生物碱衍生物作为抗乳腺癌症候选药物的潜力:在Silico研究中

Sedin Renadi, A. Pratita, R. Mardianingrum, R. Ruswanto
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引用次数: 0

摘要

癌症是全世界女性最常见的恶性肿瘤。治疗癌症的靶受体之一是雌激素、孕酮和HER2受体。已经开发出一种使用天然成分的替代治疗方法,其中一种是生物碱化合物。本研究旨在通过硅方法测定生物碱化合物作为抗癌症药物的活性。进行了虚拟筛选(AutoDock-Vina)、分子对接(AutoDock Tools)、分子动力学(Desmond)、扫描利平斯基五规则以及药代动力学和毒性参数。虚拟筛选、分子对接和分子动力学的结果表明,与其他化合物相比,daurisoline、solasodine和sambutoxin与HER2受体具有稳定的相互作用,RMSD(均方根偏差)和RMSF(均方根波动)值最低。根据所进行的研究结果,预测柔里索林、索拉索定和桑布托新可作为抗HER2候选药物用于治疗癌症。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Potency of Alkaloid Derivates as Anti-Breast Cancer Candidates: In Silico Study
Breast cancer is the most frequent malignancy in women worldwide. One of the target receptors for the treatment of breast cancer are estrogen, progesterone, and HER2 receptors. An alternative treatment using natural ingredients has been developed, one of which is alkaloid compounds. This study aims to determine the activity of alkaloid compounds as anti-breast cancer agents through an in-silico method. Virtual screening (AutoDock Vina), molecular docking (AutoDock Tools), molecular dynamics (Desmond), scanning Lipinski's rule of five, as well as pharmacokinetic and toxicity parameters, were performed. The results of virtual screening, molecular docking, and molecular dynamics show that the compounds daurisoline, solasodine, and sambutoxin have stable interactions with the HER2 receptor, with the lowest values of RMSD (Root Mean Square Deviation) and RMSF (Root Mean Square Fluctuation) compared to other compounds. Based on the results of the study conducted, it was shown that daurisoline, solasodine, and sambutoxin were predicted to be used as anti-HER2 candidates for the treatment of breast cancer.
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来源期刊
CiteScore
0.80
自引率
0.00%
发文量
15
审稿时长
24 weeks
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