Powder: -20°C for 3 years
In solvent: -80°C for 2 years
JZP-361 is a specific MAGL inhibitor with IC50s of 46 nM, 7.24 μM, and 1.79 μM for human recombinant MAGL, human recombinant FAAH, and human hABHD6. JZP-361 displays anti-histaminergic activities. JZP-361 can be used in studies about asthma.
Description | JZP-361 is a specific MAGL inhibitor with IC50s of 46 nM, 7.24 μM, and 1.79 μM for human recombinant MAGL, human recombinant FAAH, and human hABHD6. JZP-361 displays anti-histaminergic activities. JZP-361 can be used in studies about asthma. |
Targets&IC50 | H1 Receptor:6.81 (pA2), hMAGL:46 nM, hABHD6:1.79 μM, hFAAH:7.24 μM |
In vitro | JZP-361 shows the affinity of H1 antagonistic with a pA2 of 6.81). JZP-361(≤10 μM) does not show cannabinoid receptor activity. JZP-361 displays favorable interactions within the important hydrogen-bonding of the carbonyl oxygen to the oxyanion hole[1]. |
Synonyms | JZP361, JZP 361 |
Molecular Weight | 405.88 |
Formula | C22H20ClN5O |
CAS No. | 1680193-80-9 |
Powder: -20°C for 3 years
In solvent: -80°C for 2 years
Ethanol: 36.5 mg/mL (90.0 mM)
DMSO: 7.3 mg/mL (18.0 mM)
( < 1 mg/ml refers to the product slightly soluble or insoluble )
You can also refer to dose conversion for different animals. More
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JZP-361 1680193-80-9 Metabolism Lipase JZP361 JZP 361 Inhibitor inhibitor inhibit