Literature DB >> 27281691

Specific Synergist for Neonicotinoid Insecticides: IPPA08, a cis-Neonicotinoid Compound with a Unique Oxabridged Substructure.

Haibo Bao1, Xusheng Shao2, Yixi Zhang1, Yayun Deng2, Xiaoyong Xu2, Zewen Liu1, Zhong Li2.   

Abstract

Insecticide synergists are key components to increase the control efficacy and reduce active ingredient use. Here, we describe a novel insecticide synergist with activity specific for insecticidal neonicotinoids. The synergist IPPA08, a cis configuration neonicotinoid compound with a unique oxabridged substructure, could increase the toxicity of most neonicotinoid insecticides belonging to the Insecticide Resistance Action Committee (IRAC) 4A subgroup against a range of insect species, although IPPA08 itself was almost inactive to insects at synergistic concentrations. Unfortunately, similar effects were observed on the honey bee (Apis mellifera) and the brown planthopper (Nilaparvata lugens), resistant to imidacloprid. IPPA08 did not show any effects on toxicity of insecticides with different targets, which made us define it as a neonicotinoid-specific synergist. Unlike most insecticide synergists, by inhibition of activities of detoxification enzymes, IPPA08 showed no effects on enzyme activities. The results revealed that IPPA08 worked as a synergist through a distinct way. Although the modulating insect nicotinic acetylcholine receptors (nAChRs, targets of neonicotinoid insecticides) were supposed as a possible mode of action for IPPA08 as a neonicotinoid-specific synergist, direct evidence is needed in further studies. In insect pest control, IPPA08 acts as a target synergist to increase neonicotinoid toxicity and reduce the amount of neonicotinoid used. Combinations of IPPA08 and insecticidal neonicotinoids may be developed into new insecticide formulations. In summary, combining an active ingredient with a "custom" synergist appears to be a very promising approach for the development of effective new insecticide products.

Entities:  

Keywords:  detoxification enzyme; insecticide synergist; neonicotinoid; nicotinic acetylcholine receptors

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Substances:

Year:  2016        PMID: 27281691     DOI: 10.1021/acs.jafc.6b01512

Source DB:  PubMed          Journal:  J Agric Food Chem        ISSN: 0021-8561            Impact factor:   5.279


  5 in total

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Authors:  Qin Luo; Rong Huang; Qiang Xiao; Ling-Bin Kong; Jun Lin; Sheng-Jiao Yan
Journal:  ACS Omega       Date:  2019-04-11

2.  Site-Selective Reaction of Enaminones and Enamine Esters for the Synthesis of Novel Diverse Morphan Derivatives.

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Journal:  ACS Omega       Date:  2018-06-04

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Journal:  RSC Adv       Date:  2018-01-08       Impact factor: 3.361

4.  The Mechanism by Which Dodecyl Dimethyl Benzyl Ammonium Chloride Increased the Toxicity of Chlorpyrifos to Spodoptera exigua.

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Authors:  Chiara Giorio; Anton Safer; Francisco Sánchez-Bayo; Andrea Tapparo; Andrea Lentola; Vincenzo Girolami; Maarten Bijleveld van Lexmond; Jean-Marc Bonmatin
Journal:  Environ Sci Pollut Res Int       Date:  2017-11-05       Impact factor: 4.223

  5 in total

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