Fluvastatin Sodium is a synthetic indole-heptanoic-acid-derived inhibitor of hepatic HMG-CoA reductase with IC50 of 8 nM.

Lovastatin hydroxy acid sodium是一种高效 HMG-CoA 还原酶抑制剂，Ki 值为 0.6 nM，主要用于降低胆固醇合成，是抗高脂血症治疗中的重要药物。

Simvastatin hydroxy acid sodium是一种有效的 HMG-CoA 还原酶 (HMGCR) 抑制剂，能够显著降低吲哚酚硫酸盐介导的活性氧 (ROS) 生成，同时调节心肌细胞及 OATP3A1 转染 HEK293 细胞的 OATP3A1 表达，具有心血管保护作用。

Atorvastatin是一种口服活性HMG-CoA还原酶抑制剂，有效降低血脂。阿托伐他汀抑制人类SV-SMC增殖和侵袭的IC50值分别为0.39 μM和2.39 μM。

Meglutol is an antilipemic agent which lowers cholesterol, triglycerides, serum beta-lipoproteins and phospholipids, and inhibits the activity of hydroxymethylglutarryl CoA reductases, which is the rate limiting enzyme in the biosynthesis of cholesterol.

Rosuvastatin Calcium is a competitive and synthetic HMG-CoA reductase inhibitor with IC50 value of 11 nM.

Mevastatin is the first discovered statin-class HMG-CoA reductase inhibitor used as a cholesterol-lowering agent isolated from Penicillium citinium.

Lovastatin是一种用于降低胆固醇的细胞渗透性 HMG-CoA 还原酶抑制剂。

Atorvastatin hemicalcium salt（CI-981）是一种口服活性的3-羟基-3-甲基戊二酰辅酶A（HMG-CoA）还原酶抑制剂，有效降低血脂。它抑制人SV-SMC增殖和侵袭的IC50值分别为0.39 μM和2.39 μM。

SR-12813 is a pregnane X receptor (PXR) agonist and HMG-CoA reductase inhibitor with an IC50 of 850 nM.

Rosuvastatin D3 Sodium是一种 HMG-CoA 还原酶抑制剂，常用于治疗高胆固醇血症和预防心血管疾病。Rosuvastatin-d3 适用于药物代谢和药物动力学研究。

(3S,5R)-Pitavastatin calcium是 Pitavastatin 的对映体，Pitavastatin 是一种有效的 HMG-CoA 还原酶抑制剂，广泛用于高胆固醇血症和心血管疾病的治疗研究。

Swertiamarine is a naturally occuring secoiridoid glycoside which could inhibit HMG-CoA reductase activity.

Simvastatin（MK 733）是一种HMG-CoA还原酶的竞争性抑制剂，Ki为0.2 nM。

β-Amyrin palmitate是一种具有 HMG-CoA 还原酶抑制活性和抗糖尿病活性的化合物，广泛用于与糖脂代谢和糖尿病相关的研究。

Atorvastatin Calcium Salt Trihydrate是一种广泛使用的降胆固醇药物，主要通过抑制HMG-CoA还原酶来降低血清胆固醇水平。它用于治疗高胆固醇血症和相关心血管疾病。

Atorvastatin lactone is a prodrug form of atorvastatin. Atorvastatin is an orally active 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase inhibitor.

Pitavastatin Calcium is a potent and competitive inhibitor of HMG-CoA reductase with Ki value of 1.7nM, which can block cholesterol synthesis.

alpha-Asarone is a naturally occuring inhibitor of both HMG-CoA reductase (IC50 = 3 mM) and certain isoforms of the cytochrome P450 superfamily of enzymes (IC50 = 55.2 and 65.2 μg/ml for CYP2D6 and CYP3A4, respectively), with neuroprotective, anti-oxidative, anticonvulsive and cognitive enhancing action.

Pravastatin Sodium is a competitive HMG-CoA reductase inhibitor with IC50 value of 5.6 μM.