| 溶解性 | 25°C: DMSO 120mg/mL ;Water <1mg/mL; Ethanol <1mg/mL |
| 存贮条件 | 储存温度-20°C |
| 生化机理 | IC50 Value: 1±0.3μM. Toremifene is a second-generation selective estrogen-receptor modulator (SERM) in development for the prevention of osteoporosis and other adverse effects resulting from ADT in men with prostate cancer [1]. in vitro: The growth of Ac-1 cells was inhibited by tamoxifen, toremifene and atamestane in vitro with IC50values of 1.8±1.3μM, 1±0.3μM and 60.4±17.2μM, respectively. The combination of toremifene plusatamestane was found to be better than toremifene or atamestane alone in vitro[2]. in vivo: The effect of this combination was then studied in vivo using Ac-1 xenografts grown in ovariectomized female SCID mice. The mice were injected with toremifene (1000μg/day), atamestane (1000μg/day), tamoxifen (100μg/day), or the combination of toremifene plus atamestane. In this study, our results indicate that the combination of toremifene plus atamestane was as effective as toremifene or tamoxifen alone but may not provide any additional benefit over toremifene alone or tamoxifen alone[2]. Clinical trial: Prostate cancer diagnosis among men with isolated high-grade intraepithelial neoplasia enrolled onto a 3-year prospective phase III clinical trial of oral toremifene[3]. |
托瑞米芬
Toremifene （订货以英文为准）
编号：T126260
CAS号：89778-26-7
分子式：C26H28CLNO
分子量：405.96
| 产品名称 | Toremifene |
| 中文名称 | 托瑞米芬 |
| CAS号 | 89778-26-7 |
| 分子式（M.F.） | C26H28CLNO |
| 分子量（M.W.） | 405.96 |
| 储存条件 | 避光;-20°C储存;充氩 |
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