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Synonyms:

| 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 | GRK2 modulator 1 is an orally active, brain-penetrant, and selective GRK2 modulator that promotes the active, non-phosphorylated form of GRK2 and prevents aggregation of mitochondrial GRK2 and TOMM6. It enhances non-amyloidogenic APP processing, inhibits PHF-tau, neurodegeneration, and neuronal loss, reduces the senescence marker UPAR, lowers Alzheimer disease (AD)-related mortality, prolongs survival, exerts neuroprotective effects through HDAC6 inhibition, and counteracts age-related cardiac dysfunction for Alzheimer disease (AD) research. |
| Molecular Weight | 363.363 |
| Formula | C21H17NO5 |
| Cas No. | 2234900-83-3 |
| Smiles | O=C1C(C(=O)C2CC2)=C(O)C(C=3C=CC=CC3)N1C4=CC=C5OCOC5=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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