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SCD1-IN-1, a potent inhibitor of SCD1 (IC50: 5.8 nM), is valuable in dermatologic research [1].

| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 25 mg | $1,520 | 6-8 weeks | 6-8 weeks | |
| 50 mg | $1,980 | 6-8 weeks | 6-8 weeks | |
| 100 mg | $2,500 | 6-8 weeks | 6-8 weeks |
| Description | SCD1-IN-1, a potent inhibitor of SCD1 (IC50: 5.8 nM), is valuable in dermatologic research [1]. |
| In vitro | SCD1-IN-1 (compound I, 6 days) effectively inhibits SCD1 enzyme activity in intact human cells, with an IC50 of 6.8 nM [1]. |
| In vivo | SCD1-IN-1 (compound I, 1.5% w/v, 25 μL), applied to the ventral surfaces of both ears of the hamster ear model [1] at a dosage of 1.5% in a vehicle of propylene glycol/transcutanol/ethanol (20/20/60, w/v, 25 μL), twice daily for two weeks, significantly reduces cholesterol ester (CE) and wax ester (WE) production by 62% and 82%, respectively, indicating its effectiveness in modulating sebum production and sebaceous gland size in this model. |
| Molecular Weight | 395.37 |
| Formula | C20H20F3NO4 |
| Cas No. | 1111078-63-7 |
| Smiles | O(C1=C(C(F)(F)F)C=CC=C1)[C@@H]2CN(C(COC3=CC=C(CO)C=C3)=O)CC2 |
| 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.
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