Publication | Closed Access
PPAR Modulating Polyketides from a Chinese <i>Plakortis simplex</i> and Clues on the Origin of Their Chemodiversity
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Citations
36
References
2016
Year
Molecular PharmacologyPlakilactone DerivativesBiochemistryTheir ChemodiversityNatural SciencesMedicineChemical DerivativeMolecular BiologyNatural Product BiosynthesisVicinal DiepoxidePpar Modulating PolyketidesChemistryChemical BiologyPharmacologyPharmaceutical ChemistryFifteen PolyketidesDrug DiscoveryNatural Product Synthesis
Fifteen polyketides, including the first hydroxylated plakortone (12) and plakdiepoxide (15), the first polyketide to embed a vicinal diepoxide, have been isolated from the Chinese sponge Plakortis simplex. The structures of the new metabolites were elucidated by analysis of spectroscopic data, Mosher's derivatization, and DFT computational calculations. The reactivity of the major endoperoxide of this sponge was investigated, suggesting that furan, furanylidene, and plakilactone derivatives, well-known classes of natural products, could actually be chemical degradation products. Plakdiepoxide is a potent and selective modulator of peroxisome proliferator-activated receptor (PPAR)-γ, while the diunsaturated C12 fatty acid monotriajaponide (13) activates both PPAR-α and PPAR-γ, a dual activity of potential great importance for the treatment of metabolic disorders.
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