New derivatives of quinazolinone as an object in the search for substances that exhibit a multi-target effect

A. A. Starikova, A. A. Tsibizova, N. V. Zolotareva, D. Merezhkina, A. Ozerov, M. Samotrueva
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Abstract

Due to the rapid growth in the number of patients with diabetes in a complicated epidemiological picture, the question of the possibility of exposure of a substance to several targets becomes more important. It is noted that the most common infectious diseases in patients with diabetes mellitus are infections of the respiratory and urinary tract, skin and soft tissues, diabetic foot ulcers, otitis media and periodontal infections. Antimicrobial agents can have both direct and indirect hypoglycemic effects. Quinazolinones belonging to the group of heterocyclic derivatives exhibit a wide range of pharmacological activity. The use of the PASS program for the purpose of computer prediction of pharmacological activity showed a high probability of the hypoglycemic effect of new derivatives. The obtained results motivated the authors to search for the relationship between antimicrobial action and hypoglycemic effect within the general direction of studying the multi-targeting of drug ligands. Analysis of the literature data, as well as own studies of new quinazolinone derivative pharmacological activity make it possible to divide all ligands into functional groups that cause additional binding to the target molecule. The quinazolinone fragment, characterized by the uniqueness of its structure, can be reasonably attributed to multi-target ligands. The triazole cycle and the sulfonamide group can also purposefully bind to the target molecule. A carbamide residue, a fragment of sulfonylurea and an acetamide group, depending on the structure of the substance they are part of, can function both as a specific ligand and as a functional group involved in the stabilization of the intermediate transition state. The results obtained by the authors, as well as other researchers, allow us to formulate an assumption about the relationship between the mechanisms of antimicrobial and hyperglycemic activity.
以喹唑啉酮的新衍生物为对象,寻找具有多靶效应的物质
由于在复杂的流行病学情况下糖尿病患者人数迅速增加,一种物质可能接触到多个目标的问题变得更加重要。据悉,糖尿病患者最常见的传染病是呼吸道和泌尿道感染、皮肤和软组织感染、糖尿病足溃疡、中耳炎和牙周感染。抗菌剂既有直接降糖作用,也有间接降糖作用。属于杂环衍生物类的喹唑啉酮具有广泛的药理活性。使用 PASS 程序进行药理活性计算机预测显示,新衍生物具有降血糖作用的可能性很高。这些结果促使作者在研究药物配体多靶点作用的大方向下,寻找抗菌作用与降血糖作用之间的关系。通过对文献数据的分析,以及自己对新的喹唑啉酮衍生物药理活性的研究,可以将所有配体分为能与靶分子产生额外结合的官能团。喹唑啉酮片段具有结构独特的特点,可以合理地归结为多目标配体。三唑循环和磺酰胺基团也可以有目的地与目标分子结合。碳酰胺残基、磺酰脲片段和乙酰胺基团,根据它们所组成物质的结构,既可以作为特定配体,也可以作为参与稳定中间过渡态的官能团。作者和其他研究人员获得的结果使我们能够对抗菌和降血糖活性机制之间的关系做出假设。
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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