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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.
Afiliação
  • Campos PE; Laboratoire de Chimie et de Biotechnologie des Produits Naturels, Faculté des Sciences et Technologies, Université de La Réunion, 15 Avenue René Cassin, CS 92003, CEDEX 9, 97744 Saint-Denis, France.
  • Herbette G; Institut de Chimie Organique et Analytique, Université d'Orléans-CNRS-Pôle de Chimie, Rue de Chartres-UMR 6759, BP6759, CEDEX 2, 45067 Orléans, France.
  • Fougère L; CNRS, Aix-Marseille Université, Centrale Marseille, FSCM, Spectropole, Campus de St Jérôme-Service 511, 13397 Marseille, France.
  • Clerc P; Institut de Chimie Organique et Analytique, Université d'Orléans-CNRS-Pôle de Chimie, Rue de Chartres-UMR 6759, BP6759, CEDEX 2, 45067 Orléans, France.
  • Tintillier F; Laboratoire de Chimie et de Biotechnologie des Produits Naturels, Faculté des Sciences et Technologies, Université de La Réunion, 15 Avenue René Cassin, CS 92003, CEDEX 9, 97744 Saint-Denis, France.
  • de Voogd NJ; Laboratoire de Chimie et de Biotechnologie des Produits Naturels, Faculté des Sciences et Technologies, Université de La Réunion, 15 Avenue René Cassin, CS 92003, CEDEX 9, 97744 Saint-Denis, France.
  • Le Goff G; Naturalis Biodiversity Center, Darwinweg 2, 2333 CR Leiden, The Netherlands.
  • Ouazzani J; Institute of Environmental Sciences, Leiden University, Einsteinweg 2, 2333 CC Leiden, The Netherlands.
  • Gauvin-Bialecki A; CNRS, Institut de Chimie des Substances Naturelles, UPR 2301, Université Paris-Sud, Université Paris-Saclay, 1, Av. de la Terrasse, 91198 Gif-sur-Yvette, France.
Mar Drugs ; 20(10)2022 Oct 13.
Article em En | MEDLINE | ID: mdl-36286460
ABSTRACT
A chemical study of the CH2Cl2-MeOH (11) 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.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Poríferos / Alcaloides Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Poríferos / Alcaloides Idioma: En Ano de publicação: 2022 Tipo de documento: Article