Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Villano, Rosaria, Tinto, Francesco, Di Marzo, Vincenzo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
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
_version_ 1784669327945891840
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
work_keys_str_mv AT villanorosaria facileandsustainablesynthesisofcommendamideanditsanalogues
AT tintofrancesco facileandsustainablesynthesisofcommendamideanditsanalogues
AT dimarzovincenzo facileandsustainablesynthesisofcommendamideanditsanalogues