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An in silico perception for newly isolated flavonoids from peach fruit as privileged avenue for a countermeasure outbreak of COVID-19

机译:在桃子水果中为新分离的黄酮类动物的硅感知,作为特权大道,用于抵抗Covid-19

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3′-Hydroxy-4′-methoxy-chroman-7- O -β- D -glucopyranoside 4 was first isolated from a natural source, together with three known compounds, the ferulic acid heptyl ester 1 , naringenin 2 , and 4,2′,4′-trihydroxy-6′-methoxychalcone-4′- O -β- D -glucopyranoside 3 , which were isolated from peach [ Prunus persica (L.) Batsch] fruits. These compounds were subjected to different virtual screening strategies in order to examine their activity to combat the COVID-19 outbreak. The study design composed of some major aspects: (a) docking with main protease ( M ~(pro) ), (b) docking with spike protein, (c) 3D shape similarity study (Rapid Overlay Chemical Similarity-ROCS) to the clinically used drugs in COVID-19 patients, and finally, (d) the rule of five and the estimated pre-ADMT properties of the separated flavonoids. Docking study with M ~(pro) of SARS-CoV-2 (PDB ID:6LU7, and 6Y2F) showed that compound 3 , its aglycone part, and compound 4 have a strong binding mode to a protease receptor with key amino acids, especially Gln:166AA, and having a similar docking pose to co-crystalized ligands. Docking with the spike protein of SARS-CoV-2 illustrated that compounds 3 and 4 have a good binding affinity to PDB ID:6VSB through the formation of HBs with Asp:467A and Asn:422A. According to ROCS analysis, compounds 1 , 3 , and 4 displayed high similarities to drugs that prevent SARS-Co2 entry to the lung cells or block the inflammatory storm causing lung injury. Compounds 3 and 4 are good candidates for drug development especially because they showed predicted activity against SARS-CoV-2 through different mechanisms either by preventing genome replication or by blocking inflammatory storm that trigger lung injury. These compounds were isolated from peach fruit, and the study supports data and continues with the recommendation of peach fruits in controlling and managing COVID-19 cases.
机译:首先将3'-羟基-4'-甲氧基 - Chroman-7-O-β-D-葡糖醇苷4与三种已知的化合物,阿魏酸庚基酯1,柚皮蛋白2和4,2分离',4'-三羟基-6'-甲氧基霉酮-4'-β-D-葡糖醇3,其从桃[prunus persica(l。)果实中分离。这些化合物进行了不同的虚拟筛选策略,以检查他们的活动,以打击Covid-19爆发。该研究设计由一些主要方面组成:(a)与主要蛋白酶(m〜(pro)),(b)与尖峰蛋白,(c)3d形状相似性研究(快速覆盖化学相似性-rocs)对接到临床上在Covid-19患者中使用的药物,最后,(d)的五个和估计的异种类黄酮的预期性能。与SARS-COV-2(PDB ID:6LU7和6Y2F)的M〜(PRO)的对接研究表明,化合物3,其糖苷酮部分和化合物4具有强氨基酸的蛋白酶受体的强结合模式,尤其是GLN:166AA,并具有与共结晶配体相似的对接姿势。通过SARS-COV-2的尖峰蛋白对接,所示的化合物3和4通过在具有ASP:467A和ASN:422A的HBS形成HBS的PDB ID:6VSB具有良好的结合亲和力。根据Rocs分析,化合物1,3和4显示与防止SARS-CO2进入肺细胞的药物的高相似性,或阻断导致肺损伤的炎症风暴。化合物3和4是药物开发的良好候选者,特别是因为通过防止基因组复制或阻断触发肺损伤的炎症风暴,它们通过不同机制显示了对SARS-COV-2的预测活性。这些化合物与桃果分离,研究支持数据并继续桃子果实在控制和管理Covid-19例中的建议。

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