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Design, Synthesis and Evaluation of New Multifunctional Benzothiazoles as Photoprotective, Antioxidant and Antiproliferative Agents

A current trend of research in the health field is toward the discovery of multifunctional compounds, capable of interacting with multiple biological targets, thus simplifying multidrug therapies and improving patient compliance. The aim of this work was to synthesize new multifunctional chemical en...

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Autores principales: Barbari, Riccardo, Tupini, Chiara, Durini, Elisa, Gallerani, Eleonora, Nicoli, Francesco, Lampronti, Ilaria, Baldisserotto, Anna, Manfredini, Stefano
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9822352/
https://www.ncbi.nlm.nih.gov/pubmed/36615480
http://dx.doi.org/10.3390/molecules28010287
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author Barbari, Riccardo
Tupini, Chiara
Durini, Elisa
Gallerani, Eleonora
Nicoli, Francesco
Lampronti, Ilaria
Baldisserotto, Anna
Manfredini, Stefano
author_facet Barbari, Riccardo
Tupini, Chiara
Durini, Elisa
Gallerani, Eleonora
Nicoli, Francesco
Lampronti, Ilaria
Baldisserotto, Anna
Manfredini, Stefano
author_sort Barbari, Riccardo
collection PubMed
description A current trend of research in the health field is toward the discovery of multifunctional compounds, capable of interacting with multiple biological targets, thus simplifying multidrug therapies and improving patient compliance. The aim of this work was to synthesize new multifunctional chemical entities bearing a benzothiazole nucleus, a structure that has attracted increasing interest for the great variety of biological actions that it can perform, and already used as a scaffold in several multifunctional drugs. Compounds are reported, divided into two distinct series, synthetized and tested in vitro for the antioxidant, and include UV-filtering and antitumor activities. DPPH and FRAP tests were chosen to outline an antioxidant activity profile against different radical species. The UV-filtering activity was investigated, pre- and post-irradiation, through evaluation of a O/W sunscreen standard formulation containing 3% of the synthetic compounds. The antitumor activity was investigated both on human melanoma cells (Colo-38) and on immortalized human keratinocytes as a control (HaCat). A good antiproliferative profile in terms of IC(50) was chosen as a mandatory condition to further investigate apoptosis induction as a possible cytotoxicity mechanism through the Annexin V test. Compound BZTcin4 was endowed with excellent activity and a selectivity profile towards Colo-38, supported by a good antioxidant capacity and an excellent broad-spectrum photoprotective profile.
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spelling pubmed-98223522023-01-07 Design, Synthesis and Evaluation of New Multifunctional Benzothiazoles as Photoprotective, Antioxidant and Antiproliferative Agents Barbari, Riccardo Tupini, Chiara Durini, Elisa Gallerani, Eleonora Nicoli, Francesco Lampronti, Ilaria Baldisserotto, Anna Manfredini, Stefano Molecules Article A current trend of research in the health field is toward the discovery of multifunctional compounds, capable of interacting with multiple biological targets, thus simplifying multidrug therapies and improving patient compliance. The aim of this work was to synthesize new multifunctional chemical entities bearing a benzothiazole nucleus, a structure that has attracted increasing interest for the great variety of biological actions that it can perform, and already used as a scaffold in several multifunctional drugs. Compounds are reported, divided into two distinct series, synthetized and tested in vitro for the antioxidant, and include UV-filtering and antitumor activities. DPPH and FRAP tests were chosen to outline an antioxidant activity profile against different radical species. The UV-filtering activity was investigated, pre- and post-irradiation, through evaluation of a O/W sunscreen standard formulation containing 3% of the synthetic compounds. The antitumor activity was investigated both on human melanoma cells (Colo-38) and on immortalized human keratinocytes as a control (HaCat). A good antiproliferative profile in terms of IC(50) was chosen as a mandatory condition to further investigate apoptosis induction as a possible cytotoxicity mechanism through the Annexin V test. Compound BZTcin4 was endowed with excellent activity and a selectivity profile towards Colo-38, supported by a good antioxidant capacity and an excellent broad-spectrum photoprotective profile. MDPI 2022-12-29 /pmc/articles/PMC9822352/ /pubmed/36615480 http://dx.doi.org/10.3390/molecules28010287 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Barbari, Riccardo
Tupini, Chiara
Durini, Elisa
Gallerani, Eleonora
Nicoli, Francesco
Lampronti, Ilaria
Baldisserotto, Anna
Manfredini, Stefano
Design, Synthesis and Evaluation of New Multifunctional Benzothiazoles as Photoprotective, Antioxidant and Antiproliferative Agents
title Design, Synthesis and Evaluation of New Multifunctional Benzothiazoles as Photoprotective, Antioxidant and Antiproliferative Agents
title_full Design, Synthesis and Evaluation of New Multifunctional Benzothiazoles as Photoprotective, Antioxidant and Antiproliferative Agents
title_fullStr Design, Synthesis and Evaluation of New Multifunctional Benzothiazoles as Photoprotective, Antioxidant and Antiproliferative Agents
title_full_unstemmed Design, Synthesis and Evaluation of New Multifunctional Benzothiazoles as Photoprotective, Antioxidant and Antiproliferative Agents
title_short Design, Synthesis and Evaluation of New Multifunctional Benzothiazoles as Photoprotective, Antioxidant and Antiproliferative Agents
title_sort design, synthesis and evaluation of new multifunctional benzothiazoles as photoprotective, antioxidant and antiproliferative agents
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9822352/
https://www.ncbi.nlm.nih.gov/pubmed/36615480
http://dx.doi.org/10.3390/molecules28010287
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