SYNTHESIS, CHARACTERIZATION AND ANTIMICROBIAL EVALUATION OF NOVEL BIS-HETERO CYCLIC DERIVATIVES

Q4 Pharmacology, Toxicology and Pharmaceutics INDIAN DRUGS Pub Date : 2023-05-28 DOI:10.53879/id.60.05.13553
Sathish K. Konidala, G. Kamala, Srinivasan Nagarajan, Durga R. Gunna
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引用次数: 0

Abstract

The present research outlines a series of bis-hetero cyclic derivatives (a1-6) synthesized from methyl-1-(2, 5-dioxopyrrolidin-1-yl) -6- methyl -2- oxo -4- phenyl -1, 2, 3, 4- tetrahydro pyrimidine -5- carboxylate treated with different aromatic aldehydes under acidic environment. The synthesized titled derivatives were confirmed by determination of physicochemical properties, by different spectral data and they were evaluated for in vitro antibacterial activity against Bacillus subtilis, Staphylococcus aureus, Escherichia coli and Pseudomonas aeruginosa and antifungal activity against Aspergillus niger and Candida albicans organisms at 25, 50, 100 µg mL-1 concentrations using streptomycin and fluconazole as reference standard drug respectively, through cup plate method. The in vitro antimicrobial assay results indicated that the derivatives a1, a2 and a3 showed significant antimicrobial activity, whereas the remaining derivatives showed moderate antimicrobial activities compared to the standard drugs. Further extension of this research to the cellular level is required to describe the mechanism of action, efficacy, and structural activity of these derivatives for antimicrobial activity.
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新型双杂环衍生物的合成、表征及抗菌性能评价
本研究概述了以甲基-1-(2,5-二氧代吡咯烷-1-基)-6-甲基-2-氧代-4-苯基-1,2,3,4-四氢嘧啶-5-羧酸酯为原料,在酸性环境中用不同的芳香醛处理合成的一系列双杂环衍生物(a1-6)。通过物理化学性质的测定和不同的光谱数据证实了合成的标题衍生物,并评估了它们在25、50、60℃时对枯草芽孢杆菌、金黄色葡萄球菌、大肠杆菌和铜绿假单胞菌的体外抗菌活性以及对黑曲霉和白色念珠菌的抗真菌活性,100µg mL-1浓度,分别使用链霉素和氟康唑作为参考标准药物,通过杯板法。体外抗菌测定结果表明,与标准药物相比,衍生物a1、a2和a3显示出显著的抗菌活性,而其余衍生物显示出中等的抗菌活性。需要将这项研究进一步扩展到细胞水平,以描述这些衍生物的抗菌活性的作用机制、功效和结构活性。
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来源期刊
INDIAN DRUGS
INDIAN DRUGS Pharmacology, Toxicology and Pharmaceutics-Pharmaceutical Science
CiteScore
0.30
自引率
0.00%
发文量
98
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