2. Metabolic Enzyme/Protease
  3. Acyltransferase
  4. YM17E

YM17E is an inhibitor of acyl CoA:cholesterol acyltransferase (ACAT), with IC50 of 44 nM in rabbit liver microsomes in vitro.

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YM17E

YM17E 構造式

CAS 番号 : 124900-72-7

容量 価格（税別） 在庫状況 数量
Solid + Solvent (Highly Recommended)
10 mM * 1 mL in DMSO
ready for reconstitution
 USD 158 在庫あり
Solution
10 mM * 1 mL in DMSO USD 158 在庫あり
Solid
5 mg $110 在庫あり
10 mg $150 在庫あり
25 mg $260 在庫あり
50 mg $380 在庫あり
100 mg   お問い合わせ  
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YM17E 関連抗体

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Acyltransferase アイソフォーム固有の製品をすべて表示:

すべてのアイソフォームを表示
ACAT1 ACAT2 MGAT2 ACAT DGAT1 DGAT2

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製品説明

YM17E is an inhibitor of acyl CoA:cholesterol acyltransferase (ACAT), with IC50 of 44 nM in rabbit liver microsomes in vitro.

IC50 & Target

IC50: 44 nM (ACAT in rabbit liver microsomes)[1]
体外実験

YM17E is as potent in inhibiting ACAT activity in the liver as in the intestine, with IC50 values of 45 and 34 nM, respectively[2].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

YM17E 関連抗体
体内実験

YM17E (3, 10 and 30 mg/kg per day, p.o.) decreases total cholesterol, cholesteryl ester and non-HDL cholesterol in a dose-dependent manner. Total cholesterol and cholesteryl ester levels in liver do not decrease significantly after intravenous administration of YM17E, but do decrease significantly and in a dose-dependent manner after oral administration. YM17E (3, 5, 10 mg/kg, i.v.) significantly inhibits hepatic ACAT activities in a dose-dependent manner. YM17E produces a significant increase in 125I-LDL clearance in atherogenic diet-fed rats after both oral and intravenous administration[1]. YM17E inhibits production of [14C]cholesteryloleate from [14C]oleoyl CoA in a dose-dependent manner in both liver and intestinal microsomes used as enzyme sources[2].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
分子量

652.91

分子式

C40H56N6O2
CAS 番号
Appearance

Solid

Color

White to off-white

SMILES

O=C(NC1=CC=C(N(C)C)C=C1)N(CC2=CC=CC(CN(C3CCCCCC3)C(NC4=CC=C(N(C)C)C=C4)=O)=C2)C5CCCCCC5
輸送条件

Room temperature in continental US; may vary elsewhere.
保管条件
Powder -20°C 3 years
In solvent -80°C 6 months
  -20°C 1 month
溶剤 & 溶解度
体外: 

DMSO : ≥ 125 mg/mL (191.45 mM; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO)

*"≥" means soluble, but saturation unknown.

Preparing
Stock Solutions
Concentration Solvent Mass 1 mg 5 mg 10 mg
1 mM 1.5316 mL 7.6580 mL 15.3160 mL
5 mM 0.3063 mL 1.5316 mL 3.0632 mL
10 mM 0.1532 mL 0.7658 mL 1.5316 mL
View the Complete Stock Solution Preparation Table

* Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month. When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.

  • Molarity Calculator

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Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

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Concentration
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Volume
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Molecular Weight *

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

一般には略語で表示されます：C1V1 = C2V2

濃度 （開始）

C1

×
体積 （開始）

V1

=
濃度 （終了）

C2

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体積 （終了）

V2

In Vivo Dissolution Calculator
Please enter the basic information of animal experiments:

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Calculation results:
Working solution concentration: mg/mL
純度とドキュメンテーション

純度: 98.34%

COA (246 KB) HNMR (283 KB) LCMS (283 KB)

取扱説明書 (2659 KB)
参考文献
動物実験
[1]

YM17E is administered to rats fed an atherogenic diet at intravenous doses of 0, 3, 5 and 10 mg/kg per day for 5 days or oral doses of 0, 3, 10 and 30 mg/kg per day for 5 days. At 2 h after final administration, all the blood and liver are removed. Serum is obtained from the blood by centrifugation and serum total cholesterol and free cholesterol are measured by an enzymatic method. Serum HDL is prepared by the heparin-Mn method.

MedChemExpress (MCE) はこれらの方法の精度を確認していません。 こちらは参照専用です。
参考文献

Complete Stock Solution Preparation Table

* Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month. When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.

Optional Solvent Concentration Solvent Mass 1 mg 5 mg 10 mg 25 mg
DMSO 1 mM 1.5316 mL 7.6580 mL 15.3160 mL 38.2901 mL
5 mM 0.3063 mL 1.5316 mL 3.0632 mL 7.6580 mL
10 mM 0.1532 mL 0.7658 mL 1.5316 mL 3.8290 mL
15 mM 0.1021 mL 0.5105 mL 1.0211 mL 2.5527 mL
20 mM 0.0766 mL 0.3829 mL 0.7658 mL 1.9145 mL
25 mM 0.0613 mL 0.3063 mL 0.6126 mL 1.5316 mL
30 mM 0.0511 mL 0.2553 mL 0.5105 mL 1.2763 mL
40 mM 0.0383 mL 0.1915 mL 0.3829 mL 0.9573 mL
50 mM 0.0306 mL 0.1532 mL 0.3063 mL 0.7658 mL
60 mM 0.0255 mL 0.1276 mL 0.2553 mL 0.6382 mL
80 mM 0.0191 mL 0.0957 mL 0.1915 mL 0.4786 mL
100 mM 0.0153 mL 0.0766 mL 0.1532 mL 0.3829 mL
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YM17E Related Classifications

  • Molarity Calculator

  • Dilution Calculator

The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

質量   濃度   体積   分子量 *
= × ×

The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

一般には略語で表示されます：C1V1 = C2V2

濃度 （開始） × 体積 （開始） = 濃度 （終了） × 体積 （終了）
× = ×
C1   V1   C2   V2
Help & FAQs
  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

Keywords:

YM17E124900-72-7AcyltransferaseDiacylglycerol acyltransferaseDiglyceride acyltransferaseacyl-CoA:cholesterol acyltransferasemono- acylglycerol acyltransferaseInhibitorinhibitorinhibit

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製品名:
YM17E
製品番号:
HY-101627
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