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Synthesis, Structural Characterization, Antimicrobial Activity, and In Vitro Biocompatibility of New Unsaturated Carboxylate Complexes with 2,2′-Bipyridine

The synthesis, structural characterization, cytotoxicity, and antimicrobial properties of four new complexes formed by employing acrylate anion and 2,2′-bipyridine are reported herein. X-ray crystallography revealed the trinuclear nature of [Mn(3)(2,2′-bipy)(2)(C(3)H(3)O(2))(6)] (1), meanwhile compl...

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Autores principales: Vasile Scăețeanu, Gina, Chifiriuc, Mariana Carmen, Bleotu, Coralia, Kamerzan, Crina, Măruţescu, Luminiţa, Daniliuc, Constantin G., Maxim, Cătălin, Calu, Larisa, Olar, Rodica, Badea, Mihaela
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6017882/
https://www.ncbi.nlm.nih.gov/pubmed/29329277
http://dx.doi.org/10.3390/molecules23010157
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author Vasile Scăețeanu, Gina
Chifiriuc, Mariana Carmen
Bleotu, Coralia
Kamerzan, Crina
Măruţescu, Luminiţa
Daniliuc, Constantin G.
Maxim, Cătălin
Calu, Larisa
Olar, Rodica
Badea, Mihaela
author_facet Vasile Scăețeanu, Gina
Chifiriuc, Mariana Carmen
Bleotu, Coralia
Kamerzan, Crina
Măruţescu, Luminiţa
Daniliuc, Constantin G.
Maxim, Cătălin
Calu, Larisa
Olar, Rodica
Badea, Mihaela
author_sort Vasile Scăețeanu, Gina
collection PubMed
description The synthesis, structural characterization, cytotoxicity, and antimicrobial properties of four new complexes formed by employing acrylate anion and 2,2′-bipyridine are reported herein. X-ray crystallography revealed the trinuclear nature of [Mn(3)(2,2′-bipy)(2)(C(3)H(3)O(2))(6)] (1), meanwhile complexes with general formula [M(2,2′-bipy)(C(3)H(3)O(2))(2)(H(2)O)(x)]∙yH(2)O ((2) M: Ni, x = 1, y = 0; (3) M: Cu, x = 1, y = 0; (4) M: Zn, x = 0, y = 1; 2,2′-bipy: 2,2′-bipyridine; C(3)H(3)O(2): acrylate anion) were shown to be mononuclear. The lowest minimum inhibitory concentration (MIC) of 128 μg mL(−1) was recorded for all four tested complexes against Candida albicans, for complex (3) against Escherichia coli, and for complex (4) against Staphylocococcus aureus. Compounds (3) and (4) were also potent efflux pumps activity inhibitors (EPI), proving their potential for use in synergistic combinations with antibiotics. Complexes (1)–(4) revealed that they were not cytotoxic to HCT-8 cells. They also proved to interfere with the cellular cycle of tumour HCT-8 cells by increasing the number of cells found in the S and G2/M phases. Taken together, these results demonstrate the potential of zinc and copper complexes for use in the development of novel antimicrobial and anti-proliferative agents.
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spelling pubmed-60178822018-11-13 Synthesis, Structural Characterization, Antimicrobial Activity, and In Vitro Biocompatibility of New Unsaturated Carboxylate Complexes with 2,2′-Bipyridine Vasile Scăețeanu, Gina Chifiriuc, Mariana Carmen Bleotu, Coralia Kamerzan, Crina Măruţescu, Luminiţa Daniliuc, Constantin G. Maxim, Cătălin Calu, Larisa Olar, Rodica Badea, Mihaela Molecules Article The synthesis, structural characterization, cytotoxicity, and antimicrobial properties of four new complexes formed by employing acrylate anion and 2,2′-bipyridine are reported herein. X-ray crystallography revealed the trinuclear nature of [Mn(3)(2,2′-bipy)(2)(C(3)H(3)O(2))(6)] (1), meanwhile complexes with general formula [M(2,2′-bipy)(C(3)H(3)O(2))(2)(H(2)O)(x)]∙yH(2)O ((2) M: Ni, x = 1, y = 0; (3) M: Cu, x = 1, y = 0; (4) M: Zn, x = 0, y = 1; 2,2′-bipy: 2,2′-bipyridine; C(3)H(3)O(2): acrylate anion) were shown to be mononuclear. The lowest minimum inhibitory concentration (MIC) of 128 μg mL(−1) was recorded for all four tested complexes against Candida albicans, for complex (3) against Escherichia coli, and for complex (4) against Staphylocococcus aureus. Compounds (3) and (4) were also potent efflux pumps activity inhibitors (EPI), proving their potential for use in synergistic combinations with antibiotics. Complexes (1)–(4) revealed that they were not cytotoxic to HCT-8 cells. They also proved to interfere with the cellular cycle of tumour HCT-8 cells by increasing the number of cells found in the S and G2/M phases. Taken together, these results demonstrate the potential of zinc and copper complexes for use in the development of novel antimicrobial and anti-proliferative agents. MDPI 2018-01-12 /pmc/articles/PMC6017882/ /pubmed/29329277 http://dx.doi.org/10.3390/molecules23010157 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Vasile Scăețeanu, Gina
Chifiriuc, Mariana Carmen
Bleotu, Coralia
Kamerzan, Crina
Măruţescu, Luminiţa
Daniliuc, Constantin G.
Maxim, Cătălin
Calu, Larisa
Olar, Rodica
Badea, Mihaela
Synthesis, Structural Characterization, Antimicrobial Activity, and In Vitro Biocompatibility of New Unsaturated Carboxylate Complexes with 2,2′-Bipyridine
title Synthesis, Structural Characterization, Antimicrobial Activity, and In Vitro Biocompatibility of New Unsaturated Carboxylate Complexes with 2,2′-Bipyridine
title_full Synthesis, Structural Characterization, Antimicrobial Activity, and In Vitro Biocompatibility of New Unsaturated Carboxylate Complexes with 2,2′-Bipyridine
title_fullStr Synthesis, Structural Characterization, Antimicrobial Activity, and In Vitro Biocompatibility of New Unsaturated Carboxylate Complexes with 2,2′-Bipyridine
title_full_unstemmed Synthesis, Structural Characterization, Antimicrobial Activity, and In Vitro Biocompatibility of New Unsaturated Carboxylate Complexes with 2,2′-Bipyridine
title_short Synthesis, Structural Characterization, Antimicrobial Activity, and In Vitro Biocompatibility of New Unsaturated Carboxylate Complexes with 2,2′-Bipyridine
title_sort synthesis, structural characterization, antimicrobial activity, and in vitro biocompatibility of new unsaturated carboxylate complexes with 2,2′-bipyridine
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6017882/
https://www.ncbi.nlm.nih.gov/pubmed/29329277
http://dx.doi.org/10.3390/molecules23010157
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