吡咯喹啉-1,3-二胺作为靶向β- n -乙酰-d -己糖氨酸酶的双功能杀虫剂的发现。

IF 3.5 4区 医学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Xi Jiang, Zhijun Zhang, Kanglv Tang, Han Zhou, Dengtuo Wang, Huijie Xie, Yingqian Liu, Tian Liu
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引用次数: 0

摘要

背景:β- n -乙酰- d -己糖氨酸酶(Hex)在昆虫的生长发育、真菌的细胞增殖和病原体入侵中起着至关重要的作用。针对Hexs的抑制剂的发现为开发生态友好型农用化学品带来了巨大的希望。方法:采用酶促法从玉米螟(Ostrinia furnacalis)中鉴定出新的昆虫Hex抑制剂(OfHex1)。采用分子对接的方法来阐明抑制剂的结合机制。通过对玉米螟(Ostrinia furnacalis) 3龄幼虫和农业病原菌禾谷镰刀菌(Fusarium graminearum)进行体内和体外生物活性评价。结果:吡咯喹啉-1,3-二胺(PQDs)在微摩尔水平上是OfHex1的竞争性抑制剂。通过氢键和疏水相互作用,pqd被结合在OfHex1的活性位点内。结果表明:PQDs对OfHex1具有明显的抑制作用,且具有很强的杀虫和杀真菌活性,是开发双功能杀虫剂的理想候选物。结论:PQDs对OfHex1具有显著的抑制活性,具有很强的杀虫和杀真菌活性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Discovery of Pyrroloquinazoline-1,3-diamines as Dual-function Insecticide Candidates Targeting β-N-acetyl-D-hexosaminidase.

Background: β-N-acetyl-D-hexosaminidase (Hex) plays crucial roles in insect growth and development, as well as in cell proliferation and pathogen invasion in fungi. The discovery of inhibitors targeting Hexs holds great promise for the development of eco-friendly agrochemicals.

Methods: Novel inhibitors of insect Hex from Ostrinia furnacalis (OfHex1) were identified through enzymatic assays. Molecular docking was employed to elucidate the binding mechanisms of the inhibitors. The biological activities of identified inhibitors were assessed in vivo and in vitro by administration of the compounds to the 3rd instar larvae of Ostrinia furnacalis and the agricultural pathogen Fusarium graminearum, respectively.

Results: Pyrroloquinazoline-1,3-diamines (PQDs) were identified as competitive inhibitors of OfHex1 at the micromolar level. Through hydrogen bonding and hydrophobic interactions, PQDs were bound within the active sites of OfHex1. The most potent compound, designated as 4h, demonstrated an insecticidal efficacy of 86.7% against the 3rd instar larvae of O. furnacalis when administered at 2 mM. Additionally, 4a displayed complete inhibition of mycelium spreading at 1 mM.

Conclusion: PQDs exhibited significant inhibitory activity against OfHex1 and demonstrated substantial insecticidal and fungicidal potency, positioning PQDs as promising candidates for the development of dual-function insecticide candidates.

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来源期刊
Current medicinal chemistry
Current medicinal chemistry 医学-生化与分子生物学
CiteScore
8.60
自引率
2.40%
发文量
468
审稿时长
3 months
期刊介绍: Aims & Scope Current Medicinal Chemistry covers all the latest and outstanding developments in medicinal chemistry and rational drug design. Each issue contains a series of timely in-depth reviews and guest edited thematic issues written by leaders in the field covering a range of the current topics in medicinal chemistry. The journal also publishes reviews on recent patents. Current Medicinal Chemistry is an essential journal for every medicinal chemist who wishes to be kept informed and up-to-date with the latest and most important developments.
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