Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1254169 | Chinese Chemical Letters | 2014 | 4 Pages |
One new 6,7-seco-ent-kaurane diterpenoid, sculponin T (1), was isolated from the aerial parts of Isodon sculponeatus, along with four known analogs, sculponeatin J (2), sculponeatin K (3), sculponeatin C (4), and sculponeatin Q (5). Their structures were elucidated by extensive spectroscopic analysis and by comparison with data reported in the literature. Significant cytotoxic activity was observed for compound 2 against five human tumor cell lines with IC50 values ranging from 1.8 μmol/L to 3.3 μmol/L, and it also inhibited NO production in LPS-stimulated RAW264.7 cells, with IC50 value of 3.3 μmol/L.
Graphical abstractOne new 6,7-seco-ent-kaurane diterpenoid, namely sculponin T (1), along with another four known analogs (2–5), were isolated from the aerial parts of Isodon sculponeatus. Compound 2 exhibited significant cytotoxic activity against HL-60, SMMC-7721, A-549, MCF-7, and SW-480 cell lines, while compounds 1 and 4 showed moderate cytotoxicity.Figure optionsDownload full-size imageDownload as PowerPoint slide