SYNTHESIS AND INVESTIGATION OF ANTIMICROBIAL ACTIVITY OF THE NEW CLASS OF ACYLHYDROSONES (QUINOLIN-8-YL) OF GLYCOLIC ACID

V. Chornous, A. M. Grosav, M. Bratenko, S. Deineka, О.І. Gavrilyuk
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Abstract

Antibiotic resistance of pathogenic strains of microorganisms is one of the most difficultproblems of modern medicine. An effective way to solve it is the synthesis of new classesof antibacterial and antifungal drugs with a wide spectrum of antiseptic action.Purpose of the research – synthesis of the new types of glycolic acid acylhydrazones(quinolin-8-yl)and investigation of their antimicrobe activity.Material and methods. The analysis of their antibacterial and antifungal activity wascarried out and the dependence of the antimicrobial action of the synthesized drugson the structure of the molecule, the type of heterocyclic fragment and the type ofmicroorganisms was investigated.Results. It was proposed a convenient method for the synthesis of new types of acylhydrosones (quinolin-8-yl) glycolic acid, which is realized by condensation ofhydrozides (quinolin-8-yl) of glycolic acid with a series of heterocyclic aldehydes.Conclusion. The results obtained indicate that this class of compounds is promising aspotential antimicrobial drugs.
新型乙醇酸酰基氢酮(喹啉-8-基)的合成及抗菌活性研究
微生物病原菌对抗生素的耐药性是现代医学中最困难的问题之一。解决这一问题的有效途径是合成具有广谱抗菌作用的新型抗菌和抗真菌药物。目的研究新型乙醇酸酰腙(喹啉-8-基)的合成及其抑菌活性。材料和方法。对其抑菌和抗真菌活性进行了分析,并考察了合成药物的抑菌作用与分子结构、杂环片段类型和微生物类型的依赖关系。提出了一种由羟基乙酸氢化物(喹啉-8-基)与一系列杂环醛缩合而成的新型酰氢酮(喹啉-8-基)乙醇酸的简便方法。结果表明,这类化合物是很有潜力的抗菌药物。
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