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  3. Biochemical Assay Reagents
  4. 52549-17-4

52549-17-4

Pranoprofen Chemical Structure

52549-17-4

Chemical Structure

  • Pranoprofen
  • CAS No: 52549-17-4
    Formula: C15H13NO3
    Molecular Weight: 255.27
  • IUPAC Name: 2-(5H-chromeno[2,3-b]pyridin-7-yl)propanoic acid
  • InChIKey: TVQZAMVBTVNYLA-UHFFFAOYSA-N
  • SMILES: CC(C(O)=O)C1=CC2=C(C=C1)OC3=NC=CC=C3C2

Biological Activity: Pranoprofen is a non-steroidal anti-inflammatory agent (NSAID) for the research of keratitis or other ophthalmology diseases. Pranoprofen inhibit COX-1 and COX-2 enzymes, thus blocking arachidonic acid converted to eicosanoids and reducing prostaglandins synthesis[1][2].

Cat. No. Product Name Purity Description
HY-B0336 Pranoprofen 98.65% Pranoprofen is a non-steroidal anti-inflammatory agent (NSAID) for the research of keratitis or other ophthalmology diseases. Pranoprofen inhibit COX-1 and COX-2 enzymes, thus blocking arachidonic acid converted to eicosanoids and reducing prostaglandins synthesis.
HY-B0336R Pranoprofen (Standard) ≥98% Pranoprofen (Standard) is the analytical standard of Pranoprofen. This product is intended for research and analytical applications. Pranoprofen is a non-steroidal anti-inflammatory agent (NSAID) for the research of keratitis or other ophthalmology diseases. Pranoprofen inhibit COX-1 and COX-2 enzymes, thus blocking arachidonic acid converted to eicosanoids and reducing prostaglandins synthesis.
HY-165662S Pranoprofen-13C-d3 Pranoprofen-13C-d3 (Pyaopofe-13C-d3) is 13C and deuterium labeled Pranoprofen.

References

[1]. Toru Hosoi, et al. Effect of pranoprofen on endoplasmic reticulum stress in the primary cultured glial cells. Neurochem Int. 2009 Jan;54(1):1-6. [Content Brief]
[2]. Minting Chen, et al. The Therapeutic Effects and Possible Mechanism of Pranoprofen in Mouse Model of Corneal Alkali Burns. J Ophthalmol. 2020 Apr 6;2020:7485912. [Content Brief]

Keywords:

PranoprofenPranoprofen (Standard)Pranoprofen-13C-d3