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吡啶酰胺类化合物对按蚊的气相驱避和杀虫活性

Vapor phase repellency and insecticidal activity of pyridinyl amides against anopheline mosquitoes.

作者信息

Cuba Ingeborg H, Richoux Gary R, Norris Edmund J, Bernier Ulrich R, Linthicum Kenneth J, Bloomquist Jeffrey R

机构信息

Emerging Pathogens Institute, Entomology and Nematology Department, 2055 Mowry Road, University of Florida, Gainesville, FL, 32610-0009, USA.

USDA/ARS Center for Medical, Agricultural, and Veterinary Entomology, Gainesville, FL, 32610-0009, USA.

出版信息

Curr Res Parasitol Vector Borne Dis. 2021 Nov 18;1:100062. doi: 10.1016/j.crpvbd.2021.100062. eCollection 2021.

Abstract

It is important to identify repellents that can provide reliable protection from arthropod biting and prevent arthropod-borne diseases, such as malaria. In the present study, the spatial repellent activity and toxicity of two novel pyridinyl amides ( and ) were evaluated against , , and . In vapor repellency bioassays, compound was generally more effective than DEET and 2-undecanone, while compound was about as active as these standards. Overall, transfluthrin was the most active compound for inducing anopheline mosquito repellency, knockdown, and lethality. Although they were not the most active repellents, the two experimental amides produced the largest electroantennographic responses in female antennae. They also displayed modest toxicity to anopheline mosquitoes. Significant synergism of repellency was observed for the mixture of a pyrethroid-derived acid and the repellent 2-undecanone against anopheline mosquitoes, similar to that observed previously in . Overall, this study provides insight for further synthesis of alternative amide compounds for use as spatial treatments.

摘要

识别能够提供可靠防护以抵御节肢动物叮咬并预防节肢动物传播疾病(如疟疾)的驱避剂非常重要。在本研究中,评估了两种新型吡啶基酰胺( 和 )对 、 和 的空间驱避活性及毒性。在气相驱避生物测定中,化合物 通常比避蚊胺和2-十一酮更有效,而化合物 的活性与这些标准品相当。总体而言,甲氧苄氟菊酯是诱导按蚊驱蚊、击倒和致死的最具活性的化合物。尽管这两种实验性酰胺不是最具活性的驱避剂,但它们在雌蚊触角中产生了最大的电触角图反应。它们对按蚊也表现出适度的毒性。观察到拟除虫菊酯衍生酸与驱避剂2-十一酮的混合物对按蚊有显著的驱避协同作用,类似于先前在 中观察到的情况。总体而言,本研究为进一步合成用作空间处理的替代酰胺化合物提供了见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ea7/8906123/83332e8c54cc/ga1.jpg

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