(±)-(3R′,5S′,6E)-7-[3-(4-Fluorophenyl)-1-isopropylindol-2-yl]-3,5-dihydroxy-6-heptenoate, sodium Light yellow solid. PROTECT FROM LIGHT. PACKAGED UNDER INERT GAS. A synthetic HMG-CoA reductase inhibitor (IC50 = 40-100 nM for human liver microsomes) that acts as an anti-hypercholesterolemic agent. Decreases the basal MMP-1 levels in culture media of endothelial cells in a time- and dose-dependent manner. Inhibits the formation of TBA-reactive substances in Fe(II)-supported peroxidation of liposomes (IC50 = 12 µM). Purity: ≥98% by HPLC. RTECS MJ9675050, CAS 93957-55-2. Merck Index: 14, 4218 Ref.: Yamamoto, A., et al. 2001. J. Pharm. Pharmacol. 53, 227. Dansette, P.M., et al. 2000. Exp. Toxicol. Pathol. 52, 145. Ikeda, U., et al. 2000. Hypertension 36, 325. Levy, R.I., et al. 1993. Circulation 87 (4 Suppl.), III45. Tse, F.L.S. et al. 1992. J. Clin. Pharmacol. 32, 630. Yuan, J., et al. 1991. Atherosclerosis 87, 147. R: 61; S: 36/37/39-45 |