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JZP 361, >99%, Tocris Bioscience™
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Quantity:
10mg
50 mg
Description
Potent and selective reversible MAGL inhibitor (IC50 = 46 nM). Exhibits 35-fold and 150-fold higher selectivity over human FAAH and ABHD6, respectively (IC50 values are 1.79 and 7.24 μM, respectively). Displays affinity for H1 receptors (pA2 = 6.81). Exhibits no activity at cannabinoid receptors at 10 μM.
Specifications
Specifications
Chemical Name or Material | [4-(8-Chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)-1-piperidinyl](1H-1,2,4- |
CAS | 1680193-80-9 |
Purity Grade Notes | >99% |
Molecular Formula | C22H20ClN5O |
Linear Formula | C22H20ClN5O |
Quantity | 10mg |
Synonym | 4-8-chloro-5,6-dihydro-11h-benzo 5,6 cyclohepta 1,2-b pyridin-11-ylidene-1-piperidinyl 1h-1,2,4-triazol-1-yl methanone |
Solubility Information | Soluble to 100mM in DMSO and to 20mM in ethanol |
InChI Key | GAVZCGTYRWKKDV-UHFFFAOYSA-N |
SMILES | C1CC2=C(C=CC(=C2)Cl)C(=C3CCN(CC3)C(=O)N4C=NC=N4)C5=C1C=CC=N5 |
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