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141799-76-0

中文名称 141799-76-0
英文名称 E 5324
CAS 141799-76-0
分子式 C26H34N4O2
分子量 434.57
MOL 文件 141799-76-0.mol
141799-76-0 结构式 141799-76-0 结构式

基本信息

中文别名
化合物 T15187
英文别名
E 5324
Urea, N-butyl-N'-[2-[3-(5-ethyl-4-phenyl-1H-imidazol-1-yl)propoxy]-6-methylphenyl]-

物理化学性质

沸点637.4±55.0 °C(Predicted)
密度1.11±0.1 g/cm3(Predicted)
储存条件-20°C储存
溶解度溶于二甲基亚砜
酸度系数(pKa)14.20±0.46(Predicted)

安全数据

危险性符号(GHS)
GHS07
警示词警告
危险性描述H302-H315-H319-H335

常见问题列表

生物活性
E-5324 是一个强效的酰基辅酶 A:胆固醇酰基转移酶 (ACAT) 抑制剂,其 IC50 值在 44 至 190 nM 之间。
靶点

IC50: 44 to 190 nM (ACAT)

体外研究

E-5324 is a potent ACAT inhibitor with IC 50 s of 44 to 190 nM in microsomes. E-5324 shows no effect on triglyceride synthesis up to 10 μM. E-5324 also has no effect on bovine pancreatic cholesterol esterase or lecithin: cholesterol acyltransferase (LCAT) up to 10 μM. E-5324 inhibits the incorporation of [ 3 H]oleate into cholesteryl [ 3 H]oleate in a concentration-dependent manner with an IC 50 of 0.44 μM. E-5324 also inhibits [ 3 H]cholesteryl ester synthesis with an IC 50 of 0.41 μM.

体内研究

The areas under the cholesterol-time curves for duration of this study (AUC) for control, E-5324 0.02% and E-5324 0.1% are 104985±4411, 106096±4476 and 105231±4 348 mg×day/dL, respectively. The high dose of E-5324 (0.1%) significantly reduces the surface involvement by 34% and 54% in the aortic arch and thoracic aorta, respectively. E-5324 treatment significantly reduces the wet weight and protein content. In the aortic arch, the high dose of E-5324 (0.1%) significantly reduces both cholesteryl ester and total cholesterol by 60% and 59%, respectively. The high dose of E-5324 (0.1%) markedly reduces the ACAT activities in the aortic arch and thoracic aorta by 35% and 44%, respectively.

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