Larvicidal potential of Knoevenagel adducts against Aedes aegypti: theoretical study and in vitro validation.

IF 3.2 4区 医学 Q3 CHEMISTRY, MEDICINAL
Future medicinal chemistry Pub Date : 2025-05-01 Epub Date: 2025-05-05 DOI:10.1080/17568919.2025.2498877
Paloma G Abrantes, Poliana G Abrantes, Renata R Magalhães, Gildilayne M Silva, Natália F Sousa, Marcus T Scotti, Renan T Leite, Jheison M C Francelino, Fabíola C Nunes, Juliana A Vale
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引用次数: 0

Abstract

Aim: This study investigated the larvicidal potential of Knoevenagel adducts against Aedes aegypti larvae to develop sustainable alternatives for controlling disease vectors like dengue.

Methods: Larvicidal activity of Knoevenagel adducts (1a-l) was evaluated on fourth-stage Aedes aegypti larvae. Additional analyses included nitric oxide measurement, cell profiling, toxicity assessment, molecular docking, molecular dynamics simulation, and ADMET (Absorption, Distribution, Metabolism, and Toxicity) evaluation.

Results: Compounds 1c and 1g showed high larvicidal efficacy, with LC50 values of 3.39 and 5.13 ppm. Hemolymph analysis revealed altered hemocyte composition, indicating an immune response, though nitric oxide levels remained unchanged. Molecular docking identified strong interactions between the Aedes aegypti FKBP12 enzyme (PDB: 3UQI) and Knoevenagel adducts. Compound 1g had the highest activity probability and binding affinity, while 1c showed strong interactions validated by biological assays. Molecular dynamics confirmed stable interactions of 1c and FKBP12, with both 1c and 1g displaying significant van der Waals contributions. ADMET analysis highlighted 1c as a less toxic compound, with minimal mutagenic risk, favorable pharmacokinetics, and high bioavailability.

Conclusions: Knoevenagel adducts 1c and 1g are promising candidates for effective, selective, and environmentally friendly larvicides.

Knoevenagel加合物对埃及伊蚊的杀幼虫潜力:理论研究和体外验证。
目的:研究Knoevenagel加合物对埃及伊蚊幼虫的杀灭潜力,为登革热等疾病媒介的控制提供可持续的替代品。方法:测定Knoevenagel加合物(1a- 1)对埃及伊蚊4期幼虫的杀幼虫活性。其他分析包括一氧化氮测量、细胞谱分析、毒性评估、分子对接、分子动力学模拟和ADMET(吸收、分布、代谢和毒性)评估。结果:化合物1c和1g具有较好的杀虫效果,LC50值分别为3.39和5.13 ppm。血淋巴分析显示血细胞组成改变,表明免疫反应,尽管一氧化氮水平保持不变。分子对接发现埃及伊蚊FKBP12酶(PDB: 3UQI)与Knoevenagel加合物之间存在强相互作用。化合物1g具有最高的活性概率和结合亲和力,而化合物1c经生物实验证实具有很强的相互作用。分子动力学证实1c和FKBP12稳定的相互作用,1c和1g都表现出显著的范德华贡献。ADMET分析强调1c是一种毒性较低的化合物,具有最小的致突变风险、良好的药代动力学和高生物利用度。结论:Knoevenagel加合物1c和1g是有效的、选择性的、环境友好的杀幼虫剂。
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来源期刊
Future medicinal chemistry
Future medicinal chemistry CHEMISTRY, MEDICINAL-
CiteScore
5.80
自引率
2.40%
发文量
118
审稿时长
4-8 weeks
期刊介绍: Future Medicinal Chemistry offers a forum for the rapid publication of original research and critical reviews of the latest milestones in the field. Strong emphasis is placed on ensuring that the journal stimulates awareness of issues that are anticipated to play an increasingly central role in influencing the future direction of pharmaceutical chemistry. Where relevant, contributions are also actively encouraged on areas as diverse as biotechnology, enzymology, green chemistry, genomics, immunology, materials science, neglected diseases and orphan drugs, pharmacogenomics, proteomics and toxicology.
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