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JZL195

Chemical Structure : JZL195

CAS No.: 1210004-12-8

JZL195 (JJKK-004, JZL 195)

Catalog No.: PC-20487Not For Human Use, Lab Use Only.

JZL195 (JJKK-004) is a potent, selective dual fatty acid amide hydrolase (FAAH) and monoacylglycerol lipase (MAGL) inhibitor with IC50s of 2 and 4 nM, respectively.

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Purity & Documentation Purity: >98% (HPLC) Select Batch:

Biological Activity

JZL195 (JJKK-004) is a potent, selective dual fatty acid amide hydrolase (FAAH) and monoacylglycerol lipase (MAGL) inhibitor with IC50s of 2 and 4 nM, respectively.
JZL195 produces near-complete blockade of FP-Rh labeling of both mouse brain FAAH and MAGL with IC50 of 13 and 19 nM, respectively.
JZL195 inhibits rat and human FAAH and MAGL enzymes with IC50 values in the range of 10-100 nM based on competitive ABPP assays.
JZL195 (20 mg/kg; i.p.) produces an antinociceptive response in the tail immersion assays.

Physicochemical Properties

M.Wt 433.46
Formula C24H23N3O5
Appearance Solid
CAS No.
Storage
Solide Powder
-20°C 12 Months; 4°C 6 Months
In Solvent
-80°C 6 Months; -20°C 6 Months
Shipping
Solubility

10 mM in DMSO

Chemical Name/SMILES

4-nitrophenyl 4-(3-phenoxybenzyl)piperazine-1-carboxylate

References

1. Long JZ, et al. Proc Natl Acad Sci U S A. 2009 Dec 1;106(48):20270-5.

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