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双胍-磺酰胺衍生物的合成、表征及对乙酰胆碱酯酶抑制、抗氧化和 DNA/BSA 结合性质的研究。

The biguanide-sulfonamide derivatives: synthesis, characterization and investigation of anticholinesterase inhibitory, antioxidant and DNA/BSA binding properties.

机构信息

Chemistry Department, Kahramanmaras Sutcu Imam University, Kahramanmaras, Turkey.

出版信息

J Biomol Struct Dyn. 2023;41(24):14952-14967. doi: 10.1080/07391102.2023.2184637. Epub 2023 Mar 1.

Abstract

A number of new biguanidine-sulfonamide derivatives () were synthesized and their structures were characterized by spectroscopic and analytical methods. Crystal structures of the compounds , , , and were determined by single crystal X-ray diffraction studies. X-ray crystallographic data showed the π-electron delocalization through the biguanide units. The AChE and BChE cholinesterase inhibitor, DPPH antioxidant and DNA/BSA binding properties of the synthesized compounds were evaluated. Results of cholinesterase inhibitory properties have shown that the compounds containing electron-withdrawing (-F, -Cl) groups have higher AChE/BChE inhibitory and antioxidant activities. Compound showed higher BChE inhibitory activity than tacrine with IC value of 28.4 µM. The compounds interact with DNA minor groove binding mode. The compounds with a naphthyl group in its structure strongly binds with DNA/BSA biomolecules.Communicated by Ramaswamy H. Sarma.

摘要

合成了一系列新的双胍-磺酰胺衍生物(),并通过光谱和分析方法对其结构进行了表征。通过单晶 X 射线衍射研究确定了化合物、、、和的晶体结构。X 射线晶体学数据表明,通过双胍单元实现了π 电子离域。评估了合成化合物的 AChE 和 BChE 胆碱酯酶抑制剂、DPPH 抗氧化剂和 DNA/BSA 结合特性。胆碱酯酶抑制特性的结果表明,含有吸电子(-F、-Cl)基团的化合物具有更高的 AChE/BChE 抑制和抗氧化活性。化合物对 BChE 的抑制活性高于他克林,IC 值为 28.4 μM。这些化合物与 DNA 小沟结合模式相互作用。结构中带有萘基的化合物与 DNA/BSA 生物分子强烈结合。由 Ramaswamy H. Sarma 传达。

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