针对登革热RNA依赖RNA聚合酶药物靶点的天然产物的计算机发现

IF 0.4 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY Chem-Bio Informatics Journal Pub Date : 2021-03-15 DOI:10.1273/CBIJ.21.11
J. Billones, N. A. B. Clavio
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引用次数: 0

摘要

登革热病毒(DENV)引起的病毒感染是世界热带地区最具挑战性的疾病之一。由于迄今为止缺乏治疗登革热的药物,因此需要加紧努力,发现和开发这种蚊媒疾病的令人垂涎的治疗方法。最具吸引力的抗病毒靶点之一是DENV RNA依赖的RNA聚合酶(RdRp),它催化黄病毒RNA基因组的从头起始和延伸。在这项工作中,近5000种天然产物与DENV RdRp对接。将结合能大于已知配体的197个分子进一步聚类,形成35类分子结构。这些具有令人满意的预测药物性质和已知天然来源的化合物可以进一步探索,为第一种抗登革热药物铺平道路。
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In Silico Discovery of Natural Products Against Dengue RNA-Dependent RNA Polymerase Drug Target
The viral infection caused by the dengue virus (DENV) is one of the most challenging diseases in the tropical regions of the world. The absence of drugs for dengue to this date calls for intense efforts to discover and develop the much coveted therapeutics for this mosquito-borne disease. One of the most attractive antiviral targets is the DENV RNAdependent RNA polymerase (RdRp), which catalyzes the de novo initiation as well as elongation of the flavivirus RNA genome. In this work, almost 5000 natural products were docked to DENV RdRp. The top 197 molecules with greater binding energies than the known ligand of the target were further clustered down to furnish 35 classes of molecular structures. These compounds with satisfactory predicted drug properties and with known natural origin can be further explored to pave the way for the first anti-dengue drug.
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来源期刊
Chem-Bio Informatics Journal
Chem-Bio Informatics Journal BIOCHEMISTRY & MOLECULAR BIOLOGY-
CiteScore
0.60
自引率
0.00%
发文量
8
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