Synthesis, Docking Study, and Structural Characterization of New Bioactive Thiazolidine-4-one Derivatives as Antibacterial and Antioxidant Agents

IF 1.1 4区 化学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY
Zainab Y. Kadhim, Hasanain Gomhor J. Alqaraghuli
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引用次数: 0

Abstract

Objective: This study involved the design and synthesis of new thiazolidine-4-one derivatives, as well as testing their antioxidant activity and evaluating their potential as antibacterial agents. Methods: Thiazolidine-4-one compounds (T-1) and (T-2) were synthesized by reacting 2-mercaptoacetic acid with the synthesized imines, (Im-1) and (Im-2), respectively. The synthesized compounds were characterized by physicochemical and spectrophotometric data (UV-Vis, FT-IR, 1H, 13C NMR, and CHN analysis). Pseudomonas aeruginosa (P. aeruginosa), Staphylococcus aureus (S. aureus), and Escherichia coli (E. coli) were used as test organisms for the antibacterial activity of (T-1) and (T-2). Molecular docking experiments were performed to gain an understanding of the affinity and interaction between thiazolidine-4-one molecules and glucosamine-6-phosphate synthase (GA6PS). Hemolysis assays and DPPH·/ABTS·+ scavenging activity of (T-1) and (T-2) were studied. Results and Discussion: The results showed strong antibacterial activity of (T-2) compared to ciprofloxacin as a standard in inhibiting the growth of P. aeruginosa and E. coli, while its antibacterial effect in inhibiting the growth of S. aureus was stronger than ciprofloxacin. The data obtained from the docking studies were in perfect agreement with the data from the in vitro antibacterial test. Compound (T-2) showed good binding affinity to GA6PS, which is an important enzyme for bacterial cell wall synthesis, making (T-2) a promising antibacterial agent. The thiazolidine-4-ones (T-1) and (T-2) showed strong antioxidant activity, and non-toxicity was confirmed by the hemolysis method. Conclusions: We propose that one of the mechanisms behind the antibacterial activity of the synthesized thiazolidin-4-ones is the disruption of bacterial cytoplasmic membrane integrity, and therefore, these compounds have favorable properties for potential biomedical applications and positive future prospects.

Abstract Image

新型生物活性噻唑烷-4-酮类抗菌抗氧化衍生物的合成、对接研究及结构表征
目的:设计和合成新的噻唑烷-4- 1衍生物,测试其抗氧化活性,评价其作为抗菌药物的潜力。方法:将合成的亚胺(Im-1)和(Im-2)分别与2-巯基乙酸反应合成噻唑烷-4-酮化合物(T-1)和(T-2)。通过物理化学和分光光度(UV-Vis, FT-IR, 1H, 13C NMR和CHN分析)对合成的化合物进行了表征。以铜绿假单胞菌(P. aeruginosa)、金黄色葡萄球菌(S. aureus)和大肠埃希菌(E. coli)作为(T-1)和(T-2)的抑菌活性试验菌。通过分子对接实验,了解噻唑烷-4- 1分子与氨基葡萄糖-6-磷酸合成酶(GA6PS)的亲和力和相互作用。研究溶血实验及(T-1)和(T-2)对DPPH·/ABTS·+的清除活性。结果与讨论:结果表明(T-2)对铜绿假单胞菌和大肠杆菌的抑菌活性比环丙沙星强,对金黄色葡萄球菌的抑菌作用比环丙沙星强。对接研究得到的数据与体外抗菌试验的数据完全一致。化合物(T-2)与细菌细胞壁合成的重要酶GA6PS具有良好的结合亲和力,是一种很有前景的抗菌剂。噻唑烷-4-酮(T-1)和(T-2)具有较强的抗氧化活性,溶血法证实其无毒。结论:我们认为所合成的噻唑烷-4-ones抗菌活性的机制之一是破坏细菌细胞质膜的完整性,因此这些化合物具有良好的生物医学应用潜力和积极的前景。
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来源期刊
Russian Journal of Bioorganic Chemistry
Russian Journal of Bioorganic Chemistry 生物-生化与分子生物学
CiteScore
1.80
自引率
10.00%
发文量
118
审稿时长
3 months
期刊介绍: Russian Journal of Bioorganic Chemistry publishes reviews and original experimental and theoretical studies on the structure, function, structure–activity relationships, and synthesis of biopolymers, such as proteins, nucleic acids, polysaccharides, mixed biopolymers, and their complexes, and low-molecular-weight biologically active compounds (peptides, sugars, lipids, antibiotics, etc.). The journal also covers selected aspects of neuro- and immunochemistry, biotechnology, and ecology.
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