| 貨號(hào) | 規(guī)格 | 價(jià)格 | 上海 | 北京 | 武漢 | 南京 | 購(gòu)買(mǎi)數(shù)量 |
|---|---|---|---|---|---|---|---|
| S82289-1mg | 98% | ￥200.00 | 8 | - | - | - |
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| S82289-2mg | 98% | ￥300.00 | 8 | - | - | - |
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| S82289-5mg | 98% | ￥490.00 | 8 | - | - | - |
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| S82289-10mg | 98% | ￥790.00 | 6 | - | - | - |
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| S82289-25mg | 98% | ￥1590.00 | 5 | - | - | - |
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| S82289-50mg | 98% | ￥2590.00 | 貨期：2-3天 | - | - | - |
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Endoxifen E-isomer hydrochloride (E-Endoxifen hydrochloride), an E-isomer of Endoxifen, is an impurity in Endoxifen Z-isomer agent substance. Endoxifen E-isomer hydrochloride exhibits antiestrogenic effects
| 產(chǎn)品描述： | Endoxifen E-isomer hydrochloride (E-Endoxifen hydrochloride), an E-isomer of Endoxifen, is an impurity in Endoxifen Z-isomer agent substance. Endoxifen E-isomer hydrochloride exhibits antiestrogenic effects | ||||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 靶點(diǎn)： | Estrogen Receptor/ERR;EstrogenReceptor/ERR;?Estrogen/progestogenReceptor | ||||||||||||||||||||
| 體外研究： | Endoxifen E-isomer (1-1000 nM; 12 h) inhibits PGR gene expression in E2-induced MCF-7 cells | ||||||||||||||||||||
| 參考文獻(xiàn)： | 1. Elkins P, et, al. Characterization of the isomeric configuration and impurities of (Z)-endoxifen by 2D NMR, high resolution LC?MS, and quantitative HPLC analysis. J Pharm Biomed Anal. 2014 Jan;88:174-9. 2. Zheng Y, et, al. Elimination of antiestrogenic effects of active tamoxifen metabolites by glucuronidation. Drug Metab Dispos. 2007 Oct;35(10):1942-8. | ||||||||||||||||||||
| 溶解性： | soluble in DMSO | ||||||||||||||||||||
| 保存條件： | -20℃ | ||||||||||||||||||||
| 配置溶液濃度參考： |
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| 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權(quán)威性，僅供客戶參考交流研究之用。 |
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