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Synonyms:
Aromatase-IN-1
| 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 | Aromatase-IN-1 is a competitive inhibitor of aromatase (P450arom) with an IC50 of 40 nM and a Ki of 1.05 nM against human targets. It binds to the heme iron of aromatase via an imidazole nitrogen atom. Aromatase-IN-1 is applicable for studies related to breast cancer. |
| In vitro | Aromatase-IN-1 (Compound 22e) effectively inhibits human placental aromatase with an IC₅₀ of 0.040 μM and a Ki of 1.05 nM, achieving a 99% inhibition rate at 25 μM. At 2.5 μM, Aromatase-IN-1 only weakly inhibits human testicular P450 17, with an inhibition rate of 4%. |
| Molecular Weight | 321.29 |
| Formula | C17H11N3O4 |
| Cas No. | 331684-05-0 |
| Smiles | O=C1C=2C=CC=CC2OC=3C(=CC=C(C13)N(=O)=O)CN4C=NC=C4 |
| 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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