Compounds which are useful as inhibitors of cholesterol biosynthesis and thus as hypocholesterolemic agents are provided which have a quinoline or a pyridine anchor attached by means of a linker to a binding domain sidechain, which compounds inhibit the enzyme 3-hydroxy-3-methylglutaryl-coenzyme A reductase.
本研究提供了可作为
胆固醇生物合成
抑制剂从而作为低
胆固醇血症药物的化合物,这些化合物具有一个
喹啉或
吡啶锚,通过连接物与结合域侧链相连,这些化合物可抑制 3-羟基-3-
甲基戊二酰
辅酶 A 还原酶。