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141799-76-0

中文名稱 141799-76-0
英文名稱 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 結(jié)構(gòu)式 141799-76-0 結(jié)構(gòu)式

基本信息

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

物理化學(xué)性質(zhì)

沸點(diǎn)637.4±55.0 °C(Predicted)
密度1.11±0.1 g/cm3(Predicted)
儲(chǔ)存條件-20°C儲(chǔ)存
溶解度溶于二甲基亞砜
酸度系數(shù)(pKa)14.20±0.46(Predicted)

安全數(shù)據(jù)

危險(xiǎn)性符號(hào)(GHS)GHS hazard pictograms
GHS07
警示詞警告
危險(xiǎn)性描述H302-H315-H319-H335

常見問題列表

生物活性
E-5324 是一個(gè)強(qiáng)效的?;o酶 A:膽固醇酰基轉(zhuǎn)移酶 (ACAT) 抑制劑,其 IC50 值在 44 至 190 nM 之間。
靶點(diǎn)

IC50: 44 to 190 nM (ACAT)

體外研究

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.

體內(nèi)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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