一种恶二唑衍生物(5(4-羟基苯基)-2-(n -苯基氨基)-1,3,4-恶二唑)的生物学特性:体外、计算机和网络药理学方法。

IF 3.2 4区 医学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Tugce Duran, Irem Balikci, Busra Buyukkosucu, Ibrahim Furkan Gunes, Hatice Kubra Pekgonul, Necati Vardar, Mahmut Deniz Yilmaz, Gunes Ak, Gokhan Zengin
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引用次数: 0

摘要

恶二唑类化合物引起人们极大的兴趣,因为它们具有从抗氧化剂到抗癌剂的一系列生物活性。在此背景下,我们想要证明5(4-羟基苯基)-2-(n -苯基氨基)-1,3,4-恶二唑(Hppo)的抗氧化、酶抑制和抗癌作用。通过自由基清除和还原能力测试来测定抗氧化能力。研究了胆碱酯酶、酪氨酸酶、淀粉酶和葡萄糖苷酶的酶抑制作用。对胰腺癌细胞系(PANC-1、CRL-169)和HEK293细胞系进行了抑癌实验。该化合物显示出显著的抗氧化活性(特别是在CUPRAC(铜酸还原抗氧化能力)测定中)和酶抑制特性(特别是葡萄糖苷酶抑制)。在抗肿瘤实验中,化合物对具有凋亡信号通路的胰腺癌表现出较强的抗肿瘤活性。这些结果得到了分子模型和生物信息学工具的证实。因此,我们的发现可以为制药工业中多向药物的开发提供新的和多用途的化合物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Biological Characterization of One Oxadiazole Derivative (5(4-Hydroxyphenyl)-2-(N-Phenyl Amino)-1,3,4-Oxadiazole): In Vitro, In Silico, and Network Pharmacological Approaches

Oxadiazole compounds are of great interest because they have a range of biological activities ranging from antioxidants to anticancer agents. Against this background, we wanted to demonstrate the antioxidant, enzyme inhibitory, and anticancer effects of 5(4-hydroxyphenyl)-2-(N-phenylamino)-1,3,4-oxadiazole (Hppo). Antioxidant abilities were measured through free radical scavenging and reducing power tests. Enzyme inhibitory effects were studied by cholinesterases, tyrosinase, amylase, and glucosidase. The anticancer effect was tested on pancreatic cancer cell lines (PANC-1, CRL-169) and on HEK293 cell lines. The compound showed significant antioxidant activity (particularly in the CUPRAC (cupric acid-reducing antioxidant capacity) assay) and enzyme inhibitory properties (particularly glucosidase inhibition). In the anticancer test, the compound showed strong anticancer activity in pancreatic cancer with apoptotic signaling pathways. These results were confirmed by molecular modeling and bioinformatics tools. Thus, our findings can provide novel and versatile compounds for the development of multidirectional drugs in the pharmaceutical industry.

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来源期刊
Chemical Biology & Drug Design
Chemical Biology & Drug Design 医学-生化与分子生物学
CiteScore
5.10
自引率
3.30%
发文量
164
审稿时长
4.4 months
期刊介绍: Chemical Biology & Drug Design is a peer-reviewed scientific journal that is dedicated to the advancement of innovative science, technology and medicine with a focus on the multidisciplinary fields of chemical biology and drug design. It is the aim of Chemical Biology & Drug Design to capture significant research and drug discovery that highlights new concepts, insight and new findings within the scope of chemical biology and drug design.
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