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7-Ethoxycoumarin (CAS 31005-02-4)

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Application:
7-Ethoxycoumarin is a substrate for CYP2B6
CAS Number:
31005-02-4
Molecular Weight:
190.20
Molecular Formula:
C11H10O3
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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7-Ethoxycoumarin (7-EC) is a derivative of coumarin that is found in numerous plant species. Laboratory experiments have employed 7-Ethoxycoumarin to investigate the biological effects associated with coumarin derivatives. Although the precise mechanism of action for 7-Ethoxycoumarin remains incompletely understood, it is hypothesized to function through modulating the activity of various enzymes and proteins that play roles in inflammation and cancer regulation. For instance, 7-Ethoxycoumarin has the ability to inhibit cyclooxygenase-2 (COX-2), an enzyme involved in the generation of inflammatory mediators.


7-Ethoxycoumarin (CAS 31005-02-4) References

  1. Highly sensitive high-performance liquid chromatographic assay for coumarin 7-hydroxylation and 7-ethoxycoumarin O-deethylation by human liver cytochrome P450 enzymes.  |  Yamazaki, H., et al. 1999. J Chromatogr B Biomed Sci Appl. 721: 13-9. PMID: 10027632
  2. 7-ethoxycoumarin deethylation activity in perfused isolated rat brain.  |  Chikaoka, Y. and Tamura, M. 1999. J Biochem. 125: 634-40. PMID: 10050054
  3. Use of 7-ethoxycoumarin to monitor multiple enzymes in the human CYP1, CYP2, and CYP3 families.  |  Waxman, DJ. and Chang, TK. 2006. Methods Mol Biol. 320: 153-6. PMID: 16719387
  4. Hydrogen peroxide-mediated dealkylation of 7-ethoxycoumarin by cytochrome P450 (CYP107AJ1) from Streptomyces peucetius ATCC27952.  |  Niraula, NP., et al. 2011. Enzyme Microb Technol. 48: 181-6. PMID: 22112829
  5. Metabolism of 7-ethoxycoumarin, safrole, flavanone and hydroxyflavanone by cytochrome P450 2A6 variants.  |  Uno, T., et al. 2013. Biopharm Drug Dispos. 34: 87-97. PMID: 23112005
  6. Metabolism of 7-ethoxycoumarin, flavanone and steroids by cytochrome P450 2C9 variants.  |  Uno, T., et al. 2017. Biopharm Drug Dispos. 38: 486-493. PMID: 28758225
  7. In vitro Drug Metabolism Investigation of 7-Ethoxycoumarin in Human, Monkey, Dog and Rat Hepatocytes by High Resolution LC-MS/MS.  |  Feng, WY., et al. 2018. Drug Metab Lett. 12: 33-53. PMID: 29669508
  8. Stimulation of mixed-function oxidation of 7-ethoxycoumarin in periportal and pericentral regions of the perfused rat liver by xylitol.  |  Belinsky, SA., et al. 1983. Eur J Biochem. 137: 1-6. PMID: 6606574
  9. The metabolism of 7-ethoxycoumarin and 7-hydroxycoumarin by rat and hairless mouse skin strips.  |  Moloney, SJ., et al. 1982. Biochem Pharmacol. 31: 4005-9. PMID: 6984334
  10. Metabolism of coumarin and 7-ethoxycoumarin by rat, mouse, guinea pig, cynomolgus monkey and human precision-cut liver slices.  |  Steensma, A., et al. 1994. Xenobiotica. 24: 893-907. PMID: 7810171
  11. Comparison of the metabolism of 7-ethoxycoumarin and coumarin in precision-cut rat liver and lung slices.  |  Price, RJ., et al. 1995. Food Chem Toxicol. 33: 233-7. PMID: 7896234
  12. Diverse functions of aromatase: O-deethylation of 7-ethoxycoumarin.  |  Toma, Y., et al. 1996. Endocrinology. 137: 3791-6. PMID: 8756548
  13. Induction of cytochrome P450 1A1 in rat liver slices by 7-ethoxycoumarin and 4-methyl-7-ethoxycoumarin.  |  Kuhn, UD., et al. 1998. Exp Toxicol Pathol. 50: 491-6. PMID: 9784028

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

7-Ethoxycoumarin, 25 mg

sc-207170
25 mg
$41.00

7-Ethoxycoumarin, 100 mg

sc-207170A
100 mg
$71.00