The Identification of Suberosin from Prangos pabularia Essential Oil and Its Mosquito Activity Against Aedes aegypti
A detailed analysis of Prangos pabularia Lindl. (Apiaceae) fruit oil was performed by gas chromatography (GC-FID) and gas chromatography-mass spectrometry (GC-MS). Bicyclogermacrene (21%), (Z)- b -ocimene (19%), a -humulene (8%), a -pinene (8%) and spathulenol (6%) were the main constituents of the...
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description | A detailed analysis of Prangos pabularia Lindl. (Apiaceae) fruit oil was performed by gas chromatography (GC-FID) and gas chromatography-mass spectrometry (GC-MS). Bicyclogermacrene (21%), (Z)- b -ocimene (19%), a -humulene (8%), a -pinene (8%) and spathulenol (6%) were the main constituents of the oil. One compound with 1.8% at RI 3420 remained unidentified or tentatively identified as suberosin from the Wiley GC-MS Library. T he assumed compound, suberosin was synthesized in two steps and its structure was confirmed by 1D NMR and GC- MS analyses. As part of our continued research to discover new chemicals for use in mosquito control agents as repellents and larvicides, suberosin and its parent compound coumarin were investigated for the mosquito biting deterrent and larvicidal activity against Aedes aegypti. Both suberosin and coumarin showed biting deterrent activity but the activity was lower than the positive control, DEET (N,N-diethyl-3-methylbenzamide). In larval bioassays, suberosin with LC 50 value of 8.1 ppm was significantly more toxic than c oumarin (LC 50 = 49.6 ppm) at 24-h post treatment. These results indicate that suberosin may be useful for use as mosquito larvicidal agent . |
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(Apiaceae) fruit oil was performed by gas chromatography (GC-FID) and gas chromatography-mass spectrometry (GC-MS). Bicyclogermacrene (21%), (Z)- b -ocimene (19%), a -humulene (8%), a -pinene (8%) and spathulenol (6%) were the main constituents of the oil. One compound with 1.8% at RI 3420 remained unidentified or tentatively identified as suberosin from the Wiley GC-MS Library. T he assumed compound, suberosin was synthesized in two steps and its structure was confirmed by 1D NMR and GC- MS analyses. As part of our continued research to discover new chemicals for use in mosquito control agents as repellents and larvicides, suberosin and its parent compound coumarin were investigated for the mosquito biting deterrent and larvicidal activity against Aedes aegypti. Both suberosin and coumarin showed biting deterrent activity but the activity was lower than the positive control, DEET (N,N-diethyl-3-methylbenzamide). In larval bioassays, suberosin with LC 50 value of 8.1 ppm was significantly more toxic than c oumarin (LC 50 = 49.6 ppm) at 24-h post treatment. 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In larval bioassays, suberosin with LC 50 value of 8.1 ppm was significantly more toxic than c oumarin (LC 50 = 49.6 ppm) at 24-h post treatment. These results indicate that suberosin may be useful for use as mosquito larvicidal agent .</description><subject>Chromatography</subject><subject>Diuretics</subject><subject>Education</subject><subject>Entomology</subject><subject>Hemorrhoids</subject><subject>Investigations</subject><subject>Libraries</subject><subject>Literature reviews</subject><subject>Mass spectrometry</subject><subject>Mosquitoes</subject><subject>NMR</subject><subject>Nuclear magnetic resonance</subject><subject>Oils & fats</subject><subject>Pharmacy</subject><subject>Retention</subject><subject>Scientific imaging</subject><subject>Temperature</subject><issn>1307-6167</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><recordid>eNotjctKw0AUQIMgWKv_cMF1YB6ZR5ahVA1UKljX5Sa5iVPiTJqZCP17FV2d1TnnKltxyUyuuTY32W2MJ8a0tKZYZenwQVB35JPrXYvJBQ-hh7eloTlE56Gfwye8zuiHEGHCZhlxdgjbGH8dHGHvRkDfQZ0ivIR4XlwKULXJfbl0gWpA52OCijqKgDRcpuTususex0j3_1xn74_bw-Y53-2f6k21yyduZcq5VIKpxrSd5S0xxrhWRLbkqjdtQb1tS6sKgSXqBrVgjbIoGCOBaFRZklxnD3_daQ7nhWI6nsIy-5_lkVsmhdSlsPIbiFtXHA</recordid><startdate>20160101</startdate><enddate>20160101</enddate><creator>Tabanca, Nurhayat</creator><creator>Tsikolia, Maia</creator><creator>Ozek, Gulmira</creator><creator>Temel Ozek</creator><creator>Abbas, Ali</creator><creator>Bernier, Ulrich R</creator><creator>Duran, Ahmet</creator><creator>K Husnu Can Baser</creator><creator>Khan, Ikhlas A</creator><general>ACG Publications</general><scope>3V.</scope><scope>7WY</scope><scope>7XB</scope><scope>883</scope><scope>8FK</scope><scope>8FL</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>BEZIV</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FRNLG</scope><scope>K60</scope><scope>K6~</scope><scope>M0F</scope><scope>PIMPY</scope><scope>PQBIZ</scope><scope>PQBZA</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope></search><sort><creationdate>20160101</creationdate><title>The Identification of Suberosin from Prangos pabularia Essential Oil and Its Mosquito Activity Against Aedes aegypti</title><author>Tabanca, Nurhayat ; 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(Apiaceae) fruit oil was performed by gas chromatography (GC-FID) and gas chromatography-mass spectrometry (GC-MS). Bicyclogermacrene (21%), (Z)- b -ocimene (19%), a -humulene (8%), a -pinene (8%) and spathulenol (6%) were the main constituents of the oil. One compound with 1.8% at RI 3420 remained unidentified or tentatively identified as suberosin from the Wiley GC-MS Library. T he assumed compound, suberosin was synthesized in two steps and its structure was confirmed by 1D NMR and GC- MS analyses. As part of our continued research to discover new chemicals for use in mosquito control agents as repellents and larvicides, suberosin and its parent compound coumarin were investigated for the mosquito biting deterrent and larvicidal activity against Aedes aegypti. Both suberosin and coumarin showed biting deterrent activity but the activity was lower than the positive control, DEET (N,N-diethyl-3-methylbenzamide). In larval bioassays, suberosin with LC 50 value of 8.1 ppm was significantly more toxic than c oumarin (LC 50 = 49.6 ppm) at 24-h post treatment. These results indicate that suberosin may be useful for use as mosquito larvicidal agent .</abstract><cop>Gebze</cop><pub>ACG Publications</pub><oa>free_for_read</oa></addata></record> |
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subjects | Chromatography Diuretics Education Entomology Hemorrhoids Investigations Libraries Literature reviews Mass spectrometry Mosquitoes NMR Nuclear magnetic resonance Oils & fats Pharmacy Retention Scientific imaging Temperature |
title | The Identification of Suberosin from Prangos pabularia Essential Oil and Its Mosquito Activity Against Aedes aegypti |
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