JZP-MA-13 is a selective alpha/beta-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].
Molecular Weight:
338.36
CAS Number:
[3034900-00-7]
Formula:
C14H15FN4O3S
Target:
MAGL
Application Notes:
MCE Product type: Reference compound
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