Details
Stereochemistry | ACHIRAL |
Molecular Formula | C27H28N2O4 |
Molecular Weight | 444.5222 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 1 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
COC1=CC=C(C=C1)C(=C(C2=CC=CC=C2)[N+]([O-])=O)C3=CC=C(OCCN4CCCC4)C=C3
InChI
InChIKey=MFKMXUFMHOCZHP-RQZHXJHFSA-N
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/b27-26-
Molecular Formula | C27H28N2O4 |
Molecular Weight | 444.5222 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 1 |
Optical Activity | NONE |
Nitromiphene (NIT; CI 628) is a triarylethylene antiestrogen shown to be effective in treatment of experimental breast cancer. Nitromiphene is one of the earliest nonsteroidal selective estrogen receptor modulators (SERMs). It is an anti-estrogen capable to translocate the estrogen receptor to the nucleus and to induce the replenishment of the cytosol receptor. Nitromiphene inhibited the uptake of [3H]-estradiol in rat whole homogenates and isolated cell nuclei tissues and the pituitary, and inhibited estradiol-induced female sexual behavior. Nitromiphene has thus been shown to suppress the growth of chemically induced and ransplantedmammary tumors in rodents. Also, Nitromiphene was shown to have potent, prolonged antiuterotropic effects in immature rats. Nitromiphene has been shown to undergo conversion to demethyl Nitromiphene (CI628M), a phenolic metabolite which had greater affinity for estrogen receptors and greater biological potency in vitro than did Nitromiphene. However, the in vivo antiestrogenic effects of Nitromiphene and demethyl Nitromiphene were similar, possibly due to facile O-demethylation of the former compound after administration.
Approval Year
PubMed
Title | Date | PubMed |
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Effects of anti-estrogens on testosterone stimulated male sexual behavior and peripheral target tissues in the castrate male rat. | 1975 Jun |
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Effect of subcutaneous vs intraperitoneal administration of an anti-estrogen, CI-628, estradiol-and estradiol benzoate-stimulated lordosis in the ovariectomized rat. | 1976 Oct |
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Anti-oestrogen action: uterine nuclear retention of the CI-628 anti-oestrogen receptor complex in vitro. | 1977 Feb |
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Biological potency and uterine estrogen receptor interactions of the metabolites of the antiestrogens CI628 and U23,469. | 1981 Jan |
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Formation of benzophenone and alpha, alpha-diarylacetophenone metabolites of the antiestrogen nitromiphene (CI628) in the presence of rat cecal contents. | 1983 Sep 12 |
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Sexual preference and feminine and masculine sexual behavior of male rats prenatally exposed to antiandrogen or antiestrogen. | 1995 Jun |
Patents
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/856418
Rats: Nitromiphene was injected intraperitoneally 2 h prior to an intravenous injection of [3H]estradiol, and the animals were killed 2 h after the estradiol.
Route of Administration:
Intraperitoneal
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/6391811
Curator's Comment: CI-628 citrate (1.5 ug/ml) significantly inhibited the transformation of rabbit morulae to blastocysts. https://www.ncbi.nlm.nih.gov/pubmed/6230443
Nitromiphene (CI-628) on the morphology and 17 beta-hydroxysteroid dehydrogenase (17 beta-HSD) activity of mouse blastocysts were compared in culture. When Day 4 mouse blastocysts were cultured in Eagle's medium containing 214 ng 3H-estradiol (E2) and CI-628 at 0, 1.5, 3, 6, 12 and 18 ug/ml, shedding of the zona pellucida was prevented by CI-628. The effect of CI-628 on the morphology was dose-dependent: little effects were seen at 1.5 and 3 ug/ml during the first 2 days, but the blastocysts became small, dense and eventually collapsed inside the zona. At 6 ug/ml and higher, the effect was quite pronounced. The earliest change was seen at 10 hours in 12 and 18 ug/ml CI-628 medium when 1/3 of the embryos became dense and smaller.
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 16:24:40 GMT 2023
by
admin
on
Fri Dec 15 16:24:40 GMT 2023
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Record UNII |
5FS1NJ6Q8N
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Record Status |
Validated (UNII)
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Record Version |
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-
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Systematic Name | English |
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NCI_THESAURUS |
C481
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C90720
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Nitromifene
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100000084122
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DTXSID50883143
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10448-84-7
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SUB09327MIG
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5FS1NJ6Q8N
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CHEMBL2105203
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3773
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22150
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Related Record | Type | Details | ||
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SALT/SOLVATE -> PARENT |
Related Record | Type | Details | ||
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ACTIVE MOIETY |