Green hemi-synthesis of novel thiazole derivatives from Ammodaucus leucotrichus Coss. & Dur. and Cuminum cyminum L. essential oils: stereochemistry, molecular fluorescence spectroscopy, in vitro biologicial activity, and molecular docking study

•New thiazole derivatives from natural product (Ammodaucus leucotrichus and Cuminum cyminum) were hemi-synthesized.•Chemical characterization of the obtained compounds was performed using FTIR, 1D and 2D NMR.•DFT calculation study confirmed the structural stability of the obtained compounds.•New thi...

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Veröffentlicht in:Journal of molecular structure 2022-10, Vol.1265, p.133376, Article 133376
Hauptverfasser: Hassaine, Ridha, El Haci, Imad Abdelhamid, Bouchama, Abdelghani, Boukenna, Leϊla, Aissaoui, Mohammed, Djafri, Ahmed, Haffas, Maamar, Benabdellah, Mohammed, Choukchou-Braham, Noureddine, Bachari, Khaldoun, Taibi, Nadia
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Sprache:eng
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Zusammenfassung:•New thiazole derivatives from natural product (Ammodaucus leucotrichus and Cuminum cyminum) were hemi-synthesized.•Chemical characterization of the obtained compounds was performed using FTIR, 1D and 2D NMR.•DFT calculation study confirmed the structural stability of the obtained compounds.•New thiazole derivatives exhibited moderate antioxidant activity, while their antibacterial one was much more interesting against some bacterial strains.•Molecular docking study revealed that the new thiazole derivatives can be good candidates to inhibit TNF-α. This paper reports the hemi-synthesis of a new thiazole derivatives from 3-allylrhodanine under green chemical conditions (solvent free and ambient temperature). Two targeted molecules: perillaldehyde and cuminaldehyde from essential oils of Ammodaucus leucotrichus Coss. & Dur. and Cuminum cyminum L. were used. Thiazole derivatives (HRP11, 12) were obtained and characterized by FTIR, 1H NMR, 13C NMR, 2D NMR. In addition, stereochemistry of HRP11, 12 was characterized by using 2D NMR and their structural stability was confirmed by DFT calculation. Furthermore, the new products were screened for their in vitro biological activity and in silico interaction with TNF-α by using molecular docking study. A moderate antioxidant activity was found for the two obtained products evaluated by DPPH and ABTS radical scavenging techniques. Against all odds, HRP12 revealed an interesting antibacterial activity against Escherichia coli, Citrobacter freundii, and Salmonella typhimurium. Thereby, a molecular fluorescence spectroscopy was carried out to compare the fluorescence of gentamicin and that of HRP11, 12. Molecular docking performed on the Tumor Necrosis Factor (TNF-α) demonstrated sensitivity towards the thiazole derivatives obtained. [Display omitted]
ISSN:0022-2860
1872-8014
DOI:10.1016/j.molstruc.2022.133376