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Investigation of Premyrsinane and Myrsinane Esters in Euphorbia cupanii and Euphobia pithyusa with MS2LDA and Combinatorial Molecular Network Annotation Propagation.
Nothias-Esposito, Mélissa; Nothias, Louis Felix; Da Silva, Ricardo R; Retailleau, Pascal; Zhang, Zheng; Leyssen, Pieter; Roussi, Fanny; Touboul, David; Paolini, Julien; Dorrestein, Pieter C; Litaudon, Marc.
Affiliation
  • Nothias-Esposito M; Laboratory of Natural Products Chemistry, UMR CNRS SPE 6134 , University of Corsica , 20250 , Corte , France.
  • Nothias LF; Institute of Natural Substances Chemistry, CNRS UPR 2301 , University of Paris-Saclay , 91198 , Gif-sur-Yvette , France.
  • Da Silva RR; Collaborative Mass Spectrometry Innovation Center, Skaggs School of Pharmacy and Pharmaceutical Sciences , University of California San Diego , La Jolla , California 92093 , United States.
  • Retailleau P; Collaborative Mass Spectrometry Innovation Center, Skaggs School of Pharmacy and Pharmaceutical Sciences , University of California San Diego , La Jolla , California 92093 , United States.
  • Zhang Z; Collaborative Mass Spectrometry Innovation Center, Skaggs School of Pharmacy and Pharmaceutical Sciences , University of California San Diego , La Jolla , California 92093 , United States.
  • Leyssen P; Institute of Natural Substances Chemistry, CNRS UPR 2301 , University of Paris-Saclay , 91198 , Gif-sur-Yvette , France.
  • Roussi F; Collaborative Mass Spectrometry Innovation Center, Skaggs School of Pharmacy and Pharmaceutical Sciences , University of California San Diego , La Jolla , California 92093 , United States.
  • Touboul D; Laboratory for Virology and Experimental Chemotherapy, Rega Institute for Medical Research , KU Leuven , 3000 Leuven , Belgium.
  • Paolini J; Institute of Natural Substances Chemistry, CNRS UPR 2301 , University of Paris-Saclay , 91198 , Gif-sur-Yvette , France.
  • Dorrestein PC; Institute of Natural Substances Chemistry, CNRS UPR 2301 , University of Paris-Saclay , 91198 , Gif-sur-Yvette , France.
  • Litaudon M; Laboratory of Natural Products Chemistry, UMR CNRS SPE 6134 , University of Corsica , 20250 , Corte , France.
J Nat Prod ; 82(6): 1459-1470, 2019 06 28.
Article in En | MEDLINE | ID: mdl-31181921
ABSTRACT
The species Euphorbia pithyusa and Euphorbia cupanii are two closely related Mediterranean spurges for which their taxonomic relationships are still being debated. Herein, the diterpene ester content of E. cupanii was investigated using liquid chromatography coupled to tandem mass spectrometry. The use of molecular networking coupled to unsupervised substructure annotation ( MS2LDA) indicated the presence of new premyrsinane/myrsinane diterpene esters in the E. cupanii fractions. A structure-guided isolation procedure yielded 16 myrsinane (11a-h, 12, and 13) and premyrsinane esters (14a-c and 15a-c), along with four 4ß-phorbol esters (16a-c and 17) that showed inhibitory activity against chikungunya virus replication. The structures of the 16 new compounds (11a-c, 11h, 12, 13, 14a-c, 15a-c, 16a-c, and 17) were characterized by NMR spectroscopy and X-ray crystallography. To further uncover the diterpene ester content of these two species, the concept of combinatorial network annotation propagation (C-NAP) was developed. By leveraging the fact that the diterpene esters of Euphorbia species are made up of limited building blocks, a combinatorial database of theoretical structures was created and used for C-NAP that made possible the annotation of 123 premyrsinane or myrsinane esters, from which 74% are not found in any compound database.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Virus Replication / Chikungunya virus / Euphorbia / Diterpenes Language: En Journal: J Nat Prod Year: 2019 Document type: Article Affiliation country: France

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Virus Replication / Chikungunya virus / Euphorbia / Diterpenes Language: En Journal: J Nat Prod Year: 2019 Document type: Article Affiliation country: France
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