Details
Stereochemistry | ACHIRAL |
Molecular Formula | C25H24F3NO2 |
Molecular Weight | 427.4588 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 1 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
OCCNCCOC1=CC=C(C=C1)C(=C(/C2=CC=CC=C2)C(F)(F)F)\C3=CC=CC=C3
InChI
InChIKey=MHXVDXXARZCVRK-WCWDXBQESA-N
InChI=1S/C25H24F3NO2/c26-25(27,28)24(21-9-5-2-6-10-21)23(19-7-3-1-4-8-19)20-11-13-22(14-12-20)31-18-16-29-15-17-30/h1-14,29-30H,15-18H2/b24-23+
Panomifene (also known as GYKI-13504 or EGIS-5660), a triphenyl-alkene derivative that was studied as an antiestrogen. This drug binds to specific estrogen receptors and exhibits inhibitory effects on experimental mammary tumors both in vitro and in vivo. Panomifene reached phase II clinical trials for the treatment of breast cancer before development was terminated.
Originator
Approval Year
PubMed
Title | Date | PubMed |
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Influence of GYKI-13504, a new antioestrogen, on the responsiveness of isolated uterus removed from oestradiol pretreated rats to PGF2 alpha. | 1985 Dec |
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Determination of panomifene in human plasma by high-performance liquid chromatography. | 1994 May 13 |
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Antiestrogens, antiandrogens. | 1996 |
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A highly regio- and stereoselective carbocupration of fluoroalkylated internal alkynes: a short total synthesis of the antiestrogenic drug panomifene. | 2004 Mar 18 |
Patents
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/7519764
12 mg and 120 mg
Route of Administration:
Oral
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NCI_THESAURUS |
C481
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Panomifene
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ACTIVE MOIETY
METABOLITE (PARENT)
METABOLITE (PARENT)