Published January 30, 2015 | Version v1
Journal article Open

In vitro Antioxidant and Antiproliferative Activities of Flavonoids from Ailanthus excelsa (Roxb.) (Simaroubaceae) Leaves

  • 1. Pharmacognosy Department, National Research Centre, Dokki, Giza, Egypt
  • 2. Pharmaceutical Sciences Department, Faculty of Pharmacy, Nutrition and Health Sciences, University of Calabria, Arcavacata Rende 87036 (CS), Italy. Fax: +3 99 84 49 32 98
  • 3. Phytochemistry and Plant Systematic Department, National Research Centre, Dokki, Giza, Egypt
  • 4. Chemistry Department, Faculty of Science, Menoufi a University, Shebin El-Khom, Egypt
  • 5. Pharmaceutical Sciences Institute, Pharmaceutical Chemistry Department, University of Graz, Schubertstr. 1, A-8010 Graz, Austria

Description

The present study aimed to investigate the chemical composition, and the antioxidant and antiproliferative activities of Ailanthus excelsa, a plant used in Egyptian traditional medicine. Chromatographic separation of a methanol extract of A. excelsa leaves yielded four fl avones, namely apigenin (1), apigenin 7-O-β-glucoside (2), luteolin (3), and luteolin 7-O-β-glucoside (4), and seven fl avonols, namely kaempferol (5), kaempferol 3-O-α-arabinoside (6), kaempferol 3-O-β-galactoside (7), quercetin (8), quercetin 3-O-α-arabinoside (9), quercetin 3-O-β- galactoside (10), and quercetin 3-O-rutinoside (11). The A. excelsa extract tested in different in vitro systems (DPPH and FRAP assays) showed significant antioxidant activity. The potential antiproliferative activity of the A. excelsa extract and isolated flavonoids against five human cancer cell lines such as ACHN, COR-L23, A375, C32, and A549 was investigated in vitro by the SRB assay in comparison with one normal cell line, 142BR. The extract exhibited the highest inhibitory activity against C32 cells with an IC50 value of 36.5 μg ml-1. Interesting activity against COR-L23 was found with 10 (IC50 value of 3.2 μg ml-1). Compounds 1 and 3 inhibited cell growth in both amelanotic melanoma and malignant melanoma cells.

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