Comparison

Estriol European Partner

€95.00
Excl. VAT
Item no. S2466-50
Manufacturer Selleckchem
CASRN 50-27-1
Amount 50 mg
Category
Type Inhibitors
Specific against other
ECLASS 10.1 32160490
ECLASS 11.0 32160490
UNSPSC 12000000
Alias NSC-12169, GPR30;Estrogen/progestogen Receptor
Similar products Estriol
Available
Administration
Administrated via s.c.
Animal Models
mPTEN+/- and wild-type mice
Cell lines
SkBr3 cells
Clinical Trials
Estriol is currently under investigation in Phase I clinical trials, dealing with the vaginal environment of pre-menopausal women.
Concentrations
ca.100 nM
Description
Estriol is an antagonist of the G-protein coupled estrogen receptor in estrogen receptor-negative breast cancer cells.
Dosages
4 ug/g/day
Formulation
Estriol is dissolved in ethanol and corn oil.
In vitro
MTT assays using G-1 shows that, in SkBr3 cells, the proliferative effect induced by 100 nM G-1 is abolished in the presence of 1 uM estriol which acts as an antagonist of GPR30-dependent pathway. [1], A cell-free transcription assay demonstrates that the antiestrogenic activity exhibited by estriol is because of interferring with estradiol-induced positive cooperative binding and receptor dimerization, , binding of hER complexes to ERE, as well as reducing estradiol-dependent transcription in a dose-dependent manner. [2], A recent study shows that estrogen (estrone, estradiol, and estriol) inhibits Alzheimer's disease-associated low-order Abeta oligomer formation, and among them, estriol shows the strongest in vitro activity. [3]
In vivo
In mPTEN+/- mice, estriol treatments resulted in a 187.54% gain in the relative ratio of uterine wet weight to body weight, , estriol also increases the ratio to 176.88% in wild-type mice. [4], Estriol treatment (20 mg/kg ip), in vivo, sensitizes Kupffer cells to LPS via mechanisms dependent on an increase in CD14 by elevated portal blood endotoxin caused by increased gut permeability in rats, while one-half of the rats given estriol intraperitoneally 24 hours before an injection of a sublethal dose of LPS (5 mg/kg) died within 24 hours. [5]
Incubation Time
6 days
Method
For the 3-(4, 5-dimethylthiazol-2-yl)-2, 5-diphenyltetrazolium bromide (MTT) assay, cells are cultured in plastic 96-well plates under 200 uL of growth medium and at an initial density of 10, 000 cells per well. Cells are washed once they have attached and further incubated in medium containing 2.5% charcoal-stripped FBS with the indicated treatment. The medium is changed every 2 days (with treatment). Where applicable, 200 ng of the indicated plasmids are transfected every 2 days before treatments using Fugene6 Reagent, as recommended by the manufacturer. Following 6 days of incubation, the assay mixture (10uL per well) containing 1mg/mL 3-(4, 5-dimethylthiazol-2-yl)-2, 5-diphenyltetrazolium bromide (MTT) is added to each well and incubated, at 37 C for 4 h in a 5% CO2 atmosphere. The yellow tetrazolium MTT, reduced by metabolically active cells, results in intracellular purple formazan, which is released after overnight incubation with 200 uL 1% sodium dodecyl sulfate in 0.01N HCL and quantified spectrophotometrically by reading absorbance at 570nm using an enzyme-linked immunosorbent assay plate reader.
Molecular Weight (MW)
288, 39
Picture ChemicalStructure Description
Estriol Chemical Structure
Solubility (25C)
DMSO 57 mg/mL, Water <1 mg/mL, Ethanol 10 mg/mL
Storage
2 years -20CPowder, 2 weeks4Cin DMSO, 2 months-80Cin DMSO

Note: The presented information and documents (Manual, Product Datasheet, Safety Datasheet and Certificate of Analysis) correspond to our latest update and should serve for orientational purpose only. We do not guarantee the topicality. We would kindly ask you to make a request for specific requirements, if necessary.

All products are intended for research use only (RUO). Not for human, veterinary or therapeutic use.

Amount: 50 mg
Available: In stock
Listprice: €95.00
Price: €95.00
available

Delivery expected until 8/28/2025 

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