In silico Pharmacokinetic and Toxicity Prediction of Compounds from Andrographis paniculata (Burm.f.) Nees.

Izatunnafis Izatunnafis, Y. B. Murti, Bambang Sulistyo Ari Sudarmanto
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Abstract

Many compounds have been isolated from Andrographis paniculata (Burm. f.) Nees (AP). In drug discovery and development, plant secondary metabolites are popular as resources for drug candidates. A high-quality drug candidate should not only be effective against the therapeutic target, but it should also be safe and have good pharmacokinetic features. This study aimed to predict the pharmacokinetic features and toxicity potencies of 46 compounds from AP using the pKCSM online tool. According to pKCSM prediction, among the forty-six compounds from AP, compound 1 (14-Deoxy-11,12-didehydroandrographolide), compound 2 (14-Deoxyandrographolide), and compound 39 ((-)-beta-Sitosterol) have good pharmacokinetic features and do not have potencies to be mutagenic and hepatotoxic agents. The lethal dosage values (LD50) of compounds 1, 2, and 39, are 1935, 2053, and 2424 (mol/kg), respectively. However, further research is still needed to confirm these predictions.
穿心莲(Burm.f. Nees.)化合物的硅学药代动力学和毒性预测
从穿心莲(Andrographis paniculata (Burm. f.) Nees)(AP)中分离出了许多化合物。在药物发现和开发过程中,植物次生代谢物作为候选药物资源备受青睐。优质的候选药物不仅要对治疗靶点有效,还要安全且具有良好的药代动力学特征。本研究旨在利用 pKCSM 在线工具预测 46 种来自 AP 的化合物的药代动力学特征和毒性效力。根据 pKCSM 预测结果,在 46 个来自 AP 的化合物中,化合物 1(14-脱氧-11,12-二脱氢穿心莲内酯)、化合物 2(14-脱氧穿心莲内酯)和化合物 39((-)-beta-谷甾醇)具有良好的药代动力学特征,不具有诱变性和肝毒性。化合物 1、2 和 39 的致死剂量值(LD50)分别为 1935、2053 和 2424(mol/kg)。不过,仍需要进一步的研究来证实这些预测。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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