1. Metabolic Enzyme/Protease
  2. Phospholipase
  3. Ecopladib

Ecopladib  (Synonyms: PLA 725)

目录号: HY-U00037 纯度: 95.0%
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Ecopladib 是一种胞浆磷脂酶 A2α (phospholipase A2α) 抑制剂,在 GLU micelle 和大鼠全血细胞中,IC50 值分别为 0.15 μM 和 0.11 μM。

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Ecopladib Chemical Structure

Ecopladib Chemical Structure

CAS No. : 381683-92-7

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查看 Phospholipase 亚型特异性产品:

  • 生物活性

  • 实验参考方法

  • 纯度 & 产品资料

  • 参考文献

生物活性

Ecopladib is a sub-micromolar inhibitor of cytosolic phospholipase A2α (cPLA2α), with IC50s of 0.15 μM and 0.11 μM in the GLU micelle and rat whole blood assays, respectively.

IC50 & Target

IC50: 0.15 μM (cPLA2α, in GLU micelle), 0.11 μM (cPLA2α, rat blood)[1]

体外研究
(In Vitro)

Ecopladib 在37 nM的浓度下能够抑制cPLA2α达73%,而在1 μM的浓度下对sPLA2的抑制率仅为16%。Ecopladib 对前列腺素(PGF2α)和白三烯(LTB4 和 LTC4/D4/E4)的产生的抑制作用具有相似的IC50值,约为20?30 nM。在20 μM的浓度下,Ecopladib 对COX-1和COX-2无活性,这个浓度大约是其在MC-9细胞中IC50值的100倍。此外,Ecopladib 能够抑制由花生四烯酸通过12-和15-脂氧合酶途径生成的12-和15-HETE,其IC50值约为0.3 μM[1]

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

体内研究
(In Vivo)

Ecopladib 在此模型中口服有效,ED50 为 8 mg/kg,表明它可以抑制体内 COX-2 衍生的 PGE2 形成。口服 Ecopladib 可有效减少角叉菜胶引起的爪肿胀:根据剂量-反应研究,确定 ED50 为 40 mg/kg[1]

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

分子量

748.11

Formula

C39H33Cl3N2O5S

CAS 号
性状

固体

颜色

White to off-white

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式
Powder -20°C 3 years
4°C 2 years
In solvent -80°C 6 months
-20°C 1 month
纯度 & 产品资料
参考文献
Animal Administration
[1]

Male Sprague−Dawley rats are anesthetized, and 10−20 mL of filtered air is injected subcutaneously under the dorsal skin to form a pouch. Three and six days later, the pouches are reinflated with 10−15 mL of sterile air. On the seventh day, the test compound is dissolved in vehicle (55.5% Phosal 53 MCT, 5.6% Tween 80, 16.7% Labrasol, and 22.2% propylene carbonate) to give 37.5 mg of test compound per mL of vehicle. This test compound in vehicle is diluted with water to the appropriate concentration and dosed at 4 mL/kg. Vehicle treated animals receives the same amount of vehicle as the animals treated with the highest dose of compound. Two hours later, 2 mL of a 1% solution of carrageenan (Viscarin carrageenan type GP-209NF) in saline is injected into the pouch. Six hours after the carrageenan injection, the rats are individually sacrificed and the contents of the pouch are harvested. The amount of fluid recovered is measured. An aliquot of the exudate is centrifuged at 6500 rpm for 10 min, and 300 μL of each supernatant is precipitated with MeOH (800 μL) precooled to 0°C. The samples are well vortexed and are kept at −80°C overnight. The samples are centrifuged again and assayed for PGE2 to locate the PGE2 production within the linear range of the PGE2 standard curve. To minimize the difference in binding environments for the standards and samples, the standard curve is generated in a 1% solution of carrageenan that is mixed with assay buffer to the same dilution as the samples. The approximate ED50 value is extrapolated from the dose−response curve.

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

参考文献
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  • 稀释计算器

The molarity calculator equation

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

质量   浓度   体积   分子量 *
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The dilution calculator equation

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

This equation is commonly abbreviated as: C1V1 = C2V2

浓度 (start) × 体积 (start) = 浓度 (final) × 体积 (final)
× = ×
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.

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