2-芳基-7,7-二甲基-5-氧代-5,6,7,8-四氢喹啉-4-羧酸及其与取代肼反应产物的合成和抗缺氧活性

K. V. Namyatova, S. S. Zykova, D. S. Ovchinnikov, S. Shurov
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The purpose of this study is to synthesize and investigate the antihypoxic activity of 2-aryl-7,7-dimethyl-5-oxo-5,6,7,8-tetrahydroquinoline-4-carboxylic acids and their reaction products with substituted hydrazines.Materials and methods. 2-Aryl-7,7-dimethyl-5-oxo-5,6,7,8-tetrahydroquinoline-4-carboxylic acids (I–VI) were obtained with high yields as a result of the interaction of 4-aroyl-2,4-dioxobutane acids with 3-amino-5,5-dimethylcyclohex-2-enone. Interaction of 2-aryl-7,7-dimethyl-5-oxo-5,6,7,8-tetrahydroquinoline-4-carboxylic acids with benzyl- and (2-phenylethyl)hydrazines 5-aryl-2-benzyl- and 2-(2-phenylethyl)-8,8-dimethyl-3,7,8,9-tetrahydro-2H-pyrido[4,3,2-de]cinnoline-3-ones (VII–XII) were obtained. As a result, 12 compounds were synthesized. The study of the antihypoxic activity of the obtained compounds was carried out in vivo on a model of normobaric hypoxia with hypercapnia.Results and discussion. 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引用次数: 0

摘要

导言。缺氧是指当氧气供应不足或在生物氧化过程中氧气的利用受到干扰时,组织中的氧化过程受到破坏。慢性缺氧损伤在各种疾病的发生和发展中起着重要作用,因此有必要合成具有抗缺氧活性的新化合物。本研究的目的是合成并研究 2-芳基-7,7-二甲基-5-氧代-5,6,7,8-四氢喹啉-4-羧酸及其与取代肼的反应产物的抗缺氧活性。通过 4-芳酰基-2,4-二氧代丁烷酸与 3-氨基-5,5-二甲基环己-2-烯酮的相互作用,高产率地获得了 2-芳基-7,7-二甲基-5-氧代-5,6,7,8-四氢喹啉-4-羧酸(I-VI)。2-芳基-7,7-二甲基-5-氧代-5,6,7,8-四氢喹啉-4-羧酸与苄基和(2-苯基乙基)肼相互作用,得到 5-芳基-2-苄基和 2-(2-苯基乙基)-8,8-二甲基-3,7,8,9-四氢-2H-吡啶并[4,3,2-de]噌啉-3-酮(VII-XII)。因此,共合成了 12 个化合物。在常压缺氧和高碳酸血症模型上对所获化合物的体内抗缺氧活性进行了研究。对合成的化合物进行了抗缺氧作用测试。化合物 VI 和 VIII 具有最明显的抗缺氧活性,它们在 C5 苯基取代基的对位上分别有一个甲氧基和一个甲基。化合物 III 的结构中含有氯,化合物 X 中含有氟,以及不含取代基(化合物 I 和 VII),都有助于产生缺氧效应。根据研究结果,喹啉羧酸和吡啶噌啉类化合物都是潜在的抗缺氧物质。对合成化合物的抗缺氧活性进行了比较分析,确定了它们的结构与作用严重程度之间的关系,并确定了最有效的物质。
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Synthesis and Antihypoxic Activity of 2-aryl-7,7-dimethyl-5-oxo-5,6,7,8-tetrahydroquinoline-4-carboxylic Acids and Their Reaction Products with Substituted Hydrazines
Introduction. Hypoxia is a violation of oxidative processes in tissues that occur when oxygen is insufficiently supplied to them or when its utilization is disrupted during biological oxidation. Chronic hypoxic damage plays an important role in the occurrence and development of various diseases, which necessitates the synthesis of new compounds with antihypoxic activity.Aim. The purpose of this study is to synthesize and investigate the antihypoxic activity of 2-aryl-7,7-dimethyl-5-oxo-5,6,7,8-tetrahydroquinoline-4-carboxylic acids and their reaction products with substituted hydrazines.Materials and methods. 2-Aryl-7,7-dimethyl-5-oxo-5,6,7,8-tetrahydroquinoline-4-carboxylic acids (I–VI) were obtained with high yields as a result of the interaction of 4-aroyl-2,4-dioxobutane acids with 3-amino-5,5-dimethylcyclohex-2-enone. Interaction of 2-aryl-7,7-dimethyl-5-oxo-5,6,7,8-tetrahydroquinoline-4-carboxylic acids with benzyl- and (2-phenylethyl)hydrazines 5-aryl-2-benzyl- and 2-(2-phenylethyl)-8,8-dimethyl-3,7,8,9-tetrahydro-2H-pyrido[4,3,2-de]cinnoline-3-ones (VII–XII) were obtained. As a result, 12 compounds were synthesized. The study of the antihypoxic activity of the obtained compounds was carried out in vivo on a model of normobaric hypoxia with hypercapnia.Results and discussion. The synthesized compounds were tested for the presence of antihypoxic action. The most pronounced antihypoxic activity is characteristic of compounds VI and VIII, which have a methoxy group and a methyl radical in the para-position of the phenyl substituent at C5, respectively. The presence of chlorine in the structure of compound III, fluorine in compound X and the absence of substituents (compounds I and VII) contribute to the prohypoxic effect. According to the results of the study, both quinolincarboxylic acids and pyridocinnolines are potential antihypoxants.Conclusion. A comparative analysis of the antihypoxic activity of the synthesized compounds was carried out, the relationship between their structure and severity of action was established, the most active substances were identified.
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