5,6,7-Trihydroxyflavone Yellow solid. A cell-permeable flavone that inhibits the activity of 12-lipoxygenase (IC50 = 120 nM) and reverse transcriptase. Protects cortical neurons from b-amyloid induced toxicity. Reduces leukotriene biosynthesis and inhibits the release of lysosomal enzymes. Also inhibits cellular Ca2+ uptake and mobilization, and adjuvant-induced arthritis. Reported to inhibit microsomal lipid peroxidation by forming an iron-baicalein complex. Inhibits topoisomerase II and induces cell death in hepatocellular carcinoma cell lines. Potentiates contractile responses to nerve stimulation. Inhibits protein tyrosine kinase and PMA-stimulated protein kinase C. Purity: ≥98% by TLC. CAS 491-67-8. Merck Index: 14, 942 Ref.: Leabeau, A., et al. 2001. Neuroreport 12, 2199. Gao, D., et al. 1996. Biochem. Mol. Biol. Int. 39, 215. Matsuzaki, Y., et al. 1996. Jpn. J. Cancer Res. 87, 170. Huang, H.C., et al. 1994. Eur. J. Pharmacol. 268, 73. Butenko, I.G., et al. 1993. Agents Actions 39, C49. Abe, K., et al. 1990. Chem. Pharm. Bull. 38, 209. Kimura, Y., et al. 1987. Biochim. Biophys. Acta 922, 278. Sekiya, K., and Okuda, H. 1982. Biochem. Biophys. Res. Commun. 105, 1090. R: 36/37/38; S: 26-36 |