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首页> 外文期刊>Asian Journal of Pharmaceutical and Clinical Research >QUINIC ACID AS A POTENT DRUG CANDIDATE FOR PROSTATE CANCER – A COMPARATIVE PHARMACOKINETIC APPROACH
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QUINIC ACID AS A POTENT DRUG CANDIDATE FOR PROSTATE CANCER – A COMPARATIVE PHARMACOKINETIC APPROACH

机译:奎尼酸作为前列腺癌的强效候选药物—药代动力学的比较方法

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Objective: Phytotherapy is growing importance with the emergence of deadly diseases. Prostate cancer is one such disease which is the most prevalent cancer afflicting men. Therapeutic application of plant is better understood with the pharmacological investigation of its phytoconstituents. Quinic acid is a prominent bioconstituent of flowers of Moringa oleifera Lam, a traditional plant of high nutritional and medicinal values. The present study analyzes the pharmacokinetic properties of this phytocomponent for its therapeutic application in prostate cancer.Methods: In silico tools were used to screen the physicochemical, Lipinski-type and drug properties of Quinic acid from the other compounds used for comparison. The M. oleifera flower compound, Quinic acid and the standard therapeutic Curcumin were the ultimate compounds selected for further studies on their Adsorption-Distribution-Metabolism-Excretion (ADME) characteristics and toxicity parameters.Results: The overall pharmacokinetics results indicated that Quinic acid had more number of advantages over Curcumin and the other compounds studied. Quinic acid possessed greater values of drug score and drug likeness with lesser brain penetration and lesser toxicity effects.Conclusion: The study suggested that the pharmacokinetic properties of Quinic acid were more preferable to be used as a potent drug candidate to combat prostate cancer.
机译:目的:随着致命疾病的出现,植物疗法变得越来越重要。前列腺癌就是一种这样的疾病,它是困扰男性的最普遍的癌症。通过对其植物成分的药理研究,可以更好地理解植物的治疗应用。奎宁酸是辣木(Moringa oleifera Lam)花的重要生物成分,该花是一种具有高营养和药用价值的传统植物。本研究分析了该植物成分在前列腺癌治疗中的药代动力学特性。方法:使用计算机软件,从其他用于比较的化合物中筛选奎尼酸的理化性质,Lipinski型和药物性质。油松花化合物,奎尼酸和标准的治疗性姜黄素是最终选择的化合物,其吸附-分布-代谢-排泄(ADME)特性和毒性参数进一步研究。结果:总体药代动力学结果表明奎尼酸具有与姜黄素和其他研究化合物相比,具有更多的优势。奎尼酸具有较高的药物得分和相似度值,具有较低的脑渗透性和较小的毒性作用。结论:研究表明,奎尼酸的药代动力学特性更适合用作对抗前列腺癌的有效候选药物。

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