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« Previous AbstractDiscovery of the aggregation pheromone of the brown marmorated stink bug (Halyomorpha halys) through the creation of stereoisomeric libraries of 1-bisabolen-3-ols    Next AbstractAbsolute Configurations of Stink Bug- and Plant-Produced Sesquipiperitols via Synthesis of All Stereoisomers »

J Nat Prod


Title:Absolute Configurations of Zingiberenols Isolated from Ginger (Zingiber officinale) Rhizomes
Author(s):Khrimian A; Shirali S; Guzman F;
Address:"Invasive Insect Biocontrol and Behavior Laboratory, U.S. Department of Agriculture, Agricultural Research Service , Northeast Area, Bldg 007, Rm 301, BARC-West, 10300 Baltimore Avenue, Beltsville, Maryland 20705, United States"
Journal Title:J Nat Prod
Year:2015
Volume:20151125
Issue:12
Page Number:3071 - 3074
DOI: 10.1021/acs.jnatprod.5b00638
ISSN/ISBN:1520-6025 (Electronic) 0163-3864 (Linking)
Abstract:"Two stereoisomeric zingiberenols in ginger were identified as (3R,6R,7S)-1,10-bisaboladien-3-ol (2) and (3S,6R,7S)-1,10-bisaboladien-3-ol (5). Absolute configurations were assigned by utilizing 1,10-bisaboladien-3-ol stereoisomers and two gas-chromatography columns: a 25 m Hydrodex-beta-6TBDM and 60 m DB-5MS. The C-6 and C-7 absolute configurations in both zingiberenols match those of zingiberene present abundantly in ginger rhizomes. Interestingly, zingiberenol 2 has recently been identified as a male-produced sex pheromone of the rice stink bug, Oebalus poecilus, thus indicating that ginger plants may be a potential source of the sex pheromone of this bug"
Keywords:"Animals Gas Chromatography-Mass Spectrometry Ginger/*chemistry Heteroptera/drug effects/metabolism Male Molecular Structure Monocyclic Sesquiterpenes Oils, Volatile Pheromones/chemistry/*isolation & purification/pharmacology Rhizome/*chemistry Sesquiterpe;"
Notes:"MedlineKhrimian, Ashot Shirali, Shyam Guzman, Filadelfo eng Research Support, U.S. Gov't, Non-P.H.S. 2015/11/26 J Nat Prod. 2015 Dec 24; 78(12):3071-4. doi: 10.1021/acs.jnatprod.5b00638. Epub 2015 Nov 25"

 
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