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48-602MAG
Buffer Detection Kit for Magnetic Beads
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530538
Sigma-AldrichcPLA2α Inhibitor II, Pyrrophenone - CAS 341973-06-6 - Calbiochem
A cell-permeable, highly potent, and reversible inhibitor of cytosolic phospholipase A2a (IC₅₀ = 4.2 nM).
More>>A cell-permeable, highly potent, and reversible inhibitor of cytosolic phospholipase A2a (IC₅₀ = 4.2 nM). Less<<
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Description
Overview
A cell-permeable, non-toxic, pyrolidine derivative that acts as a highly potent, and reversible inhibitor of cytosolic phospholipase A2a (cPLA2a; IC50 = 4.2 nM). Does not inhibit the activities of PLA IB and IIA groups even at higher concentrations (~250 µM). Unlike AACOCF3 (Cat. No. 100109), its action is shown to be rapid and does not require a pre-incubation period. Diminishes the release of arachidonic acid (IC50 = 24 nM), prostaglandin E2 (PGE2; IC50 = 25 nM) and leukotriene C4 (IC50 = 14 nM) in A23187 stimulated THP-1 cells. Its effects on production of PGE2 and thromboxane B2 are comparable to those of indomethacin. Also shown to inhibit the lysophospholipase and esterase activity of cPLA2&alpha.
Please note that the molecular weight for this compound is batch-specific due to variable water content.
Catalogue Number
530538
Brand Family
Calbiochem®
Synonyms
Phospholipase A2α Inhibitor
References
References
Ono, T., et al. 2002. Biochem. J.363, 727. Seno, K., et al. 2001. Bioorg. Med. Chem. Lett.11, 587.
Note that this data sheet is not lot-specific and is representative of the current specifications for this product. Please consult the vial label and the certificate of analysis for information on specific lots. Also note that shipping conditions may differ from storage conditions.
Revision
31-October-2014 JSW
Synonyms
Phospholipase A2α Inhibitor
Description
A cell-permeable, non-toxic, pyrolidine derivative that acts as a highly potent, and reversible inhibitor of cytosolic phospholipase A2a (cPLA2a; IC50 = 4.2 nM). Does not inhibit the activities of PLA IB and IIA groups even at higher concentrations (~250 µM). Unlike AACOCF3 (Cat. No. 100109), its action is shown to be rapid and does not require a pre-incubation period. Diminishes the release of arachidonic acid (IC50 = 24 nM), prostaglandin E2 (PGE2; IC50 = 25 nM) and leukotriene C4 (IC50 = 14 nM) in A23187 stimulated THP-1 cells. Its effects on production of PGE2 and thromboxane B2 are comparable to those of indomethacin. Also shown to inhibit the lysophospholipase and esterase activity of cPLA2&alpha.
Form
Off-white powder
Intert gas (Yes/No)
Packaged under inert gas
CAS number
341973-06-6
Chemical formula
C₄₉H₃₇F₂N₃O₅S₂
Purity
≥98% by HPLC
Solubility
DMSO (100 mg/ml)
Storage
Protect from light -20°C
Do Not Freeze
Ok to freeze
Special Instructions
Following reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 3 months at -20°C.
Toxicity
Standard Handling
References
Ono, T., et al. 2002. Biochem. J.363, 727. Seno, K., et al. 2001. Bioorg. Med. Chem. Lett.11, 587.
