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- W3126088899 endingPage "127819" @default.
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- W3126088899 abstract "In this study, we have designed and synthesized 2-((5-acetyl-1-(phenyl)-4-methyl-1H-imidazol-2-yl)thio)-N-(4-((benzyl)oxy)phenyl) acetamide derivatives. Antimicrobial activities of all the imidazole derivatives have been examined against Gram-positive and Gram-negative bacteria and results showed that the conjugates have appreciable antibacterial activity. Besides, several analogous were evaluated for their in vitro antiresistant bacterial strains such as Extended-spectrum beta-lactamases (ESBL), Vancomycin-resistant Enterococcus (VRE), and Methicillin-resistant Staphylococcus aureus (MRSA). The SAR revealed that the 12l compound resulted in potency against all bacterial strains as well as ESBL, VRE, and MRSA strains. Lipinski’s rule of five, and ADME studies were preformed for all the synthesized compounds with Staphylococcus aureus dihydropteroate synthase (saDHPS) protein (PDB ID: 6CLV) and were found standard drug-likeness properties of conjugates. Moreover, the binding mode of the ligands with the protein study has been examined by molecular docking and results are quite promising. Besides, all the analogous were tested for their in vitro antituberculosis, antimalarial, and antioxidant activity." @default.
- W3126088899 created "2021-02-01" @default.
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- W3126088899 date "2021-03-01" @default.
- W3126088899 modified "2023-09-24" @default.
- W3126088899 title "Structure based design, synthesis, and biological evaluation of imidazole derivatives targeting dihydropteroate synthase enzyme" @default.
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- W3126088899 doi "https://doi.org/10.1016/j.bmcl.2021.127819" @default.
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