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Globunoids A-D,来自 Knema globularia 茎的未描述的双查耳酮和双黄烷类化合物,具有α-葡萄糖苷酶和α-淀粉酶抑制活性。

Globunoids A-D, undescribed bichalconoid and biflavanoids with α-glucosidase and α-amylase inhibitory activities from Knema globularia stems.

机构信息

Center of Excellence in Natural Products Chemistry, Department of Chemistry, Chulalongkorn University, Pathumwan, Bangkok, 10330, Thailand.

Graduate School of Bioagricultural Sciences, Nagoya University, Nagoya, 464-8601, Japan.

出版信息

Phytochemistry. 2024 May;221:114066. doi: 10.1016/j.phytochem.2024.114066. Epub 2024 Mar 15.

Abstract

A bichalconoid, globunoid A (1) and three biflavanones, globunoids B-D (2-4), previously undescribed, were isolated from the stems of Knema globularia, along with fourteen known analogues 5-18. The chemical structures of 1-4 were elucidated by the comprehensive spectroscopic analysis including UV, IR, HRESIMS, and NMR; the absolute configurations were determined based on their NOESY data, DP4+ statistical analysis, and ECD calculation. Up to now, compounds 2 and 3 represent the first 3,3″-linked biflavanone structures. Among the isolated compounds, 2, 3, and 2,3-dihydrocalodenin B (6) potently inhibited α-glucosidase and α-amylase activities, with IC values in the range 1.1-7.5 μM. Furthermore, the most active compound 6 was found to be a non-competitive inhibitor against these two enzymes.

摘要

一种双查耳酮、球形 A(1)和三种双二氢黄酮醇,球形 B-D(2-4),以前未被描述过,从 Knema globularia 的茎中分离出来,同时还分离出了 14 种已知类似物 5-18。通过包括 UV、IR、HRESIMS 和 NMR 的综合光谱分析,阐明了 1-4 的化学结构;根据它们的 NOESY 数据、DP4+统计分析和 ECD 计算确定了绝对构型。到目前为止,化合物 2 和 3 代表了第一个 3,3″-连接的双二氢黄酮醇结构。在分离得到的化合物中,2、3 和 2,3-二氢白头翁素 B(6)强烈抑制α-葡萄糖苷酶和α-淀粉酶的活性,IC 值在 1.1-7.5 μM 范围内。此外,发现最活性化合物 6 对这两种酶均为非竞争性抑制剂。

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