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JZP-361

Catalog No. T27703   CAS 1680193-80-9
Synonyms: JZP361, JZP 361

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.

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JZP-361 Chemical Structure
JZP-361, CAS 1680193-80-9
Pack Size Availability Price/USD Quantity
5 mg In stock $ 64.00
10 mg In stock $ 98.00
25 mg In stock $ 197.00
50 mg In stock $ 328.00
100 mg In stock $ 493.00
500 mg In stock $ 1,070.00
1 mL * 10 mM (in DMSO) In stock $ 70.00
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Purity: 99.41%
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Biological Description
Chemical Properties
Storage & Solubility Information
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 FAAH (human):7.24 μM, ABHD6 (human):1.79 μM, MAGL (human):46 nM, H1 receptor:6.81 (pA2)
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

Storage

Powder: -20°C for 3 years | In solvent: -80°C for 1 year

Solubility Information

Ethanol: 36.5 mg/mL (90.0 mM)

DMSO: 7.3 mg/mL (18.0 mM)

TargetMolReferences and Literature

1. Jayendra Z Patel, et al. Loratadine analogues as MAGL inhibitors. Bioorg Med Chem Lett. 2015 Apr 1;25(7):1436-42.

Related compound libraries

This product is contained In the following compound libraries:
Inhibitor Library Bioactive Compound Library Bioactive Compounds Library Max

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Keywords

JZP-361 1680193-80-9 Metabolism Lipase JZP361 JZP 361 inhibitor inhibit

 

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