2-(2-肼基)噻唑类潜在抗氧化、抗炎和抗癌药物的合成、分子对接及生物学评价

IF 1.2 Q4 PHARMACOLOGY & PHARMACY
Dattatraya G Raut, Raghunath B Bhosale, Anjana S Lawand, Mahesh G Hublikar, Vikas D Kadu, Sandeep B Patil, Prafulla B Choudhari
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引用次数: 0

摘要

背景:近年来,研究人员致力于开发以聚乙二醇为绿色溶剂合成生物活性杂环化合物的新方法。在此背景下,我们报道了合成的2-(2-肼基)噻唑的体外抗氧化、体外抗炎和体外抗癌活性。目的:开发新型抗氧化、抗炎、抗癌药物。方法:首先用PEG-400 (20 mL)在5 mol%冰醋酸存在下缩合取代苯乙酮1、硫代氨基脲2和α-卤酮3,得到硫代氨基脲中间体。然后,这些硫代氨基脲与α-卤酮3反应,得到合适的2-(2-肼基)噻唑。合成的化合物在体外测试了其抗氧化、抗炎和抗癌活性。结果:体外评价报告显示,几乎所有分子均具有潜在的抗氧化活性,可清除2,2-二苯基-1-吡啶肼(DPPH)、一氧化氮(NO)、超氧自由基(SOR)和过氧化氢(H2O2)自由基。与作为参考标准的双氯芬酸钠相比,大多数2-(2-肼基)噻唑衍生物显示出潜在的抗炎活性。与阿霉素相比,2-(2-肼基)噻唑类衍生物对人白血病细胞株K-562具有显著的抗癌活性。结论:所有化合物均具有清除2,2-二苯基-1-吡啶酰肼(DPPH)和一氧化氮(NO)自由基的活性。其中4b、4d和4e表现出良好的过氧化氢能力,4b、4e、4f和4g表现出优异的超氧自由基清除能力。此外,4b, 4e和4g化合物显示出对标准双氯芬酸钠药物有效的体外抗炎活性。2-(2-肼基)噻唑衍生物4c和4d对人白血病细胞K-562具有明显的抗癌活性。因此,这些分子为设计和开发新的抗氧化、抗炎和抗癌药物提供了一个有趣的模板。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Syntheses, Molecular Docking and Biological Evaluation of 2-(2- hydrazinyl)thiazoles as Potential Antioxidant, Anti-Inflammatory and Significant Anticancer Agents.

Background: Recently, researchers have worked on the development of new methods for the synthesis of bioactive heterocycles using polyethylene glycol as a green solvent. In this context, we report the synthesized 2-(2-hydrazinyl) thiazoles for their in vitro antioxidant, in vitro anti-inflammatory and in vitro anti-cancer activities.

Objective: The objective of the study was to develop novel antioxidant, anti-inflammatory and anti-cancer drugs.

Methods: At the outset, the condensation of substituted acetophenones 1, thiosemicarbazide 2, and α-haloketones 3 was carried out using PEG-400 (20 mL) in the presence of 5 mol% glacial acetic acid to afford thiosemicarbazones intermediate. Furthermore, these thiosemicarbazones were reacted with α-haloketones 3 to obtain appropriate 2-(2-hydrazinyl) thiazoles. The synthesized compounds were in vitro tested for their antioxidant, anti-inflammatory, and anti-cancer activity.

Results: In vitro evaluation report showed that nearly all molecules possessed potential antioxidant activity against 2,2-Diphenyl-1-picrylhydrazyl (DPPH), nitric oxide (NO), superoxide radical (SOR) and hydrogen peroxide (H2O2) radical scavenging activity. Most 2-(2-hydrazinyl) thiazoles derivatives have shown potential anti-inflammatory activity as compared to diclofenac sodium as a reference standard. 2-(2-Hydrazinyl) thiazoles derivatives showed significant anticancer activity for human leukemia cell line K-562 compared to adriamycin as a reference standard.

Conclusion: All tested compounds showed potential 2,2-Diphenyl-1-picrylhydrazyl (DPPH) and nitric oxide (NO) radical scavenging activity. Among the tested series, 4b, 4d and 4e exhibited good hydrogen peroxide and 4b, 4e, 4f and 4g showed excellent superoxide radical scavenging activity. In addition, the 4b, 4e and 4g compounds revealed potent in vitro anti-inflammatory activity against standard diclofenac sodium drug. 2-(2-Hydrazinyl) thiazole derivatives, such as 4c and 4d, showed significant anticancer activity against human leukemia cell line K-562. Thus, these molecules provide an interesting template for the design and development of new antioxidant, anti-inflammatory, and anti-cancer agents.

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