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Self-Assembly and Multifaceted Bioactivity of a Silver(I) Quinolinate Coordination Polymer
[Image: see text] Coordination polymers have emerged as a new class of potent biologically active agents due to a variety of important characteristics such as the presence of bioactive metal centers and linkers, low toxicity, stability, tailorable structures, and bioavailability. The research on int...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8527454/ https://www.ncbi.nlm.nih.gov/pubmed/34546735 http://dx.doi.org/10.1021/acs.inorgchem.1c02110 |
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author | Jaros, Sabina W. Krogul-Sobczak, Agnieszka Bażanów, Barbara Florek, Magdalena Poradowski, Dominik Nesterov, Dmytro S. Śliwińska-Hill, Urszula Kirillov, Alexander M. Smoleński, Piotr |
author_facet | Jaros, Sabina W. Krogul-Sobczak, Agnieszka Bażanów, Barbara Florek, Magdalena Poradowski, Dominik Nesterov, Dmytro S. Śliwińska-Hill, Urszula Kirillov, Alexander M. Smoleński, Piotr |
author_sort | Jaros, Sabina W. |
collection | PubMed |
description | [Image: see text] Coordination polymers have emerged as a new class of potent biologically active agents due to a variety of important characteristics such as the presence of bioactive metal centers and linkers, low toxicity, stability, tailorable structures, and bioavailability. The research on intermediate metabolites has also been explored with implications toward the development of selective anticancer, antimicrobial, and antiviral therapeutic strategies. In particular, quinolinic acid (H(2)quin) is a recognized metabolite in kynurenine pathway and potent neurotoxic molecule, which has been selected in this study as a bioactive building block for assembling a new silver(I) coordination polymer, [Ag(Hquin)(μ-PTA)](n)·H(2)O (1). This product has been prepared from silver oxide, H(2)quin, and 1,3,5-triaza-7-phosphaadamantane (PTA), and fully characterized by standard methods including single-crystal X-ray diffraction. Compound 1 has revealed distinctive bioactive features, namely (i) a remarkable antiviral activity against herpes simplex virus type 1 (HSV-1) and adenovirus 36 (Ad-36), (ii) a significant antibacterial activity against clinically important bacteria (Staphylococcus aureus, Escherichia coli, and Pseudomonas aeruginosa), and (iii) a selective cytotoxicity against HeLa (human cervix carcinoma) cell line. The present work widens a growing family of bioactive coordination polymers with potent antiviral, antibacterial, and antiproliferative activity. |
format | Online Article Text |
id | pubmed-8527454 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-85274542021-10-20 Self-Assembly and Multifaceted Bioactivity of a Silver(I) Quinolinate Coordination Polymer Jaros, Sabina W. Krogul-Sobczak, Agnieszka Bażanów, Barbara Florek, Magdalena Poradowski, Dominik Nesterov, Dmytro S. Śliwińska-Hill, Urszula Kirillov, Alexander M. Smoleński, Piotr Inorg Chem [Image: see text] Coordination polymers have emerged as a new class of potent biologically active agents due to a variety of important characteristics such as the presence of bioactive metal centers and linkers, low toxicity, stability, tailorable structures, and bioavailability. The research on intermediate metabolites has also been explored with implications toward the development of selective anticancer, antimicrobial, and antiviral therapeutic strategies. In particular, quinolinic acid (H(2)quin) is a recognized metabolite in kynurenine pathway and potent neurotoxic molecule, which has been selected in this study as a bioactive building block for assembling a new silver(I) coordination polymer, [Ag(Hquin)(μ-PTA)](n)·H(2)O (1). This product has been prepared from silver oxide, H(2)quin, and 1,3,5-triaza-7-phosphaadamantane (PTA), and fully characterized by standard methods including single-crystal X-ray diffraction. Compound 1 has revealed distinctive bioactive features, namely (i) a remarkable antiviral activity against herpes simplex virus type 1 (HSV-1) and adenovirus 36 (Ad-36), (ii) a significant antibacterial activity against clinically important bacteria (Staphylococcus aureus, Escherichia coli, and Pseudomonas aeruginosa), and (iii) a selective cytotoxicity against HeLa (human cervix carcinoma) cell line. The present work widens a growing family of bioactive coordination polymers with potent antiviral, antibacterial, and antiproliferative activity. American Chemical Society 2021-09-21 2021-10-18 /pmc/articles/PMC8527454/ /pubmed/34546735 http://dx.doi.org/10.1021/acs.inorgchem.1c02110 Text en © 2021 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Jaros, Sabina W. Krogul-Sobczak, Agnieszka Bażanów, Barbara Florek, Magdalena Poradowski, Dominik Nesterov, Dmytro S. Śliwińska-Hill, Urszula Kirillov, Alexander M. Smoleński, Piotr Self-Assembly and Multifaceted Bioactivity of a Silver(I) Quinolinate Coordination Polymer |
title | Self-Assembly and Multifaceted Bioactivity of a Silver(I)
Quinolinate Coordination Polymer |
title_full | Self-Assembly and Multifaceted Bioactivity of a Silver(I)
Quinolinate Coordination Polymer |
title_fullStr | Self-Assembly and Multifaceted Bioactivity of a Silver(I)
Quinolinate Coordination Polymer |
title_full_unstemmed | Self-Assembly and Multifaceted Bioactivity of a Silver(I)
Quinolinate Coordination Polymer |
title_short | Self-Assembly and Multifaceted Bioactivity of a Silver(I)
Quinolinate Coordination Polymer |
title_sort | self-assembly and multifaceted bioactivity of a silver(i)
quinolinate coordination polymer |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8527454/ https://www.ncbi.nlm.nih.gov/pubmed/34546735 http://dx.doi.org/10.1021/acs.inorgchem.1c02110 |
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