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JZP-MA-13

JZP-MA-13 is a selective α/β-hydrolase domain 6 (ABHD6) inhibitor with an IC50 of 392 nM. JZP-MA-13 shows no inhibition of MAGL, ABHD12, FAAH, or other serine hydrolases. JZP-MA-13 is a positron emission tomography (PET) ligand for in vivo imaging of the ABHD6[1].

Product Specifications

CAS Number

3034900-00-7

UNSPSC

12352005

Target

MAGL

Type

Reference compound

Related Pathways

Metabolic Enzyme/Protease

Applications

Neuroscience-Neuromodulation

Field of Research

Neurological Disease

Assay Protocol

https://www.medchemexpress.com/jzp-ma-13.html

Solubility

10 mM in DMSO

Smiles

FC1=CC=C(C=C1)N(C)C(OC2=NSN=C2N3CCOCC3)=O

Molecular Formula

C14H15FN4O3S

Molecular Weight

338.36

References & Citations

[1]Karine Mardon, et al. Utilizing PET and MALDI Imaging for Discovery of a Targeted Probe for Brain Endocannabinoid α/ β-Hydrolase Domain 6 (ABHD6) . J Med Chem. 2022 Dec 14.

Shipping Conditions

Room temperature

Scientific Category

Reference compound1

Clinical Information

No Development Reported

Frequently Asked Questions

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