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Synonyms:
ERβ agonist-2
| Pack Size | Price | USA Stock | Global Stock | Quantity |
|---|---|---|---|---|
| 10 mg | Inquiry | 10-14 weeks | 10-14 weeks | |
| 50 mg | Inquiry | 10-14 weeks | 10-14 weeks |
| Description | ERβagonist-2 (Page 72) is a selective ERβ agonist with an EC50 of 800 nM or less. This compound specifically inhibits the activation and/or proliferation of T cells, thereby reducing circulating T cell levels in subjects, without significantly affecting levels of circulating neutrophils, monocytes, or B cells. ERβagonist-2 is applicable in research on chronic heart failure post-myocardial infarction, graft-versus-host disease, multiple sclerosis, and experimental autoimmune encephalomyelitis. |
| Targets & IC50 | ERβ:< 800 nM (EC50) |
| In vitro | ERβ agonist-2 has an EC₅₀ of 800 nM or lower when acting on the estrogen receptor β (ERβ). |
| Molecular Weight | 304.34 |
| Formula | C19H16N2O2 |
| Cas No. | 628321-25-5 |
| Smiles | OC1=CC=C(C=C1)C=2C=3C=CC=CC3NC2C=4C(=NOC4C)C |
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year Shipping with blue ice/Shipping at ambient temperature. |
Dissolve 2 mg of the compound in 100 μL DMSO
to obtain a stock solution at a concentration of 20 mg/mL . If the required concentration exceeds the compound's known solubility, please contact us for technical support before proceeding.
1) Add 100 μL of the DMSO
stock solution to 400 µL PEG300
and mix thoroughly until the solution becomes clear.
2) Add 50 µL Tween 80 and mix well until fully clarified.
3) Add 450 µL Saline,PBS or ddH2O
and mix thoroughly until a homogeneous solution is obtained.
| Size | Quantity | Unit Price | Amount | Operation |
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