A cell permeable acetylpiperazine derivative that acts as a selective and reversible inhibitor of lysophopholipase 2 (LYPLA2; IC50 = 510 nM, Ki = 230 nM) without affecting the activity of LYPLA1 and 25 other serine hydrolases in mouse BW5147 T cell hydridoma proteome. Shown to cause an almost complete inhibition (+90%) of LYPLA2 activity in lung, heart, and kidney (50 mg/kg, 3 h), and in HEK293T, and mouse T cells (~ 5 µM for 3 h).
A cell permeable, selective, and reversisble inhibitor of lysophopholipase 2 (LYPLA2; IC₅₀ = 510 nM, Ki = 230 nM). Does not affect LYPLA1.
Biochem/physiol Actions
Cell permeable: yes
Primary Target APT2
Warning
Toxicity: Standard Handling (A)
Reconstitution
Following reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 3 months at -20°C.
Other Notes
Adibekian, A., et al. 2012. J. Am. Chem. Soc.134, 10345.
Legal Information
CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany
Storage Class
11 - Combustible Solids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
Certificates of Analysis (COA)
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