Lovastatin 洛伐他汀
Lovastatin是一种HMG-CoA还原酶抑制剂,无细胞试验中IC50为3.4 nM,用于降胆固醇(降脂药)。Lovastatin 可触发自噬。
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货号:
TK0538 -
规格:
- 10mg
- 50mg
- 100mg
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价格:
¥0.00
Lovastatin是一种HMG-CoA还原酶抑制剂,无细胞试验中IC50为3.4 nM,用于降胆固醇(降脂药)。Lovastatin 可触发自噬。
| CAS No. | 75330-75-5 |
| 生物活性 | Lovastatin is a cell-permeable HMG-CoA reductase inhibitor used to lower cholesterol. |
| 分子式 | C24H36O5 |
| 分子量 | 404.54 |
| 运输条件 | Room temperature in continental US; may vary elsewhere. |
| 储存条件 | Powder, -20°C ,3 years |
| 溶解性数据 | DMSO : ≥ 100 mg/mL (247.19 mM) |
| 体内研究 | Lovastatin is an inactive lactone that is hydrolyzed in the liver to an active f3-hydroxyacid form. This principal metabolite is the inhibitor of the enzyme HMG-CoA reductase. The Ki is 1 nM. Lovastatin and its β-hydroxyacid metabolite are highly bound to human plasma proteins. Lovastatin crosses the blood-brain and placental barriers. Lovastatin produces a profound reduction of apolipoprotein-B-containing lipoproteins, especially LDL cholesterol and, to a lesser extent, plasma triglycerides, and a small increase in HDL cholesterol. |
| 体外研究 | Lovastatin (10 μM; 72 hours) efficiently reduces viability of HepG2 cells.Lovastatin (10 μM; 48 hours) induces apoptosis in HepG2 cells. |
| 纯度及产品资料 | 98% |