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2-甲氧基苯甲酰基硫脲的合成、抗菌活性评估、基于高效液相色谱的化合物积累及对接研究

Synthesis, antimicrobial evaluation, HPLC-based compound accumulation and docking studies of 2-methoxybenzoyl thioureas.

作者信息

Erol Gunal Sule, Çeçen Selen Duygu, Kaplan Engin

机构信息

Faculty of Pharmacy, Department of Pharmaceutical Chemistry, Istanbul University-Cerrahpaşa, Istanbul, Türkiye.

Faculty of Pharmacy, Department of Analytical Chemistry, Istanbul University-Cerrahpaşa, Istanbul, Türkiye.

出版信息

Future Med Chem. 2025 May;17(10):1119-1129. doi: 10.1080/17568919.2025.2504332. Epub 2025 May 15.

Abstract

INTRODUCTION

In this study, we presented the synthesis, antimicrobial activity, High Performance Liquid Chromatography (HPLC)-based compound accumulation and molecular docking of 2-methoxybenzoyl substituted thiourea derivatives.

MATERIALS AND METHODS

The antimicrobial activity of a total of eight synthesized compounds was evaluated against seven species of bacteria and fungi. HPLC-based compound accumulation assay, molecular docking, in silico toxicity and ADME analyses were performed for selected compounds for further evaluation of compound activity relationship.

RESULTS AND DISCUSSION

The compounds exhibited greater activity against fungi than bacteria, with compounds , , , and showing particularly strong activity against species. Compounds , , , and that had varying biological activities were selected for further analyses. Compounds , , and accumulated intracellularly reaching up to 36.77% within 1 hours. Molecular docking studies revealed compatible interactions among the compounds in comparison to their varying biological activities. Additionally, all compounds had low toxicity and showed no physicochemical violations when compared to Lipinski's rule of five.

CONCLUSION

The results suggest that optimizing the position of substituents on the phenyl rings of acyl thioureas could enhance the antimicrobial activity of our compounds.

摘要

引言

在本研究中,我们介绍了2-甲氧基苯甲酰基取代硫脲衍生物的合成、抗菌活性、基于高效液相色谱(HPLC)的化合物积累以及分子对接。

材料与方法

总共八种合成化合物的抗菌活性针对七种细菌和真菌进行了评估。对选定的化合物进行了基于HPLC的化合物积累测定、分子对接、计算机模拟毒性和ADME分析,以进一步评估化合物的活性关系。

结果与讨论

这些化合物对真菌的活性比对细菌的活性更强,化合物 、 、 和 对 菌种表现出特别强的活性。选择具有不同生物活性的化合物 、 、 和 进行进一步分析。化合物 、 和 在细胞内积累,1小时内达到36.77%。分子对接研究表明,与它们不同的生物活性相比,这些化合物之间存在相容的相互作用。此外,与Lipinski的五规则相比,所有化合物的毒性都很低,并且没有显示出物理化学违规情况。

结论

结果表明,优化酰基硫脲苯环上取代基的位置可以提高我们化合物的抗菌活性。

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