Biochem/physiol Actions
Cell permeable: no
Reversible: no
Target Ki: 5-10 µM against phosphatidylcholine (PC)-specific phospholipase C
Product does not compete with ATP.
Primary Targetpc-specificphopholipase c
General description
Selective inhibitor of phosphatidylcholine-specific phospholipase C (PC-PLC) (Bacillus cereus, Ki = 5-10 µM). Does not inhibit (up to 50 µM) phosphatidylinositol-specific phospholipase C, phospholipase A2, and phospholipase D. Inhibitor of the sphingomyelinase activity. Also inhibits angiogenesis by preventing the synthesis of basement membrane (BM).
Selective inhibitor of phosphatidylcholine (PC)-specific phospholipase C (Ki = 5-10 µM). Does not inhibit phosphatidylinositol-specific phospholipase C, phospholipase A, or phospholipase D. Also reported to inhibit LPS-stimulated ERK activation via its inhibitory effect on PLC. Inhibits angiogenesis by preventing the synthesis of basement membrane.
Legal Information
CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany
Other Notes
Monick, M.M., et al. 1999. J. Immunol. 162, 3005.Lozanski, G., et al. 1997. Biochem. J.328, 271.Maragoudakis, M.E., et al. 1993. Kidney Int. 43, 147.Doppler, C., et al. 1992. AIDS Res. Human Retroviruses8, 245.Schutze, S., et al. 1992. Cell71, 765.Sauer, G., et al. 1990. Cancer Lett.53, 97.Muller-Decker, K. 1989. Biochem. Biophys. Res. Commun.162, 198.Amtmann, E., et al. 1987. Biochem. Pharmacol.36, 1545.Sauer, G., et al. 1984. Proc. Natl. Acad. Sci. USA81, 3263.
Packaging
5 mg in Plastic ampoule
Preparation Note
tissue culture media should be at neutral pH, since product is active only at or slightly below pH 7.0. The compound is inactive at pH 7.4 and above, and it is hydrolyzed below pH 6.0. HEPES buffer should not be used as it renders D609 toxic.
Reconstitution
Material is very labile once in solution (1.5 day half-life in tissue culture medium).
Warning
Toxicity: Standard Handling (A)
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