Enfenamic acid

• Description :

  Enfenamic acid is a nonsteroidal anti-inflammatory agent and a prostaglandin synthetase inhibitor, inhibiting hepatic gluconeogenesis in Swiss albino mice. Enfenamic acid suppresses wound healing[1][2][3].

• Product Name Alternative :

  Tromaril; RH 8

• UNSPSC :

  12352005

• Hazard Statement :

  H302-H315-H319-H335

• Target :

  Others

• Type :

  Reference compound

• Related Pathways :

  Others

• Applications :

  COVID-19-immunoregulation

• Field of Research :

  Inflammation/Immunology

• Assay Protocol :

  https://www.medchemexpress.com/enfenamic-acid.html

• Solubility :

  10 mM in DMSO

• Smiles :

  O=C(O)C1=CC=CC=C1NCCC2=CC=CC=C2

• Molecular Formula :

  C15H15NO2

• Molecular Weight :

  241.29

• Precautions :

  P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362-P403+P233-P405-P501

• References & Citations :

  [1]Rao CM, et al. Effects of enfenamic acid and its zinc salt on wound-healing. Indian J Physiol Pharmacol. 1988;32 (1) :61-66.|[2]Diwan PV, et al. Effects of nonsteroidal antiinflammatory agents (NSAIAs) on wound healing. Indian J Exp Biol. 1986;24 (10) :640-643.|[3]Sreenath TL, et al. The inhibitory effect of enfenamic acid (Tromaril) on hepatic gluconeogenesis in Swiss albino mice. Biochem Int. 1985 Dec;11 (6) :885-91.|[4]Srivastava K, et al. Role of plasminogen activators and leukocytes in IUD-induced inflammation: effect of some anti-inflammatory agents. Adv Contracept. 1989 Sep;5 (3) :173-8.

• Shipping Conditions :

  Room temperature

• Scientific Category :

  Reference compound1

• Clinical Information :

  No Development Reported

• CAS Number :

  [23049-93-6]