Bedoukian   RussellIPM   RussellIPM   Piezoelectric Micro-Sprayer


Home
Animal Taxa
Plant Taxa
Semiochemicals
Floral Compounds
Semiochemical Detail
Semiochemicals & Taxa
Synthesis
Control
Invasive spp.
References

Abstract

Guide

Alphascents
Pherobio
InsectScience
E-Econex
Counterpart-Semiochemicals
Print
Email to a Friend
Kindly Donate for The Pherobase

« Previous AbstractA mechanism for the coordination of proliferation and differentiation by spatial regulation of Fus2p in budding yeast    Next AbstractEffects of Indoor Air Pollutants on Atopic Dermatitis »

Sci Rep


Title:Bursaphelenchus xylophilus is killed by homologues of 2-(1-undecyloxy)-1-ethanol
Author(s):Kim J; Lee SM; Park CG;
Address:"Institute of Agriculture and Life Science, Gyeongsang National University, Jinju 52828, Republic of Korea. SM Biovision Co., Jinju 52828, Republic of Korea. Institute of Life Science, Gyeongsang National University, Jinju 52828, Republic of Korea. Division of Applied Life Science (BK21+ Program) Gyeongsang National University, Jinju 52828, Republic of Korea"
Journal Title:Sci Rep
Year:2016
Volume:20160711
Issue:
Page Number:29300 -
DOI: 10.1038/srep29300
ISSN/ISBN:2045-2322 (Electronic) 2045-2322 (Linking)
Abstract:"2-(1-Undecyloxy)-1-ethanol, monochamol, is a male-produced aggregation pheromone of the Monochamus species, which are efficient vectors of the pine wood nematode (PWN), Bursaphelenchus xylophilus, which cause devastating damage to pines worldwide. The nematicidal activity of synthetic monochamol and its homologues (ROEtOH: R = C7-C13) were investigated to find potential alternatives to the currently used PWN control agents abamectin and emamectin. Compounds with C7-C13 chain length alkyl groups exhibited 100% nematicidal activity at a concentration of 1000 mg/L. At a concentration of 100 mg/L, 2-(1-nonyloxy)-1-ethanol (C9OEtOH), 2-(1-decyloxy)-1-ethanol (C10OEtOH), 2-(1-undecyloxy)-1-ethanol (C11OEtOH), and 2-(1-dodecyloxy)-1-ethanol (C12OEtOH) showed 100% nematicidal activity, but the others showed weaker activities. C11OEtOH showed similar nematicidal activity to abamectin in terms of LD90 values, which were 13.30 and 12.53 mg/L, respectively. However, C9OEtOH, C10OEtOH, and C12OEtOH (LC90 values: 53.63, 38.18, and 46.68 mg/L, respectively) were less effective than C11OEtOH and abamectin. These results indicate that monochamol could be an effective alternative agent against PWN. The relationship of insecticidal and nematicidal activity to different carbon chain lengths in compounds is discussed"
Keywords:Animals Antinematodal Agents/*administration & dosage Coleoptera/*parasitology Disaccharides/therapeutic use Disease Vectors Ecosystem Ethanol/administration & dosage/*analogs & derivatives/chemistry Ethers/*administration & dosage/chemistry Insecticides/;
Notes:"MedlineKim, Junheon Lee, Sang-Myeong Park, Chung Gyoo eng England 2016/07/13 Sci Rep. 2016 Jul 11; 6:29300. doi: 10.1038/srep29300"

 
Back to top
 
Citation: El-Sayed AM 2024. The Pherobase: Database of Pheromones and Semiochemicals. <http://www.pherobase.com>.
© 2003-2024 The Pherobase - Extensive Database of Pheromones and Semiochemicals. Ashraf M. El-Sayed.
Page created on 28-12-2024