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Contact and Fumigant Toxicities of 3‑Methylphenol Isolated from Ostericum koreanum and Its Derivatives against House Dust Mites

The acaricidal activities of an active constituent derived from Ostericum koreanum roots and its derivatives were determined using fumigant and direct-contact toxicity bioassays against Dermatophagoides farinae and Dermatophagoides pteronyssinus. This was compared with that of a commercial acaricide...

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Published in:Journal of agricultural and food chemistry 2012-12, Vol.60 (50), p.12349-12354
Main Authors: Jeon, Ju-Hyun, Yang, Ji-Yeon, Chung, Namhyun, Lee, Hoi-Seon
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Language:English
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cited_by cdi_FETCH-LOGICAL-a369t-bffb1ea25fb7b2cebbca66df12940b2f783ab5d90c5b9706f42da0926adf0dc43
cites cdi_FETCH-LOGICAL-a369t-bffb1ea25fb7b2cebbca66df12940b2f783ab5d90c5b9706f42da0926adf0dc43
container_end_page 12354
container_issue 50
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creator Jeon, Ju-Hyun
Yang, Ji-Yeon
Chung, Namhyun
Lee, Hoi-Seon
description The acaricidal activities of an active constituent derived from Ostericum koreanum roots and its derivatives were determined using fumigant and direct-contact toxicity bioassays against Dermatophagoides farinae and Dermatophagoides pteronyssinus. This was compared with that of a commercial acaricide (benzyl benzoate). In the fumigant toxicity bioassay, 4-chloro-6-isopropyl-3-methylphenol (0.29 μg/cm2) was 37.17 times more effective than benzyl benzoate (10.78 μg/cm2) against D. farinae, followed by 6-fluoro-3-methylphenol (0.57 μg/cm2), 3-methylphenol (0.63 μg/cm2), 4-chloro-3-methylphenol (0.75 μg/cm2), and 4-isopropyl-3-methylphenol (0.78 μg/cm2). In the direct-contact toxicity bioassay, 4-chloro-6-isopropyl-3-methylphenol (0.21 μg/cm2) was 36.81 times more toxic than benzyl benzoate (7.73 μg/cm2) against D. farinae, followed by 6-fluoro-3-methylphenol (0.40 μg/cm2), 3-methylphenol (0.41 μg/cm2), 4-isopropyl-3-methylphenol (0.56 μg/cm2), and 4-chloro-3-methylphenol (0.60 μg/cm2). The acaricidal effects of 3-methyphenol derivatives against D. pteronyssinus were similar to those against D. farinae. In structure–activity relationships, acaricidal activities could be related to the introduction of chloro, fluoro, and isopropyl functional groups onto the 3-methylphenol skeleton. These results indicate that naturally occurring 3-methylphenol and its derivatives are potential house dust mite control agents.
doi_str_mv 10.1021/jf3044296
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Agric. Food Chem</addtitle><description>The acaricidal activities of an active constituent derived from Ostericum koreanum roots and its derivatives were determined using fumigant and direct-contact toxicity bioassays against Dermatophagoides farinae and Dermatophagoides pteronyssinus. This was compared with that of a commercial acaricide (benzyl benzoate). In the fumigant toxicity bioassay, 4-chloro-6-isopropyl-3-methylphenol (0.29 μg/cm2) was 37.17 times more effective than benzyl benzoate (10.78 μg/cm2) against D. farinae, followed by 6-fluoro-3-methylphenol (0.57 μg/cm2), 3-methylphenol (0.63 μg/cm2), 4-chloro-3-methylphenol (0.75 μg/cm2), and 4-isopropyl-3-methylphenol (0.78 μg/cm2). In the direct-contact toxicity bioassay, 4-chloro-6-isopropyl-3-methylphenol (0.21 μg/cm2) was 36.81 times more toxic than benzyl benzoate (7.73 μg/cm2) against D. farinae, followed by 6-fluoro-3-methylphenol (0.40 μg/cm2), 3-methylphenol (0.41 μg/cm2), 4-isopropyl-3-methylphenol (0.56 μg/cm2), and 4-chloro-3-methylphenol (0.60 μg/cm2). The acaricidal effects of 3-methyphenol derivatives against D. pteronyssinus were similar to those against D. farinae. In structure–activity relationships, acaricidal activities could be related to the introduction of chloro, fluoro, and isopropyl functional groups onto the 3-methylphenol skeleton. 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Psychology</topic><topic>Gas Chromatography-Mass Spectrometry</topic><topic>Insecticides - chemistry</topic><topic>Insecticides - pharmacology</topic><topic>mite control</topic><topic>Plant Extracts - pharmacology</topic><topic>Pyroglyphidae - drug effects</topic><topic>roots</topic><topic>toxicity</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jeon, Ju-Hyun</creatorcontrib><creatorcontrib>Yang, Ji-Yeon</creatorcontrib><creatorcontrib>Chung, Namhyun</creatorcontrib><creatorcontrib>Lee, Hoi-Seon</creatorcontrib><collection>AGRIS</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><jtitle>Journal of agricultural and food chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jeon, Ju-Hyun</au><au>Yang, Ji-Yeon</au><au>Chung, Namhyun</au><au>Lee, Hoi-Seon</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Contact and Fumigant Toxicities of 3‑Methylphenol Isolated from Ostericum koreanum and Its Derivatives against House Dust Mites</atitle><jtitle>Journal of agricultural and food chemistry</jtitle><addtitle>J. Agric. Food Chem</addtitle><date>2012-12-19</date><risdate>2012</risdate><volume>60</volume><issue>50</issue><spage>12349</spage><epage>12354</epage><pages>12349-12354</pages><issn>0021-8561</issn><eissn>1520-5118</eissn><coden>JAFCAU</coden><abstract>The acaricidal activities of an active constituent derived from Ostericum koreanum roots and its derivatives were determined using fumigant and direct-contact toxicity bioassays against Dermatophagoides farinae and Dermatophagoides pteronyssinus. This was compared with that of a commercial acaricide (benzyl benzoate). In the fumigant toxicity bioassay, 4-chloro-6-isopropyl-3-methylphenol (0.29 μg/cm2) was 37.17 times more effective than benzyl benzoate (10.78 μg/cm2) against D. farinae, followed by 6-fluoro-3-methylphenol (0.57 μg/cm2), 3-methylphenol (0.63 μg/cm2), 4-chloro-3-methylphenol (0.75 μg/cm2), and 4-isopropyl-3-methylphenol (0.78 μg/cm2). In the direct-contact toxicity bioassay, 4-chloro-6-isopropyl-3-methylphenol (0.21 μg/cm2) was 36.81 times more toxic than benzyl benzoate (7.73 μg/cm2) against D. farinae, followed by 6-fluoro-3-methylphenol (0.40 μg/cm2), 3-methylphenol (0.41 μg/cm2), 4-isopropyl-3-methylphenol (0.56 μg/cm2), and 4-chloro-3-methylphenol (0.60 μg/cm2). The acaricidal effects of 3-methyphenol derivatives against D. pteronyssinus were similar to those against D. farinae. In structure–activity relationships, acaricidal activities could be related to the introduction of chloro, fluoro, and isopropyl functional groups onto the 3-methylphenol skeleton. These results indicate that naturally occurring 3-methylphenol and its derivatives are potential house dust mite control agents.</abstract><cop>Washington, DC</cop><pub>American Chemical Society</pub><pmid>23194135</pmid><doi>10.1021/jf3044296</doi><tpages>6</tpages></addata></record>
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ispartof Journal of agricultural and food chemistry, 2012-12, Vol.60 (50), p.12349-12354
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1520-5118
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source American Chemical Society:Jisc Collections:American Chemical Society Read & Publish Agreement 2022-2024 (Reading list)
subjects acaricidal properties
Animals
Apiaceae - chemistry
benzyl benzoate
bioassays
Biological and medical sciences
Cresols - chemistry
Cresols - pharmacology
Dermatophagoides farinae
Dermatophagoides pteronyssinus
dust mites
Food industries
fumigants
Fundamental and applied biological sciences. Psychology
Gas Chromatography-Mass Spectrometry
Insecticides - chemistry
Insecticides - pharmacology
mite control
Plant Extracts - pharmacology
Pyroglyphidae - drug effects
roots
toxicity
title Contact and Fumigant Toxicities of 3‑Methylphenol Isolated from Ostericum koreanum and Its Derivatives against House Dust Mites
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