YM17E
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货号：A1176487
YM17E 是一种酰基辅酶A:胆固醇酰基转移酶 (AC AT
YM17E 化学结构
YM17E 3D分子结构
规格
价格
会员价
库存
数量
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YM17E 纯度/质量文件 产品仅供科研
货号：A1176487
标准纯度：
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产品说明书
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YM17E 质控信息
Penfluridol
+
Dopamine receptor, Ki: 1.6 μM
98%
Ansofaxine HCl
++
Dopamine receptor, IC50: 491 nM
98%
Tetrahydroberberine,THB
+
98+%
Prochlorperazine Maleate
✔
95%
Olanzapine
✔
99+%
Trifluoperazine
++++
Dopamine D2 receptor, IC50: 1.1 nM
98%
Ropinirole hydrochloride
++
99%
Lurasidone
++++
98%
Levosulpiride
✔
99+%
Pridopidine
✔
95%
Metoclopramide
✔
✔
99+%
Molindone HCl
✔
98%
Sulpiride
✔
99+%
Perospirone
++++
99%
Perospirone HCl
++++
98+%
Phenothiazine
✔
98%
Pimozide
+
Dopamine D1 receptor, Ki: 6600 nM
+++
Dopamine D2 receptor, Ki: 3.0 nM
++++
Dopamine D3 receptor, Ki: 0.83 nM
98%
Rotundine
++
D1 receptor, IC50: 166 nM
+
D2 receptor, IC50: 1.47 μM
+
D3 receptor, IC50: 3.25 μM
98%
Domperidone
✔
99+%
ONC206
✔
97%
Pimethixene maleate
++
Dopamine D1 Receptor, pKi: 6.37
+++
Dopamine D2 Receptor, pKi: 8.19
++
Dopamine D4.4 Receptor, pKi: 7.54
97%
Loxapine succinate
++
D2 receptor (Human), Ki: 62 nM
D1 receptor (human), Ki: 26 nM
++
D2 receptor (bovine), Ki: 26 nM
D2 receptor (human), Ki: 24 nM
+++
D4 receptor (human), Ki: 7.5 nM
99%
Chlorprothixene
+++
+++
+++
+++
98%
SCH-23390 HCl
++++
D1 dopamine receptor, Ki: 0.2 nM
++++
D5 dopamine receptor, Ki: 0.3 nM
98%
MPP+ iodide
✔
97%
σ1 Receptor antagonist-1
+
97%
Benztropine mesylate
++
98%
Azaperone
✔
98%
Ziprasidone HCl
✔
98+%
Paliperidone
✔
98%
Alizapride HCl
✔
99+%
Amisulpride
✔
98%
Quetiapine hemifumarate
✔
Adrenergic Receptor
98%
Clozapine N-oxide
✔
99%
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1. 鼠标悬停在“+”上可以显示相关IC50的具体数值。"+"越多，抑制作用越强。2. "✔"表示该化合物对相应的亚型有抑制作用，但抑制强度暂时没有相关数据。
YM17E 生物活性
描述
YM17E is equally effective in inhibiting ACAT activity in the liver as it is in the intestines, with IC50 values of 45 and 34 nM, respectively[2]
YM17E 动物研究
Animal study
Administered orally at doses of 3, 10, and 30 mg/kg daily, YM17E reduces total cholesterol, cholesterol esters, and non-HDL cholesterol in a dose-dependent manner. Intravenous injection of YM17E does not significantly lower total cholesterol and cholesterol ester levels in the liver, but oral administration does, and it is dose-dependent. Under the administration route of intravenous injection, YM17E significantly inhibits hepatic ACAT activity in a dose-dependent manner at doses of 3, 5, and 10 mg/kg. Following both oral and intravenous administration, YM17E significantly increases the clearance rate of 125 I-LDL in rats fed an atherosclerotic diet[1]
YM17E 参考文献
YM17E 实验方案
计算器
摩尔计算器
总药量计算器
工作液计算器
存储液制备
1mg
5mg
10mg
1 mM
5 mM
10 mM
1.53mL
0.31mL
0.15mL
7.66mL
1.53mL
0.77mL
15.32mL
3.06mL
1.53mL
YM17E 技术信息
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