亚精胺
精胺
生物
生物化学
化学
萜类
立体化学
酶
作者
Wei Jiang,Dongdong Wang,Brice A. P. Wilson,Donna Voeller,Heidi R. Bokesch,Emily A. Smith,Stanley Lipkowitz,Barry R. O’Keefe,Kirk R. Gustafson
标识
DOI:10.1021/acs.jnatprod.1c00367
摘要
An extract of a Sinularia sp. soft coral showed inhibitory activity against the E3-ubiquitin ligase casitas B-lineage lymphoma proto-oncogene B (Cbl-b). Subsequent bioassay-guided separation of the extract provided a series of terpenoid-derived spermidine and spermine amides that were named sinularamides A–G (1–7). Compounds 1–7 represent new natural products; however, sinularamide A (1) was previously reported as a synthetic end product. The structures of sinularamides A–G (1–7) were elucidated by analysis of spectroscopic and spectrometric data from NMR, IR, and HRESIMS experiments and by comparison with literature data. All of the isolated compounds showed Cbl-b inhibitory activities with IC50 values that ranged from approximately 6.5 to 33 μM.
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