2-Methoxyestradiol

2-Methoxyestradiol
Systematic (IUPAC) name

(8R,9S,13S,14S,17S)-2-Methoxy-13-methyl-6,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthrene-3,17-diol
Identifiers
CAS Number	362-07-2^N
PubChem	CID 66414
ChemSpider	59788^Y
UNII	6I2QW73SR5^Y
ChEBI	CHEBI:28955^Y
ChEMBL	CHEMBL299613^Y
Chemical data
Formula	C₁₉H₂₆O₃
Molar mass	302.408 g/mol
SMILES Oc1cc3c(cc1OC)[C@H]2CC[C@@]4([C@@H](O)CC[C@H]4[C@@H]2CC3)C
InChI InChI=1S/C19H26O3/c1-19-8-7-12-13(15(19)5-6-18(19)21)4-3-11-9-16(20)17(22-2)10-14(11)12/h9-10,12-13,15,18,20-21H,3-8H2,1-2H3/t12-,13+,15-,18-,19-/m0/s1^Y Key:CQOQDQWUFQDJMK-SSTWWWIQSA-N^Y
^NY (what is this?) (verify)

2-Methoxyestradiol (2ME2) is a natural metabolite of estradiol. As an experimental drug candidate, it is being developed under the tradename of Panzem.^[1] It prevents the formation of new blood vessels that tumors need in order to grow (angiogenesis), hence it is an angiogenesis inhibitor.^[2]

It also acts as a vasodilator.

2ME2 is derived from estrogen, although it binds poorly to known estrogen receptors.^[3]

It induces apoptosis in some cancer cell lines.^[4]

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.^[5]

Preclinical models also suggest that 2ME2 could also be effective against inflammatory diseases such as rheumatoid arthritis. Several studies have been conducted showing 2ME2 is a microtubule-inhibitor^[6] and effective against prostate cancer in rodents.

The CAS name for 2ME2 is (17 beta)-2-methoxyestra-1,3,5(10)-triene-3,17-diol.

References

↑ EntreMed's Product Information Site Archived May 4, 2005 at the Wayback Machine
↑ 2-Methoxyestradiol: an endogenous antiangiogenic and antiproliferative drug candidate. Pribluda VS, et al. Cancer Metastasis Rev. 2000;19(1-2):173-9. Review.
↑ Dose-response effects of 2-methoxyestradiol on estrogen target tissues in the ovariectomized rat. Sibonga JD et al. Endocrinology. 2003 Mar;144(3):785-92. PMID 12586754
↑ LaValee; et al. (2003). "2-Methoxyestradiol Up-Regulates Death Receptor 5 and Induces Apoptosis through Activation of the Extrinsic Pathway" 63 (2): 468–75. PMID 12543804.
↑ "EntreMed Presents Results for Panzem® NCD Phase 2 Ovarian Cancer Study". Archived from the original on July 17, 2012.
↑ Lakhani, NJ; Sarkar, MA; Venitz, J; Figg, WD (2003). "2-Methoxyestradiol, a promising anticancer agent". Pharmacotherapy 23 (2): 165–72. doi:10.1592/phco.23.2.165.32088. PMID 12587805.

External links

Chemical Information and Structure from the Comparative Toxicogenomics Database
2-Methoxyestradiol 4 journal refs as URLs

This article is issued from Wikipedia - version of the Saturday, January 09, 2016. The text is available under the Creative Commons Attribution/Share Alike but additional terms may apply for the media files.