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      Thorectandrols A and B, new cytotoxic sesterterpenes from the marine sponge Thorectandra species.

      Journal of Natural Products
      Animals, Antineoplastic Agents, chemistry, isolation & purification, pharmacology, Circular Dichroism, Drug Screening Assays, Antitumor, Humans, Magnetic Resonance Spectroscopy, Molecular Conformation, Porifera, Spectrometry, Mass, Fast Atom Bombardment, Terpenes, Tumor Cells, Cultured

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          Abstract

          Two new sesterterpenes, thorectandrol A (1) and B (2), were isolated from extracts of the marine sponge Thorectandra sp. The structures were determined by extensive NMR spectral data analysis. NOE correlations were used to define the relative stereochemistry of 1 and 2, while CD data were used to suggest their absolute stereochemistry. Both compounds 1 and 2 inhibited the growth of MALME-3M (melanoma) and MCF-7 (breast) cancer cell lines in the range 30-40 microg/mL. The known compound palauolol (3) was isolated as well and was also cytotoxic.

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