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Synonyms:
Org 214444-0
| 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 | Org 214444-0 is an orally active, highly potent, and selective agonist of FSHR, exhibiting EC50 values of 2.0 nM and 1.2 nM in human and rat (measured in CHO cells), respectively. It activates human granulosa cells in vitro, promotes follicular development in rats, and induces ovulation in vivo, supporting its use in infertility research. |
| Molecular Weight | 664.558 |
| Formula | C30H32BrF2N3O5S |
| Cas No. | 914093-78-0 |
| Smiles | C(#N)C=1[C@H](C2=C(C[C@H](CCC)CC2=O)NC1C)C3=CC(OCC)=C(OCC4=C(NS(C)(=O)=O)C=C(F)C(F)=C4)C(Br)=C3 |
| 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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