Oral dictyoceratin-C (1) and A (2), hypoxia-selective growth inhibitors, showed potent in vivo antitumor effects in mice subcutaneously inoculated with sarcoma S180 cells. Structurally modified analogs were synthesized to assess the structure-activity relationship of the natural compounds 1 and 2 isolated from a marine sponge. Biological evaluation of these analogs showed that the exo-olefin and hydroxyl and methyl ester moieties were important for the hypoxia-selective growth inhibitory activities of 1 and 2. Thus far, only substitution of the methyl ester with propargyl amide in 1 was found to be effective for the synthesis of probe molecules for target identification.
CITATION STYLE
Sumii, Y., Kotoku, N., Fukuda, A., Kawachi, T., Arai, M., & Kobayashi, M. (2015). Structure-activity relationship and in vivo anti-tumor evaluations ofdictyoceratin-A and-C,hypoxia-selective growth inhibitors from marine sponge. Marine Drugs, 13(12), 7419–7432. https://doi.org/10.3390/md13127074
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