Εμφάνιση απλής εγγραφής

dc.creatorMatiadis D., Liggri P.G.V., Kritsi E., Tzioumaki N., Zoumpoulakis P., Papachristos D.P., Balatsos G., Sagnou M., Michaelakis A.en
dc.date.accessioned2023-01-31T08:57:58Z
dc.date.available2023-01-31T08:57:58Z
dc.date.issued2021
dc.identifier10.3390/ijms22168915
dc.identifier.issn16616596
dc.identifier.urihttp://hdl.handle.net/11615/76419
dc.description.abstractVector-borne diseases have appeared or re-emerged in many Southern Europe countries making the transmission of infectious diseases by mosquitoes (vectors) one of the greatest worldwide health threats. Larvicides have been used extensively for the control of Aedes (Stegomyia) albopictus (Skuse, 1895) (Diptera: Culicidae) and Culex pipiens Linnaeus, 1758 (Diptera: Culicidae) mosquitoes in urban and semi-urban environments, causing the increasing resistance of mosquitoes to commercial insecticides. In this study, 27 curcuminoids and monocarbonyl curcumin derivatives were synthesised and evaluated as potential larvicidal agents against Cx. pipiens and Ae. albopictus. Most of the compounds were more effective against larvae of both mosquito species. Four of the tested compounds, curcumin, demethoxycurcumin, curcumin-BF2 complex and a monocarbonyl tetramethoxy curcumin derivative exhibited high activity against both species. In Cx. pipiens the recorded LC50 values were 6.0, 9.4, 5.0 and 32.5 ppm, respectively, whereas in Ae. albopictus they exhibited LC50 values of 9.2, 36.0, 5.5 and 23.6 ppm, respectively. No conclusive structure activity relationship was evident from the results and the variety of descriptors values generated in silico provided some insight to this end. © 2021 by the authors. Licensee MDPI, Basel, Switzerland.en
dc.language.isoenen
dc.sourceInternational Journal of Molecular Sciencesen
dc.source.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85112751337&doi=10.3390%2fijms22168915&partnerID=40&md5=190317b7a277b68b365bfa393cfe792f
dc.subjectcurcuminen
dc.subjectcurcumin bf 2 complexen
dc.subjectdemethoxycurcuminen
dc.subjectlarvicidal agenten
dc.subjectmonocarbonyl tetramethoxy curcumin derivativeen
dc.subjectunclassified drugen
dc.subjectcurcuminen
dc.subjectinsecticideen
dc.subjectnonsteroid antiinflammatory agenten
dc.subjectAedes albopictusen
dc.subjectArticleen
dc.subjectchemical analysisen
dc.subjectclinical effectivenessen
dc.subjectclinical evaluationen
dc.subjectcomputer modelen
dc.subjectCulex pipiensen
dc.subjectincubation timeen
dc.subjectlarvaen
dc.subjectlarvicidal activityen
dc.subjectLC50en
dc.subjectmosquito vectoren
dc.subjectnonhumanen
dc.subjectphysical chemistryen
dc.subjectstructure activity relationen
dc.subjectsynthesisen
dc.subjectAedesen
dc.subjectanimalen
dc.subjectchemistryen
dc.subjectCulexen
dc.subjectdrug effecten
dc.subjectfemaleen
dc.subjectAedesen
dc.subjectAnimalsen
dc.subjectAnti-Inflammatory Agents, Non-Steroidalen
dc.subjectCulexen
dc.subjectCurcuminen
dc.subjectFemaleen
dc.subjectInsecticidesen
dc.subjectLarvaen
dc.subjectMosquito Vectorsen
dc.subjectMDPIen
dc.titleCurcumin derivatives as potential mosquito larvicidal agents against two mosquito vectors, culex pipiens and aedes albopictusen
dc.typejournalArticleen


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