1. Membrane Transporter/Ion Channel Cytoskeleton Metabolic Enzyme/Protease
  2. Fat Mass and Obesity-associated Protein (FTO) Potassium Channel Gap Junction Protein Endogenous Metabolite
  3. Meclofenamic acid sodium hydrate

Meclofenamic acid sodium hydrate  (Synonyms: Meclofenamate sodium hydrate)

目录号: HY-117275A
产品使用指南

Meclofenamic acid (Meclofenamate) sodium hydrate 是一种非甾体抗炎剂。Meclofenamic acid sodium hydrate 是一种高选择性的脂肪和肥胖相关酶 (FTO) 抑制剂。Meclofenamic acid sodium hydrate 与 FTO 竞争,与含有 m(6)A 的核酸结合。Meclofenamic acid sodium hydrate 是一种非选择性的缝隙连接 (gap-junction) 阻滞剂。Meclofenamic acid sodium hydrate 抑制 hKv2.1hKv1.1,其 IC50 分别为 56.0 和 155.9 μM。

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Meclofenamic acid sodium hydrate Chemical Structure

Meclofenamic acid sodium hydrate Chemical Structure

CAS No. : 67254-91-5

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Meclofenamic acid sodium hydrate 的其他形式现货产品:

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MCE 顾客使用本产品发表的 1 篇科研文献

  • 生物活性

  • 纯度 & 产品资料

  • 参考文献

生物活性

Meclofenamic acid (Meclofenamate) sodium hydrate is a non-steroidal anti-inflammatory agent. Meclofenamic acid sodium hydrate is a highly selective FTO (fat mass and obesity-associated) enzyme inhibitor. Meclofenamic acid sodium hydrate competes with FTO binding for the m(6)A-containing nucleic acid. Meclofenamic acid sodium hydrate is a non-selective gap-junction blocker. Meclofenamic acid sodium hydrate inhibits hKv2.1 and hKv1.1, with IC50 values of 56.0 and 155.9 μM, respectively[1][2][3][4].

IC50 & Target

IC50: 1 μM (cyclooxygenase), 56.0 μM (hKv2.1), 155.9 μM (hKv1.1)[3]

体外研究
(In Vitro)

Meclofenamic acid sodium hydrate (0-100 μM, 24 h) inhibits FTO demethylation in a dose-response manner[1].
Meclofenamic acid sodium hydrate inhibits enzyme cyclooxygenase, with an IC50 about 1 μM, thereby inhibiting the production of prostaglandins[2].
Meclofenamic acid sodium hydrate inhibits the release of 5-HETE and LTB4 from human neutrophils stimulated with calcium ionophore and antagonizes the response of tissues to certain prostaglandins[2].

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

Western Blot Analysis[1]

Cell Line: HeLa cells
Concentration: 0, 12.5, 25, 50, 100 μM
Incubation Time: 24 h
Result: Inhibited FTO demethylation in a dose-response manner, and elevates the levels of cellular m6A in mRNA by targeting FTO.
Clinical Trial
分子量

336.15

Formula

C14H12Cl2NNaO3

CAS 号
结构分类
初始来源
运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

Please store the product under the recommended conditions in the Certificate of Analysis.

纯度 & 产品资料
参考文献
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  • 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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Meclofenamic acid sodium hydrate
目录号:
HY-117275A
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