In Silico Anti- HIV Analysis of FTIR identified Bioactive compounds present in Vitex altissima L and Vitex leucoxylon L

C. Masi, S. Naganathan, A. Natarajan, Vivek Pazhamalai, M. Tafesse
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Abstract

The knowledge of the traditional plants in India is a collection over millennia by our ancient people. The Siddha System of Medicine (Traditional Tamil System of medicine) is the foremost of all other medical systems in the world which provide service to the humanity for more than 5000 years in combating diseases and also in maintaining its physical, mental and moral health. Vitex species were used in siddha for its anti- viral activity for several years. However, the present study deals with the Human Immunodeficiency Virus because of its complexity and killing effects. FTIR analysis of Vitex altissima L and Vitex leucoxylon L revealed the presence of 21 and 17 bioactive compounds respectively. These compounds were analysed further for its binding affinity mechanism against one of the virulence causing protein, reverse transcriptase (target protein) of Human Immunodeficiency Virus (HIV) by using molecular docking and bioinformatics tools. Interaction rate was determined between bioactive compounds against the protein target based on binding free energy requirements. Molecular docking was also made to the commercially available drugs (Zidovudine, Stavudine, and Nevirapine) against the target protein. By comparing the results between bioactive compounds in the Vitex species and the commercially available drugs, it was clear that the bioactive compounds were much more effective than the commercially available drugs, thereby suitable for the treatment of AIDS. Hence, this study will form the basis for promoting therapeutic lead molecules from the traditional plants which restore the tradition and also eliminates the harmful side effects.
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白荆和白荆中生物活性化合物的红外光谱分析
印度传统植物的知识是贵国古人几千年来的积累。悉达医学体系(传统泰米尔医学体系)是世界上最重要的医疗体系,它为人类提供了5000多年的治疗疾病和保持身体、精神和道德健康的服务。牡荆属植物因其抗病毒作用已被广泛应用于中药中。然而,由于人类免疫缺陷病毒的复杂性和杀伤作用,本研究涉及人类免疫缺陷病毒。通过FTIR分析,白荆和白荆分别含有21种和17种活性成分。利用分子对接和生物信息学手段进一步分析了这些化合物与人类免疫缺陷病毒(HIV)致毒蛋白之一逆转录酶(靶蛋白)的结合亲和力机制。根据结合自由能需求确定生物活性化合物与蛋白质靶标之间的相互作用速率。分子对接也进行了市售药物(齐多夫定,司他夫定,奈韦拉平)针对靶蛋白。通过对牡荆属植物和市售药物生物活性成分的比较,发现牡荆属植物的生物活性成分比市售药物有效得多,适合用于艾滋病的治疗。因此,本研究将为从传统植物中提取治疗性铅分子,在恢复传统的同时消除有害的副作用奠定基础。
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