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UCB-J is a radioligand for the synaptic vesicle protein 2A (SV2A), utilized in positron emission tomography (PET)[4].


| Description | UCB-J is a radioligand for the synaptic vesicle protein 2A (SV2A), utilized in positron emission tomography (PET)[4]. |
| In vivo | UCB-J demonstrates a significant unbound fraction (0.46 ± 0.02) and undergoes moderate metabolic rates in plasma, with 39% ± 5% and 24% ± 3% of the parent compound remaining after 30 and 90 minutes, respectively[3]. This compound also exhibits substantial uptake and rapid kinetics within the monkey brain[3]. Notably, pretreatment of an animal with UCB-J (150 μg/kg, iv) results in a reduction of the whole brain Standard Uptake Value (SUV) to levels comparable to those of the centrum semiovale, thereby highlighting [18F]7's in vivo binding specificity towards SV2A[4]. |
| Molecular Weight | 320.315 |
| Formula | C17H15F3N2O |
| Cas No. | 1604786-87-9 |
| Smiles | Cc1cnccc1CN1CC(CC1=O)c1cc(F)c(F)c(F)c1 |
| Relative Density. | no data available |
| 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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