Meclofenamic acid

CAS No. 644-62-2

Meclofenamic acid( Meclofenamate )

Catalog No. M26293 CAS No. 644-62-2

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.

Purity : >98% (HPLC)

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Biological Information

  • Product Name
    Meclofenamic acid
  • Note
    Research use only, not for human use.
  • Brief Description
    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.
  • Description
    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.
  • In Vitro
    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.
  • In Vivo
    ——
  • Synonyms
    Meclofenamate
  • Pathway
    Others
  • Target
    Other Targets
  • Recptor
    Major prion protein
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    644-62-2
  • Formula Weight
    296.15
  • Molecular Formula
    C14H11Cl2NO2
  • Purity
    >98% (HPLC)
  • Solubility
    In Vitro:?DMSO : 100 mg/mL (337.67 mM)
  • SMILES
    Cc1ccc(Cl)c(Nc2ccccc2C(O)=O)c1Cl
  • Chemical Name
    ——

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • Stability
    ≥ 2 years

Reference

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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