Overview of Piperidine and Morpholine Derivatives as Promising Sources of Biologically Active Compounds (Review)

Q3 Pharmacology, Toxicology and Pharmaceutics
A. E. Khamitova, D. A. Berillo
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引用次数: 0

Abstract

Introduction. The search for new, effective and safe pharmacologically active substances remains an urgent task in the field of pharmacy. Many compounds of the piperidine and morpholine series are widely used in medical practice and belong to an important group of biologically active compounds. An informational, literature search on the synthesis of new derivatives of piperidine and morpholine was carried out. The article summarizes the results of studies of new derivatives of piperidine and morpholine as potential sources of biologically active substances. Text. The review is devoted to the relationship between the pharmacological activity of the N-derivatives of piperidine and morpholine in relation to various biological targets and the structure of the substance, the importance of the piperidine and morpholine rings in the design and development of drugs is highlighted. Piperidine and morpholine are considered as prerogative structures not only for increasing activity, but also for obtaining biological substances with desired therapeutic properties and improved pharmacokinetics. Conclusion. The literature review shows the current trend towards the study of morpholine and piperidine derivatives, reveals their high pharmacophore activity. The review will provide researchers with the necessary knowledge base to make chemical structural changes to the structures of drug leaders to enhance pharmacological activities.
哌啶和Morpholine衍生物作为生物活性化合物的前景来源(综述)
介绍。寻找新的、有效的、安全的药理活性物质仍然是药学领域的一项紧迫任务。哌啶和morpholine系列化合物广泛应用于医学实践,是一类重要的生物活性化合物。对哌啶和啉类新衍生物的合成进行了信息性的文献检索。综述了哌啶和啉类新衍生物作为生物活性物质潜在来源的研究成果。文本。本文综述了哌啶和morpholine的n -衍生物与各种生物靶点的药理活性与物质结构之间的关系,强调了哌啶和morpholine环在药物设计和开发中的重要性。哌啶和吗啡啉被认为是特权结构,不仅可以增加活性,而且可以获得具有理想治疗特性和改善药代动力学的生物物质。结论。本文综述了目前对吗啡啉和哌啶衍生物的研究趋势,揭示了它们具有较高的药效团活性。该综述将为研究人员对药物先导物结构进行化学结构改变以增强药理活性提供必要的知识基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Drug Development and Registration
Drug Development and Registration Pharmacology, Toxicology and Pharmaceutics-Pharmaceutical Science
CiteScore
1.20
自引率
0.00%
发文量
61
审稿时长
8 weeks
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