“…The antibacterial activities of newly synthesized compounds 20-40 were determined by well plate method in Mueller-Hinton Agar [27][28][29]. The antibacterial activity was carried out against 24 h old cultures of bacterial strains like Escherichia coli, Staphylococcus aureus, and Pseudomonas aeroginosa.…”
Section: Antibacterial Studiesmentioning
confidence: 99%
“…The antimicrobial activity of newly synthesized compounds 20-40 were determined by well plate method [27][28][29]. The supremacy of the synthesized compounds as antimicrobials was assessed for their antibacterial studies against different human pathogenic strains of bacteria namely Escherichia coli (ATCC25922), Staphylococcus aureus (ATCC25923), and Pseudomonas aeruginosa (ATCC27853).…”
Section: Antimicrobial Activitymentioning
confidence: 99%
“…Molecular docking studies of compound 38 and 39 into S. aureus tyrosyl-tRNA synthetase active site was performed, and the tight fitting of the compounds in the active site and the associated high binding energy might be the reason for their antimicrobial activity. On the other hand, compounds [28][29][30] were found to exert positive efficacy towards antioxidant activity comparable to butylated hydroxy anisole.…”
“…The antibacterial activities of newly synthesized compounds 20-40 were determined by well plate method in Mueller-Hinton Agar [27][28][29]. The antibacterial activity was carried out against 24 h old cultures of bacterial strains like Escherichia coli, Staphylococcus aureus, and Pseudomonas aeroginosa.…”
Section: Antibacterial Studiesmentioning
confidence: 99%
“…The antimicrobial activity of newly synthesized compounds 20-40 were determined by well plate method [27][28][29]. The supremacy of the synthesized compounds as antimicrobials was assessed for their antibacterial studies against different human pathogenic strains of bacteria namely Escherichia coli (ATCC25922), Staphylococcus aureus (ATCC25923), and Pseudomonas aeruginosa (ATCC27853).…”
Section: Antimicrobial Activitymentioning
confidence: 99%
“…Molecular docking studies of compound 38 and 39 into S. aureus tyrosyl-tRNA synthetase active site was performed, and the tight fitting of the compounds in the active site and the associated high binding energy might be the reason for their antimicrobial activity. On the other hand, compounds [28][29][30] were found to exert positive efficacy towards antioxidant activity comparable to butylated hydroxy anisole.…”
“…Recently a number of articles have published on the synthesis of 1, 4-dihydropyridines [6][7][8][9][10][11][12] . Heterogeneous catalysts have gained and have been widely used as a stable and an efficient catalyst for synthesis of organic compound.…”
We introduce Cu [(L)proline] 2 as a Novel Catalyst, cheap, environmentally friendly, and easy separation for Synthesis of 1, 4-Dihydropyridines under solvent-free condition. IR spectra Confirms formation complex of Cu [(L)proline] 2 .
“…Recently a number of articles have published on the synthesis of 1, 4-dihydropyridines [6][7][8][9][10][11][12][13] . Heterogeneous catalysts have gained and have been widely used as a stable and an efficient catalyst for synthesis of organic compound.…”
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