Petrosaspongiolides M−R:  New Potent and Selective Phospholipase A2 Inhibitors from the New Caledonian Marine Sponge Petrosaspongia n igra

• Published in: Journal of natural products (Washington, D.C.) Vol. 61; no. 5; pp. 571 - 575
• Main Authors: Randazzo, Antonio, Debitus, Cécile, Minale, Luigi, García Pastor, P, Alcaraz, Maria J, Payá, M, Gomez-Paloma, Luigi
• Format: Journal Article
• Language: English
• Published: American Chemical Society 22-05-1998
• ISSN: 0163-3864; 1520-6025
• DOI: 10.1021/np9704922

Five new bioactive sesterterpenes (1−5) have been isolated from the New Caledonian marine sponge Petrosaspongia nigra Bergquist and named petrosaspongiolides M−R. Their chemical structures were determined from 1D and 2D NMR studies and MS data. All compounds inhibited different preparations of phospholipase A2 (PLA2) by irreversibly blocking these enzymes (particularly human synovial and bee venom, see Table ), with IC50 values in the micromolar range. Interestingly, these compounds displayed a much lower activity (or no activity at all) toward porcine pancreas and Naja naja venom PLA2 enzymes. The most potent compound, 1 (IC50 1.6 and 0.6 μM for human synovial and bee venom PLA2 enzymes, respectively), was slightly more active than manoalide (6) (IC50 3.9 and 7.5 μM) under our experimental conditions. Compound 3 is more selective, inhibiting human synovial PLA2 to a greater extent than bee venom PLA2.