Biochem/physiol Actions
Target IC50: 3.7 µM against 5-lipoxygenase
Reversible: no
Product does not compete with ATP.
Primary Target5-lipoxygenase
Cell permeable: yes
General description
A natural dietary compound reported to have anti-carcinogenic and anti-inflammatory properties. A cell-permeable, selective, non-competitive inhibitor of 5-lipoxygenase (ID50 = 3.7 µM). Inhibits Cu2+-induced LDL oxidation in the initiation phase but acts as a prooxidant in the propagation phase. An irreversible inhibitor of glutathione S-transferases and a non-competitive inhibitor of xanthine oxidase.
A cell-permeable natural dietary compound reported to have anti-carcinogenic and anti-inflammatory properties. A selective, non-competitive inhibitor of 5-lipoxygenase (ID50 = 3.7 µM). Inhibits Cu2+-induced LDL oxidation in the initiation phase but acts as a prooxidant in the propagation phase. An effective irreversible inhibitor of glutathione S-transferases and a non-competitive inhibitor of xanthine oxidase.
Legal Information
CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany
Other Notes
Yamanaka, N., et al. 1997. FEBS Lett.405, 186.Chan, W.S., et al. 1995. Anticancer Res.15, 703.Ploemen, J.H., et al. 1993. Food Chem. Toxicol.31, 475.Koshihara, Y., et al. 1984. Biochim. Biophys. Acta792, 92.
Packaging
Packaged under inert gas
500 mg in Plastic ampoule
Reconstitution
Following reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 3 months at -20°C.
Warning
Toxicity: Carcinogenic / Teratogenic (D)
This product has met the following criteria: