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Design, Synthesis, and Biological Evaluation Studies of Novel Naphthalene-Chalcone Hybrids As Antimicrobial, Anticandidal, Anticancer, and VEGFR-2 Inhibitors

[Image: see text] Cancer is a progressive disease that is frequently encountered worldwide. The incidence of cancer is increasing with the changing living conditions around the world. The side-effect profile of existing drugs and the resistance developing in long-term use increase the need for novel...

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Autores principales: Osmaniye, Derya, Sağlık, Begüm Nurpelin, Khalilova, Narmin, Levent, Serkan, Bayazıt, Gizem, Gül, Ülküye Dudu, Özkay, Yusuf, Kaplancıklı, Zafer Asım
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2023
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9947975/
https://www.ncbi.nlm.nih.gov/pubmed/36844559
http://dx.doi.org/10.1021/acsomega.2c07256
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author Osmaniye, Derya
Sağlık, Begüm Nurpelin
Khalilova, Narmin
Levent, Serkan
Bayazıt, Gizem
Gül, Ülküye Dudu
Özkay, Yusuf
Kaplancıklı, Zafer Asım
author_facet Osmaniye, Derya
Sağlık, Begüm Nurpelin
Khalilova, Narmin
Levent, Serkan
Bayazıt, Gizem
Gül, Ülküye Dudu
Özkay, Yusuf
Kaplancıklı, Zafer Asım
author_sort Osmaniye, Derya
collection PubMed
description [Image: see text] Cancer is a progressive disease that is frequently encountered worldwide. The incidence of cancer is increasing with the changing living conditions around the world. The side-effect profile of existing drugs and the resistance developing in long-term use increase the need for novel drugs. In addition, cancer patients are not resistant to bacterial and fungal infections due to the suppression of the immune system during the treatment. Rather than adding a new antibacterial or antifungal drug to the current treatment plan, the fact that the drug with anticancer activity has these effects (antibacterial and antifungal) will increase the patient’s quality of life. For this purpose, in this study, a series of 10 new naphthalene-chalcone derivatives were synthesized and their anticancer-antibacterial-antifungal properties were investigated. Among the compounds, compound 2j showed activity against the A549 cell line with an IC(50) = 7.835 ± 0.598 μM. This compound also has antibacterial and antifungal activity. The apoptotic potential of the compound was measured by flow cytometry and showed apoptotic activity of 14.230%. The compound also showed 58.870% mitochondrial membrane potential. Compound 2j inhibited VEGFR-2 enzyme with IC(50) = 0.098 ± 0.005 μM. Molecular docking studies of the compounds were carried out by in silico methods against VEGFR-2 and caspase-3 enzymes.
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spelling pubmed-99479752023-02-24 Design, Synthesis, and Biological Evaluation Studies of Novel Naphthalene-Chalcone Hybrids As Antimicrobial, Anticandidal, Anticancer, and VEGFR-2 Inhibitors Osmaniye, Derya Sağlık, Begüm Nurpelin Khalilova, Narmin Levent, Serkan Bayazıt, Gizem Gül, Ülküye Dudu Özkay, Yusuf Kaplancıklı, Zafer Asım ACS Omega [Image: see text] Cancer is a progressive disease that is frequently encountered worldwide. The incidence of cancer is increasing with the changing living conditions around the world. The side-effect profile of existing drugs and the resistance developing in long-term use increase the need for novel drugs. In addition, cancer patients are not resistant to bacterial and fungal infections due to the suppression of the immune system during the treatment. Rather than adding a new antibacterial or antifungal drug to the current treatment plan, the fact that the drug with anticancer activity has these effects (antibacterial and antifungal) will increase the patient’s quality of life. For this purpose, in this study, a series of 10 new naphthalene-chalcone derivatives were synthesized and their anticancer-antibacterial-antifungal properties were investigated. Among the compounds, compound 2j showed activity against the A549 cell line with an IC(50) = 7.835 ± 0.598 μM. This compound also has antibacterial and antifungal activity. The apoptotic potential of the compound was measured by flow cytometry and showed apoptotic activity of 14.230%. The compound also showed 58.870% mitochondrial membrane potential. Compound 2j inhibited VEGFR-2 enzyme with IC(50) = 0.098 ± 0.005 μM. Molecular docking studies of the compounds were carried out by in silico methods against VEGFR-2 and caspase-3 enzymes. American Chemical Society 2023-02-13 /pmc/articles/PMC9947975/ /pubmed/36844559 http://dx.doi.org/10.1021/acsomega.2c07256 Text en © 2023 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 Osmaniye, Derya
Sağlık, Begüm Nurpelin
Khalilova, Narmin
Levent, Serkan
Bayazıt, Gizem
Gül, Ülküye Dudu
Özkay, Yusuf
Kaplancıklı, Zafer Asım
Design, Synthesis, and Biological Evaluation Studies of Novel Naphthalene-Chalcone Hybrids As Antimicrobial, Anticandidal, Anticancer, and VEGFR-2 Inhibitors
title Design, Synthesis, and Biological Evaluation Studies of Novel Naphthalene-Chalcone Hybrids As Antimicrobial, Anticandidal, Anticancer, and VEGFR-2 Inhibitors
title_full Design, Synthesis, and Biological Evaluation Studies of Novel Naphthalene-Chalcone Hybrids As Antimicrobial, Anticandidal, Anticancer, and VEGFR-2 Inhibitors
title_fullStr Design, Synthesis, and Biological Evaluation Studies of Novel Naphthalene-Chalcone Hybrids As Antimicrobial, Anticandidal, Anticancer, and VEGFR-2 Inhibitors
title_full_unstemmed Design, Synthesis, and Biological Evaluation Studies of Novel Naphthalene-Chalcone Hybrids As Antimicrobial, Anticandidal, Anticancer, and VEGFR-2 Inhibitors
title_short Design, Synthesis, and Biological Evaluation Studies of Novel Naphthalene-Chalcone Hybrids As Antimicrobial, Anticandidal, Anticancer, and VEGFR-2 Inhibitors
title_sort design, synthesis, and biological evaluation studies of novel naphthalene-chalcone hybrids as antimicrobial, anticandidal, anticancer, and vegfr-2 inhibitors
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9947975/
https://www.ncbi.nlm.nih.gov/pubmed/36844559
http://dx.doi.org/10.1021/acsomega.2c07256
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