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New antibacterial, non-genotoxic materials, derived from the functionalization of the anti-thyroid drug methimazole with silver ions

The new silver(I) compound {[AgBr(μ2-S-MMI)(TPP))]2} (1) and the known one [AgCl(TPP)2(MMI)] (2) were obtained by refluxing toluene solutions of silver(I) halide with triphenylphosphine (TPP) and the anti-thyroid drug 2-mercapto-1-methyl-imidazole or methimazole (MMI). The complexes were characteriz...

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Published in:Journal of inorganic biochemistry 2016-07, Vol.160, p.114-124
Main Authors: Sainis, I., Banti, C.N., Owczarzak, A.M., Kyros, L., Kourkoumelis, N., Kubicki, M., Hadjikakou, S.K.
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container_title Journal of inorganic biochemistry
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creator Sainis, I.
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description The new silver(I) compound {[AgBr(μ2-S-MMI)(TPP))]2} (1) and the known one [AgCl(TPP)2(MMI)] (2) were obtained by refluxing toluene solutions of silver(I) halide with triphenylphosphine (TPP) and the anti-thyroid drug 2-mercapto-1-methyl-imidazole or methimazole (MMI). The complexes were characterized by m.p., vibrational spectroscopy (mid-FT-IR), 1H, 31P-NMR, UV–Vis spectroscopic techniques and X-ray crystallography. The antibacterial effect of 1 and 2 against the bacterial species Pseudomonas aeruginosa (PAO) and Escherichia coli was evaluated. Compound 1 exhibits comparable activity to the corresponding one of the silver nitrate which is an antibacterial drug in use. The in vivo genotoxicity of 1–2 by the mean of Allium cepa test shows no alterations in the mitotic index values due to the absence of chromosomal aberrations. The mechanism of action of the title compounds is evaluated. The DNA binding tests indicate the ability of the complexes 1–2 to modify the activity of the bacteria. The binding constants of 1–2 towards CT-DNA indicate interaction through opening of the hydrogen bonds of DNA. Docking studies on DNA-complexes interactions confirm the binding of both complexes 1–2 in the major groove of the CT-DNA. In conclusion the silver complex 1 is an anti-bacterial and non-genotoxic material, which can be applied to antibacterial drug in the future. Mixed ligand silver(I) complexes of the antithyroid drug methimazole (MMI): {[AgBr(μ2-S-MMI)(TPP))]2} (1) and [AgCl(TPP)2(MMI)] (2) (TPP=triphenylphosphine, were evaluated for their antibacterial effect against the bacterial species Pseudomonas aeruginosa (PAO) and Escherichia coli (E. coli). The in vivo genotoxicity of 1–2 was evaluated by Allium cepa test. [Display omitted] •Synthesis and characterization of silver(I) complexes•Antimicrobial activity of silver complexes and their interaction with CT-DNA•The steric effect of arylphosphines towards the antimicrobial activity of the complexes•Genotoxicity
doi_str_mv 10.1016/j.jinorgbio.2015.12.013
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The complexes were characterized by m.p., vibrational spectroscopy (mid-FT-IR), 1H, 31P-NMR, UV–Vis spectroscopic techniques and X-ray crystallography. The antibacterial effect of 1 and 2 against the bacterial species Pseudomonas aeruginosa (PAO) and Escherichia coli was evaluated. Compound 1 exhibits comparable activity to the corresponding one of the silver nitrate which is an antibacterial drug in use. The in vivo genotoxicity of 1–2 by the mean of Allium cepa test shows no alterations in the mitotic index values due to the absence of chromosomal aberrations. The mechanism of action of the title compounds is evaluated. The DNA binding tests indicate the ability of the complexes 1–2 to modify the activity of the bacteria. The binding constants of 1–2 towards CT-DNA indicate interaction through opening of the hydrogen bonds of DNA. Docking studies on DNA-complexes interactions confirm the binding of both complexes 1–2 in the major groove of the CT-DNA. In conclusion the silver complex 1 is an anti-bacterial and non-genotoxic material, which can be applied to antibacterial drug in the future. Mixed ligand silver(I) complexes of the antithyroid drug methimazole (MMI): {[AgBr(μ2-S-MMI)(TPP))]2} (1) and [AgCl(TPP)2(MMI)] (2) (TPP=triphenylphosphine, were evaluated for their antibacterial effect against the bacterial species Pseudomonas aeruginosa (PAO) and Escherichia coli (E. coli). The in vivo genotoxicity of 1–2 was evaluated by Allium cepa test. 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All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c441t-220c522d5dfd4032fa7f4fb8a9f3ddafc27f0f1b49f0ffdf3c9cbf8cc15eda93</citedby><cites>FETCH-LOGICAL-c441t-220c522d5dfd4032fa7f4fb8a9f3ddafc27f0f1b49f0ffdf3c9cbf8cc15eda93</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26765999$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Sainis, I.</creatorcontrib><creatorcontrib>Banti, C.N.</creatorcontrib><creatorcontrib>Owczarzak, A.M.</creatorcontrib><creatorcontrib>Kyros, L.</creatorcontrib><creatorcontrib>Kourkoumelis, N.</creatorcontrib><creatorcontrib>Kubicki, M.</creatorcontrib><creatorcontrib>Hadjikakou, S.K.</creatorcontrib><title>New antibacterial, non-genotoxic materials, derived from the functionalization of the anti-thyroid drug methimazole with silver ions</title><title>Journal of inorganic biochemistry</title><addtitle>J Inorg Biochem</addtitle><description>The new silver(I) compound {[AgBr(μ2-S-MMI)(TPP))]2} (1) and the known one [AgCl(TPP)2(MMI)] (2) were obtained by refluxing toluene solutions of silver(I) halide with triphenylphosphine (TPP) and the anti-thyroid drug 2-mercapto-1-methyl-imidazole or methimazole (MMI). The complexes were characterized by m.p., vibrational spectroscopy (mid-FT-IR), 1H, 31P-NMR, UV–Vis spectroscopic techniques and X-ray crystallography. The antibacterial effect of 1 and 2 against the bacterial species Pseudomonas aeruginosa (PAO) and Escherichia coli was evaluated. Compound 1 exhibits comparable activity to the corresponding one of the silver nitrate which is an antibacterial drug in use. The in vivo genotoxicity of 1–2 by the mean of Allium cepa test shows no alterations in the mitotic index values due to the absence of chromosomal aberrations. The mechanism of action of the title compounds is evaluated. The DNA binding tests indicate the ability of the complexes 1–2 to modify the activity of the bacteria. The binding constants of 1–2 towards CT-DNA indicate interaction through opening of the hydrogen bonds of DNA. Docking studies on DNA-complexes interactions confirm the binding of both complexes 1–2 in the major groove of the CT-DNA. In conclusion the silver complex 1 is an anti-bacterial and non-genotoxic material, which can be applied to antibacterial drug in the future. Mixed ligand silver(I) complexes of the antithyroid drug methimazole (MMI): {[AgBr(μ2-S-MMI)(TPP))]2} (1) and [AgCl(TPP)2(MMI)] (2) (TPP=triphenylphosphine, were evaluated for their antibacterial effect against the bacterial species Pseudomonas aeruginosa (PAO) and Escherichia coli (E. coli). The in vivo genotoxicity of 1–2 was evaluated by Allium cepa test. 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The complexes were characterized by m.p., vibrational spectroscopy (mid-FT-IR), 1H, 31P-NMR, UV–Vis spectroscopic techniques and X-ray crystallography. The antibacterial effect of 1 and 2 against the bacterial species Pseudomonas aeruginosa (PAO) and Escherichia coli was evaluated. Compound 1 exhibits comparable activity to the corresponding one of the silver nitrate which is an antibacterial drug in use. The in vivo genotoxicity of 1–2 by the mean of Allium cepa test shows no alterations in the mitotic index values due to the absence of chromosomal aberrations. The mechanism of action of the title compounds is evaluated. The DNA binding tests indicate the ability of the complexes 1–2 to modify the activity of the bacteria. The binding constants of 1–2 towards CT-DNA indicate interaction through opening of the hydrogen bonds of DNA. Docking studies on DNA-complexes interactions confirm the binding of both complexes 1–2 in the major groove of the CT-DNA. In conclusion the silver complex 1 is an anti-bacterial and non-genotoxic material, which can be applied to antibacterial drug in the future. Mixed ligand silver(I) complexes of the antithyroid drug methimazole (MMI): {[AgBr(μ2-S-MMI)(TPP))]2} (1) and [AgCl(TPP)2(MMI)] (2) (TPP=triphenylphosphine, were evaluated for their antibacterial effect against the bacterial species Pseudomonas aeruginosa (PAO) and Escherichia coli (E. coli). The in vivo genotoxicity of 1–2 was evaluated by Allium cepa test. [Display omitted] •Synthesis and characterization of silver(I) complexes•Antimicrobial activity of silver complexes and their interaction with CT-DNA•The steric effect of arylphosphines towards the antimicrobial activity of the complexes•Genotoxicity</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>26765999</pmid><doi>10.1016/j.jinorgbio.2015.12.013</doi><tpages>11</tpages></addata></record>
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ispartof Journal of inorganic biochemistry, 2016-07, Vol.160, p.114-124
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source ScienceDirect Freedom Collection
subjects Allium cepa
Anti-Bacterial Agents - chemical synthesis
Anti-Bacterial Agents - pharmacology
Antithyroid Agents - chemical synthesis
Antithyroid Agents - pharmacology
Binding Sites
Coordination Complexes - chemical synthesis
Coordination Complexes - pharmacology
CT-DNA
DNA - chemistry
Drug Repositioning
Escherichia coli
Escherichia coli - drug effects
Escherichia coli - growth & development
Genotoxicity
Hydrogen Bonding
Methimazole
Methimazole - chemical synthesis
Methimazole - pharmacology
Microbial Sensitivity Tests
Mitotic Index
Molecular Docking Simulation
Onions - cytology
Onions - drug effects
Onions - genetics
Organophosphorus Compounds - chemistry
Pseudomonas aeruginosa
Pseudomonas aeruginosa - drug effects
Pseudomonas aeruginosa - growth & development
Pseudomonas aeruginosa and Escherichia coli
Silver - chemistry
Silver Nitrate - pharmacology
Silver(I) compounds
Toluene - chemistry
title New antibacterial, non-genotoxic materials, derived from the functionalization of the anti-thyroid drug methimazole with silver ions
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