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Hyperforin and deoxycohumulone as a larvicidal agent against culex pipiens (diptera: Culicidae)

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dc.contributor.author Mitsopoulou, KP en
dc.contributor.author Vidali, VP en
dc.contributor.author Koliopoulos, G en
dc.contributor.author Couladouros, EA en
dc.contributor.author Michaelakis, A en
dc.date.accessioned 2014-06-06T06:53:04Z
dc.date.available 2014-06-06T06:53:04Z
dc.date.issued 2014 en
dc.identifier.issn 00456535 en
dc.identifier.uri http://dx.doi.org/10.1016/j.chemosphere.2013.11.073 en
dc.identifier.uri http://62.217.125.90/xmlui/handle/123456789/6342
dc.subject Hypericum perforatum en
dc.subject Larvicidal activity en
dc.subject Piperonyl butoxide en
dc.subject Sub-lethal effect en
dc.subject West Nile virus (WNV) en
dc.title Hyperforin and deoxycohumulone as a larvicidal agent against culex pipiens (diptera: Culicidae) en
heal.type journalArticle en
heal.identifier.primary 10.1016/j.chemosphere.2013.11.073 en
heal.publicationDate 2014 en
heal.abstract The larvicidal effect of hyperforin (1), a bioactive compound of Hypericum perforatum, and deoxycohumulone (2) (biosynthetic precursor of hyperforin) were evaluated against Culex pipiens (Diptera: Culicidae) for the first time. All the acetate analogues (3-6) of hyperforin (1) and deoxycohumulone (2) were also synthesized and bioassayed to provide information on structural requirements for the tested compounds. Larvicidal results revealed that hyperforin (1) and deoxycohumulone (2) exhibited potent activity with LC50 value of 26.72 and 51.03mgL-1, respectively. The monoacetyl-deoxycohumulone (4) displayed lower activity with LC50 value of 135.92mgL-1, while all other acetate analogues were inactive at concentrations even as high as 150mgL-1, indicating that the free hydroxyl groups are essential for the larvicidal activity. The mortality values were increased, more than 80%, when 10mgL-1 piperonyl butoxide were added in hyperforin (1) or deoxycohumulone (2) bioassays. Finally, sub-lethal survival analysis is conducted for three doses of hyperforin (1) and deoxycohumulone (2) and results are discussed. © 2013 Elsevier Ltd. en
heal.journalName Chemosphere en
dc.identifier.volume 100 en
dc.identifier.doi 10.1016/j.chemosphere.2013.11.073 en
dc.identifier.spage 124 en
dc.identifier.epage 129 en


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