Isolation of eudesmane type sesquiterpene ketone from Prangos heyniae H.Duman & M.F.Watson essential oil and mosquitocidal activity of the essential oils

Author:

Özek Gülmira1,Bedir Erdal2,Tabanca Nurhayat34,Ali Abbas4,Khan Ikhlas A.4,Duran Ahmet5,Başer Kemal H.C.6,Özek Temel17

Affiliation:

1. Department of Pharmacognosy, Faculty of Pharmacy, Anadolu University, Eskişehir, 26470, Turkey

2. Department of Bioengineering, Izmir Institute of Technology, Urla, 35430, Izmir, Turkey

3. USDA-ARS, Subtropical Horticulture Research Station, 13601 Old Cutler Rd., Miami, FL 33158, USA

4. National Center for Natural Products Research, The University of Mississippi, University, MS 38677, Miami, USA

5. Sancak District, Veysel Karani Street, Ataşehir Homes, Blok K/38, Selçuklu / konya, Turkey

6. Department of Pharmacognosy, Faculty of Pharmacy, Near East University, Lefkoşa (Nicosia) TRNC, Mersin 10, Mersin, Turkey

7. Anadolu University, Medicinal Plant Drug and Scientific Research Center (AUBIBAM), 26470-Eskişehir, Turkey

Abstract

AbstractIn the present work, an endemic species Prangos heyniae collected in four locations from Turkey was subjected to hydrodistillation in Clevenger type apparatus to obtain the essential oils (EO1-4). The gas-chromatography/mass spectrometry (GC/MS) and gas-chromatography-flame ionization detector (GC/FID) analyses showed that the EOs were rich in sesquiterpenes, germacrene D (10.3-12.1%), β-bisabolene (14.4%), kessane (26.9%), germacrene B (8.2%), elemol (3.4-46.9%), β-bisabolenal (1.4-70.7%), β-bisabolenol (8.4%) and an eudesmane type sesquiterpene (1) (16.1%) with [M+218]. This unidentified compound (1) was isolated in a rapid one-step manner with >95.0% purity using Preparative Capillary Gas Chromatography (PCGC) with an HP Innowax column connected to a Preparative Fraction Collector (PFC) system. Structure determination was accomplished from 1D- and 2D-NMR spectroscopic data which determined a new eudesmane type sesquiterpene, 3,7(11)-eudesmadien-2-one (1). Using a biting deterrent bioassay, the mean proportion not biting (PNB) values of the P. heyniae EO1-4 were 0.88 for EO1 and 0.80 for EO2 which were similar to the positive control DEET (N,N-diethyl-3-methylbenzamide). The EO3 and EO4 had lower PNB values of 0.64 and 0.44, respectively. P. heyniae EO1-4 showed good larvicidal activity at 125 and 62.5 ppm whereas EO1-3 were slightly less effective at the dose of 31.25 ppm and EO4 was not active at 31.25 ppm against 1st instar Aedes aegypti.

Publisher

Walter de Gruyter GmbH

Subject

Materials Chemistry,General Chemistry

Reference184 articles.

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4. Comparative evaluation of cytotoxic and apoptogenic effects of several coumarins on human cancer cell lines: osthole induces apoptosis in p53-deficient H1299 cells;Adv. Pharmacol. Sci.,2014

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