Molecular structure of Fenoprofen calcium salt, CAS Number: 53746-45-5
Fenoprofen calcium salt (CAS 53746-45-5)
Alternate Names:
(±)-2-(3-Phenoxyphenyl)propionic acid
CAS Number:
53746-45-5
Molecular Weight:
522.60
Molecular Formula:
C30H26O6•Ca
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.
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Fenoprofen calcium salt hydrate may function nonsteroidal anti-inflammatory. Its mechanism of action involves inhibiting the activity of cyclooxygenase enzymes, particularly COX-1 and COX-2, which are responsible for the production of prostaglandins from arachidonic acid. By blocking these enzymes, fenoprofen calcium salt hydrate reduces the synthesis of prostaglandins, which are involved in the inflammatory response. At the cellular level, fenoprofen calcium salt hydrate interferes with the production of inflammatory mediators, providing insights into the underlying mechanisms of inflammatory processes.
Fenoprofen calcium salt (CAS 53746-45-5) References
- Chiral inversion of R(-) fenoprofen and ketoprofen enantiomers in cats. | Castro, E., et al. 2000. J Vet Pharmacol Ther. 23: 265-71. PMID: 11106999
- Multiresidue analysis of acidic and polar organic contaminants in water samples by stir-bar sorptive extraction-liquid desorption-gas chromatography-mass spectrometry. | Quintana, JB., et al. 2007. J Chromatogr A. 1174: 27-39. PMID: 17727869
- Effect of n-octanol in the mobile phase on lipophilicity determination by reversed-phase high-performance liquid chromatography on a modified silica column. | Benhaim, D. and Grushka, E. 2008. J Chromatogr A. 1209: 111-9. PMID: 18814882
- Investigating the chlorination of acidic pharmaceuticals and by-product formation aided by an experimental design methodology. | Quintana, JB., et al. 2010. Water Res. 44: 243-55. PMID: 19800649
- Characterization of Ascentis RP-Amide column: Lipophilicity measurement and linear solvation energy relationships. | Benhaim, D. and Grushka, E. 2010. J Chromatogr A. 1217: 65-74. PMID: 19939395
- Anti-nociceptive activity and toxicity evaluation of Cu(II)-fenoprofenate complexes in mice. | Gumilar, F., et al. 2012. Eur J Pharmacol. 675: 32-9. PMID: 22169772
- Hyphenation of ionic liquid albumin glassy carbon biosensor or protein label-free sensor with differential pulse stripping voltammetry for interaction studies of human serum albumin with fenoprofen enantiomers. | Abd El-Hady, D. and Youssef, AK. 2013. Anal Chim Acta. 772: 68-74. PMID: 23540249
- Oxidation of non-steroidal anti-inflammatory drugs with aqueous permanganate. | Rodríguez-Álvarez, T., et al. 2013. Water Res. 47: 3220-30. PMID: 23582668
- Enhanced analgesic properties and reduced ulcerogenic effect of a mononuclear copper(II) complex with fenoprofen in comparison to the parent drug: promising insights in the treatment of chronic inflammatory diseases. | Agotegaray, M., et al. 2014. Biomed Res Int. 2014: 505987. PMID: 25050353
- A supramolecular topical gel derived from a non-steroidal anti-inflammatory drug, fenoprofen, is capable of treating skin inflammation in mice. | Majumder, J., et al. 2015. Org Biomol Chem. 13: 2300-9. PMID: 25554116
- The pharmacokinetics of oral ketoprofen in patients after gastric resection. | Porażka, J., et al. 2017. Pharmacol Rep. 69: 296-299. PMID: 28178590
- Fate of five pharmaceuticals under different infiltration conditions for managed aquifer recharge. | Silver, M., et al. 2018. Sci Total Environ. 642: 914-924. PMID: 29929143
- Influence of obesity on pharmacokinetics and analgesic effect of ketoprofen administered intravenously to patients after laparoscopic cholecystectomy. | Porażka, J., et al. 2020. Pharmacol Rep. 72: 763-768. PMID: 32048255
- Effect of Substitution Degree and Homogeneity on Cyclodextrin-Ligand Complex Stability: Comparison of Fenbufen and Fenoprofen Using CD and NMR Spectroscopy. | Kraszni, M., et al. 2023. Int J Mol Sci. 24: PMID: 37108706
- A liquid chromatographic method for the determination of fenoprofen in equine plasma and urine. | Delbeke, FT. and Debackere, M. 1994. Biomed Chromatogr. 8: 29-31. PMID: 8130630
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
Fenoprofen calcium salt, 5 g | sc-239989 | 5 g | $56.00 |