体外测试抗病毒化合物硅学数据库的开发与特征描述

Nicolas Porto Felix, Caio Cheohen, M. E. Esteves, Manuela Leal da Silva
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引用次数: 0

摘要

抗病毒药物是抑制病毒感染或病毒复制的物质,是治疗病毒性疾病的药物。然而,由于病原体的多样性,寻找新的抗病毒药物非常重要。与传统的研发方法相比,将已获批准的药物重新定位是一种成本更低、速度更快的策略。由于缺乏有关这些药物的汇编和标准化数据,这项工作旨在建立一个体外抗病毒测试数据库。因此,我们通过体外测试抗病毒药物方法的出版物获得了化合物及其信息,并创建了六个数据库,涵盖 SMILES、MOL、SDF 2D、MOL2、PDB 和 PDBQT 扩展库,按是否具有抗病毒活性进行分类。每个文件都包含其 IUPAC 名称和多达三个维度的结构数据。
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Development and Characterization of an In Silico Database of In Vitro Tested Antiviral Compounds
Antivirals are substances that inhibit viral infection or virus replication, acting as drugs to treat viral diseases. However, due the diversity of pathogens, it is important to seek new antivirals. Among the options, repositioning already approved drugs is a cheaper and faster strategy when compared to classical research and development methods. Since there is a lack of compiled and standardized data on these drugs, this work aims to build a database of in vitro antiviral tests. Thus, the compounds and their information were obtained through publications of in vitro methods for testing antiviral drugs, we created six databases covering SMILES, MOL, SDF 2D, MOL2, PDB and PDBQT extensions, classified by the presence and/or absence of antiviral activity. Each file contains its IUPAC name and structural data in up to three dimensions.
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