Abstract
An Irish strain of the dinoflagellate Amphidinium carterae was previously shown to produce antibacterial amphidinol derivatives of unknown masses. Inspection of the major metabolites present in a bulk culture of this strain led to the isolation and structure elucidation of a new amphidinol derivative named amphidinol C featuring an unprecedented tetrahydropyran ring between the positions C-7 and C-11. The structure was determined using extensive analyses of NMR and MS data and comparison with data of analogues. The new ring was proposed to stem from a nucleophilic substitution of the sulphate present on the side chain of Amphidinol B. The major metabolites isolated were tested for their antibacterial and antifungal activities and Amphidinol C showed moderate fungicidal activity against yeast and filamentous fungi at 8–16 µg mL−1.
Original language | English |
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Pages (from-to) | 104-108 |
Number of pages | 5 |
Journal | Phytochemistry Letters |
Volume | 51 |
DOIs | |
Publication status | Published - Oct 2022 |
Keywords
- Amphidinium carterae
- Amphidinol
- Fungicidal
- Polyketide