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  •   Ιδρυματικό Αποθετήριο Πανεπιστημίου Θεσσαλίας
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  •   Ιδρυματικό Αποθετήριο Πανεπιστημίου Θεσσαλίας
  • Επιστημονικές Δημοσιεύσεις Μελών ΠΘ (ΕΔΠΘ)
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ.
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Ιδρυματικό Αποθετήριο Πανεπιστημίου Θεσσαλίας
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Curcumin derivatives as potential mosquito larvicidal agents against two mosquito vectors, culex pipiens and aedes albopictus

Thumbnail
Συγγραφέας
Matiadis D., Liggri P.G.V., Kritsi E., Tzioumaki N., Zoumpoulakis P., Papachristos D.P., Balatsos G., Sagnou M., Michaelakis A.
Ημερομηνία
2021
Γλώσσα
en
DOI
10.3390/ijms22168915
Λέξη-κλειδί
curcumin
curcumin bf 2 complex
demethoxycurcumin
larvicidal agent
monocarbonyl tetramethoxy curcumin derivative
unclassified drug
curcumin
insecticide
nonsteroid antiinflammatory agent
Aedes albopictus
Article
chemical analysis
clinical effectiveness
clinical evaluation
computer model
Culex pipiens
incubation time
larva
larvicidal activity
LC50
mosquito vector
nonhuman
physical chemistry
structure activity relation
synthesis
Aedes
animal
chemistry
Culex
drug effect
female
Aedes
Animals
Anti-Inflammatory Agents, Non-Steroidal
Culex
Curcumin
Female
Insecticides
Larva
Mosquito Vectors
MDPI
Εμφάνιση Μεταδεδομένων
Επιτομή
Vector-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.
URI
http://hdl.handle.net/11615/76419
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  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ. [19735]

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