Shweta Tiwari, Gul Naz Fatima, Vimlesh Kumar, Shailendra K Saraf
{"title":"<i>In-silico</i> and <i>in-vitro</i> evaluation of diazenyl compounds as anti-bacterial agents.","authors":"Shweta Tiwari, Gul Naz Fatima, Vimlesh Kumar, Shailendra K Saraf","doi":"10.1080/17568919.2025.2504319","DOIUrl":null,"url":null,"abstract":"<p><strong>Aim: </strong>The diazenyls are interesting scaffold in medicinal chemistry displaying a wide range of pharmacological activities including anti-microbial, anti-cancer, anti-inflammatory, and analgesic-antipyretic, among others. These diverse attributes have reinitiated the interest of the researchers in them. Studies suggest that incorporating heterocyclic ring system into diazenyl scaffold helps to improve the biological property of the drug-like substances. The present study aims to synthesize novel diazinyl-triazole adducts, with an intent to obtain compounds with enhanced anti-bacterial potential.</p><p><strong>Materials and methods: </strong>All synthesized compounds were characterized using physicochemical methods and spectroscopic techniques. The compounds were evaluated <i>in-vitro</i> against two Gram-positive and two Gram-negative bacterial strains, demonstrating good to moderate efficacy. <i>In-silico</i> prediction study was also carried out for the synthesized series of compounds.</p><p><strong>Results and conclusion: </strong>The molecular docking data are aligned with the <i>in-vitro</i> experimental results. The ADMET predictions suggested the compounds are both efficacious and safe. The study presents new compounds as potential anti-bacterial agents with desirable pharmacological profile.</p>","PeriodicalId":12475,"journal":{"name":"Future medicinal chemistry","volume":" ","pages":"1013-1022"},"PeriodicalIF":3.2000,"publicationDate":"2025-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12091933/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Future medicinal chemistry","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1080/17568919.2025.2504319","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/5/15 0:00:00","PubModel":"Epub","JCR":"Q3","JCRName":"CHEMISTRY, MEDICINAL","Score":null,"Total":0}
引用次数: 0
Abstract
Aim: The diazenyls are interesting scaffold in medicinal chemistry displaying a wide range of pharmacological activities including anti-microbial, anti-cancer, anti-inflammatory, and analgesic-antipyretic, among others. These diverse attributes have reinitiated the interest of the researchers in them. Studies suggest that incorporating heterocyclic ring system into diazenyl scaffold helps to improve the biological property of the drug-like substances. The present study aims to synthesize novel diazinyl-triazole adducts, with an intent to obtain compounds with enhanced anti-bacterial potential.
Materials and methods: All synthesized compounds were characterized using physicochemical methods and spectroscopic techniques. The compounds were evaluated in-vitro against two Gram-positive and two Gram-negative bacterial strains, demonstrating good to moderate efficacy. In-silico prediction study was also carried out for the synthesized series of compounds.
Results and conclusion: The molecular docking data are aligned with the in-vitro experimental results. The ADMET predictions suggested the compounds are both efficacious and safe. The study presents new compounds as potential anti-bacterial agents with desirable pharmacological profile.
期刊介绍:
Future Medicinal Chemistry offers a forum for the rapid publication of original research and critical reviews of the latest milestones in the field. Strong emphasis is placed on ensuring that the journal stimulates awareness of issues that are anticipated to play an increasingly central role in influencing the future direction of pharmaceutical chemistry. Where relevant, contributions are also actively encouraged on areas as diverse as biotechnology, enzymology, green chemistry, genomics, immunology, materials science, neglected diseases and orphan drugs, pharmacogenomics, proteomics and toxicology.