中文名 | EPISILVESTROL |
英文名 | Episilvestrol |
别名 | 化合物 T11215 5MYC-UTR-LUC抑制剂(EPISILVESTROL) |
英文别名 | Episilvestrol EPISILVESTROL (1R,2R,3S,3aR,8bS)-6-[[(2S,3R,6R)-6-[(1S)-1,2-Dihydroxyethyl]-3-methoxy-1,4-dioxan-2-yl]oxy]-2,3,3a,8b-tetrahydro-1,8b-dihydroxy-8-methoxy-3a-(4-methoxyphenyl)-3-phenyl-1H-cyclopenta[b]benzofuran-2-carboxylic acid methyl ester 1H-Cyclopenta[b]benzofuran-2-carboxylic acid, 6-[[(2S,3R,6R)-6-[(1S)-1,2-dihydroxyethyl]-3-methoxy-1,4-dioxan-2-yl]oxy]-2,3,3a,8b-tetrahydro-1,8b-dihydroxy-8-methoxy-3a-(4-methoxyphenyl)-3-phenyl-, methyl ester, (1R,2R,3S,3aR,8bS)- |
CAS | 697235-39-5 |
化学式 | C34H38O13 |
分子量 | 654.66 |
存储条件 | 2-8℃ |
体外研究 | Episilvestrol is a specific eIF4A-targeting translation inhibitor, with antitumor activity. Episilvestrol is cytotoxic activity against several human cancer cell lines, such as Lu1, LNCaP, MCF-7 and HUVEC cells, with ED 50 s of 3.8, 3.8, 5.5 and 15.3 nM, respectively. The GI 50 s of Episilvestrol against the cell proliferation of NCI-H460 and MCF-7 cels are 17.96 nM and 17.96 nM after first test and 15.6 nM and 18.7 nM after 2 months via SRB assay. Episilvestrol also suppresses HK1 cells and EBV-positive C666.1 NPC cells. |
1mg | 5mg | 10mg | |
---|---|---|---|
1 mM | 1.528 ml | 7.638 ml | 15.275 ml |
5 mM | 0.306 ml | 1.528 ml | 3.055 ml |
10 mM | 0.153 ml | 0.764 ml | 1.528 ml |
5 mM | 0.031 ml | 0.153 ml | 0.306 ml |
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