香蒲
植物化学
水烛
花粉
混合的
化学
量子化学
IC50型
立体化学
植物
传统医学
体外
生物
有机化学
生物化学
分子
生态学
医学
湿地
作者
Chao Wang,Yu‐Peng Li,Xu Gong,Li‐She Gan,Hua Zhang
标识
DOI:10.1080/14786419.2023.2248352
摘要
AbstractTwo rarely occurring diphenylheptanoid-phenylheptanoid hybrid dimers (1 and 2) and one new oxygenated fatty acid (3), as well as two known fatty acid analogues (4 and 5), were isolated from the 70% EtOH extract of the pollen of Typha angustifolia. Their planar structures were established by interpretation of MS and NMR spectroscopic data, and the absolute configurations of 1 and 2 were determined by Mosher’s method and quantum chemical TD-DFT calculations of ECD spectra. An in vitro anti-diabetic evaluation of these isolates revealed that compounds 1 and 2 exhibited promising inhibitory activity against α-glucosidase with IC50 values of 11.85 ± 0.69 and 17.06 ± 3.08 μM, respectively. It is the first report on both diphenylheptanoid constituents and α-glucosidase inhibitors from the title plant, which represents a significant phytochemical progress of this herbal species and may serve as a reference for its future medicinal applications.Keywords: typha angustifoliadiphenylheptanoidphenylheptanoidα-glucosidase inhibitionabsolute configuration Disclosure statementNo potential conflict of interest was reported by the author(s).Additional informationFundingFinancial supports from Natural Science Foundation of Shandong Province [No. JQ201721], the Young Taishan Scholars Program [No. tsqn20161037] and National Natural Science Foundation of China (22077111) are greatly acknowledged.
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