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Bazedoxifene

SKU: orb3027356

Description

Bazedoxifene is a non-steroidal, orally active selective estrogen receptor modulator that exhibits activity against ERα and ERβ with IC50 values of 26 nM and 99 nM, respectively. Bazedoxifene also inhibits IL-6/GP130 protein interactions. Bazedoxifene is utilized in research on postmenopausal osteoporosis and pancreatic cancer, serving as a dual-purpose compound for hormonal and cytokine pathway investigations.

Research Area

Immunology & Inflammation, Metabolism Research

Images & Validation

Key Properties

CAS Number198481-32-2
MW470.61
Purity98.79%
FormulaC30H34N2O3
SMILESOC=1C=CC(=CC1)C2=C(C3=CC(O)=CC=C3N2CC4=CC=C(OCCN5CCCCCC5)C=C4)C
TargetOthers,Estrogen/progestogen Receptor,IL Receptor,Estrogen Receptor/ERR
SolubilityDMSO:80 mg/mL (169.99 mM);10% DMSO+40% PEG300+5% Tween-80+45% Saline:3.3 mg/mL (7.01 mM)

Bioactivity

Target IC50
ERα:26 nM|ERβ:99 nM
In Vivo
In the Capan-1 and HPAF-II pancreatic carcinoma xenograft models in mice, Bazedoxifene (5mg/kg/d, administered continuously for 18 days) significantly inhibited tumor growth and induced tumor cell apoptosis. The effect was more pronounced when used in combination with chemotherapeutic agents .
In Vitro
In PANC-1, AsPC-1, and HPAF-II pancreatic carcinoma cells, Bazedoxifene (5-20μM, 2 hours) can inhibit IL-6 and IL-11-induced STAT3 phosphorylation in a dose-dependent manner .

Storage & Handling

Storagestore at low temperature | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Expiration Date12 months from date of receipt.
DisclaimerFor research use only

Alternative Names

Bazedoxifene, TSE424, TSE-424

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Bazedoxifene (orb3027356)

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% DMSO +
%+
% Tween 80 +
%

Available Sizes

Select a size below

1 mg
$ 80.00
1 ml x 10 mM (in DMSO)
$ 130.00
5 mg
$ 130.00
10 mg
$ 170.00
25 mg
$ 280.00
50 mg
$ 360.00
100 mg
$ 540.00
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