Toremifene (Z-Toremifene) is a second-generation selectiveestrogen-receptor modulator (SERM)in development for the prevention of osteoporosis. Toremifene also potent inhibits infectiousEBOV ZaireandMarburg (MARV)withIC₅₀of 0.07 μM and 2.6 μM, respectively^[1][2].

Toremifene is a second-generation selective estrogen-receptor modulator (SERM) in development for the prevention of osteoporosis and other adverse effects resulting from ADT with prostate cancer^[1].
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^[3].

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^[3].

405.96

C₂₆H₂₈ClNO

89778-26-7

托瑞米芬；涛瑞米芬

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