Bioactivity of semisynthetic eugenol derivatives against Spodoptera frugiperda (Lepidoptera: Noctuidae) larvae infesting maize in Colombia

dc.contributor.authorVargas-Méndez, Leonor Y.
dc.contributor.authorSanabria-Flórez, Pedro L.
dc.contributor.authorSaavedra- Reyes, Laura M.
dc.contributor.authorMerchan-Arenas, Diego R.
dc.contributor.authorKouznetsov, Vladimir V.
dc.date.accessioned2019-07-05T20:02:59Z
dc.date.available2019-07-05T20:02:59Z
dc.date.issued2018-09-27
dc.description.abstractThe anti-acetylcholinesterase, larvicidal, antifeedant activities and general toxicity of 15 semisynthetic eugenol derivatives based on clove oil (including the own oil), were evaluated against the maize armyworm, Spodoptera frugiperda (J.E. Smith). Therefore, promising eugenol molecules were classified with larvicidal, anti-acetylcholinesterase and antifeedant activities for controlling this pest. During structure–activity relationship studies and physicochemical profile analysis, it was found that among tested molecules 1-15, eugenol 1, prenyl eugenol 4, isoeugenol 8 and isoeugenol acetate 11 exhibited lethal effects LD50 at concentrations < 1 mg/g of insect. On the other hand, eugenol 1, metallyl eugenol 3, isoeugenol 8 and isoeugenol acetate 11 showed a good antifeedant activity (CE50 =158-209 μg/mL) with a high antifeedant index (70-78 %) at concentration 1000 μg/mL, possessing a weak antiacetylcholinesterase activity (IC50 = 21-31 g/mL). According to their ecotoxicological profiles (LC50 = 2033.1-6303.8 μg/mL on Artemia salina larvae), isoeugenol 8 and its acetate derivative 11 could be potential used in control of the growth, feeding, or reproduction of S. frugiperda larvae, acting as moderate insecticidal acetylcholinesterase inhibitors and/or antifeedant molecules. Such structure–activity relationship studies could stimulate the identification of lead structures from natural sources for the development of larvicidal and deterrent products against S. frugiperda and related insect pests.spa
dc.description.domainhttp://unidadinvestigacion.usta.edu.cospa
dc.format.mimetypeapplication/pdf
dc.identifier.citationMerchan-Arenas, D. R., Vargas-Méndez, L. Y., Sanabria-Flórez, P. L., Saavedra- Reyes, L. M., & Kouznetsov, V. V. (2018). Bioactivity of semisynthetic eugenol derivatives against spodoptera frugiperda (lepidoptera: Noctuidae) larvae infesting maize in colombia. Bogotá: doi:10.1016/j.sjbs.2018.09.010spa
dc.identifier.doihttps://doi.org/10.1016/j.sjbs.2018.09.010spa
dc.identifier.urihttp://hdl.handle.net/11634/17462
dc.publisher.branchCRAI-USTA Bogotáspa
dc.relation.referencesAbbassy, M.A., Abdelgaleil, S.A.M., Rabie, R.Y.A., 2009. Insecticidal and synergistic effects of Majorana hortensis essential oil and some of its major constituents. Entomol. Exp. Appl. 131 (3), 225–232.spa
dc.relation.referencesAhmad, M., Saleem, M.A., Sayyed, A.H., 2009. Efficacy of insecticide mixtures against pyrethroid- and organophosphate-resistant populations of Spodoptera litura (Lepidoptera: Noctuidae). Pest Manag. Sci. 65 (3), 266–274.spa
dc.relation.referencesBarbosa, J.D.F., Silva, V.B., Alves, P.B., Gumina, G., Santos, R.L.C., Sousa, D.P., Cavalcanti, S.C.H., 2012. Structure–activity relationships of eugenol derivatives against Aedes aegypti (Diptera:Culicidae) larvae. Pest Manag. Sci. 68 (11), 1478–1483.spa
dc.relation.referencesBhagat, D.S., Mathur, K.R., 1982. Synthesis of new derivatives of eugenol and isoeugenol. J. Chem. Eng. Data 27 (2), 209–210.spa
dc.relation.referencesCarballo, J.L., Hernández-Inda, Z.L., Pérez, P., García-Grávalos, M.D., 2002. A comparison between two brine shrimp assays to detect in vitro cytotoxicity in marine natural products. BMC Biotechnology 2 (1), 1–7.spa
dc.relation.referencesChorus, I., Bartram, J., 1999. Toxic Cyanobacteria in Water: A guide to their public health consequences, monitoring and management. E & FN Spon, London, pp. 377–380.spa
dc.relation.referencesDayan, F.E., Cantrell, C.L., Duke, S.O., 2009. Natural products in crop protection. Bioorg. Med. Chem. 17 (12), 4022–4034.spa
dc.relation.referencesDenholm, I., Horowitz, A.R., Cahill, M., Ishaaya, I., 1998. Management of Resistance to Novel Insecticides, in: Ishaaya, I., Degheele, D. (Eds.), Insecticides with Novel Modes of Action. Springer, Berlin, pp. 260–282.spa
dc.relation.referencesEl-Aswad, A.F., Abdelgaleil, S.A.M., Nakatani, M., 2003. Feeding deterrent and growth inhibitory properties of limonoids from Khaya senegalensis against the cotton leafworm, Spodoptera littoralis. Pest Manag. Sci. 60 (2), 199–203.spa
dc.relation.referencesFurniss, B., Hannaford, A., Smith, P., Tatchell A., 1989. Vogel’s Textbook of Practical Organic Chemistry; Prentice Hall: London, pp 135-241.spa
dc.relation.referencesHao, G., Dong, Q., Yang, G., 2011. A comparative study on the constitutive properties of marketed pesticides. Mol. Inform. 30 (6‐ 7), 614–622.spa
dc.relation.referencesIsman, M.B., 2005. Problems and opportunities for the commercialization of insecticides, in: by Regnault-Roger, C., Philogene, B.J.R., Vincent, R. (Eds.), Biopesticides of plant origin. Lavoisier, Paris, pp. 283–291.spa
dc.relation.referencesKiran, S.R., Reddy, A.S., Devi, P.S, Reddy, K.J., 2006. Insecticidal, antifeedant and oviposition deterrent effects of the essential oil and individual compounds from leaves of Chloroxylon swietenia DC. Pest Manag. Sci. 62 (11), 1116–1121.spa
dc.relation.referencesLamberth, C., Jeanmart, S., Luksch, T., Plant, A., 2013. Current challenges and trends in the discovery of agrochemicals. Science 341 (6147), 742-746.spa
dc.relation.referencesMclaughlin, L.J., Rogers, L., Anderson, J.E., 1998. The use of biological assays to evaluate botanicals. Drug Inform. J. 32 (2), 513–524.spa
dc.relation.referencesPandey, S.K., Tandon, S., Ahmad, A., Singh, A.K., Tripathi, A.K., 2013. Structure–activity relationships of monoterpenes and acetyl derivatives against Aedes aegypti (Diptera: Culicidae) larvae. Pest Manag. Sci. 69 (11), 1235–1238.spa
dc.relation.referencesSimmonds, M., Blaney, W.M., Esquivel, B., Rodriguez-Hahn, L., 1996. Effect of Clerodane- Type Diterpenoids Isolated from Salvia spp. on the feeding behaviour of Spodoptera littoralis. Pestic. Sci. 47 (1), 17–23.spa
dc.relation.referencesTewary, D.K., Bhardwaj, A., Sharma, A., Sinha, A.K., Shanker, A., 2006. Bioactivity and structure–activity relationship of natural methoxylated phenylpropenes and their derivatives against Aphis craccivora Koch (Hemiptera: Aphididae). J. Pest Sci. 79(4), 209– 214.spa
dc.relation.referencesWalsh, S.B., Dolden, T.A., Moores, G.D., Kristensen, M., Lewis, T., Devonshire, A.L., Williamson, M.S., 2001. Identification and characterization of mutations in housefly (Musca domestica) acetylcholinesterase involved in insecticide resistance. Biochem. J. 359, 175–181.spa
dc.relation.referencesXu, H.X., Zheng, X.S., Yang, Y.J., Tian, J.C., Tan, K.H., Heong, K.L., Lu, Z.X., 2015. Methyl eugenol bioactivities as a new potential botanical insecticide against major insect pests and their natural enemies on rice (Oriza sativa). Crop Protection 72, 144–149.spa
dc.rightsAtribución-NoComercial-CompartirIgual 2.5 Colombia
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/2.5/co/
dc.subject.keywordSpodoptera frugiperdaspa
dc.subject.keywordEugenol derivativesspa
dc.subject.keywordClove oilspa
dc.subject.keywordAcetylcholinesterase activityspa
dc.subject.keywordInsecticidal activityspa
dc.subject.keywordAntifeedant activityspa
dc.subject.keywordToxicity on Artemia salina larvaespa
dc.titleBioactivity of semisynthetic eugenol derivatives against Spodoptera frugiperda (Lepidoptera: Noctuidae) larvae infesting maize in Colombiaspa
dc.type.categoryGeneración de Nuevo Conocimiento: Artículos publicados en revistas especializadas - Electrónicosspa

Archivos

Bloque original

Mostrando 1 - 1 de 1
Cargando...
Miniatura
Nombre:
Bioactivity of semisynthetic eugenol derivatives against Spodoptera frugiperda (Lepidoptera: Noctuidae) larvae infesting maize in Colombia.pdf
Tamaño:
905.38 KB
Formato:
Adobe Portable Document Format
Descripción:
Artículo SCOPUS

Bloque de licencias

Mostrando 1 - 1 de 1
Cargando...
Miniatura
Nombre:
license.txt
Tamaño:
807 B
Formato:
Item-specific license agreed upon to submission
Descripción: