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Estriol is a G-protein coupled estrogen receptor antagonist. It is one of the three main estrogens produced by the human body. It can be a weak or strong estrogen depending on if it is given acutely or chronically when given to immature animals, but is an antagonist when given in combination with estradiol. It may play a role in the development of breast cancer, but based on in vitro research does appear to act as an antagonist to the G-protein coupled estrogen receptor
Expert Opin Ther Targets. 2020 Apr;24(4):389-402.
Cepharanthine hydrochloride induces mitophagy targeting GPR30 in hepatocellular carcinoma (HCC)
Estriol purchased from AbMole
| Cell Experiment | |
|---|---|
| Cell lines | SkBr3 cells |
| Preparation method | For the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay, culturing cells in 96-well plates under 200 μL of growth medium and at an initial density of 10,000 cells per well. Washing cells once they have attached and further incubated in medium which contains 2.5% charcoal-stripped FBS with the indicated treatment. Changing the medium every 2 days (with treatment). Where applicable,transfecting 200 ng of the indicated plasmids every 2 days before treatments using Fugene6 Reagent, as recommended by the manufacturer. Following 6 days of incubation, adding the assay mixture (10µL per well) which contains 1mg/mL 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) 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 µL 1% sodium dodecyl sulfate in 0.01N HCL and quantified spectrophotometrically by reading absorbance at 570nm using an enzyme-linked immunosorbent assay plate reader. |
| Concentrations | ~100 nM |
| Incubation time | 6 days |
| Animal Experiment | |
|---|---|
| Animal models | mPTEN+/- and wild-type mice |
| Formulation | Estriol is dissolved in ethanol and corn oil. |
| Dosages | 4 μg/g/day |
| Administration | Administrated via s.c.SkBr3 细胞 |
| Molecular Weight | 288.39 |
| Formula | C18H24O3 |
| CAS Number | 50-27-1 |
| Solubility (25°C) | DMSO 45 mg/mL |
| Storage |
Powder -20°C 3 years ; 4°C 2 years In solvent -80°C 6 months ; -20°C 1 month |
[1] M Taylor. Unconventional estrogens: estriol, biest, and triest
[2] G P Vooijs, et al. Review of the endometrial safety during intravaginal treatment with estriol
| Related Estrogen Receptor Products |
|---|
| Fulvestrant
Fulvestrant is a Estrogen receptor (ER) antagonist with IC50 of 0.094 nM. Fulvestrant can also induce autophagy and apoptosis, and has anti-tumor effect. |
| LY500307
LY500307 is a potent, selective estrogen receptor beta agonist with an EC50 of 0.66 nM. |
| Calcitriol
Calcitriol is an Active metabolite of vitamin D3 that activates the vitamin D receptor. *The compound is unstable in solutions, freshly prepared is recommended |
| Tamoxifen Citrate (ICI 46474)
Tamoxifen Citrate is an antagonist of the estrogen receptor by competitive inhibition of estrogen binding. |
| 20-Hydroxyecdysone
20-Hydroxyecdysone (Ecdysterone, 20E) is a naturally occurring ecdysteroid hormone which controls the ecdysis (moulting) and metamorphosis of arthropods. |
All AbMole products are for research use only, cannot be used for human consumption or veterinary use. We do not provide products or services to individuals. Please comply with the intended use and do not use AbMole products for any other purpose.
Products are for research use only. Not for human use. We do not sell to patients.
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