Date published: 2026-4-23

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5-Hydroxy Diclofenac (CAS 69002-84-2)

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Alternate Names:
2-[(2,6-Dichlorophenyl)amino]-5-hydroxy-benzeneacetic acid
Application:
5-Hydroxy Diclofenac is a metabolite of diclofenac
CAS Number:
69002-84-2
Molecular Weight:
312.15
Molecular Formula:
C14H11Cl2NO3
Supplemental Information:
This is classified as a Dangerous Good for transport and may be subject to additional shipping charges.
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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5-Hydroxy Diclofenac is a metabolite of Diclofenac, a nonsteroidal anti-inflammatory compound that is believed to function via inhibiton of cyclooxygenase (COX). One study using mouse models showed that 5-Hydroxy Diclofenac forms a quinoneimine conjugate that stimulates proliferation of lymph node cells. Other similar studies have found that Diclofenac and its derivatives can be useful in the deconvolution of cytochrome activities.


5-Hydroxy Diclofenac (CAS 69002-84-2) References

  1. Diclofenac and its derivatives as tools for studying human cytochromes P450 active sites: particular efficiency and regioselectivity of P450 2Cs.  |  Mancy, A., et al. 1999. Biochemistry. 38: 14264-70. PMID: 10572000
  2. Syntheses and characterization of the acyl glucuronide and hydroxy metabolites of diclofenac.  |  Kenny, JR., et al. 2004. J Med Chem. 47: 2816-25. PMID: 15139759
  3. Investigation of the immunogenicity of diclofenac and diclofenac metabolites.  |  Naisbitt, DJ., et al. 2007. Toxicol Lett. 168: 45-50. PMID: 17123753
  4. Biosynthesis of drug metabolites using microbes in hollow fiber cartridge reactors: case study of diclofenac metabolism by Actinoplanes species.  |  Osorio-Lozada, A., et al. 2008. Drug Metab Dispos. 36: 234-40. PMID: 18006646
  5. Occurrence of diclofenac and selected metabolites in sewage effluents.  |  Stülten, D., et al. 2008. Sci Total Environ. 405: 310-6. PMID: 18640705
  6. Liquid chromatography-tandem mass spectrometric assay for diclofenac and three primary metabolites in mouse plasma.  |  Sparidans, RW., et al. 2008. J Chromatogr B Analyt Technol Biomed Life Sci. 872: 77-82. PMID: 18674973
  7. Celecoxib inhibits 5-lipoxygenase.  |  Maier, TJ., et al. 2008. Biochem Pharmacol. 76: 862-72. PMID: 18692027
  8. Identification of quinone imine containing glutathione conjugates of diclofenac in rat bile.  |  Waldon, DJ., et al. 2010. Chem Res Toxicol. 23: 1947-53. PMID: 21053927
  9. Discovery and Optimization of 5-Hydroxy-Diclofenac toward a New Class of Ligands with Nanomolar Affinity for the CaMKIIα Hub Domain.  |  Tian, Y., et al. 2022. J Med Chem. 65: 6656-6676. PMID: 35500061
  10. Microbial oxidative metabolism of diclofenac: production of 4'-hydroxydiclofenac using Epiccocum nigrum IMI354292.  |  Webster, R., et al. 1998. Appl Microbiol Biotechnol. 49: 371-6. PMID: 9615477

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

5-Hydroxy Diclofenac, 1 mg

sc-207033
1 mg
$349.00

5-Hydroxy Diclofenac, 5 mg

sc-207033A
5 mg
$411.00

5-Hydroxy Diclofenac, 25 mg

sc-207033B
25 mg
$806.00

5-Hydroxy Diclofenac, 100 mg

sc-207033C
100 mg
$1603.00