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Nitromifene

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
Nitromifene
Clinical data
Other namesCI-628; CN-5518; CN-55945
Identifiers
  • 1-[2-[4-[1-(4-Methoxyphenyl)-2-nitro-2-phenylethenyl]phenoxy]ethyl]pyrrolidine
CAS Number
PubChemCID
ChemSpider
UNII
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC27H28N2O4
Molar mass444.531 g·mol−1
3D model (JSmol)
  • COC1=CC=C(C=C1)C(=C(C2=CC=CC=C2)[N+](=O)[O-])C3=CC=C(C=C3)OCCN4CCCC4
  • InChI=1S/C27H28N2O4/c1-32-24-13-9-21(10-14-24)26(27(29(30)31)23-7-3-2-4-8-23)22-11-15-25(16-12-22)33-20-19-28-17-5-6-18-28/h2-4,7-16H,5-6,17-20H2,1H3
  • Key:MFKMXUFMHOCZHP-UHFFFAOYSA-N

Nitromifene (INNTooltip International Nonproprietary Name; also as thecitratesaltnitromifene citrate (USANTooltip United States Adopted Name), developmental code namesCI-628,CN-5518,CN-55945) is anonsteroidalselective estrogen receptor modulator (SERM) related totriphenylethylenes liketamoxifen that was never marketed.[1] It is a mixture of (E)- and (Z)-isomers that possess similarantiestrogenic activity.[2] The drug was described in 1966.[1] Along with tamoxifen,nafoxidine, andclomifene, it was one of the earliest SERMs.[3]

Nitromifene has been found to dissociate from theestrogen receptor 250-fold faster thanestradiol.[4] This may be involved in its antagonistic activity at the estrogen receptor.[4]

References

[edit]
  1. ^abElks J (14 November 2014).The Dictionary of Drugs: Chemical Data: Chemical Data, Structures and Bibliographies. Springer. pp. 880–.ISBN 978-1-4757-2085-3.
  2. ^Kirk RE, Othmer DF (1980).Encyclopedia of chemical technology. Wiley. p. 676.ISBN 978-0-471-02065-3.
  3. ^Jordan VC, Morrow M (June 1999)."Tamoxifen, raloxifene, and the prevention of breast cancer".Endocrine Reviews.20 (3):253–278.doi:10.1210/edrv.20.3.0368.PMID 10368771.
  4. ^abDe Boer W, Notides AC, Katzenellenbogen BS, Hayes JR, Katzenellenbogen JA (January 1981). "The capacity of the antiestrogen CI-628 to activate the estrogen receptor in vitro".Endocrinology.108 (1):206–212.doi:10.1210/endo-108-1-206.PMID 7007019.
ERTooltip Estrogen receptor
Agonists
Mixed
(SERMsTooltip Selective estrogen receptor modulators)
Antagonists
GPERTooltip G protein-coupled estrogen receptor
Agonists
Antagonists
Unknown
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