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Facile and Sustainable Synthesis of Commendamide and its Analogues
Commendamide, or N-(3-hydroxypalmitoyl)-glycine 1a, is a gut microbiota-derived bioactive metabolite, structurally similar to long-chain N-acyl-amino acids which belong to the complex lipid signaling system known as endocannabinoidome and play important roles in mammals through activation of, inter...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8921460/ https://www.ncbi.nlm.nih.gov/pubmed/35300384 http://dx.doi.org/10.3389/fchem.2022.858854 |
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author | Villano, Rosaria Tinto, Francesco Di Marzo, Vincenzo |
author_facet | Villano, Rosaria Tinto, Francesco Di Marzo, Vincenzo |
author_sort | Villano, Rosaria |
collection | PubMed |
description | Commendamide, or N-(3-hydroxypalmitoyl)-glycine 1a, is a gut microbiota-derived bioactive metabolite, structurally similar to long-chain N-acyl-amino acids which belong to the complex lipid signaling system known as endocannabinoidome and play important roles in mammals through activation of, inter alia, G-protein-coupled receptors (GPCRs). In this work, we describe a simple, green and economic method for the preparation of commendamide 1a, a GPCR G2A/132 agonist. The developed protocol is general and could also be applied to the synthesis of deuterated commendamide 1b, as well as to other minor microbiota-derived metabolites, such as the analog 2. |
format | Online Article Text |
id | pubmed-8921460 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-89214602022-03-16 Facile and Sustainable Synthesis of Commendamide and its Analogues Villano, Rosaria Tinto, Francesco Di Marzo, Vincenzo Front Chem Chemistry Commendamide, or N-(3-hydroxypalmitoyl)-glycine 1a, is a gut microbiota-derived bioactive metabolite, structurally similar to long-chain N-acyl-amino acids which belong to the complex lipid signaling system known as endocannabinoidome and play important roles in mammals through activation of, inter alia, G-protein-coupled receptors (GPCRs). In this work, we describe a simple, green and economic method for the preparation of commendamide 1a, a GPCR G2A/132 agonist. The developed protocol is general and could also be applied to the synthesis of deuterated commendamide 1b, as well as to other minor microbiota-derived metabolites, such as the analog 2. Frontiers Media S.A. 2022-03-01 /pmc/articles/PMC8921460/ /pubmed/35300384 http://dx.doi.org/10.3389/fchem.2022.858854 Text en Copyright © 2022 Villano, Tinto and Di Marzo. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Chemistry Villano, Rosaria Tinto, Francesco Di Marzo, Vincenzo Facile and Sustainable Synthesis of Commendamide and its Analogues |
title | Facile and Sustainable Synthesis of Commendamide and its Analogues |
title_full | Facile and Sustainable Synthesis of Commendamide and its Analogues |
title_fullStr | Facile and Sustainable Synthesis of Commendamide and its Analogues |
title_full_unstemmed | Facile and Sustainable Synthesis of Commendamide and its Analogues |
title_short | Facile and Sustainable Synthesis of Commendamide and its Analogues |
title_sort | facile and sustainable synthesis of commendamide and its analogues |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8921460/ https://www.ncbi.nlm.nih.gov/pubmed/35300384 http://dx.doi.org/10.3389/fchem.2022.858854 |
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