lovastatinMevinolin from Aspergillus sp.2-Methyl-1,2,3,7,8,8a-hexahydro-3,7-dimethyl-8-[2-(tetrahydro-4-hydroxy-6-oxo-2H-pyran-2-yl)ethyl]-1-naphthalenyl ester butanoic acid6-α-MethylcompactinMonacolin K
Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
保存温度
2-8°C
GHS危险品标识
急性毒性(口服,皮肤接触,吸入),类别4
皮肤刺激,类别2
眼刺激,类别2
皮肤过敏,类别1
特定目标器官毒性 -一次接触,类别3
产品相关信息
Empirical Formula (Hill Notation)
C24H36O5
产品质量级别
PREMIUM
纯度
≥98% (HPLC)
药理学性质
相关基因信息
human ... HMGCR(3156)rat ... Hmgcr(25675)
描述信息
Biochem/physiol Actions Lovastatin is a cholesterol lowering drug and competitive inhibitor of HMG-CoA reductase, a rate limiting enzyme in cholesterol synthesis. Blocks the production of mevalonate, a critical compound in the production of cholesterol and isoprenoids. This product is a substrate of Pgp and CYP3A. It increases cellular resistance to anticancer agents such as doxorubicin and induces apoptosis in myeloma cells. The roles of Pgp and CYP3A, possible connection between drug resistance, regulation of the mevalonate pathway, and iosprenylation of signaling proteins in these observations remain to be resolved. The product induces apoptosis in numerous cancer cell lines perhaps, in part, by inhibiting the isoprenylation of Rho family GTPases. It causes cell cycle arrest in G1 and G2/M phases.