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Synthesis of Tetracyclic Spirooxindolepyrrolidine-Engrafted Hydantoin Scaffolds: Crystallographic Analysis, Molecular Docking Studies and Evaluation of Their Antimicrobial, Anti-Inflammatory and Analgesic Activities.
Toumi, Amani; Abdella, Faiza I A; Boudriga, Sarra; Alanazi, Tahani Y A; Alshamari, Asma K; Alrashdi, Ahlam Abdulrahman; Dbeibia, Amal; Hamden, Khaled; Daoud, Ismail; Knorr, Michael; Kirchhoff, Jan-Lukas; Strohmann, Carsten.
Affiliation
  • Toumi A; Laboratory of Heterocyclic Chemistry Natural Product and Reactivity (LR11ES39), Department of Chemistry, Faculty of Science of Monastir, University of Monastir, Monastir 5019, Tunisia.
  • Abdella FIA; Department of Chemistry, College of Science, Ha'il University, Ha'il 81451, Saudi Arabia.
  • Boudriga S; Laboratory of Heterocyclic Chemistry Natural Product and Reactivity (LR11ES39), Department of Chemistry, Faculty of Science of Monastir, University of Monastir, Monastir 5019, Tunisia.
  • Alanazi TYA; Department of Chemistry, College of Science, Ha'il University, Ha'il 81451, Saudi Arabia.
  • Alshamari AK; Department of Chemistry, College of Science, Ha'il University, Ha'il 81451, Saudi Arabia.
  • Alrashdi AA; Department of Chemistry, College of Science, Ha'il University, Ha'il 81451, Saudi Arabia.
  • Dbeibia A; Laboratory of Analysis, Treatment and Valorization of Environmental Pollutants and Products, Faculty of Pharmacy, University of Monastir, Monastir 5019, Tunisia.
  • Hamden K; Laboratory of Bioresources: Integrative Biology and Valorization, Higher Institute of Biotechnology of Monastir, University of Monastir, Monastir 5000, Tunisia.
  • Daoud I; Department of Matter Sciences, University of Mohamed Khider, BP 145 RP, Biskra 07000, Algeria.
  • Knorr M; Laboratory of Natural and Bio-Actives Substances, Faculty of Science, Tlemcen University, P.O. Box 119, Tlemcen 13000, Algeria.
  • Kirchhoff JL; Institut UTINAM-UMR CNRS 6213, Université de Franche-Comté, 16 Route de Gray, 25030 Besançon, France.
  • Strohmann C; Faculty of Chemistry, Inorganic Chemistry, Technical University Dortmund, Otto-Hahn-Strasse 6, 44227 Dortmund, Germany.
Molecules ; 28(21)2023 Nov 06.
Article in En | MEDLINE | ID: mdl-37959862
ABSTRACT
In a sustained search for novel potential drug candidates with multispectrum therapeutic application, a series of novel spirooxindoles was designed and synthesized via regioselective three-component reaction between isatin derivatives, 2-phenylglycine and diverse arylidene-imidazolidine-2,4-diones (Hydantoins). The suggested stereochemistry was ascertained by an X-ray diffraction study and NMR spectroscopy. The resulting tetracyclic heterocycles were screened for their in vitro and in vivo anti-inflammatory and analgesic activity and for their in vitro antimicrobial potency. In vitro antibacterial screening revealed that several derivatives exhibited remarkable growth inhibition against different targeted microorganisms. All tested compounds showed excellent activity against the Micrococccus luteus strain (93.75 µg/mL ≤ MIC ≤ 375 µg/mL) as compared to the reference drug tetracycline (MIC = 500 µg/mL). Compound 4e bearing a p-chlorophenyl group on the pyrrolidine ring exhibited the greatest antifungal potential toward Candida albicans and Candida krusei (MIC values of 23.43 µg/mL and 46.87 µg/mL, respectively) as compared to Amphotericin B (MIC = 31.25 and 62.50 µg/mL, respectively). The target compounds were also tested in vitro against the lipoxygenase-5 (LOX-5) enzyme. Compounds 4i and 4l showed significant inhibitory activity with IC50 = 1.09 mg/mL and IC50 = 1.01 mg/mL, respectively, more potent than the parent drug, diclofenac sodium (IC50 = 1.19 mg/mL). In addition, in vivo evaluation of anti-inflammatory and analgesic activity of these spirooxindoles were assessed through carrageenan-induced paw edema and acetic acid-induced writhing assays, respectively, revealing promising results. In silico molecular docking and predictive ADMET studies for the more active spirocompounds were also carried out.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Hydantoins / Anti-Infective Agents Language: En Journal: Molecules Journal subject: BIOLOGIA Year: 2023 Document type: Article Affiliation country: Tunisia

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Hydantoins / Anti-Infective Agents Language: En Journal: Molecules Journal subject: BIOLOGIA Year: 2023 Document type: Article Affiliation country: Tunisia