新型1,2,4-三唑衍生物的生物学特性(文献综述)

M. V. Ohloblina
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引用次数: 0

摘要

1,2,4-三唑的现代化学需要寻找更合理的合成生物活性物质的方法。迄今为止,已知许多有吸引力的替代方法来合成具有潜在生物活性的1,2,4-三唑衍生物的经典方法。上述化合物具有抗菌、抗真菌、抗氧化、抗炎、抗病毒等活性。在文献资料归纳的基础上,选择了一个有前景的科学研究方向。这项工作的目的是确定现代有机合成的方向,清楚地指出了1,2,4-三唑的各种化学建模的可能性以及使用其衍生物的特性。材料和方法。在工作中采用了以下方法:综合、分析、信息检索、描述、概括。该研究的材料包括文献来源,其中包含有关1,2,4-三唑进一步化学建模的相关性和前景的信息。对1,2,4-三唑类具有潜在生物活性衍生物的经典合成方法进行了探索、分析和推广。通过对大量信息的研究和近10年的专利检索,已经找到了大约700种信息来源。他们强调了来自世界各地的科学团队致力于筛选新的3-芳基-5-巯基-1,2,4-三唑和四- o-乙酰-α- d -葡萄糖吡喃基溴的抗菌活性研究的工作;在4,5-二苯基- 4h -1,2,4-三唑-3-硫醇中寻找对金黄色葡萄球菌和白色念珠菌具有明显抗菌活性的新化合物;具有镇痛和抗炎活性的噻唑[3,2-b]-1,2,4-三唑-5(6H) -1分子的新候选物的鉴定;具有中等抑菌活性和较高的抑菌活性。现代信息源的处理、系统化要素、比较和概括表明1,2,4-三唑衍生物具有较高的生物活性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Biological features of new 1,2,4-triazole derivatives (a literature review)
Modern chemistry of 1,2,4-triazoles is in need of the search for more rational ways of synthesizing biologically active substances. To date, a number of attractive alternatives to the classical methods for the synthesis of potentially biologically active derivatives among 1,2,4-triazoles are known. The above mentioned compounds demonstrate antimicrobial, antifungal, antioxidant, anti-inflammatory, antiviral activity, etc. Based on the results of literary sources generalization, a promising direction of scientific research was chosen. The aim of this work is to determine the direction of modern organic synthesis, clearly indicating the possibility of various chemical modeling of 1,2,4-triazoles and the peculiarities of using their derivatives. Materials and methods. The following methods were used in the work: synthetic, analytical, information retrieval, descriptive, generalization. The materials for the study comprised literary sources containing information on the relevance and prospects for further chemical modeling of 1,2,4-triazole. Results. A search, analysis and generalization of attractive alternatives to classical methods for the synthesis of potentially biologically active derivatives among 1,2,4-triazoles was carried out. Based on the study of a large amount of information and patent search over the past 10 years, about 700 sources of information have been found. They highlight the work of scientific teams from around the world devoted to screening studies of the antibacterial activity of new 3-aryl-5-mercapto-1,2,4-triazoles and tetra-O-acetyl-α-D-glucopyranosyl bromide; search for a number of new compounds among 4,5-diphenyl-4H-1,2,4-triazole-3-thiols with pronounced antibacterial activity against S. aureus and antifungal activity against Candida albicans; identification of new candidates among thiazolo[3,2-b]-1,2,4-triazol-5(6H)-one molecules with analgesic and anti-inflammatory activity; bringing moderate antimicrobial and fairly high antifungal activity of the above compounds. Conclusions. Processing, elements of systematization, comparison and generalization of modern information sources indicate rather high rates of biological activity of 1,2,4-triazole derivatives.
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