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黄牛木超临界提取物对登革2型病毒的体外和计算机模拟活性

In-vitro and in silico activity of (Gaur) L. supercritical extract against the dengue-2 virus.

作者信息

Kaushik Sulochana, Kaushik Samander, Kumar Ramesh, Dar Lalit, Yadav Jaya Parkash

机构信息

Department of Genetics, Maharshi Dayanand University, Rohtak, Haryana 124001 India.

Centre for Biotechnology, Maharshi Dayanand University, Rohtak, Haryana 124001 India.

出版信息

Virusdisease. 2020 Dec;31(4):470-478. doi: 10.1007/s13337-020-00624-9. Epub 2020 Aug 31.

Abstract

Our health and wealth are highly influenced by a number of viruses. Dengue is one of them having a global influence in absence of vaccines and antiviral. WHO suggested that the morbidity of dengue is increasing more than 6 times from 0.5 million in 2010 to over 3.34 million in 2016, following a sharp increase in 2019. The aim of the present study is to check the in vitro and in silico anti-dengue activity of supercritical extract in cell lines. The optimum yield of supercritical extract was obtained 0.13 g/10 g (1.3% w/w) at 40 °C temp and 15 MPa pressure and further characterized by GC-MS. The antiviral assay was performed on C6/36 cell lines with 100 copies of dengue-2 virus and maximum non-toxic dose (31.25 µg/ml) of supercritical extract and their effect was detected by real-time RT-PCR. This study revealed that supercritical extract inhibited the dengue-2 virus (99.9%). GC-MS analysis of supercritical extract showed the presence of 10 compounds. The major compounds identified were Hexadecanoic acid, 15-methyl-methyl ester (24.498%); 9,12-octadecadienoyl chloride, (,)- (23.718%); methyl dodecanoic acid (13.228%); methyl-stearate (8.696%); Tridecanoic acid, 12-methyl-, methyl-ester (8.426%), dodecanoic acid (6.102%). The study reveals that can be exploited to develop an effective, inexpensive, and specific anti-dengue. The molecular docking study demonstrated the binding energy of 1,2-benzenedicarboxylic acid, bis(2-methylpropyl) ester (- 4.1 kcal/mol), 9,12-octadecadienoyl chloride (,) (- 4.0 kcal/mol) ligands were higher than others. It is concluded that can play a major role to inhibit dengue-2 virus.

摘要

我们的健康和财富受到多种病毒的严重影响。登革热就是其中之一,在缺乏疫苗和抗病毒药物的情况下,它在全球范围内造成影响。世界卫生组织指出,登革热的发病率从2010年的50万例急剧上升,到2016年超过334万例,增长了6倍多,2019年更是急剧增加。本研究的目的是检测超临界提取物在细胞系中的体外和计算机模拟抗登革热活性。在40℃温度和15MPa压力下获得超临界提取物的最佳产量为0.13g/10g(1.3%w/w),并通过气相色谱-质谱联用仪(GC-MS)进一步表征。在含有100个登革热2型病毒拷贝的C6/36细胞系上进行抗病毒试验,并使用超临界提取物的最大无毒剂量(31.25μg/ml),通过实时逆转录聚合酶链反应(real-time RT-PCR)检测其效果。本研究表明,超临界提取物抑制了登革热2型病毒(9九十九点九%)。超临界提取物的气相色谱-质谱联用分析显示存在10种化合物。鉴定出的主要化合物为十六烷酸,15-甲基-甲酯(24.498%);9,12-十八碳二烯酰氯,(,)-(23.718%);十二烷酸甲酯(13.228%);硬脂酸甲酯(8.696%);十三烷酸,12-甲基-,甲酯(8.426%),十二烷酸(6.102%)。该研究表明,可以利用其开发一种有效、廉价且特异性的抗登革热药物。分子对接研究表明,1,2-苯二甲酸双(2-甲基丙基)酯(-4.1千卡/摩尔)、9,12-十八碳二烯酰氯(,)(-4.0千卡/摩尔)配体的结合能高于其他配体。得出的结论是,其可以在抑制登革热2型病毒方面发挥主要作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cdbc/7749025/a547cfd459b6/13337_2020_624_Fig1_HTML.jpg

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