上海源葉生物科技有限公司

主營(yíng)產(chǎn)品: S30260異硫氰酸胍,30259鹽酸胍,嗜熱菌蛋白酶

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15921386130

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聯(lián)人:
何小姐
話:
86-021-61559134
機(jī):
15921386130
真:
86-021-55068248
址:
上海市松江區(qū)長(zhǎng)塔路465號(hào)6幢
編:
200433
網(wǎng)址:
www.shyuanye.com
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http://true-witness.com/st191837/
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S80104
S80104
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更新時(shí)間:2024-07-03 21:35:13瀏覽次數(shù):133

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  • 產(chǎn)品描述: Endoxifen Z-isomer is the most important Tamoxifen metabolite responsible for eliciting the anti-estrogenic effects of this drug in breast cancer cells expressing estrogen receptor-alpha (ERα). Endoxifen inhibits hERG tail currents at 50 mV in a concentration-dependent manner with IC50 values of 1.6 μM. IC50 value: 1.6 μM Target: hERG Potassium Channel, Estrogen Receptor/ERR Endoxifen Z-isomer is considered a prodrug, since it has a much higher potency for the estrogen receptor than its parent drug. Endoxifen inhibits the hERG channel protein trafficking to the plasma membrane in a concentration-dependent manner with Endoxifen being more potent than Tamoxifen. Endoxifen is also shown to be a more potent inhibitor of estrogen target genes when ERβ is expressed. Additionally, low concentrations of Endoxifen Z-isomer observed in Tamoxifen treated patients with deficient CYP2D6 activity (20 to 40 nM) markedly inhibit estrogen-induced cell proliferation rates in the presence of ERβ, whereas much higher Endoxifen Z-isomer concentrations are needed when ERβ is absent.
  • 靶點(diǎn): Estrogen Receptor/ERR;Potassium Channel
  • 參考文獻(xiàn):
    1. Chae YJ, et al. Endoxifen, the active metabolite of tamoxifen, inhibits cloned hERG potassium channels. Eur J Pharmacol. 2015 Apr 5;752:1-7. 2. Wu X, et al. Estrogen receptor-beta sensitizes breast cancer cells to the anti-estrogenic actions of endoxifen. Breast Cancer Res. 2011 Mar 10;13(2):R27.
  • 溶解度: Soluble  in  DMSO
  • 保存條件: 2-8℃,避光
  • 配置溶液濃度參考:
    1mg 5mg 10mg
    1 mM 2.677 ml 13.387 ml 26.775 ml
    5 mM 0.535 ml 2.677 ml 5.355 ml
    10 mM 0.268 ml 1.339 ml 2.677 ml
    50 mM 0.054 ml 0.268 ml 0.535 ml
  • 注意:部分產(chǎn)品我司僅能提供部分信息,我司不保證所提供信息的性,僅供客戶參考交流研究之用。
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