ChemicalBook--->CAS DataBase List--->1032008-74-4

1032008-74-4

1032008-74-4 Structure

1032008-74-4 Structure
IdentificationBack Directory
[Name]

Endoxifen HCl
[CAS]

1032008-74-4
[Synonyms]

CS-1633
Endoxifen HCl
Endoxifen Z-isomer HCl
Endoxifen (hydrochloride)
Endoxifen (Z-isomer hydrochloride)
4-[(Z)-1-[4-[2-(methylamino)ethoxy]phenyl]-2-phenylbut-1-enyl]phenol,hydrochloride
[Molecular Formula]

C25H28ClNO2
[MOL File]

1032008-74-4.mol
[Molecular Weight]

409.95
Chemical PropertiesBack Directory
[storage temp. ]

Store at -20°C
[solubility ]

DMSO: 12.5 mg/mL (30.49 mM); Water: < 0.1 mg/mL (insoluble)
[form ]

Solid
[color ]

White to off-white
Hazard InformationBack Directory
[Uses]

Endoxifen Z-isomer hydrochloride 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 [1] Target: hERG Potassium Channel, Estrogen Receptor/ERR Endoxifen 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. [1] Endoxifen is also shown to be a more potent inhibitor of estrogen target genes when ERβ is expressed. Additionally, low concentrations of Endoxifen 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 concentrations are needed when ERβ is absent.[2]
[Biological Activity]

Endoxifen Z-isomer hydrochloride, as the active metabolite of Tamoxifen, is a potent and selective estrogen receptor antagonist.
[target]

TargetValue
Estrogen receptor
[References]

[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. DOI:10.1016/j.ejphar.2015.01.048
[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. DOI:10.1186/bcr2844
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