Literature DB >> 31420785

Insecticidal activity of indole derivatives against Plutella xylostella and selectivity to four non-target organisms.

Ângela C F Costa1, Sócrates C H Cavalcanti2, Alisson S Santana1, Ana P S Lima1, Thaysnara B Brito2, Rafael R B Oliveira2, Nathália A Macêdo2, Paulo F Cristaldo3, Ana Paula A Araújo4, Leandro Bacci5,6.   

Abstract

The diamondback moth Plutella xylostella (Linnaeus, 1758) (Lepidoptera: Plutellidae) is a destructive pest of brassica crops of economic importance that have resistance to a range of insecticides. Indole derivates can exert diverse biological activities, and different effects may be obtained from small differences in their molecular structures. Indole is the parent substance of a large number of synthetic and natural compounds, such as plant and animal hormones. In the present study, we evaluate the insecticidal activity of 20 new synthesized indole derivatives against P. xylostella, and the selectivity of these derivatives against non-target hymenopteran beneficial arthropods: the pollinator Apis mellifera (Linnaeus, 1758) (Hymenoptera: Apidae), and the predators Polybia scutellaris (White, 1841), Polybia sericea (Olivier, 1791) and Polybia rejecta (Fabricius, 1798) (Hymenoptera: Vespidae). Bioassays were performed in the laboratory to determine the lethal and sublethal effects of the compounds on P. xylostella and to examine their selectivity to non-target organisms by topical application and foliar contact. The treatments consisted of two synthesized derivatives (most and least toxic), the positive control (deltamethrin) and the negative control (solvent). The synthesized compound 4e [1-(1H-indol-3-yl)hexan-1-one] showed high toxicity (via topical application and ingestion) and decreased the leaf consumption by P. xylostella, displaying a higher efficiency than the pyrethroid deltamethrin, widely used to control this pest. In addition, the synthesized indole derivatives were selective to the pollinator A. mellifera and the predators P. scutellaris, P. sericea and P. rejecta, none of which were affected by deltamethrin. Our results highlight the promising potential of the synthesized indole derivatives for the generation of new chemical compounds for P. xylostella management.

Entities:  

Keywords:  Chemical control; Pest control; Pesticides; Tryptamine

Mesh:

Substances:

Year:  2019        PMID: 31420785     DOI: 10.1007/s10646-019-02095-1

Source DB:  PubMed          Journal:  Ecotoxicology        ISSN: 0963-9292            Impact factor:   2.823


  36 in total

1.  3-Hydroxykynurenine transaminase identity with alanine glyoxylate transaminase. A probable detoxification protein in Aedes aegypti.

Authors:  Qian Han; Jianmin Fang; Jianyong Li
Journal:  J Biol Chem       Date:  2002-03-05       Impact factor: 5.157

2.  Widespread pyrethroid resistance in Australian diamondback moth, Plutella xylostella (L.), is related to multiple mutations in the para sodium channel gene.

Authors:  N M Endersby; K Viduka; S W Baxter; J Saw; D G Heckel; S W McKechnie
Journal:  Bull Entomol Res       Date:  2011-02-23       Impact factor: 1.750

3.  Design, synthesis, and biological evaluation of (2E)-(2-oxo-1, 2-dihydro-3H-indol-3-ylidene)acetate derivatives as anti-proliferative agents through ROS-induced cell apoptosis.

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Journal:  Eur J Med Chem       Date:  2016-09-03       Impact factor: 6.514

4.  Insecticidal activities of chiral N-trifluoroacetyl sulfilimines as potential ryanodine receptor modulators.

Authors:  Sha Zhou; Yucheng Gu; Ming Liu; Changchun Wu; Sha Zhou; Yu Zhao; Zhehui Jia; Baolei Wang; Lixia Xiong; Na Yang; Zhengming Li
Journal:  J Agric Food Chem       Date:  2014-11-07       Impact factor: 5.279

5.  Design, synthesis, insecticidal activity and structure-activity relationship of 3,3-dichloro-2-propenyloxy-containing phthalic acid diamide structures.

Authors:  Mei-Li Feng; Yu-Feng Li; Hong-Jun Zhu; Jue-Ping Ni; Bin-Bin Xi; Liang Zhao
Journal:  Pest Manag Sci       Date:  2012-05-03       Impact factor: 4.845

Review 6.  Cruciferous vegetables and human cancer risk: epidemiologic evidence and mechanistic basis.

Authors:  Jane V Higdon; Barbara Delage; David E Williams; Roderick H Dashwood
Journal:  Pharmacol Res       Date:  2007-01-25       Impact factor: 7.658

7.  The tryptophan oxidation pathway in mosquitoes with emphasis on xanthurenic acid biosynthesis.

Authors:  Qian Han; Brenda T Beerntsen; Jianyong Li
Journal:  J Insect Physiol       Date:  2006-09-17       Impact factor: 2.354

8.  Plant defence responses in oilseed rape MINELESS plants after attack by the cabbage moth Mamestra brassicae.

Authors:  Ishita Ahuja; Nicole Marie van Dam; Per Winge; Marianne Trælnes; Aysel Heydarova; Jens Rohloff; Mette Langaas; Atle Magnar Bones
Journal:  J Exp Bot       Date:  2015-01-06       Impact factor: 6.992

9.  Synthesis and Antioxidant Activity of Alkyl Nitroderivatives of Hydroxytyrosol.

Authors:  Elena Gallardo; Rocío Palma-Valdés; Beatriz Sarriá; Irene Gallardo; José P de la Cruz; Laura Bravo; Raquel Mateos; José L Espartero
Journal:  Molecules       Date:  2016-05-18       Impact factor: 4.411

10.  Insecticidal and Nematicidal Activities of Novel Mimosine Derivatives.

Authors:  Binh Cao Quan Nguyen; Jamnian Chompoo; Shinkichi Tawata
Journal:  Molecules       Date:  2015-09-14       Impact factor: 4.411

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