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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
Structure of NITROMIFENE

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-

HIDE SMILES / InChI

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

PubMed

TitleDatePubMed
Effect of subcutaneous vs intraperitoneal administration of an anti-estrogen, CI-628, estradiol-and estradiol benzoate-stimulated lordosis in the ovariectomized rat.
1976 Oct
Anti-oestrogen action: uterine nuclear retention of the CI-628 anti-oestrogen receptor complex in vitro.
1977 Feb
Biological potency and uterine estrogen receptor interactions of the metabolites of the antiestrogens CI628 and U23,469.
1981 Jan
Formation of benzophenone and alpha, alpha-diarylacetophenone metabolites of the antiestrogen nitromiphene (CI628) in the presence of rat cecal contents.
1983 Sep 12
Sexual preference and feminine and masculine sexual behavior of male rats prenatally exposed to antiandrogen or antiestrogen.
1995 Jun
Patents

Patents

Sample Use Guides

In Vivo Use Guide
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
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 Fri Dec 15 16:24:40 UTC 2023
Edited
by admin
on Fri Dec 15 16:24:40 UTC 2023
Record UNII
5FS1NJ6Q8N
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
NITROMIFENE
INN  
INN  
Official Name English
nitromifene [INN]
Common Name English
1-(2-(P-(.ALPHA.-(P-METHOXYPHENYL)-.BETA.-NITROSTYRYL)PHENOXY)ETHYL)PYRROLIDINE
Common Name English
PYRROLIDINE, 1-(2-(4-(1-(4-METHOXYPHENYL)-2-NITRO-2-PHENYLETHENYL)PHENOXY)ETHYL)-
Systematic Name English
Classification Tree Code System Code
NCI_THESAURUS C481
Created by admin on Fri Dec 15 16:24:40 UTC 2023 , Edited by admin on Fri Dec 15 16:24:40 UTC 2023
Code System Code Type Description
NCI_THESAURUS
C90720
Created by admin on Fri Dec 15 16:24:40 UTC 2023 , Edited by admin on Fri Dec 15 16:24:40 UTC 2023
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WIKIPEDIA
Nitromifene
Created by admin on Fri Dec 15 16:24:40 UTC 2023 , Edited by admin on Fri Dec 15 16:24:40 UTC 2023
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SMS_ID
100000084122
Created by admin on Fri Dec 15 16:24:40 UTC 2023 , Edited by admin on Fri Dec 15 16:24:40 UTC 2023
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EPA CompTox
DTXSID50883143
Created by admin on Fri Dec 15 16:24:40 UTC 2023 , Edited by admin on Fri Dec 15 16:24:40 UTC 2023
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CAS
10448-84-7
Created by admin on Fri Dec 15 16:24:40 UTC 2023 , Edited by admin on Fri Dec 15 16:24:40 UTC 2023
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EVMPD
SUB09327MIG
Created by admin on Fri Dec 15 16:24:40 UTC 2023 , Edited by admin on Fri Dec 15 16:24:40 UTC 2023
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FDA UNII
5FS1NJ6Q8N
Created by admin on Fri Dec 15 16:24:40 UTC 2023 , Edited by admin on Fri Dec 15 16:24:40 UTC 2023
PRIMARY
ChEMBL
CHEMBL2105203
Created by admin on Fri Dec 15 16:24:40 UTC 2023 , Edited by admin on Fri Dec 15 16:24:40 UTC 2023
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INN
3773
Created by admin on Fri Dec 15 16:24:40 UTC 2023 , Edited by admin on Fri Dec 15 16:24:40 UTC 2023
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PUBCHEM
22150
Created by admin on Fri Dec 15 16:24:40 UTC 2023 , Edited by admin on Fri Dec 15 16:24:40 UTC 2023
PRIMARY
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