Pyripyropene A

Pyripyropene A is an orally active, potent and selective sterol O-acyltransferase 2 (SOAT2)/acyl-coenzyme A:cholesterol acyltransferase 2 (ACAT2) inhibitor, with an IC₅₀ of 0.07 μM. Pyripyropene A attenuates hypercholesterolemia and atherosclerosis in vivo^[1][2][3][4]. IC50 & Target:IC50: 0.07 μM (ACAT2)^[1] In Vitro:Pyripyropene A (0-100 μM; 72 hours) exhibits anti-proliferative activity against HUVECs, and with an IC₅₀ value of 1.8 μM^[1].
Pyripyropene A (10 μM ; 24 hours) inhibits VEGF (20 ng/ml)-induced migration and tubular formation of HUVECs in dose-dependent fashion^[1].
Pyripyropene A do not show growth inhibitory effects against KB3-1, K562 and Neuro2A cells^[1].
In Vivo:Pyripyropene A (10-50 mg/kg per day; p.o; 12 weeks) reduces the levels of plasma cholesterol, very-low-density lipoprotein (VLDL), and low-density lipoprotein (LDL) and hepatic cholesterol content in apolipoprotein E-knockout mice. And Pyripyropene A-treated mice display reduction of atherogenic lesion areas in the aortae and heart^[3].
Pyripyropene A inhibits the hepatic e acyl–coenzyme A:cholesterol acyltransferase 2 (ACAT2) activity in vivo^[3].
Pyripyropene A displays a half-life (t_1/2) of 0.693/λ, where λ represented the terminal slope of the log-linear portion of concentration time profile^[4].