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熊果苷和熊果苷十一烯酸酯的分子建模和对酚氧化酶的抑制活性。

Molecular modeling and phenoloxidase inhibitory activity of arbutin and arbutin undecylenic acid ester.

机构信息

Faculty of Pharmacy, Institute of Medical, Pharmaceutical and Health Sciences, Kanazawa University, Kanazawa, Japan; Faculty of Pharmacy, Hasanuddin University, Makassar, Indonesia; Faculty of Medicine, Hasanuddin University, Makassar, Indonesia.

Faculty of Pharmacy, Institute of Medical, Pharmaceutical and Health Sciences, Kanazawa University, Kanazawa, Japan; Faculty of Pharmacy, Universitas Sumatera Utara, Medan, Indonesia.

出版信息

Biochem Biophys Res Commun. 2021 Apr 2;547:75-81. doi: 10.1016/j.bbrc.2021.02.006. Epub 2021 Feb 17.

Abstract

Excessive melanin formation has been linked to various skin disorders such as hyperpigmentation and skin cancer. Tyrosinase is the most prominent target for inhibitors of melanin production. In this study, we investigated whether arbutin and its prodrug, arbutin undecylenic acid ester, might inhibit phenoloxidase (PO), a tyrosinase-like enzyme. Molecular docking simulation results suggested that arbutin and arbutin undecylenic acid ester can bind to the substrate-binding pocket of PO. Arbutin undecylenic acid ester with an IC 6.34 mM was effective to inhibit PO compared to arbutin (IC 29.42 mM). In addition, arbutin undecylenic acid ester showed low cytotoxicity in Drosophila S2 cells and the compound inhibited the melanization reaction. Therefore, the results of this study have demonstrated that arbutin undecylenic acid ester as a potential inhibitor of PO. We successfully designed a new platform utilizing Drosophila melanogaster and Bombyx mori as animal models propounding fast, cheap, and high effectiveness in method to screen tyrosinase inhibitors.

摘要

过量的黑色素形成与各种皮肤疾病有关,如色素沉着过度和皮肤癌。酪氨酸酶是黑色素生成抑制剂的最主要靶标。在这项研究中,我们研究了熊果苷及其前药十一烯酸熊果苷酯是否可以抑制酚氧化酶(PO),一种类似于酪氨酸酶的酶。分子对接模拟结果表明,熊果苷和十一烯酸熊果苷酯可以与 PO 的底物结合口袋结合。与熊果苷(IC 29.42 mM)相比,十一烯酸熊果苷酯对 PO 的抑制作用更为有效(IC 6.34 mM)。此外,十一烯酸熊果苷酯在果蝇 S2 细胞中表现出低细胞毒性,并且该化合物抑制了黑色素化反应。因此,这项研究的结果表明,十一烯酸熊果苷酯是一种潜在的 PO 抑制剂。我们成功地设计了一个新的平台,利用黑腹果蝇和家蚕作为动物模型,提出了一种快速、廉价、高效的筛选酪氨酸酶抑制剂的方法。

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