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咪唑:多功能部分的现状和未来展望。

Current and Future Prospective of a Versatile Moiety: Imidazole.

机构信息

Maharishi Markandeshwar School of Pharmacy, Maharishi Markandeshwar University, Sadopur, Ambala, 134007, Haryana, India.

SunPharma, Hill Top Area, Vill. Bhatolikalan, P.O.Barotiwala, Distt.Solan, Himachal Pardesh, 174103, India.

出版信息

Curr Drug Targets. 2020;21(11):1130-1155. doi: 10.2174/1389450121666200530203247.


DOI:10.2174/1389450121666200530203247
PMID:32472996
Abstract

Imidazole containing compounds have been a very much explored field since ancient times. Subsequently, it constitutes a significant moiety for the new drug development. A variety of compounds having imidazole moiety have been synthesized, evaluated and marketed for the treatment of various diseases such as antifungal, antiepileptic, ACE inhibitors and so on, as shown in the figure. The search for imidazole containing compounds with more selective biological potency with low side effects continues to be an active area of research in medicinal chemistry. This review is in an effort to highlight the marketed drugs with imidazole ring. The article also demonstrates the future prospective of marketed imidazoles as antifungal with potential activity targeting 14α-demethylase enzyme.

摘要

含咪唑的化合物自古以来就是一个备受关注的领域。因此,它成为了新药研发的重要组成部分。已经合成、评估和销售了多种具有咪唑部分的化合物,用于治疗各种疾病,如抗真菌药、抗癫痫药、ACE 抑制剂等,如图所示。寻找具有更高选择性生物活性和更低副作用的含咪唑化合物一直是药物化学研究的一个活跃领域。本综述旨在强调具有咪唑环的已上市药物。本文还展示了具有潜在活性的已上市咪唑类抗真菌药物的未来前景,这些药物的作用靶点是 14α-脱甲基酶。

相似文献

[1]
Current and Future Prospective of a Versatile Moiety: Imidazole.

Curr Drug Targets. 2020

[2]
Molecular Modeling Studies of Halogenated Imidazoles against 14α- Demethylase from Candida Albicans for Treating Fungal Infections.

Infect Disord Drug Targets. 2020

[3]
Molecular Docking Evaluation of Imidazole Analogues as Potent Candida albicans 14α-Demethylase Inhibitors.

Curr Comput Aided Drug Des. 2015

[4]
Imidazolylchromanones containing alkyl side chain as lanosterol 14α-demethylase inhibitors: synthesis, antifungal activity and docking study.

J Enzyme Inhib Med Chem. 2013-3-14

[5]
Carbohydrate hitched imidazoles as agents for the disruption of fungal cell membrane.

J Mycol Med. 2019-11-7

[6]
Fungal Lanosterol 14α-demethylase: A target for next-generation antifungal design.

Biochim Biophys Acta Proteins Proteom. 2019-3-6

[7]
Design, synthesis and antifungal activity of some new imidazole and triazole derivatives.

Arch Pharm (Weinheim). 2011-8-25

[8]
Synthesis of Novel 3,4-Chloroisothiazole-Based Imidazoles as Fungicides and Evaluation of Their Mode of Action.

J Agric Food Chem. 2018-7-5

[9]
Synthesis and fungicidal activity of novel imidazole-based ketene dithioacetals.

Bioorg Med Chem. 2018-3-9

[10]
Design, Synthesis and Antifungal Activity Evaluation of New Thiazolin-4-ones as Potential Lanosterol 14α-Demethylase Inhibitors.

Int J Mol Sci. 2017-1-17

引用本文的文献

[1]
Preparation of imidazole-modified paper membrane for selective extraction of gallic acid and its structural and functional analogues from .

RSC Adv. 2024-4-30

[2]
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Cent Nerv Syst Agents Med Chem. 2024

[3]
One-step synthesis of imidazoles from Asmic (anisylsulfanylmethyl isocyanide).

Beilstein J Org Chem. 2021-6-24

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