新型 6-苯氧基-4,5-二氢-1,2,6-噁唑膦 6-氧化物的简便合成、抗菌活性和硅学研究

IF 1.1 4区 化学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY Russian Journal of Bioorganic Chemistry Pub Date : 2024-12-16 DOI:10.1134/S1068162024060074
A. Wahbi, M. A. Dridi, I. Dridi, H. Alimi, S. Touil
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Convenient Synthesis, Antibacterial Activity, and In Silico Studies of Novel 6-Phenoxy-4,5-dihydro-1,2,6-oxazaphosphinine 6-Oxides

Objective: The main objective of this work was to develop a convenient synthesis of a new class of oxazaphosphorines, namely 6-phenoxy-4,5-dihydro-1,2,6-oxazaphosphinine 6-oxides (IVa–IVe), for antibacterial screening. Methods: Oxazaphosphorines (IVa–IVe) were obtained through a three-step approach involving the microwave-assisted conjugative addition of diphenyl phosphite to α,β-unsaturated ketones, followed by oximation and intramolecular cyclization. The newly synthesized oxazaphosphorines were screened for their in vitro antibacterial activity against Gram-positive (Staphylococcus aureus) and Gram-negative (Escherichia coli, Salmonella typhimurium, and Pseudomonas aeruginosa) bacteria. The obtained results were also correlated with the in silico molecular docking studies in DNA gyrase enzyme active site. Results and Discussion: Oxazaphosphorines (IVa–IVe) were obtained in 47–60% yields. The biological assays showed that these compounds exhibited appreciable antibacterial activity. Compound (IVe) was found to be the most potent antibacterial agent with an inhibition zone diameter of 9.66 ± 0.89 mm, and MIC and MBC values of 10 and 25 mg/mL respectively, when tested against S. typhimurium. We also observed a fairly good agreement between these experimental in vitro antibacterial outcomes and the in silico molecular docking results in DNA gyrase enzyme active site. Conclusions: We have successfully developed a convenient synthesis of a new class of oxazaphosphorines, namely 6-phenoxy-4,5-dihydro-1,2,6-oxazaphosphinine 6-oxides (IVa–IVe). When screened for their in vitro antibacterial activity, compound (IVe) was found to be the most potent antibacterial agent. We tried to correlate these results with those obtained in the in silico molecular docking study. The obtained results suggest that the synthesized compound (IVe) is a potential DNA gyrase inhibitor and could be used as a lead compound for developing new potent antibacterial drugs.

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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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