| CAS: | 217094-32-1 | ||||
| 分子式: | C23H32Cl2N6OS3 | ||||
| 分子量: | 575.64 | ||||
| 英文名称: |
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| 用途: | K-604 dihydrochloride 是一种有效的选择性酰基辅酶 A:胆固醇酰基转移酶 1 (ACAT-1) 抑制剂,IC50 为 0.45±0.06 μM。 |
| 货号 | 品牌 | 产品名称 | 规格 | 包装、参考价格 | 详情 | ||||||||||||||||||||||||||||
| K880401 | MACKLIN | K-604 dihydrochloride | ≥99% | 199元/1mg; 588元/5mg; 1145元/10mg; 2788元/25mg; | 展开 | ||||||||||||||||||||||||||||
储存:2-8℃ | |||||||||||||||||||||||||||||||||
| SML1837 | Sigma-Aldrich | K-604 | ≥98% (HPLC) | 1758.39元/5 MG; 7096.85元/25 MG; | 展开 | ||||||||||||||||||||||||||||
产品说明 包装 5, 25 mg in glass bottle 生化/生理作用 K-604 inhibits against acyl-coenzyme A (acyl-CoA):cholesterol O-acyltransferase-1 (ACAT1, SOAT1) activitiy in a selective (IC50 = 450 nM vs. 102.85 μ M against human ACAT1 and ACAT2, respectively) and acyl-CoA-competitive (Ki = 378 nM against oleoyl-coA) manner. K-604 inhibits cholesterol esterification in human monocyte-derived macrophages (IC50 = 68.0 nM) and enhances cholesterol efflux from THP-1 macrophages in response to HDL3 or apolipoprotein A-I. Oral administration is efficacious against macrophage foam cell formation and atherosclerosis progression among F1B hamsters on a high-fat diet (1-10 mg/kg/day) and apoE-knockout mice (60 mg/kg/day) without affecting plasma cholesterol levels. K-604 is also reported to stimulate autophagy-mediated P301L-Tau degradation in cortical neurons from 3XTg-AD mice (500 nM). 基本信息
产品性质
安全信息
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