以角鲨烯合酶为靶点,探索巴西天然产物作为抗克氏锥虫的潜在生物活性化合物

Paula Alvarez Abreu, Caroline Reis Santiago Paschoal, Vitor Won-Held Rabelo, Tamillis Figueiredo de Oliveira
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引用次数: 0

摘要

恰加斯病是一种被忽视的疾病,由原生动物克氏锥虫引起,影响全世界700万人。由于安全性和有效性问题,目前的治疗受到限制。因此,寻找新的抗寄生虫药物至关重要。角鲨烯合成酶(SQS)参与麦角甾醇的生物合成途径,是一个有吸引力的治疗靶点。在本研究中,我们利用基于配体和结构的虚拟筛选策略,在巴西的生物多样性中寻找克氏T. cruzi SQS (TcSQS)的潜在抑制剂。在NUBBE数据库中进行了虚拟筛选,其中包括来自巴西生物多样性的2200多种天然产物(NP)或半合成衍生物。然后进行分子对接和ADMET预测。一组12个NP显示与已知抑制剂观察到的TcSQS相互作用,并共享文献证据支持预测的活性。三种化合物(黄酮类化合物)作为TcSQS的潜在抑制剂表现出良好的ADMET性能。
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Exploring Brazilian Natural Products as Potential Bioactive Compounds against Trypanosoma cruzi by targeting Squalene Synthase
Chagas disease is a neglected disease caused by the protozoan Trypanosoma cruzi that affects 7 million people worldwide. The current treatment is limited due to safety and efficacy issues. Therefore, the search for new antiparasitic drugs is fundamental. The enzyme squalene synthase (SQS) is an attractive therapeutic target since it participates in the ergosterol biosynthesis pathway. In the present study, we explored the Brazilian biodiversity to search for potential inhibitors of T. cruzi SQS (TcSQS) using ligand and structure-based virtual screening strategies. A virtual screening was performed within the NUBBE database, with more than 2,200 natural products (NP) or semisynthetic derivatives from the Brazilian biodiversity. Molecular docking and ADMET predictions were then performed. A set of 12 NP showed interactions with TcSQS like those observed by known inhibitors and shared literature evidence that supports the predicted activity. Three compounds (flavonoids) showed good ADMET properties as potential inhibitors of TcSQS.
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