Neha Patil (Editor)

2 Methoxyestradiol

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CAS Number
  
362-07-2

ChemSpider
  
59788

ChEBI
  
CHEBI:28955

Molar mass
  
302.408 g/mol

PubChem CID
  
66414

UNII
  
6I2QW73SR5

Formula
  
C19H26O3

2-Methoxyestradiol 2Methoxyestradiol Wikipedia

Synonyms
  
2-Methoxyestra-1,3,5(10)-triene-3,17β-diol

2-Methoxyestradiol (2-ME2) is a natural metabolite of estradiol. As an experimental drug candidate, it is being developed under the tradename of Panzem. It prevents the formation of new blood vessels that tumors need in order to grow (angiogenesis), hence it is an angiogenesis inhibitor.

2-Methoxyestradiol 2Methoxyestradiol 2MeOE2 HIF inhibitor Read Reviews

It also acts as a vasodilator.

2-ME2 is derived from estradiol, although it binds poorly (2000-fold lower activational potency) to known estrogen receptors. However, 2-ME2 retains activity as a high-affinity agonist of the GPER (GPR30).

2-Methoxyestradiol 2Methoxyestradiol 2MeOE2 HIF inhibitor Read Reviews

It induces apoptosis in some cancer cell lines.

It has undergone Phase 1 clinical trials against breast cancer.

A phase II trial of 18 advanced ovarian cancer patients reported encouraging results in Oct 2007.

Preclinical models also suggest that 2-ME2 could also be effective against inflammatory diseases such as rheumatoid arthritis. Several studies have been conducted showing 2-ME2 is a microtubule-inhibitor and effective against prostate cancer in rodents.

2-Methoxyestradiol 2Methoxyestradiol 2MeOE2 HIF inhibitor Read Reviews

As of 2015, all clinical development of 2-ME2 has been suspended or discontinued.

2-Methoxyestradiol 2Methoxyestradiol powder SigmaAldrich

2-Methoxyestradiol File2METHOXYESTRADIOLpng Wikimedia Commons

2-Methoxyestradiol A SecondGeneration 2Methoxyestradiol Prodrug Is Effective against


2-Methoxyestradiol Does 2Methoxyestradiol Represent the New and Improved Hormone

2-Methoxyestradiol 2Methoxyestradiol C19H26O3 PubChem

2-Methoxyestradiol Syntheses of 2methoxyestradiol and eugenol template based

References

2-Methoxyestradiol Wikipedia