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Synthesis and Biological Characterization of the New Glycolipid Lactose Undecylenate (URB1418)
As a follow-up to our previous studies on glycolipid surfactants, a new molecule, that is lactose 6′-O-undecylenate (URB1418), was investigated. To this end, a practical synthesis and studies aimed at exploring its specific properties were carried out. URB1418 showed antifungal activities against Tr...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9030338/ https://www.ncbi.nlm.nih.gov/pubmed/35455453 http://dx.doi.org/10.3390/ph15040456 |
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author | Verboni, Michele Benedetti, Serena Campana, Raffaella Palma, Francesco Potenza, Lucia Sisti, Maurizio Duranti, Andrea Lucarini, Simone |
author_facet | Verboni, Michele Benedetti, Serena Campana, Raffaella Palma, Francesco Potenza, Lucia Sisti, Maurizio Duranti, Andrea Lucarini, Simone |
author_sort | Verboni, Michele |
collection | PubMed |
description | As a follow-up to our previous studies on glycolipid surfactants, a new molecule, that is lactose 6′-O-undecylenate (URB1418), was investigated. To this end, a practical synthesis and studies aimed at exploring its specific properties were carried out. URB1418 showed antifungal activities against Trichophyton rubrum F2 and Candida albicans ATCC 10231 (MIC 512 μg/mL) and no significant antibacterial activity against Staphylococcus aureus and Pseudomonas aeruginosa. At the same time, it presented anti-inflammatory properties, as documented by the dose-dependent reduction in LPS-induced NO release in RAW 264.7 cells, while a low antioxidant capacity in the range of concentrations tested (EC(50) > 200 µM) was also observed. Moreover, URB1418 offers the advantage of being more stable than the reference polyunsaturated lactose esters and of being synthesized using a “green” procedure, involving an enzymatic method, high yield and low manufacturing cost. For all these reasons and the absence of toxicity (HaCaT cells), the new glycolipid presented herein could be considered an interesting compound for applications in various fields. |
format | Online Article Text |
id | pubmed-9030338 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-90303382022-04-23 Synthesis and Biological Characterization of the New Glycolipid Lactose Undecylenate (URB1418) Verboni, Michele Benedetti, Serena Campana, Raffaella Palma, Francesco Potenza, Lucia Sisti, Maurizio Duranti, Andrea Lucarini, Simone Pharmaceuticals (Basel) Article As a follow-up to our previous studies on glycolipid surfactants, a new molecule, that is lactose 6′-O-undecylenate (URB1418), was investigated. To this end, a practical synthesis and studies aimed at exploring its specific properties were carried out. URB1418 showed antifungal activities against Trichophyton rubrum F2 and Candida albicans ATCC 10231 (MIC 512 μg/mL) and no significant antibacterial activity against Staphylococcus aureus and Pseudomonas aeruginosa. At the same time, it presented anti-inflammatory properties, as documented by the dose-dependent reduction in LPS-induced NO release in RAW 264.7 cells, while a low antioxidant capacity in the range of concentrations tested (EC(50) > 200 µM) was also observed. Moreover, URB1418 offers the advantage of being more stable than the reference polyunsaturated lactose esters and of being synthesized using a “green” procedure, involving an enzymatic method, high yield and low manufacturing cost. For all these reasons and the absence of toxicity (HaCaT cells), the new glycolipid presented herein could be considered an interesting compound for applications in various fields. MDPI 2022-04-08 /pmc/articles/PMC9030338/ /pubmed/35455453 http://dx.doi.org/10.3390/ph15040456 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 Verboni, Michele Benedetti, Serena Campana, Raffaella Palma, Francesco Potenza, Lucia Sisti, Maurizio Duranti, Andrea Lucarini, Simone Synthesis and Biological Characterization of the New Glycolipid Lactose Undecylenate (URB1418) |
title | Synthesis and Biological Characterization of the New Glycolipid Lactose Undecylenate (URB1418) |
title_full | Synthesis and Biological Characterization of the New Glycolipid Lactose Undecylenate (URB1418) |
title_fullStr | Synthesis and Biological Characterization of the New Glycolipid Lactose Undecylenate (URB1418) |
title_full_unstemmed | Synthesis and Biological Characterization of the New Glycolipid Lactose Undecylenate (URB1418) |
title_short | Synthesis and Biological Characterization of the New Glycolipid Lactose Undecylenate (URB1418) |
title_sort | synthesis and biological characterization of the new glycolipid lactose undecylenate (urb1418) |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9030338/ https://www.ncbi.nlm.nih.gov/pubmed/35455453 http://dx.doi.org/10.3390/ph15040456 |
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