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一些苯并[g]喹唑啉衍生物作为抗人轮状病毒Wa株抗病毒剂的评价:生物学筛选与对接研究

Evaluation of Some Benzo[g]Quinazoline Derivatives as Antiviral Agents against Human Rotavirus Wa Strain: Biological Screening and Docking Study.

作者信息

Abuelizz Hatem A, Bakheit Ahmed H, Marzouk Mohamed, El-Senousy Waled M, Abdellatif Mohamed M, Mostafa Gamal A E, Al-Salahi Rashad

机构信息

Department of Pharmaceutical Chemistry, College of Pharmacy, King Saud University, Riyadh 11451, Saudi Arabia.

Chemistry of Tanning Materials and Leather Technology Department, Organic Chemicals Industries Division, National Research Centre, Dokki, Cairo 12622, Egypt.

出版信息

Curr Issues Mol Biol. 2023 Mar 14;45(3):2409-2421. doi: 10.3390/cimb45030156.

Abstract

Globally, rotavirus (RV) is the most common cause of acute gastroenteritis in infants and toddlers; however, there are currently no agents available that are tailored to treat rotavirus infection in particular. Improved and widespread immunization programs are being implemented worldwide to reduce rotavirus morbidity and mortality. Despite certain immunizations, there are no licensed antivirals that can attack rotavirus in hosts. Benzoquinazolines, chemical components synthesized in our laboratory, were developed as antiviral agents, and showed good activity against herpes simplex, coxsackievirus B4 and hepatitis A and C. In this research project, an in vitro investigation of the effectiveness of benzoquinazoline derivatives - against human rotavirus Wa strains was carried out. All compounds exhibited antiviral activity, however compounds -, and showed the greatest activity (reduction percentages ranged from 50 to 66%). In-silico molecular docking of highly active compounds, which were selected after studying the biological activity of all investigated of benzo[g]quinazolines compounds, was implemented into the protein's putative binding site to establish an optimal orientation for binding. As a result, compounds , , , and are promising anti-rotavirus Wa strains that lead with Outer Capsid protein VP4 inhibition.

摘要

在全球范围内,轮状病毒(RV)是婴幼儿急性胃肠炎最常见的病因;然而,目前尚无专门用于治疗轮状病毒感染的药物。全球正在实施改进和广泛的免疫计划,以降低轮状病毒的发病率和死亡率。尽管有一定的免疫措施,但目前尚无经许可的抗病毒药物可在宿主体内攻击轮状病毒。我们实验室合成的化学成分苯并喹唑啉被开发为抗病毒剂,对单纯疱疹病毒、柯萨奇病毒B4以及甲型和丙型肝炎病毒显示出良好的活性。在本研究项目中,对苯并喹唑啉衍生物针对人轮状病毒Wa株的有效性进行了体外研究。所有化合物均表现出抗病毒活性,然而化合物 - 、 - 和 - 显示出最大的活性(降低百分比范围为50%至66%)。在研究了所有研究的苯并[g]喹唑啉化合物的生物活性后,选择了高活性化合物进行计算机模拟分子对接,将其应用于蛋白质的假定结合位点,以建立最佳的结合方向。结果,化合物 - 、 - 、 - 和 - 是有前景的抗轮状病毒Wa株药物,它们主要通过抑制外衣壳蛋白VP4发挥作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2ffe/10047800/1a1838c453fd/cimb-45-00156-g001.jpg

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