About 5 results found for searched term "Endoxifen" (0.066 seconds)
| Cat.No. | Name | Target |
|---|---|---|
| M6710 | Endoxifen Z-isomer hydrochloride | Estrogen Receptor |
| Endoxifen Z-isomer HCl | ||
| Endoxifen Z-isomer hydrochloride is a Tamoxifen metabolite and a potent estrogen receptor (ER) antagonist that concentration-dependently inhibits hERG with an IC50 value of 1.6 μM. | ||
| M9796 | Endoxifen E-isomer hydrochloride | Estrogen Receptor |
| Endoxifen E-isomer HCl | ||
| Endoxifen E-isomer hydrochloride is a tamoxifen metabolite and potent Selective Estrogen Response Modifier (SERM). | ||
| M22285 | Endoxifen hydrochloride | Estrogen Receptor |
| Endoxifen hydrochloride is a key active metabolite of Tamoxifen and an estrogen receptor (ER) modulator with high affinity and specificity for the estrogen receptor and inhibits aromatase activity.Endoxifen hydrochloride has been used in studies related to breast cancer, sclerofibroblastoma, and bipolar disorder. Research. | ||
| M22289 | Endoxifen | Estrogen Receptor |
| Endoxifen is the key active metabolite of Tamoxifen and an estrogen receptor (ER) modulator with high affinity and specificity for the estrogen receptor and inhibits aromatase activity.Endoxifen has been used in studies related to breast cancer, sclerofibroblastoma, and bipolar disorder. | ||
| M27811 | Endoxifen (Z-isomer) | Estrogen Receptor |
| 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. | ||
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