Meclofenamic acid
CAS No. 644-62-2
Meclofenamic acid ( Meclofenamate )
产品货号. M26293 CAS No. 644-62-2
甲氯芬那酸是一种非选择性间隙连接阻滞剂和选择性脂肪量和肥胖相关 (FTO) 酶抑制剂。甲氯芬那酸具有抗炎活性。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 5MG | ¥5928 | 有现货 |
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| 100MG | 获取报价 | 有现货 |
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| 200MG | 获取报价 | 有现货 |
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| 500MG | 获取报价 | 有现货 |
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| 1G | 获取报价 | 有现货 |
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生物学信息
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产品名称Meclofenamic acid
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注意事项本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
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产品简述甲氯芬那酸是一种非选择性间隙连接阻滞剂和选择性脂肪量和肥胖相关 (FTO) 酶抑制剂。甲氯芬那酸具有抗炎活性。
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产品描述Meclofenamic acid is a non-selective gap-junction blocker and a selective fat mass and obesity-associated (FTO) enzyme inhibitor. Meclofenamic acid has anti-inflammatory activities.
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体外实验Meclofenamic acid (0-100 μM, 24 h) inhibits FTO demethylation in a dose-response manner.Meclofenamic acid inhibits enzyme cyclooxygenase, with an IC50 about 1 μM, thereby inhibiting the production of prostaglandins.Meclofenamic acid inhibits the release of 5-HETE and LTB4 from human neutrophils stimulated with calcium ionophore and antagonizes the response of tissues to certain prostaglandins. Western Blot Analysis 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.
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体内实验——
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同义词Meclofenamate
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通路Others
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靶点Other Targets
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受体Major prion protein
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研究领域——
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适应症——
化学信息
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CAS Number644-62-2
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分子量296.15
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分子式C14H11Cl2NO2
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纯度>98% (HPLC)
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溶解度In Vitro:?DMSO : 100 mg/mL (337.67 mM)
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SMILESCc1ccc(Cl)c(Nc2ccccc2C(O)=O)c1Cl
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化学全称——
运输与储存
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储存条件(-20℃)
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运输条件With Ice Pack
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稳定性≥ 2 years
参考文献
1.Kimata A, et al. New series of antiprion compounds: pyrazolone derivatives have the potent activity of inhibiting protease-resistant prion protein accumulation [published correction appears in J Med Chem. 2008 Mar 13;51(5):1503]. J Med Chem. 2007;50(21):5053-5056.
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