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JJC8-088
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Catalog No. T86769Cas No. 1627576-82-2
JJC8-088, a potent DAT inhibitor, is derived from Modafinil and serves as a novel ligand. This compound is utilized in research on psychostimulant use disorders [1].
JJC8-088
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Catalog No. T86769Cas No. 1627576-82-2
JJC8-088, a potent DAT inhibitor, is derived from Modafinil and serves as a novel ligand. This compound is utilized in research on psychostimulant use disorders [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 |
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
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Product Introduction
Bioactivity
Chemical Properties
Storage & Solubility Information
| Description | JJC8-088, a potent DAT inhibitor, is derived from Modafinil and serves as a novel ligand. This compound is utilized in research on psychostimulant use disorders [1]. |
| Targets&IC50 | DAT:2.53 nM (Ki) |
| In vivo | JJC8-088, administered intraperitoneally at doses of 3-30 mg/kg for 30 to 120 minutes, effectively reduces compulsive methamphetamine self-administration in rats and enhances their locomotor activity [1]. Additionally, JJC8-088, given at 0-30 mg/kg intraperitoneally 30 minutes prior to testing, induces a rapid and significant increase in extracellular dopamine (DA) levels in rats with a history of cocaine self-administration [2]. Animal Model: Methamphetamine-addicted male Wistar rats (6-8 weeks old; weighing 200-250 g) [1]. Dosage: 0/3/10/30 mg/kg. Administration: intraperitoneal. Result: The half-life of JJC8-088 is 39 minutes, with low concentrations observed in both brain and plasma. |
| Molecular Weight | 498.63 |
| Formula | C28H32F2N2O2S |
| Cas No. | 1627576-82-2 |
| Smiles | C(S(CCN1CCN(CC(CC2=CC=CC=C2)O)CC1)=O)(C3=CC=C(F)C=C3)C4=CC=C(F)C=C4 |
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. |
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In Vivo Formulation Calculator (Clear solution)
Please enter your animal experiment information in the following box and click Calculate to obtain the stock solution preparation method and in vivo formula preparation method:
For example, if the intended dosage is 10 mg/kg for animals weighing 20 g , with a dosing volume of 100 μL per animal, and a total of 10 animals are to be administered, using a formulation of 
10% DMSO+ 40% PEG300+ 5% Tween 80+ 45% Saline/PBS/ddH2O , the resulting working solution concentration would be 2 mg/mL.Stock Solution Preparation:
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.
Preparation of the In Vivo Formulation:
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.
This example is provided solely to demonstrate the use of the In Vivo Formulation Calculator and does not constitute a recommended formulation for any specific compound. Please select an appropriate dissolution and formulation strategy based on your experimental model and route of administration.
Dose Conversion
You can also refer to dose conversion for different animals. More Dose Conversion
Tech Support
Please see Inhibitor Handling Instructions for more frequently ask questions. Topics include: how to prepare stock solutions, how to store products, and cautions on cell-based assays & animal experiments, etc
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