Lipoxygenase inhibitors flavonoids from Cyperus rotundus aerial parts

被引:0
|
作者
Sabrin R. M. Ibrahim
Gamal A. Mohamed
Khalid Z. Alshali
Rwaida A. Al Haidari
Amal A. El-Kholy
Mohamed F. Zayed
机构
[1] Taibah University,Department of Pharmacognosy and Pharmaceutical Chemistry, College of Pharmacy
[2] Assiut University,Department of Pharmacognosy, Faculty of Pharmacy
[3] King Abdulaziz University,Department of Natural Products and Alternative Medicine, Faculty of Pharmacy
[4] Al-Azhar University,Department of Pharmacognosy, Faculty of Pharmacy
[5] Assiut Branch,Department of Medicine, Faculty of Medicine
[6] King Abdulaziz University,Department of Clinical and Hospital Pharmacy, College of Pharmacy
[7] Taibah University,Department of Clinical Pharmacy, Faculty of Pharmacy
[8] Ain-Shams University,Department of Pharmaceutical Chemistry, Faculty of Pharmacy
[9] Al-Azhar University,undefined
来源
关键词
Cyperaceae; Flavonols; Myricetin derivative; 5-Lipoxygenase inhibitor; Inflammation; Structural activity relationship;
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摘要
Cyperus rotundus L. (Suada, Sueda, family: Cyperaceae) is vastly spread in several world’s subtropical and tropical regions. It had variable traditional uses and bioactivities. A new flavonol derivative: cyperaflavoside (myricetin 3,3′,5′-trimethyl ether 7-O-β-d-glucopyranoside) and five flavonoids: vitexin, orientin, cinaroside, quercetin 3-O-β-d-glucopyranoside, and myrcetin 3-O-β-d-glucopyranoside were separated from the methanolic extract of C. rotundus aerial parts. Their structures were verified based on UV, IR, NMR (1D and 2D), HRESIMS, and comparison with literature. All metabolites were assessed for their 5-lipoxygenase inhibitory potential. All compounds possessed 5-lipoxygenase inhibitory potentials with IC50s 5.1, 4.5, 5.9, 4.0, 3.7, and 2.3 μM, respectively, in comparison to indomethacin (IC50 0.98 μM). These results supported the traditional uses of C. rotundus in treating inflammation and its related symptoms.
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页码:320 / 324
页数:4
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