U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ABSOLUTE
Molecular Formula C30H35NO3
Molecular Weight 457.6038
Optical Activity ( - )
Defined Stereocenters 2 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of LEVORMELOXIFENE

SMILES

COC1=CC=C2[C@H]([C@H](C3=CC=CC=C3)C(C)(C)OC2=C1)C4=CC=C(OCCN5CCCC5)C=C4

InChI

InChIKey=XZEUAXYWNKYKPL-WDYNHAJCSA-N
InChI=1S/C30H35NO3/c1-30(2)29(23-9-5-4-6-10-23)28(26-16-15-25(32-3)21-27(26)34-30)22-11-13-24(14-12-22)33-20-19-31-17-7-8-18-31/h4-6,9-16,21,28-29H,7-8,17-20H2,1-3H3/t28-,29+/m1/s1

HIDE SMILES / InChI

Description
Curator's Comment: description was created based on several sources, including https://www.ncbi.nlm.nih.gov/pubmed/24468615 | https://www.ncbi.nlm.nih.gov/pubmed/11738564

Ormeloxifene (also known as centchroman) is a selective estrogen receptor modulator. It is a once-a-week non-steroidal oral contraceptive agent marketed in India and other countries under the brand names Novex-DS, Centron, and Sevista. Ormeloxifene has been investigated in the management of benign breast diseases such as mastalgia. The l-isomer, levormeloxifene, which has oestrogenic effects, has been investigated in the management of postmenopausal osteoporosis, but development appears to have been discontinued because of adverse effects. Recent studies have shown Ormeloxifene`s potent anti-cancer activities in breast, head and neck, and chronic myeloid leukemia cells. Several in vivo and clinical studies have reported that ormeloxifene possesses an excellent therapeutic index and has been well-tolerated, without any haematological, biochemical or histopathological toxicity, even with chronic administration. In India, ormeloxifene has been available as birth control since the early 1990s, and it is currently marketed there under the trade name Saheli. Ormeloxifene has also been licensed under the trade names Centron and Sevista. Ormeloxifene acts on oestrogen receptors. It has a weak estrogenic and potent antiestrogenic actions. It is expected to exert a contraceptive effect and normalise the bleeding from uterine cavity by regularising the expression of oestrogen receptors on the endometrium. As a contraceptive, it prevents proliferation and decidualisation of the endometrium, enhances blastocyst formation and slightly increases embryo transport through the oviducts.

Approval Year

TargetsConditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Unknown

Approved Use

Unknown
Primary
SEVISTA

Approved Use

Dysfunctional uterine bleeding

Launch Date

1992
Preventing
SEVISTA

Approved Use

Contraceptive

Launch Date

1992
Primary
Unknown

Approved Use

Unknown
PubMed

PubMed

TitleDatePubMed
Optimization of contraceptive dosage regimen of Centchroman.
2001 Jan
Centchroman, a selective estrogen receptor modulator, as a contraceptive and for the management of hormone-related clinical disorders.
2001 Jul
Interaction with anti-implantation and estrogen antagonistic activities of dl-ormeloxifene, a selective estrogen receptor modulator, by tetracycline in female Sprague-Dawley rats.
2001 Oct
Evaluation of interaction potential of certain concurrently administered drugs with pharmacological and pharmacokinetic profile of centchroman in rats.
2002 Jul
Effects of 3-phenyl-4-[[4-[2-(1-piperidinyl)ethoxy]phenyl]methyl]- 2H-1-benzopyran-7-ol (CHF 4056), a novel nonsteroidal estrogen agonist/antagonist, on reproductive and nonreproductive tissue.
2002 Mar
In vitro anti-resorptive activity and prevention of ovariectomy-induced osteoporosis in female Sprague-Dawley rats by ormeloxifene, a selective estrogen receptor modulator.
2004 Jun
Differential effects of estrogen and raloxifene on messenger RNA and matrix metalloproteinase 2 activity in the rat uterus.
2005 Apr
Modulation of estrogen action during preimplantation period and in immature estradiol-primed rat uterus by anti-implantation agent, ormeloxifene.
2005 Jun
Effect of ormeloxifene on ovariectomy-induced bone resorption, osteoclast differentiation and apoptosis and TGF beta-3 expression.
2006 Aug
Antioxidant defense system during endometrial receptivity in the guinea pig: effect of ormeloxifene, a selective estrogen receptor modulator.
2006 Jan
Modulation of estrogen receptor transactivation and estrogen-induced gene expression by ormeloxifene-a triphenylethylene derivative.
2006 Nov
Role of centchroman in regression of mastalgia and fibroadenoma.
2007 Jun
Modulation of AP-1 mediated estrogenic response by ormeloxifene in rat uterus.
2007 May
Effect of centchroman on cellular and humoral immunity.
2007 Oct-Dec
Efficacy and safety of ormeloxifene in management of menorrhagia: a pilot study.
2009 Aug
Expression of estrogen receptor co-regulators SRC-1, RIP140 and NCoR and their interaction with estrogen receptor in rat uterus, under the influence of ormeloxifene.
2009 Aug
Expression of alphaVbeta3 integrin in rat endometrial epithelial cells and its functional role during implantation.
2009 Jan 15
Effect of ormeloxifene, a selective estrogen receptor modulator, on biomarkers of endometrial receptivity and pinopode development and its relation to fertility and infertility in Indian subjects.
2009 Jun
Effects of estrogen, raloxifene, and levormeloxifene on the expression of Rho-kinase signaling molecules in urethral smooth muscle cells.
2010 Dec
Patents

Sample Use Guides

The participants were randomly assigned to double-blind therapy with levormeloxifene1.25, 5.00, 10.00 or 20.00 mg/day or placebo for 12 months.
Route of Administration: Oral
The Ishikawa cell line is grown in DMEM+10% FCS. Cells are plated in microtiter plates (1x10^5 cells/mL) in stimulation medium (DMEM+5% dextran-coated charcoal treated FSC and a total of 4.5 g/L d-glucose) and incubated for 1 day at 37 C and 5% CO2. The medium is changed and the Levormeloxifene is added in a total volume of 150 mL. The cells are incubated for another 3 days. The increased level of the alkaline phosphatase enzyme is measured as described in Littlefield et al. using pnitrophenyl phosphate as a substrate. All compounds are tested in dose–response curves from 10^6 to 10^14 M, maximal effect was achieved using 10 nM moxestrol.
Name Type Language
LEVORMELOXIFENE
INN   WHO-DD  
INN  
Official Name English
(-)-1-(2-(4-((3R,4R)-7-METHOXY-2,2-DIMETHYL-3-PHENYL-4-CHROMANYL)PHENOXY)ETHYL)PYRROLIDINE
Systematic Name English
CENTCHROMAN (-)-FORM [MI]
Common Name English
(-)-CENTCHROMAN
Common Name English
Levormeloxifene [WHO-DD]
Common Name English
L-CENTCHROMAN
Common Name English
levormeloxifene [INN]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C1821
Created by admin on Fri Dec 15 16:06:07 GMT 2023 , Edited by admin on Fri Dec 15 16:06:07 GMT 2023
Code System Code Type Description
ChEMBL
CHEMBL301327
Created by admin on Fri Dec 15 16:06:07 GMT 2023 , Edited by admin on Fri Dec 15 16:06:07 GMT 2023
PRIMARY
NCI_THESAURUS
C82904
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PRIMARY
INN
7357
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PRIMARY
MESH
C108255
Created by admin on Fri Dec 15 16:06:07 GMT 2023 , Edited by admin on Fri Dec 15 16:06:07 GMT 2023
PRIMARY
SMS_ID
100000082283
Created by admin on Fri Dec 15 16:06:07 GMT 2023 , Edited by admin on Fri Dec 15 16:06:07 GMT 2023
PRIMARY
MERCK INDEX
m3242
Created by admin on Fri Dec 15 16:06:07 GMT 2023 , Edited by admin on Fri Dec 15 16:06:07 GMT 2023
PRIMARY Merck Index
PUBCHEM
35805
Created by admin on Fri Dec 15 16:06:07 GMT 2023 , Edited by admin on Fri Dec 15 16:06:07 GMT 2023
PRIMARY
WIKIPEDIA
LEVORMELOXIFENE
Created by admin on Fri Dec 15 16:06:07 GMT 2023 , Edited by admin on Fri Dec 15 16:06:07 GMT 2023
PRIMARY
EVMPD
SUB08489MIG
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PRIMARY
CAS
78994-23-7
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PRIMARY
EPA CompTox
DTXSID301317017
Created by admin on Fri Dec 15 16:06:07 GMT 2023 , Edited by admin on Fri Dec 15 16:06:07 GMT 2023
PRIMARY
FDA UNII
9512UKZ352
Created by admin on Fri Dec 15 16:06:07 GMT 2023 , Edited by admin on Fri Dec 15 16:06:07 GMT 2023
PRIMARY