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Tamoxifen

Cat. No. M7353

All AbMole products are for research use only, cannot be used for human consumption.

Tamoxifen Structure
Synonym:

ICI47699; Z-Tamoxifen; trans-Tamoxifen

Size Price Availability Quantity
Free Sample (0.5-1 mg)  USD 0 In stock
100mg USD 25 In stock
200mg USD 35 In stock
500mg USD 60 In stock
1g USD 80 In stock
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Quality Control & Documentation
Biological Activity

Tamoxifen is an orally active, selective estrogen receptor partial agonist/antagonist. Tamoxifen is a potent Hsp90 activator and enhances the Hsp90 molecular chaperone ATPase activity. Tamoxifen also potent inhibits infectious EBOV Zaire and Marburg (MARV) with IC50 of 0.1 µM and 1.8 µM, respectively. Tamoxifen exhibits antiestrogenic effects in mammary tissue and estrogen-like effects in bone. Tamoxifen activates autophagy and induces apoptosis. Tamoxifen also can induce gene knockout of CreER(T2) transgenic mouse.

Product Citations
Protocol (for reference only)
Cell Experiment
Cell lines MCF-7 and T47D cells
Preparation method TamR cells were produced by 12-month treatment of MCF-7 and T47D cells with 4-hydroxytamoxifen (Tamoxifen, 5 μM). All cells were incubated at 37 °C with 5% CO2 in a humidified incubator.
Concentrations 5 μM
Incubation time 12 month
Animal Experiment
Animal models C57BL/6 J mice
Formulation Sunflower oil
Dosages 1 mg of tamoxifen in oil/25 g body weight, or 4 mg of tamoxifen in oil per 25 g body weight
Administration Intraperitoneal (IP) injection
Chemical Information
Molecular Weight 371.51
Formula C26H29NO
CAS Number 10540-29-1
Solubility (25°C) DMSO 30 mg/mL
Ethanol 40 mg/mL
Storage -20°C, protect from light
References

[1] Susanne Feil, et al. Methods Mol Biol. Inducible Cre mice

[2] Forbes, et al. J Med Chem. N-(1-Methyl-5-indolyl)-N'-(3-pyridyl)urea hydrochloride: the first selective 5-HT1C receptor antagonist.

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Keywords: Tamoxifen, ICI47699; Z-Tamoxifen; trans-Tamoxifen supplier, Estrogen Receptor, inhibitors, activators

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