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