Five new flavonoids and their pharmacological activities from Iris tenuifolia Pall.

被引:0
|
作者
Yan, Huijing [1 ]
Lyu, Haoyu [2 ,3 ]
Otgon, Oldokh [1 ,4 ]
Lu, Jie [1 ]
Peng, Dandan [1 ]
Zhu, Yuanhang [5 ]
Jiang, Jianqin [1 ]
机构
[1] China Pharmaceut Univ, Sch Tradit Chinese Pharm, 639 Long Mian Da Dao, Nanjing 211198, Peoples R China
[2] China Pharmaceut Univ, Sch Basic Med & Clin Pharm, 639 Long Mian Da Dao, Nanjing 211198, Peoples R China
[3] Second Mil Med Univ, Coll Pharm, Dept Pharmacol, Shanghai, Peoples R China
[4] Mongolian Natl Univ Med Sci, Sch Biomed, Dept Chem, S Zorig St 3, Ulaanbaatar 14210, Mongolia
[5] First Peoples Hosp Yunnan Prov, Dept Anesthesiol, 157 Jinbi Rd, Kunming 650034, Peoples R China
基金
中国国家自然科学基金;
关键词
Iris tenuifolia Pall; Flavonoid; Antioxidant activity; Anti-alpha-glucosidase activity; ROS; ISOFLAVONE; LEAVES;
D O I
10.1016/j.fitote.2024.106022
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Five new components including two new isoflavones, 5, 7, 2 ', 3 '-tetrahydroxy-6-methoxyisoflavone (1), 5, 7, 2 ', 3 '-tetrahydroxy-8-methoxyisoflavone (2), one flavonol 3, 5, 3 ', 4 '-tetrahydroxy-7, 2 '-dimethoxyflavonol (3), one flavanone (2S)-5, 7, 3 '-trihydroxy-2 '-methoxyflavanone (4), and one flavanonol (2R, 3R)-3, 5, 3 ', 4 '-tetrahydroxy7, 2 '-dimethoxyflavanonol (5), along with nine known flavonoids (6-14) were isolated from under ground parts of Iris tenuifolia Pall. Their structures were elucidated by NMR and HRESIMS data and by comparison of CD spectra with compounds having similar structure. The separated compounds were evaluated for in vitro antioxidant activities by DPPH and ABTS. The alpha-glucosidase inhibitory activity of the compounds were evaluated with the pNPG method, the results indicated flavonoids were potential inhibitors of alpha-glucosidase. Moreover, in vitro anti-oxidative assay using flow cytometry indicated that compounds 1-5 showed strong oxidation resistance ability on C8D1A cells without affecting the cell viability.
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页数:8
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