Date published: 2026-2-5

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4-Methoxy-17β-estradiol (CAS 26788-23-8)

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Alternate Names:
(17β)-4-Methoxy-estra-1,3,5(10)-triene-3,17-diol; 4-Methoxyestra-1,3,5(10)-triene-3,17β-diol; 4-Methoxyestradiol
Application:
4-Methoxy-17β-estradiol is a metabolite of 17β-Estradiol
CAS Number:
26788-23-8
Purity:
≥96%
Molecular Weight:
302.41
Molecular Formula:
C19H26O3
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

QUICK LINKS

4-Methoxy-17β-estradiol (4-ME2) is a metabolite of estradiol with intriguing attributes that position it uniquely in the realm of biochemical research, particularly in the study of estrogen receptor dynamics and cellular signaling pathways. This compound acts through a sophisticated mechanism, engaging estrogen receptors with a distinct affinity compared to its parent hormone, estradiol, thereby modulating gene expression in a nuanced manner. Its ability to influence various signaling cascades, beyond the classical genomic pathways typically associated with estrogens, places it at the forefront of studies aiming to elucidate the non-genomic actions of estrogen-like molecules. Importantly, 4-Methoxy-17β-estradiol has been instrumental in advancing our understanding of the delicate interplay between estrogen receptors and cell proliferation processes, making it useful in the exploration of cellular responses to estrogens in diverse biological systems. This compound′s role in research extends to probing the mechanisms underlying estrogen-induced neuroprotection, offering a window into the complex effects of estrogens on neural tissues.


4-Methoxy-17β-estradiol (CAS 26788-23-8) References

  1. Liquid chromatography-mass spectrometry (LC-MS) of steroid hormone metabolites and its applications.  |  Penning, TM., et al. 2010. J Steroid Biochem Mol Biol. 121: 546-55. PMID: 20083198
  2. Differential estimation of isomeric 2- and 4-methoxylated estrogens in serum by matrix-assisted laser desorption ionization-tandem mass spectrometry.  |  Moon, JY., et al. 2013. Anal Sci. 29: 345-51. PMID: 23474725
  3. Improved detectability of sex steroids from frozen sections of breast cancer tissue using GC-triple quadrupole-MS.  |  Moon, JY., et al. 2018. J Steroid Biochem Mol Biol. 178: 185-192. PMID: 29269263
  4. 17 beta-estradiol metabolism by hamster hepatic microsomes: comparison of catechol estrogen O-methylation with catechol estrogen oxidation and glutathione conjugation.  |  Butterworth, M., et al. 1996. Chem Res Toxicol. 9: 793-9. PMID: 8831825
  5. Formation of catechol estrogen glutathione conjugates and gamma-glutamyl transpeptidase-dependent nephrotoxicity of 17beta-estradiol in the golden Syrian hamster.  |  Butterworth, M., et al. 1997. Carcinogenesis. 18: 561-7. PMID: 9067557

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

4-Methoxy-17β-estradiol, 1 mg

sc-210108A
1 mg
$322.00

4-Methoxy-17β-estradiol, 2.5 mg

sc-210108
2.5 mg
$406.00

4-Methoxy-17β-estradiol, 5 mg

sc-210108B
5 mg
$650.00

4-Methoxy-17β-estradiol, 10 mg

sc-210108C
10 mg
$1259.00