合成N,N′-乙烯双(α甲基水杨酸酯)希夫碱衍生物抗组蛋白去乙酰化酶、抗菌、抗氧化和细胞毒活性的评价

IF 1 4区 工程技术 Q4 CHEMISTRY, MULTIDISCIPLINARY Iranian Journal of Chemistry & Chemical Engineering-international English Edition Pub Date : 2021-08-09 DOI:10.30492/IJCCE.2021.520989.4467
S. Zolghadri, Fatemeh Mosalanezhad, Mahbubeh Naderpoor, Razieh Bordbar, A. Asadzadeh, Ali Ghanbariasad, Mehdi Ghavamizadeh
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引用次数: 2

摘要

近年来,希夫碱配合物作为合成抗氧化剂,因其具有较好的抗氧化效果和较低的成本而被广泛应用。本文研究了一系列α, - me2 -salen, (N,N′-乙二(α甲基水杨酸酯))希夫碱衍生物的抗组蛋白去乙酰化酶(HDAC)、抗癌、抗菌和抗氧化活性。对于抗HDAC的研究,AUTODOCK 4.1和分子动力学(MD)模拟已经针对这些组合进行了。采用细胞毒试验、血浆铁还原能力(FRAP)、2,2-二苯基-1-吡啶肼(DPPH)和(2,2'-氮基-双(3-乙基苯并噻唑-6-磺酸))ABTS试验和琼脂扩散法分别考察了其抗癌、抗氧化和抗菌活性。结果表明,α, - me2 -salen与HDAC的对接效果最佳。此外,MD计算结果表明,α, - me2 -salen是比SAHA更有效的抑制HDAC的已知酶抑制剂。然而,α, - me2 -salen及其衍生物对任何微生物都没有抗菌活性。对mcf7细胞株的细胞毒活性分析表明,α、 - me2 -salen及其Ni (II)、Co (II)和Cu (II)衍生物具有较高的细胞毒活性,IC50分别为5、2、2和3µg ml−1。结果表明,这些化合物对DPPH、ABTS和FRAP自由基具有良好的清除活性。DPPH的抗氧化活性显示,Mn(II)配合物(IC50 = 0.13±0.50 mg/ml)的抗氧化活性最高。α、 - me2 -salen (IC50 =0.05±0.003 mg/ml)及其Ni(II)衍生物(IC50 =0.049 mg/ml)对ABTS的清除活性最高。结果表明,所有化合物均具有良好的抗癌和抗氧化活性,经进一步研究可作为候选药物使用。
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The evaluation of the anti-Histone deacetylase, antibacterial, antioxidant and cytotoxic activities of synthetic N,N´-ethylenebis(α methylsalicylideneiminate) Schiff base derivatives
Recently, Schiff base complexes as synthetic antioxidants are widely used instead of natural antioxidants because they are effective and cheaper. In this study, a series of α,ά-Me2-salen, (N,N´-ethylenebis(α methylsalicylideneiminate)) Schiff base derivatives have been investigated toward their anti-histone deacetylase (HDAC), anticancer, antibacterial and antioxidant activities. For anti HDAC studies, AUTODOCK 4.1 and Molecular Dynamics (MD) simulation have been conducted against these combinations. Cytotoxic test, ferric reducing ability of plasma (FRAP), 2,2-diphenyl-1-picrylhydrazyl (DPPH) and (2,2'-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid)) ABTS assays and Agar diffusion method have been applied to investigate anticancer, antioxidant and antibacterial activities, respectively. Based on the results, the best docking was obtained for α,ά-Me2-salen against HDAC. Also, MD calculation results demonstrated that the α,ά-Me2-salen is more effective compound for HDAC inhibiting than SAHA as a known enzyme inhibitor. However, α,ά-Me2-salen and its derivatives didn't display antibacterial activity against any of the microorganisms. Cytotoxic activity analysis toward MCF 7 cell line were apparent that α,ά-Me2-salen and its Ni (II), Co (II), and Cu (II) derivatives manifested high cytotoxic activity with IC50 5, 2, 2 and 3 µg ml−1, respectively. The antioxidant results were revealed excellent radical scavenging activities of all these compounds against DPPH, ABTS and FRAP radicals. The antioxidant activity by DPPH, showed Mn(II) complex (IC50 = 0.13 ± 0.50 mg/ml) was the most active. While, α,ά-Me2-salen (IC50 =0.05±0.003 mg/ml) and its Ni(II) derivative (IC50 =0.049 mg/ml) exhibited the highest ABTS scavenging activity. According to results, all compounds show acceptable anticancer and antioxidant activity and can be used as drug candidates after further investigations.
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来源期刊
CiteScore
2.80
自引率
22.20%
发文量
0
审稿时长
6-12 weeks
期刊介绍: The aim of the Iranian Journal of Chemistry and Chemical Engineering is to foster the growth of educational, scientific and Industrial Research activities among chemists and chemical engineers and to provide a medium for mutual communication and relations between Iranian academia and the industry on the one hand, and the world the scientific community on the other.
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