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Tocris Bioscience™ JZP 361, >99%

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Kvantitet:
10 mg
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
| Kemiskt namn eller 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 |
| Kvantitet | 10 mg |
| Löslighet | Soluble to 100mM in DMSO and to 20mM in ethanol |
| Molekylformel | C22H20ClN5O |
| Formel vikt | 405.88 |
| Renhet | >99% |
| Molekylvikt (g/mol) | 405.886 |
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