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J Chem Ecol


Title:Inhibition of male response of drugstore beetles to stegobinone by its isomer
Author(s):Kodama H; Mochizuki K; Kohno M; Ohnishi A; Kuwahara Y;
Address:"Central Research Institute, Japan Tobacco Inc., Umegaoka 6-2, Midori-ku, 227, Yokohama, Japan"
Journal Title:J Chem Ecol
Year:1987
Volume:13
Issue:8
Page Number:1859 - 1869
DOI: 10.1007/BF01013235
ISSN/ISBN:0098-0331 (Print) 0098-0331 (Linking)
Abstract:"Stegobinone, (2S, 3R, 1'R)-2,3,-dihy dro-2,3,5-trimethyl-6-(1'-methyl-2'-oxobutyl)-4H-pyran-4-one, the sex pheromone of drugstore beetles (Stegobium paniceum L.), elicited the pheromonal response from the males of the species in our bioassay system; however, the synthesized diastereomeric mixture of this compound was actually inactive to the males. Although the stegobinone isolated from the beetles of this species had significant activity, its enantiomeric [(+/-)-2S,3R,1'S-] and diatereomeric [(+/-)-2S,3S,1'RS-] isomers were inactive. Adding the (+/-)-2S,3R,1'S isomer to stegobinone significantly reduced the male response. Furthermore, the activity of Stegobinone vanished on keeping it at room temperature for two weeks. In such a stored stegobinone sample, the presence of 2S,3R,1'S isomer, the inhibitory component, was confirmed. This isomer might be produced by C-1' epimerization during storage"
Keywords:
Notes:"PubMed-not-MEDLINEKodama, H Mochizuki, K Kohno, M Ohnishi, A Kuwahara, Y eng 1987/08/01 J Chem Ecol. 1987 Aug; 13(8):1859-69. doi: 10.1007/BF01013235"

 
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