作为强效脲酶抑制剂的新型苯并咪唑基嗪衍生物:合成、体外和硅学方法。

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC
Hamidullah, Aftab Alam, Ahmed A Elhenawy, Mumtaz Ali, Abdul Latif, Ajmal Khan, Ahmed Al-Harrasi, Manzoor Ahmad
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引用次数: 0

摘要

目的:鉴于苯并咪唑和叠氮的各种生物活性,本研究重点报道了苯并咪唑核的新型衍生物:方法:对 20 种新型苯并咪唑叠氮化物进行了合成、表征和体外脲酶抑制活性测试:结果:与标准硫脲 21.14 ± 0.42 μM 相比,所有这些衍生物都表现出极好的抑制作用,IC50 值范围在 14.21 ± 1.87 到 76.11 ± 1.81 μM 之间。对目标苯并咪唑衍生物进行了 Docking 研究,以了解其结合机理。结果表明,与参考抑制剂相比,苯并咪唑衍生物具有更高的结合效力:本研究发现了新型脲酶抑制剂的潜在候选先导化合物,在工业界的支持下可用于新药开发。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Novel benzimidazole-based azine derivatives as potent urease inhibitors: synthesis, in vitro and in silico approach.

Aim: In light of various biological activities of benzimidazole and azines, this study focuses on reporting novel derivatives of benzimidazole nucleus.Methods: Twenty novel azines of benzimidazole were synthesized, characterized and tested for in vitro urease inhibitory activity.Results: All these derivatives showed excellent to good inhibition in the range of IC50 values 14.21 ± 1.87 to 76.11 ± 1.81 μM by comparing with standard thiourea 21.14 ± 0.42 μM. Docking studies were performed for the targeted benzimidazole derivatives to understand the binding mechanics. The results indicated higher binding efficacy compared with the reference inhibitor.Conclusion: This work identifies potential lead candidates for novel urease inhibitors, which with industrial support may be harnessed for the development of new drugs.

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来源期刊
CiteScore
7.20
自引率
4.30%
发文量
567
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