Copper complexes containing thiosemicarbazones derived from 6-nitropiperonal: Antimicrobial and biophysical properties. Beckford, F. A. & Webb, K. R. 2017. ISSN: 13861425 Pages: 158-171 Publication Title: Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy Volume: 183doi abstract bibtex A series of four thiosemicarbazones from 6-nitropiperonal along with the corresponding copper complexes were synthesized. The biophysical characteristics of the complexes were investigated by the binding to DNA and human serum albumin. The binding to DNA is moderate; the binding constants run from (0.49–7.50) × 104 M− 1. In relation to HSA, the complexes interact strongly with binding constants on the order of 105 M− 1. The complexes also display antioxidant behavior as determined by the ability to scavenge diphenylpicrylhydrazyl (dpph) and nitric oxide radicals. The antimicrobial profiles of the compounds, tested against a panel of microbes including five of the ESKAPE pathogens (Staphylococcus aureus, MRSA, Escherichia coli, Klebsiella pneumoniae, MDR, Acinetobacter baumannii, Pseudomonas aeruginosa) and two yeasts (Candida albicans and Cryptococcus neoformans var. grubii), are also described. The compounds contain a core moiety that is similar to oxolinic acid, a quinolone antibiotic that targets DNA gyrase and topoisomerase (IV). The binding interaction between the complexes and these important antibacterial targets were studied by computational methods, chiefly docking studies. The calculated dissociation constants for the interaction with DNA gyrase B (from Staphylococcus aureus) range from 4.32 to 24.65 μM; the binding was much stronger to topoisomerase IV, with dissociation constants ranging from 0.37 to 1.27 μM.
@misc{beckford_copper_2017,
title = {Copper complexes containing thiosemicarbazones derived from 6-nitropiperonal: {Antimicrobial} and biophysical properties},
abstract = {A series of four thiosemicarbazones from 6-nitropiperonal along with the corresponding copper complexes were synthesized. The biophysical characteristics of the complexes were investigated by the binding to DNA and human serum albumin. The binding to DNA is moderate; the binding constants run from (0.49–7.50) × 104 M− 1. In relation to HSA, the complexes interact strongly with binding constants on the order of 105 M− 1. The complexes also display antioxidant behavior as determined by the ability to scavenge diphenylpicrylhydrazyl (dpph) and nitric oxide radicals. The antimicrobial profiles of the compounds, tested against a panel of microbes including five of the ESKAPE pathogens (Staphylococcus aureus, MRSA, Escherichia coli, Klebsiella pneumoniae, MDR, Acinetobacter baumannii, Pseudomonas aeruginosa) and two yeasts (Candida albicans and Cryptococcus neoformans var. grubii), are also described. The compounds contain a core moiety that is similar to oxolinic acid, a quinolone antibiotic that targets DNA gyrase and topoisomerase (IV). The binding interaction between the complexes and these important antibacterial targets were studied by computational methods, chiefly docking studies. The calculated dissociation constants for the interaction with DNA gyrase B (from Staphylococcus aureus) range from 4.32 to 24.65 μM; the binding was much stronger to topoisomerase IV, with dissociation constants ranging from 0.37 to 1.27 μM.},
author = {Beckford, Floyd A. and Webb, Kelsey R.},
year = {2017},
doi = {10.1016/j.saa.2017.04.057},
pmid = {28448954},
note = {ISSN: 13861425
Pages: 158-171
Publication Title: Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy
Volume: 183},
keywords = {Antibacterial, Antioxidant, Molecular docking, Thiosemicarbazone},
}
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The antimicrobial profiles of the compounds, tested against a panel of microbes including five of the ESKAPE pathogens (Staphylococcus aureus, MRSA, Escherichia coli, Klebsiella pneumoniae, MDR, Acinetobacter baumannii, Pseudomonas aeruginosa) and two yeasts (Candida albicans and Cryptococcus neoformans var. grubii), are also described. The compounds contain a core moiety that is similar to oxolinic acid, a quinolone antibiotic that targets DNA gyrase and topoisomerase (IV). The binding interaction between the complexes and these important antibacterial targets were studied by computational methods, chiefly docking studies. The calculated dissociation constants for the interaction with DNA gyrase B (from Staphylococcus aureus) range from 4.32 to 24.65 μM; the binding was much stronger to topoisomerase IV, with dissociation constants ranging from 0.37 to 1.27 μM.","author":[{"propositions":[],"lastnames":["Beckford"],"firstnames":["Floyd","A."],"suffixes":[]},{"propositions":[],"lastnames":["Webb"],"firstnames":["Kelsey","R."],"suffixes":[]}],"year":"2017","doi":"10.1016/j.saa.2017.04.057","pmid":"28448954","note":"ISSN: 13861425 Pages: 158-171 Publication Title: Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy Volume: 183","keywords":"Antibacterial, Antioxidant, Molecular docking, Thiosemicarbazone","bibtex":"@misc{beckford_copper_2017,\n\ttitle = {Copper complexes containing thiosemicarbazones derived from 6-nitropiperonal: {Antimicrobial} and biophysical properties},\n\tabstract = {A series of four thiosemicarbazones from 6-nitropiperonal along with the corresponding copper complexes were synthesized. The biophysical characteristics of the complexes were investigated by the binding to DNA and human serum albumin. The binding to DNA is moderate; the binding constants run from (0.49–7.50) × 104 M− 1. In relation to HSA, the complexes interact strongly with binding constants on the order of 105 M− 1. The complexes also display antioxidant behavior as determined by the ability to scavenge diphenylpicrylhydrazyl (dpph) and nitric oxide radicals. The antimicrobial profiles of the compounds, tested against a panel of microbes including five of the ESKAPE pathogens (Staphylococcus aureus, MRSA, Escherichia coli, Klebsiella pneumoniae, MDR, Acinetobacter baumannii, Pseudomonas aeruginosa) and two yeasts (Candida albicans and Cryptococcus neoformans var. grubii), are also described. The compounds contain a core moiety that is similar to oxolinic acid, a quinolone antibiotic that targets DNA gyrase and topoisomerase (IV). The binding interaction between the complexes and these important antibacterial targets were studied by computational methods, chiefly docking studies. The calculated dissociation constants for the interaction with DNA gyrase B (from Staphylococcus aureus) range from 4.32 to 24.65 μM; the binding was much stronger to topoisomerase IV, with dissociation constants ranging from 0.37 to 1.27 μM.},\n\tauthor = {Beckford, Floyd A. and Webb, Kelsey R.},\n\tyear = {2017},\n\tdoi = {10.1016/j.saa.2017.04.057},\n\tpmid = {28448954},\n\tnote = {ISSN: 13861425\nPages: 158-171\nPublication Title: Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy\nVolume: 183},\n\tkeywords = {Antibacterial, Antioxidant, Molecular docking, Thiosemicarbazone},\n}\n\n\n\n","author_short":["Beckford, F. A.","Webb, K. 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