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      Cytotoxic aaptamine derivatives from the South China Sea sponge Aaptos aaptos.

      Journal of Natural Products
      Animals, Antineoplastic Agents, chemistry, isolation & purification, pharmacology, China, Drug Screening Assays, Antitumor, HL-60 Cells, HT29 Cells, Humans, Inhibitory Concentration 50, K562 Cells, Molecular Structure, Naphthyridines, Nuclear Magnetic Resonance, Biomolecular, Oceans and Seas, Porifera

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          Abstract

          Nine new aaptamine derivatives (1-9), together with three known related compounds (10-12), have been isolated from the South China Sea sponge Aaptos aaptos. The structures of all compounds were unambiguously elucidated on the basis of spectroscopic analyses. Structurally, compound 1 possesses a piperidinyl group fused to a demethyl(oxy)aaptamine moiety, whereas compounds 3-6 share an imidazole-fused 1H-benzo[de][1,6]naphthyridin-2(4H)-one skeleton. The cytotoxic activities of the compounds were evaluated against various human cancer cell lines, and compounds 2, 8, 11, and 12 showed potent cytotoxicities against HL60, K562, MCF-7, KB, HepG2, and HT-29 cells, with IC50 values in the range of 0.03 to 8.5 μM.

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