In silico studies of benzothiazole derivatives as potential inhibitors of Anopheles funestus and Anopheles gambiae trehalase

T. A. Ogunnupebi, G. Oduselu, O. F. Elebiju, O. Ajani, E. Adebiyi
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Abstract

In malaria management, insecticides play a crucial role in targeting disease vectors. Benzothiazole derivatives have also been reported to possess insecticidal properties, among several other properties they exhibit. The female Anopheles mosquito is responsible for transmitting the malaria parasite when infected. Anopheles gambiae (Ag) and Anopheles funestus (Af) are two of the most notable Anopheles species known to spread malaria in Nigeria. Trehalase is an enzyme that breaks down trehalose. Recent research has proposed it as a viable target for inhibition since it aids in flight and stress adaptation.This study aimed to investigate benzothiazole derivatives as potential inhibitors of trehalase of Anopheles funestus (AfTre) and Anopheles gambiae (AgTre) using toxicity profiling, molecular docking, and dynamic simulation for future insecticidal intervention. A total of 4,214 benzothiazole-based compounds were obtained from the PubChem database and subjected to screening against the 3D modelled structure of AfTre and AgTre. Compounds with some toxicity levels were optimised, and the obtained lead compounds were further investigated through molecular docking studies. Furthermore, the best hit was subjected to parameters such as RMSD, RMSF, SASA, Rg, and hydrogen bond to confirm its stability when in a complex with AfTre, and these parameters were compared to that of validamycin A (control ligand).The post-screening analysis showed binding affinities of −8.7 and −8.2 kcal/mol (compound 1), −8.2 and −7.4 kcal/mol (compound 2), compared to −6.3 and −5.1 kcal/mol (Validamycin A, a known inhibitor) against AfTre and AgTre, respectively. The molecular dynamics simulation showed that compound 1 (the best hit) had good stability when in complex with AfTre. These findings suggest that these best hits can serve as potential inhibitors for the development of novel insecticides in the control of malaria vectors.
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苯并噻唑衍生物作为疟原虫和冈比亚按蚊三卤酶潜在抑制剂的硅学研究
在疟疾防治中,杀虫剂在针对病媒方面发挥着至关重要的作用。据报道,苯并噻唑衍生物除具有其他一些特性外,还具有杀虫特性。雌性按蚊在感染后负责传播疟疾寄生虫。冈比亚按蚊(Ag)和疟蚊(Af)是已知在尼日利亚传播疟疾的两个最显著的按蚊物种。三卤糖酶是一种分解三卤糖的酶。本研究旨在通过毒性分析、分子对接和动态模拟,研究苯并噻唑衍生物作为拟南芥(AfTre)和冈比亚按蚊(AgTre)三卤糖酶的潜在抑制剂,以用于未来的杀虫干预。研究人员从 PubChem 数据库中获取了 4,214 种苯并噻唑类化合物,并根据 AfTre 和 AgTre 的三维模型结构进行了筛选。对具有一定毒性水平的化合物进行了优化,并通过分子对接研究对获得的先导化合物进行了进一步研究。此外,对最佳化合物进行了 RMSD、RMSF、SASA、Rg 和氢键等参数测试,以确认其与 AfTre 复合物的稳定性,并将这些参数与有效霉素 A(对照配体)进行了比较。筛选后分析表明,化合物 1 与 AfTre 和 AgTre 的结合亲和力分别为 -8.7 和 -8.2 kcal/mol(化合物 1)、-8.2 和 -7.4 kcal/mol(化合物 2),而 Validamycin A(已知抑制剂)则分别为 -6.3 和 -5.1 kcal/mol。分子动力学模拟显示,化合物 1(最佳化合物)与 AfTre 复合物具有良好的稳定性。这些研究结果表明,这些最佳化合物可以作为潜在的抑制剂,用于开发新型杀虫剂,控制疟疾病媒。
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Editorial: Machine learning approaches to antimicrobials: discovery and resistance RIPS (rapid intuitive pathogen surveillance): a tool for surveillance of genome sequence data from foodborne bacterial pathogens Editorial: Big data and artificial intelligence for genomics and therapeutics – Proceedings of the 19th Annual Meeting of the MidSouth Computational Biology and Bioinformatics Society (MCBIOS) In silico studies of benzothiazole derivatives as potential inhibitors of Anopheles funestus and Anopheles gambiae trehalase Predictive identification and design of potent inhibitors targeting resistance-inducing candidate genes from E. coli whole-genome sequences
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