Biomedicine Key Laboratory of Shaanxi Province, Northwest University, Xi'an, China.
Planta Med. 2010 Oct;76(15):1755-8. doi: 10.1055/s-0030-1249926. Epub 2010 May 10.
The steroids ergone (1), (22E, 24R)-ergosta-7,22-dien-3β-ol (2), 5α,8α-epidioxy-(22E,24R) -ergosta-6,22-dien-3β-ol (3), ergosta-6,22-dien-3β,5α,6β-triol (4), and polyporusterone B (5) were isolated from Polyporus umbellatus by bioassay-guided approach. They showed potent anticancer activity against HepG2 cells. Ergone displayed remarkable anticancer activity against HepG2, Hep-2, and Hela cancer cells, of which HepG2 cells were the most sensitive. Furthermore, the cytotoxic effects of ergone on normal human cells (HUVEC) were smaller than on cancer cells. The results showed that ergone had more selective cytotoxic activity against cancer cells than against normal cells.
从药用蘑菇云芝中,通过生物活性导向分离得到了甾体化合物 ergone (1), (22E, 24R)-ergosta-7,22-dien-3β-ol (2), 5α,8α-epidioxy-(22E,24R)-ergosta-6,22-dien-3β-ol (3), ergosta-6,22-dien-3β,5α,6β-triol (4), 和 polyporusterone B (5)。这些化合物对 HepG2 细胞具有很强的抗癌活性。ergone 对 HepG2、Hep-2 和 Hela 癌细胞表现出显著的抗癌活性,其中 HepG2 细胞最为敏感。此外,ergone 对正常人脐静脉内皮细胞(HUVEC)的细胞毒性作用小于对癌细胞的作用。结果表明,ergone 对癌细胞的细胞毒性活性比正常细胞更具有选择性。