Journal of Natural Products · 2002 · 44 citations · 31 references
Analysis of the Papua New Guinean sponge Theonella swinhoei afforded a new calyculinamide-related congener for which we propose the name swinhoeiamide A (1). The structure of the new compound was unambiguously established on the basis of NMR spectroscopic ((1)H, (13)C, COSY, HMBC) and mass spectrometric (FABMS) data. Swinhoeiamide A exhibited insecticidal activity toward neonate larvae of the polyphagous pest insect Spodoptera littoralis when incorporated in an artificial diet offered to the larvae in a chronic feeding bioassay (ED(50) 2.11 ppm, LD(50) 2.98 ppm). Furthermore, it was found to be fungicidal against Candida albicans and Aspergillus fumigatus (MIC 1.2 and 1.0 microg/mL, respectively).
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Yuko Kato, Nobuhiro Fusetani, Shigeki Matsunaga et al. · Journal of the American Chemical Society · 1986 · 302 citations
Bioconcentration, Pharmaceutical Science, Marine Biotechnology +14
Bertrand Favre, Patric Turowski, Brian A. Hemmings · Journal of Biological Chemistry · 1997 · 298 citations · Full text