Methods of synthesis of 1,2,4-triazole derivatives with methoxyphenyl and study the spectrum of their pharmacological activity

D. Dovbnia, A. Kaplaushenko
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引用次数: 0

Abstract

In today’s society, the work of a pharmaceutical worker is very respectful, because it is difficult to imagine the treatment of people without the use of drugs. As time passes, the number of diseases with their own characteristics only increases, so the creation of drugs of synthetic origin remains an actual task for scientists around the world. There are a large number of heterocyclic systems, the derivatives of which exhibit a wide range of pharmacological activities, namely, furan, pyrrole, pyrazole, pyridine, pyrimidine, purine, and many others. Particular attention is drawn to structures that have low toxicity. Undoubtedly, the initial heterocyclic substance must have several reactive centers in order to build the most effective pharmacophores. Studies by scientists from around the world point to the prospect of using derivatives of the 1,2,4-triazole heterocyclic system as models for new biologically active substances. The aim of the work was to summarize data on modern methods for the synthesis of 1,2,4-triazole derivatives, to determine the effect of a methoxyphenyl substituent on reactivity and changing the spectrum of pharmacological activity. Materials and methods. In the work, we used such methods as analytical, information search, descriptive, generalization. The materials of the research were information from the professional literature on the methods of synthesis and study of the biological activity of 1,2,4-triazole derivatives with methoxyphenyl. Results. A search, analysis, and generalization of information on the methods of synthesis and study of the biological activity of 1,2,4-triazole derivatives with methoxyphenyl were carried out. As a result of the studying available sources and implementation of scientific research, it was found that studies of 1,2,4-triazole derivatives with methoxyphenyl occupy an important place in the Ukrainian pharmaceutical industry, as they have a wide range of pharmacological activity. Also they show low rates of acute toxicity and are perspective to create new APIs on their base Conclusions. Processing, analysis, systematization, comparison, and generalization of modern sources of information indicate a wide synthetic variability, a fairly wide range of biological activity, and low rates of acute toxicity of 1,2,4-triazole derivatives, with methoxyphenyl at the 5th position of the nucleus of this heterocycle and a wide range of their applications.
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以甲氧基苯基为原料合成1,2,4-三唑衍生物,并研究其药理活性谱
在当今社会,药学工作者的工作是非常受人尊敬的,因为很难想象人们不使用药物的治疗。随着时间的推移,具有自身特征的疾病数量只会增加,因此,合成药物的创造仍然是世界各地科学家的一项实际任务。有大量的杂环系统,其衍生物表现出广泛的药理活性,即呋喃、吡咯、吡唑、吡啶、嘧啶、嘌呤等。特别注意的是具有低毒性的结构。毫无疑问,为了构建最有效的药效团,最初的杂环物质必须有几个反应中心。来自世界各地的科学家的研究指出了利用1,2,4-三唑杂环体系衍生物作为新的生物活性物质模型的前景。本研究的目的是总结1,2,4-三唑衍生物的现代合成方法的数据,以确定甲氧基苯基取代基对反应性的影响和改变药理学活性谱。材料和方法。在工作中,我们采用了分析、信息检索、描述、概括等方法。本研究资料来源于甲氧基苯基类1,2,4-三唑衍生物的合成方法及生物活性研究方面的专业文献。对含甲氧基苯基的1,2,4-三唑衍生物的合成方法和生物活性研究进行了检索、分析和归纳。通过对现有资源的研究和科学研究的实施,发现对1,2,4-三唑甲氧基衍生物的研究在乌克兰制药工业中占有重要地位,因为它们具有广泛的药理活性。此外,它们的急性毒性也很低,有望在其基础上开发新的原料药。对现代信息来源的处理、分析、系统化、比较和概括表明,1,2,4-三唑衍生物具有广泛的合成变异性、相当广泛的生物活性和低急性毒性,该杂环的第5位为甲氧基苯基,其应用范围广泛。
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