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Ferulone A and ferulone B: two new coumarin esters from Ferula orientalis L. roots
Authors:Seyed Mehdi Razavi  Lutfun Nahar  Hamideh Talischi  Satyajit Dey Sarker
Institution:1. Faculty of Sciences, Department of Biology, University of Mohaghegh Ardabili, Ardabil, Iranm_razavi@uma.ac.ir;3. School of Pharmacy and Biomolecular Sciences, Medicinal Chemistry and Natural Products Research Group, Liverpool John Moores University, Liverpool, UK;4. Faculty of Sciences, Department of Biology, University of Mohaghegh Ardabili, Ardabil, Iran
Abstract:Ferula orientalis (Apiaceae) is a well-known perennial herb growing wild in Iran used in traditional medicine. To perform phytochemical studies, dried ground roots of F. orientalis were sequentially Soxhlet-extracted using n-hexane, dichloromethane and methanol. A combination of vacuum liquid chromatography and preparative thin-layer chromatographic analyses were performed to isolate coumarin esters. The structures of the isolated compounds were elucidated by spectroscopic means, and in vitro free-radical-scavenging property was determined by the DPPH assay. Two new coumarin esters, 7-O-(4,8,12,16-tetrahydroxy-4,8,12,16-tetramethyl-heptadecanoyl)-coumarinand 7-O-(4-hydroxy-4,8,12-trimethyl-trideca-7,11-dienoyl)-coumarin, named ferulone A and ferulone B, respectively, were isolated from the n-hexane extract of the roots of F. orientalis. Both compounds showed a low level of free-radical-scavenging property with the RC50 values of 0.252 and 0.556 mg/mL for compounds 1 and 2, respectively, as opposed to that of the positive control (quercetin) 0.004 mg/mL. This is the first report on the purification of coumarin esters from the genus Ferula.
Keywords:Ferula orientalis  ferulone  free-radical-scavenging  DPPH  umbelliferone
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