Journal
ORGANIC & BIOMOLECULAR CHEMISTRY
Volume 5, Issue 24, Pages 3979-3986Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/b713060k
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Pericosines A-E 1-5 have been isolated from a strain of Periconia byssoides originally separated from the sea hare Aplysia kurodai. Among them, pericosines C 3 and E 5 were separated as enantiomeric mixtures. Their stereostructures, except for compound 1, have been elucidated or identified on the basis of spectroscopic analyses, including 1D and 2D NMR techniques, and X-ray analysis. In addition, conformation for all the compounds has been discussed. Compounds 1-3 exhibited significant growth inhibition against tumour cell lines. Pericosine A 1 also showed significant in vivo tumour inhibitory activity. In addition, compound 1 inhibited the protein kinase EGFR and topoisomerase II.
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