Phenolic Compound in Garlic (Allium sativum) and Black Garlic Potency as Antigout Using Molecular Docking Approach

A. Lestari, Irmanida Batubara, S. T. Wahyudi, A. Ilmiawati
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Abstract

Phenolics, including flavonoids, are bioactive components in garlic in relatively abundant amounts and are present 2–4 times more in black garlic. Both of these compounds are reported to have biological activity, with one of them acting as an antioxidant. However, its ability as an antigout is still not widely reported. Xanthine oxidase, adenine deaminase, guanine deaminase, purine nucleoside phosphorylase, and 5-Nucleotidase II are involved during the production of uric acid and causes gout. This study predicted the potential of the phenolic and flavonoid compounds in garlic and black garlic as antigout in inhibiting five target receptors through a molecular docking approach. Utilizing AutoDock Tools v.1.5.7 for receptor and ligand preparation, AutoDock Vina and AutoDock4 for molecular docking, and LigPlot+ and PyMOL for visualization. About 21 compounds from the phenolic and flavonoid groups were used as test ligands and 16 reference ligands (substrate and commercial). SwissADME predicted the pharmacokinetic parameters. The results showed that apigenin, morin, resveratrol, kaempferol, (+)-catechin, isorhamnetin, and (-)-epicatechin were predicted to have good interactions at each target receptor and had the potential to be developed as candidates for multi-target antigout. Based on the pharmacokinetic parameters, all these compounds had good scores in each, making them feasible to continue in vitro or in vivo trials.
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大蒜中酚类化合物与黑蒜抗痛风作用的分子对接研究
酚类化合物,包括黄酮类化合物,是大蒜中含量相对丰富的生物活性成分,在黑大蒜中的含量是黑大蒜的2-4倍。据报道,这两种化合物都具有生物活性,其中一种起抗氧化剂的作用。然而,它作为一种抗痛风的能力仍然没有被广泛报道。黄嘌呤氧化酶、腺嘌呤脱氨酶、鸟嘌呤脱氨酶,嘌呤核苷磷酸化酶和5-核苷酸酶II参与尿酸的产生并引起痛风。本研究通过分子对接方法预测了大蒜和黑大蒜中的酚类和黄酮类化合物作为抗痛风药物抑制五种靶受体的潜力。利用AutoDock Tools v.1.5.7进行受体和配体制备,AutoDock Vina和AutoDock4进行分子对接,LigPlot+和PyMOL进行可视化。来自酚类和类黄酮类的大约21个化合物被用作测试配体和16个参考配体(底物和商业)。SwissADME预测了药代动力学参数。结果表明,芹菜素、桑色素、白藜芦醇、山奈酚、(+)-儿茶素、异鼠李素和(-)-表儿茶素在每个靶受体上都具有良好的相互作用,有潜力开发成为多靶点抗痛风的候选药物。根据药代动力学参数,所有这些化合物在每种药物中都有良好的得分,这使得它们可以继续进行体外或体内试验。
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审稿时长
17 weeks
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