• 咨询热线
    客服服务热线 13671568941/15317326293
  • 在线咨询
  • 微信客服
    微信客服
  • 公众号
    扫码关注公众号

Toremifene

CAS No. 89778-26-7

Toremifene ( NK 622 | FC 1157a )

产品货号. M16456 CAS No. 89778-26-7

托瑞米芬(NK 622;FC 1157a)是第二代选择性雌激素受体调节剂(SERM),正在开发用于预防骨质疏松症。

纯度: >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
规格 价格/人民币 库存 数量
10MG ¥309 有现货
25MG ¥441 有现货
100MG 获取报价 有现货
200MG 获取报价 有现货
500MG 获取报价 有现货
1G 获取报价 有现货

生物学信息

  • 产品名称
    Toremifene
  • 注意事项
    本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
  • 产品简述
    托瑞米芬(NK 622;FC 1157a)是第二代选择性雌激素受体调节剂(SERM),正在开发用于预防骨质疏松症。
  • 产品描述
    Toremifene (NK 622; FC 1157a) is a second-generation selective estrogen-receptor modulator (SERM) in development for the prevention of osteoporosis.(In Vitro):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.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.(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.
  • 体外实验
    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. 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.
  • 体内实验
    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.
  • 同义词
    NK 622 | FC 1157a
  • 通路
    Endocrinology/Hormones
  • 靶点
    Estrogen Receptor/ERR
  • 受体
    ER
  • 研究领域
    Cancer
  • 适应症
    ——

化学信息

  • CAS Number
    89778-26-7
  • 分子量
    405.96
  • 分子式
    C26H28ClNO
  • 纯度
    >98% (HPLC)
  • 溶解度
    Soluble in DMSO
  • SMILES
    CN(C)CCOC1=CC=C(C=C1)/C(=C(/CCCl)\C2=CC=CC=C2)/C3=CC=CC=C3
  • 化学全称
    ——

运输与储存

  • 储存条件
    (-20℃)
  • 运输条件
    With Ice Pack
  • 稳定性
    ≥ 2 years

参考文献

1.Locci P, et al. J Interferon Cytokine Res. 2001 Nov;21(11):961-70.
产品手册
关联产品
  • LY88074

    LY88074 (Compound 88074) 是缺少基本侧链的 Raloxifene 类似物。Raloxifene 是一种选择性的雌激素受体调节剂,至少部分地通过不依赖细胞和雌激素受体的方式改善骨骼的机械特性来降低骨折风险。

  • Gestodene

    Gestodene(SHB 331;WL 70)是一种孕激素避孕药。

  • (E/Z)-GSK5182?

    (E/Z)-GSK5182 是 (E)-GSK5182 和 (Z)-GSK5182 异构体的外消旋化合物。