Date published: 2025-12-5

1-800-457-3801

SCBT Portrait Logo
Seach Input

7-Ethoxyresorufin (CAS 5725-91-7)

5.0(1)
Write a reviewAsk a question

See product citations (6)

Alternate Names:
7-ER
Application:
7-Ethoxyresorufin is a fluorometric inhibitor of vasorelaxant responses
CAS Number:
5725-91-7
Purity:
≥98%
Molecular Weight:
241.24
Molecular Formula:
C14H11NO3
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

QUICK LINKS

7-Ethoxyresorufin is a compound used in biochemical assays to assess cytochrome P450 enzyme activity, particularly CYP1A1, an enzyme involved in the metabolism of xenobiotics. The compound is a substrate for CYP1A1, and upon metabolism, it is converted to resorufin, a highly fluorescent product that can be easily quantified. This conversion process is the basis for the ethoxyresorufin-O-deethylase (EROD) assay, a widely used method to measure the induction and activity of CYP1A1. The EROD assay, utilizing 7-Ethoxyresorufin, is applied in toxicology to study the effects of environmental and chemical exposures on the induction of detoxifying enzymes. Moreover, the assay is instrumental in the field of ecotoxicology, where it is used to monitor the presence of environmental contaminants that act as inducers of cytochrome P450 enzymes in wildlife. In addition to its use in enzyme activity assays, 7-Ethoxyresorufin is also employed in research focused on understanding the metabolic pathways of xenobiotic compounds and the genetic regulation of these pathways.


7-Ethoxyresorufin (CAS 5725-91-7) References

  1. Neuronal nitric oxide synthase catalyzes the reduction of 7-ethoxyresorufin.  |  Jiang, HB. and Ichikawa, Y. 1999. Life Sci. 65: 1257-64. PMID: 10503941
  2. A study on CYP1A inhibitory action of E-2-(4'-methoxybenzylidene)-1-benzosuberone and some related chalcones and cyclic chalcone analogues.  |  Monostory, K., et al. 2003. Toxicology. 184: 203-10. PMID: 12499122
  3. Tight-binding inhibition by alpha-naphthoflavone of human cytochrome P450 1A2.  |  Cho, US., et al. 2003. Biochim Biophys Acta. 1648: 195-202. PMID: 12758162
  4. Inhibition of nitrovasodilator- and acetylcholine-induced relaxation and cyclic GMP accumulation by the cytochrome P-450 substrate, 7-ethoxyresorufin.  |  Bennett, BM., et al. 1992. Can J Physiol Pharmacol. 70: 1297-303. PMID: 1362924
  5. Dose-response studies on the induction of liver cytochromes P4501A1 and 1B1 by polycyclic aromatic hydrocarbons in arylhydrocarbon-responsive C57BL/6J mice.  |  Shimada, T., et al. 2003. Xenobiotica. 33: 957-71. PMID: 14514444
  6. Interlaboratory comparison of microsomal ethoxyresorufin and pentoxyresorufin O-dealkylation determinations: standardization of assay conditions.  |  Rutten, AA., et al. 1992. Arch Toxicol. 66: 237-44. PMID: 1514921
  7. Effects of amitraz on cytochrome P450-dependent monooxygenases and estrogenic activity in MCF-7 human breast cancer cells and immature female rats.  |  Ueng, TH., et al. 2004. Food Chem Toxicol. 42: 1785-94. PMID: 15350676
  8. Immunochemical detection of cytochrome P450 isozymes induced in rat liver by n-hexane, 2-hexanone and acetonyl acetone.  |  Nakajima, T., et al. 1991. Arch Toxicol. 65: 542-7. PMID: 1781736
  9. Redox cycling of resorufin catalyzed by rat liver microsomal NADPH-cytochrome P450 reductase.  |  Dutton, DR., et al. 1989. Arch Biochem Biophys. 268: 605-16. PMID: 2464338
  10. Phe-125 and Phe-226 of pig cytochrome P450 1A2 stabilize the binding of aflatoxin B1 and 7-ethoxyresorufin through the key CH/π interactions.  |  Zhu, S., et al. 2019. Biochem Pharmacol. 166: 292-299. PMID: 31173723
  11. Inhibitors of 7-ethoxyresorufin and 7-ethoxycoumarin de-ethylases in rat small intestinal microsomes and cells.  |  Grafstöm, R. and Stohs, SJ. 1981. Drug Chem Toxicol. 4: 147-59. PMID: 7318685
  12. A microassay for measuring cytochrome P450IA1 and P450IIB1 activities in intact human and rat hepatocytes cultured on 96-well plates.  |  Donato, MT., et al. 1993. Anal Biochem. 213: 29-33. PMID: 8238878
  13. Relaxant responses of rabbit aorta: influence of cytochrome P450 inhibitors.  |  Oyekan, AO., et al. 1994. J Pharmacol Exp Ther. 268: 262-9. PMID: 8301566

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

7-Ethoxyresorufin, 2 mg

sc-200606
2 mg
$135.00

7-Ethoxyresorufin, 10 mg

sc-200606A
10 mg
$265.00