and comparisons with the published data. All the isolates were evaluated for the α-glucosidase and tyrosinase inhibitory activities in vitro. Compounds >5, >7, >8, and >10 showed significant inhibition of α-glucosidase with IC50 values ranging between 112.3 ± 4.5 and 524.5 ± 2.7 µM (acarbose, 743. 4 ± 3.3 µM). Compounds >13 and >14 exhibited tyrosinase inhibitory effect with IC50 values of 89.0 ± 1.7 and 51.5 ± 0.6 µM, respectively (kojic acid, 46.1 ± 1.3). In the kinetic studies, compounds >5 and >14 were found to be uncompetitive inhibitors for α-glucosidase and mixed type inhibitors for tyrosinase, respectively. Furthermore, molecular docking simulations revealed the binding sites and interactions of the most active compounds with α-glucosidase and tyrosinase.
机译:沉香植物沉香的乙醚提取物提供了六种新的倍半萜,琼脂二糖Aanol- F(> 1 -> 6 ),以及四种已知的倍半萜和六种2-( 2-苯基乙基)色酮。通过详细的光谱分析,X射线衍射以及与已发表数据的比较,阐明了它们的结构。在体外评估所有分离物的α-葡萄糖苷酶和酪氨酸酶抑制活性。化合物> 5 ,> 7 ,> 8 和> 10 对α-葡萄糖苷酶具有明显的抑制作用,IC50值在112.3之间±4.5和524.5±2.7 µM(阿卡波糖,743。4±3.3 µM)。化合物> 13 和> 14 表现出酪氨酸酶抑制作用,IC50值分别为89.0±1.7和51.5±0.6μM(曲酸,46.1±1.3)。在动力学研究中,发现化合物> 5 和> 14 分别是α-葡萄糖苷酶的竞争性抑制剂和酪氨酸酶的混合型抑制剂。此外,分子对接模拟揭示了最具活性的化合物与α-葡萄糖苷酶和酪氨酸酶的结合位点和相互作用。

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