Paecilosetin derivatives as potent antimicrobial agents from Isaria farinosa
Résumé
Fifty-seven entomopathogenic microorganisms were screened against human pathogens and subjected to mass spectrometry molecular networking based dereplication. Isaria farinosa BSNB-1250, shown to produce potentially novel biologically active metabolites, was grown on a large scale on potato dextrose agar, and paecilosetin (1) and five new analogues (2–6) were subsequently isolated. The structures of the new compounds were elucidated using 1D and 2D NMR. The absolute configurations of compounds 1–6 were determined using Mosher ester derivatives (1, 3, 4), comparison of experimental and calculated ECD spectra (2–4 and 6), and single-crystal X-ray diffraction analysis (5). Compounds 1 and 5 exhibited strong antibacterial activity against MSSA and MRSA with MIC values of 1–2 μg/mL.
Domaines
Chimie| Origine | Fichiers produits par l'(les) auteur(s) |
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