Nature‐Inspired Chemistry of Complex Alkaloids: Combining Targeted Molecular Networking Approach and Semisynthetic Strategy to Access Rare Communesins in a Marine‐Derived Penicillium expansum

Author:

Hoang Thi Phuong Thuy12,Roullier Catherine1ORCID,Evanno Laurent3ORCID,Kerzaon Isabelle4ORCID,Gentil Emmanuel1ORCID,Robiou du Pont Thibaut1,Nazih El‐Hassane1,Pouchus Yves François1ORCID,Bertrand Samuel1ORCID,Poupon Erwan3ORCID,Grovel Olivier1ORCID

Affiliation:

1. Institut des Substances et Organismes de la Mer ISOMER UR 2160 Nantes Université 44000 Nantes France

2. current address: Greensea 34140 Mèze France

3. Chimie des Substances Naturelles BioCIS Université Paris-Saclay CNRS 17, avenue de la Science 91400 Orsay France

4. UMR5557 Ecologie microbienne CNRS INRAE VetAgro Sup Université Lyon Université Claude Bernard Lyon 1 69622 Villeurbanne CEDEX France

Abstract

AbstractCommunesins are rare alkaloids isolated from fungi of the genus Penicillium. In this work, the extract of a marine‐derived Penicillium expansum strain was studied using targeted molecular networking approach allowing to detect 65 communesins including 55 new ones. A fragmentation pattern for dimethylvinyl communesins was established and a script was implemented allowing to predict the structure and map all communesins in a global molecular network. A semisynthetic strategy was carried out to obtain some minor congeners from the two isolated communesins A and B. Nine communesins were then synthetised: two of them were already described as produced by the studied strain; four are new natural products which occurrence in the extracts was confirmed; three are new semi‐synthetic analogues never described so far. These communesins were evaluated for their cytotoxicity on two human cancer cell lines KB and MCF‐7 leading to a preliminary study of their structure‐activity relationships.

Publisher

Wiley

Subject

General Chemistry,Catalysis,Organic Chemistry

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