Abstract
Methyl sarcotroates A and B (3 and 4), two unprecedented diterpenoids possessing a tetradecahydrocyclopenta[3′,4′]cyclobuta[1′, 2′:4,5]cyclonona[1,2-b]oxirene ring system, along with their probable biogenetic precursor, sarcophytonolide M (1), were isolated from the Hainan soft coral Sarcophyton trocheliophorum. Their structures were elucidated by detailed spectroscopic analysis, and the absolute configuration of compound 3 was determined by TDDFT ECD calculations. Compound 4 exhibited significant inhibitory activity against protein tyrosine phosphatase 1B (PTP1B), being similar to that of positive control oleanolic acid. © 2012 American Chemical Society.
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CITATION STYLE
Liang, L. F., Kurtán, T., Mándi, A., Yao, L. G., Li, J., Zhang, W., & Guo, Y. W. (2013). Unprecedented diterpenoids as a PTP1B inhibitor from the hainan soft coral Sarcophyton trocheliophorum marenzeller. Organic Letters, 15(2), 274–277. https://doi.org/10.1021/ol303110d
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