内生真菌、uredinicola枝孢菌植物化学物质的体外和体内抗氧化、抗糖尿病、抗hiv和抗阿尔茨海默病活性

M. Govindappa, V. Thanuja, S. Tejashree, C. A. Soukhya, S. Barge, A. Manojkumar, Rai V. Ravishankar
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引用次数: 6

摘要

采用定性、薄层色谱和气相色谱-质谱等方法,鉴定了其化学成分,并对其体外抗氧化、抗hiv、抗糖尿病、抗胆碱酯酶活性进行了评价。在定性方法中发现了黄酮、单宁、生物碱、苷类、酚类、萜类和香豆素。通过GC-MS分析,鉴定出7种不同的植物化学物质,其中4种(香豆素、香豆酸、羟色胺酮、异欧前胡素)为香豆素。在DPPH(73)和FRAP(1359)法中均显示出显著的抗氧化活性。HIV-1 RT(83.81+2.14)、gp 120(80.24+2.31)、整合酶(79.43+3.14)和蛋白酶(77.63+2.14)、DPPIV、β-葡萄糖苷酶和乙酰胆碱酯酶活性显著降低。2-二苯基亚甲基氨基甲酯与氧化剂和HIV-1蛋白有明显的相互作用,而异欧前胡素与糖尿病和胆碱酯酶蛋白有明显的相互作用,其次是高结合能的膜酮。这三种植物化学物质是非致癌物,无毒,易于降解,并具有药物特性。C. uredinicola植物化学物质负责管理糖尿病,HIV-1和阿尔茨海默病。需要进一步的体内工作来证明我们的研究是正确的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
In Vitro and In Silico Antioxidant, Anti-Diabetic, Anti-HIV and Anti-Alzheimer Activity of Endophytic Fungi, Cladosporium uredinicola Phytochemicals
The present work was aimed to identify phytochemicals in C. uredinicola methanol extract from qualitative, TLC and GC-MS method and evaluated for antioxidant, anti-HIV, anti-diabetes, anti-cholinesterase activity in vitro and in silico. The C. uredinicola extract showed flavonoids, tannins, alkaloids, glycosides, phenols, terpenoids, and coumarins presence in qualitative method. From GC-MS analysis, identified seven different phytochemicals and out of seven, four (coumarin, coumarilic acid, hymecromone, alloisoimperatorin) are coumarins. The C. uredinicola extract have shown significant antioxidant activity in DPPH (73) and FRAP (1359) method. The HIV-1 RT (83.81+2.14), gp 120 (80.24+2.31), integrase (79.43+3.14) and protease (77.63+2.14), DPPIV, β-glucosidase and acetyl cholinesterase activity was significantly reduced by the extract. The 2-diphenylmethyleneamino methyl ester had shown significant interaction with oxidant and HIV-1 proteins whereas alloisoimperatorin have interacted with diabetes and cholinesterase proteins followed by hymecromone with high binding energy. These three phytochemicals are non-carcinogens, non-toxic, readily degradable and have drug likeliness properties. The C. uredinicola phytochemicals are responsible for management of diabetes, HIV-1 and Alzheimer. Further in vivo work is needed to justify our research.
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