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FZ581

Chemical Structure : FZ581

CAS No.:

FZ581 (FZ-581)

Catalog No.: PC-27819Not For Human Use, Lab Use Only.

FZ581 is a potent, pan-species inhibitor of soluble epoxide hydrolase (sEH) N-terminal phosphatase domain (sEH-P, sEH NTD) with IC50 of 59 and 490 nM for human and mouse sEH NTD, shows little to no activity against full-length sEH protein (sEH FL).

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Purity & Documentation Purity: >98% (HPLC)

Biological Activity

FZ581 is a potent, pan-species inhibitor of soluble epoxide hydrolase (sEH) N-terminal phosphatase domain (sEH-P, sEH NTD) with IC50 of 59 and 490 nM for human and mouse sEH NTD, shows little to no activity against full-length sEH protein (sEH FL).
FZ581 shows high selectivity over the soluble epoxide hydrolase activity (sEH-H).
FZ581 does not exhibit significant binding toward other 9 tested phosphatases, as well as COX-1 and COX-2, lipid phosphate phosphatases (LPPs) LPP1-3.
FZ581 exhibits inhibitory activity across different species in vitro.
FZ581 shows dose-dependent inhibition of 1-oleyl monoacyl glycerol (sn1-18:1 MAG) formation through inhibition of recombinant mouse sEH.
FZ581 (1 mg/kg) demonstrated a significant increase of main sEH-P substrate levels without affecting plasma levels of sEH-H substrates in mice and rats.

Physicochemical Properties

M.Wt 466.67
Formula C14H12ClIN2O4S
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-chloro-2-((4-iodo-3-methylphenyl)amino)-5-sulfamoylbenzoic acid

References

1. Zhu WF, et al. ACS Chem Biol. 2026 Aug 21;21(8):2053-2067.

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