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4'-Hydroxynorendoxifen

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
4'-Hydroxynorendoxifen
Clinical data
Other namesN,N-Didesmethyl-4,4'-dihydroxytamoxifen
Identifiers
  • 4,4'-(1-(4-(2-Aminoethoxy)phenyl)but-1-ene-1,2-diyl)diphenol
CAS Number
PubChemCID
ChemSpider
Chemical and physical data
FormulaC24H25NO3
Molar mass375.468 g·mol−1
3D model (JSmol)
  • CCC(=C(C1=CC=C(O)C=C1)C1=CC=C(OCCN)C=C1)C1=CC=C(O)C=C1
  • InChI=1S/C24H25NO3/c1-2-23(17-3-9-20(26)10-4-17)24(18-5-11-21(27)12-6-18)19-7-13-22(14-8-19)28-16-15-25/h3-14,26-27H,2,15-16,25H2,1H3
  • Key:VYSGWFCGFKTGQC-UHFFFAOYSA-N

4'-Hydroxynorendoxifen is asynthetic,nonsteroidalantiestrogen of thetriphenylethylene group.[1][2] It is a dualselective estrogen receptor modulator (SERM) andaromatase inhibitor (AI), and was derived fromtamoxifen, a SERM, andnorendoxifen, ametabolite of tamoxifen that has been found to act as an AI.[1][2] The drug has been suggested for potential development as a treatment forestrogen receptor (ER)-positivebreast cancer.[1][2] It wassynthesized in 2015.[1]

References

[edit]
  1. ^abcdLv W, Liu J, Skaar TC,Flockhart DA,Cushman M (March 2015)."Design and synthesis of norendoxifen analogues with dual aromatase inhibitory and estrogen receptor modulatory activities".Journal of Medicinal Chemistry.58 (6):2623–48.doi:10.1021/jm501218e.PMC 4687028.PMID 25751283.
  2. ^abcNagini S (2017). "Breast Cancer: Current Molecular Therapeutic Targets and New Players".Anti-Cancer Agents in Medicinal Chemistry.17 (2):152–163.doi:10.2174/1871520616666160502122724.PMID 27137076.
ERTooltip Estrogen receptor
Agonists
Mixed
(SERMsTooltip Selective estrogen receptor modulators)
Antagonists
GPERTooltip G protein-coupled estrogen receptor
Agonists
Antagonists
Unknown
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