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An Aminopyrimidone and Aminoimidazoles Alkaloids from the Rodrigues Calcareous Marine Sponge Ernsta naturalis
A chemical study of the CH(2)Cl(2)−MeOH (1:1) extract from the sponge Ernsta naturalis collected in Rodrigues (Mauritius) based on a molecular networking dereplication strategy highlighted one novel aminopyrimidone alkaloid compound, ernstine A (1), seven new aminoimidazole alkaloid compounds, phorb...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9604632/ https://www.ncbi.nlm.nih.gov/pubmed/36286460 http://dx.doi.org/10.3390/md20100637 |
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author | Campos, Pierre-Eric Herbette, Gaëtan Fougère, Laetitia Clerc, Patricia Tintillier, Florent de Voogd, Nicole J. Le Goff, Géraldine Ouazzani, Jamal Gauvin-Bialecki, Anne |
author_facet | Campos, Pierre-Eric Herbette, Gaëtan Fougère, Laetitia Clerc, Patricia Tintillier, Florent de Voogd, Nicole J. Le Goff, Géraldine Ouazzani, Jamal Gauvin-Bialecki, Anne |
author_sort | Campos, Pierre-Eric |
collection | PubMed |
description | A chemical study of the CH(2)Cl(2)−MeOH (1:1) extract from the sponge Ernsta naturalis collected in Rodrigues (Mauritius) based on a molecular networking dereplication strategy highlighted one novel aminopyrimidone alkaloid compound, ernstine A (1), seven new aminoimidazole alkaloid compounds, phorbatopsins D–E (2, 3), calcaridine C (4), naamines H–I (5, 7), naamidines J–K (6, 8), along with the known thymidine (9). Their structures were established by spectroscopic analysis (1D and 2D NMR spectra and HRESIMS data). To improve the investigation of this unstudied calcareous marine sponge, a metabolomic study by molecular networking was conducted. The isolated molecules are distributed in two clusters of interest. Naamine and naamidine derivatives are grouped together with ernstine in the first cluster of twenty-three molecules. Phorbatopsin derivatives and calcaridine C are grouped together in a cluster of twenty-one molecules. Interpretation of the MS/MS spectra of other compounds of these clusters with structural features close to the isolated ones allowed us to propose a structural hypothesis for 16 compounds, 5 known and 11 potentially new. |
format | Online Article Text |
id | pubmed-9604632 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-96046322022-10-27 An Aminopyrimidone and Aminoimidazoles Alkaloids from the Rodrigues Calcareous Marine Sponge Ernsta naturalis Campos, Pierre-Eric Herbette, Gaëtan Fougère, Laetitia Clerc, Patricia Tintillier, Florent de Voogd, Nicole J. Le Goff, Géraldine Ouazzani, Jamal Gauvin-Bialecki, Anne Mar Drugs Article A chemical study of the CH(2)Cl(2)−MeOH (1:1) extract from the sponge Ernsta naturalis collected in Rodrigues (Mauritius) based on a molecular networking dereplication strategy highlighted one novel aminopyrimidone alkaloid compound, ernstine A (1), seven new aminoimidazole alkaloid compounds, phorbatopsins D–E (2, 3), calcaridine C (4), naamines H–I (5, 7), naamidines J–K (6, 8), along with the known thymidine (9). Their structures were established by spectroscopic analysis (1D and 2D NMR spectra and HRESIMS data). To improve the investigation of this unstudied calcareous marine sponge, a metabolomic study by molecular networking was conducted. The isolated molecules are distributed in two clusters of interest. Naamine and naamidine derivatives are grouped together with ernstine in the first cluster of twenty-three molecules. Phorbatopsin derivatives and calcaridine C are grouped together in a cluster of twenty-one molecules. Interpretation of the MS/MS spectra of other compounds of these clusters with structural features close to the isolated ones allowed us to propose a structural hypothesis for 16 compounds, 5 known and 11 potentially new. MDPI 2022-10-13 /pmc/articles/PMC9604632/ /pubmed/36286460 http://dx.doi.org/10.3390/md20100637 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 Campos, Pierre-Eric Herbette, Gaëtan Fougère, Laetitia Clerc, Patricia Tintillier, Florent de Voogd, Nicole J. Le Goff, Géraldine Ouazzani, Jamal Gauvin-Bialecki, Anne An Aminopyrimidone and Aminoimidazoles Alkaloids from the Rodrigues Calcareous Marine Sponge Ernsta naturalis |
title | An Aminopyrimidone and Aminoimidazoles Alkaloids from the Rodrigues Calcareous Marine Sponge Ernsta naturalis |
title_full | An Aminopyrimidone and Aminoimidazoles Alkaloids from the Rodrigues Calcareous Marine Sponge Ernsta naturalis |
title_fullStr | An Aminopyrimidone and Aminoimidazoles Alkaloids from the Rodrigues Calcareous Marine Sponge Ernsta naturalis |
title_full_unstemmed | An Aminopyrimidone and Aminoimidazoles Alkaloids from the Rodrigues Calcareous Marine Sponge Ernsta naturalis |
title_short | An Aminopyrimidone and Aminoimidazoles Alkaloids from the Rodrigues Calcareous Marine Sponge Ernsta naturalis |
title_sort | aminopyrimidone and aminoimidazoles alkaloids from the rodrigues calcareous marine sponge ernsta naturalis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9604632/ https://www.ncbi.nlm.nih.gov/pubmed/36286460 http://dx.doi.org/10.3390/md20100637 |
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