Miproxifene: Difference between revisions

From WikiMD's Wellness Encyclopedia

CSV import
CSV import
Line 72: Line 72:
{{antineoplastic-drug-stub}}
{{antineoplastic-drug-stub}}
{{dictionary-stub1}}
{{dictionary-stub1}}
<gallery>
File:Miproxifene.svg|Miproxifene
</gallery>
<gallery>
<gallery>
File:Miproxifene.svg|Miproxifene
File:Miproxifene.svg|Miproxifene
</gallery>
</gallery>

Revision as of 01:41, 20 February 2025

Miproxifene
INN
Drug class
Routes of administration
Pregnancy category
Bioavailability
Metabolism
Elimination half-life
Excretion
Legal status
CAS Number 129612-87-9
PubChem 3037015
DrugBank
ChemSpider 2300875
KEGG


Miproxifene (INN) (former developmental code name DP-TAT-59) is a nonsteroidal selective estrogen receptor modulator (SERM) of the triphenylethylene group that was never marketed.<ref name="AdisInsight">http://webcache.googleusercontent.com/search?q=cache:FyhxGXFiLogJ:adisinsight.springer.com/drugs/800000796+&cd=1&hl=en&ct=clnk&gl=us</ref><ref name="StellaBorchardt2007">,

 Prodrugs: Challenges and Rewards. online version, 
  
 Springer Science & Business Media, 
  
  
  
 ISBN 978-0-387-49782-2, 
  
  
  
 Pages: 168–169,</ref> It is a derivative of afimoxifene (4-hydroxytamoxifen) in which an additional 4-isopropyl group is present in the β-phenyl ring.<ref name="OettelSchillinger2012">, 
  
 Estrogens and Antiestrogens I: Physiology and Mechanisms of Action of Estrogens and Antiestrogens. online version, 
  
 Springer Science & Business Media, 
  
  
  
 ISBN 978-3-642-58616-3, 
  
  
  
 Pages: 58–60,</ref> The drug has been found to be 3- to 10-fold more potent than tamoxifen in inhibiting breast cancer cell growth in in vitro models.<ref name="AdisInsight" /><ref name="KelloffHawk2008">, 
  
 Cancer Chemoprevention: Volume 2: Strategies for Cancer Chemoprevention. online version, 
  
 Springer, 
  
  
  
 ISBN 978-1-59259-768-0, 
  
  
  
 Pages: 251–,</ref><ref name="OttowWeinmann2008">, 
  
 Nuclear Receptors as Drug Targets. online version, 
  
 John Wiley & Sons, 
  
  
  
 ISBN 978-3-527-62330-3, 
  
  
  
 Pages: 90–,</ref> Miproxifene is the active metabolite of miproxifene phosphate (TAT-59), a phosphate ester and prodrug of miproxifene that was developed to improve its water solubility.<ref name="AdisInsight" /><ref name="StellaBorchardt2007" /><ref name="StromgaardKrogsgaard-Larsen2016">, 
  
 Textbook of Drug Design and Discovery, Fifth Edition. online version, 
  
 CRC Press, 
  
  
  
 ISBN 978-1-4987-0279-9, 
  
  
  
 Pages: 162–,</ref><ref name="YangYeh2013">, 
  
 Enzyme Technologies: Pluripotent Players in Discovering Therapeutic Agent. online version, 
  
 Wiley, 
  
  
  
 ISBN 978-1-118-73989-1, 
  
  
  
 Pages: 166–,</ref> Miproxifene phosphate was under development for the treatment of breast cancer and reached phase III clinical trials for this indication but development was discontinued.<ref name="AdisInsight" />

References

<references group="" responsive="0"></references>




Stub icon
   This article is a drug stub. You can help WikiMD by expanding it!



This article is a medical stub. You can help WikiMD by expanding it!
PubMed
Wikipedia
Stub icon
   This article is a medical stub. You can help WikiMD by expanding it!