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Synonyms:
L-797591 hydrochloride
| 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 | L-797591 hydrochloride is a selective sst1 agonist. It potently inhibits cAMP accumulation stimulated by Forskolin or CRH, mimicking the effects of SRIF-14 and SRIF-28. |
| In vitro | L-797591 hydrochloride (10^-7 M) inhibits Forskolin-induced cAMP accumulation in cortical neuron monolayers. Additionally, L-797591 hydrochloride (1 μM; 1 h) suppresses CRH-induced cAMP accumulation in E17-18 cortical neurons. |
| Molecular Weight | 644.29 |
| Formula | C38H50ClN5O2 |
| Cas No. | 3026641-74-4 |
| Smiles | C([C@@H](NC(N(CCC1=CC=CC=C1)CCC2=CC=CC=N2)=O)C(NCC(CC(CCN)C)(C)C)=O)C=3C4=C(C=CC3)C=CC=C4.Cl |
| 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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