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Phenolics of Cyperus alopecuroides Rottb. inflorescences and their biological activities

مؤلف البحث
Hanaa M. Sayed, Mahmoud H. Mohamed, Salwa F. Farag, Gamal A. Mohamed, Rainer Ebel, Olanrewaju R. M. Omobuwajo and Peter Proksch
قسم البحث
مجلة البحث
Bulletin of Pharmaceutical Sciences
الناشر
Assiut University
تصنيف البحث
2
عدد البحث
29 (1)
سنة البحث
2006
المشارك في البحث
ملخص البحث

Sixteen phenolic compounds, scopoletin (1), isoliquiritigenin 4-methyl ether (2), luteolin 5,3-dimethyl ether (3), luteolin 7,3-dimethyl ether (4), aureusidin 4-methyl ether (5), apigenin (6), luteolin (7), trans- ferulic acid (8), luteolin 4-O--D-glucopyranoside (9), luteolin 7-O--D-glucopyranoside (10), quercetin 3-O--D-glucopyranoside (11), apigenin 7-O-neohesperidoside (12), kaempferol 3-O-rutinoside (13), quercetin 3-O-rutinoside (14), kaempferol 3-O-[2-O-D-xylopyranosyl-6-O--L-rhamnopyranosyl]--D-glucopyranoside (15) and kaempferol 3-O-[2-O-D-glucopyranosyl-6-O--L-rhamnopyranosyl]--D-glucopyranoside (16) were isolated from the methanolic extract of the inflorescences of Cyperus alopecuroides Rottb. for the first time. Their structures have been established on basis of physical, chemical and spectroscopic methods in addition to comparison with literature data and/or authentic samples. The antioxidant and cytotoxic activities in addition to -amylase inhibitory activity of the isolated compounds have been studied.