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Details

Stereochemistry ABSOLUTE
Molecular Formula C29H33NO3
Molecular Weight 443.5772
Optical Activity ( - )
Defined Stereocenters 2 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 7-DESMETHYLORMELOXIFENE, (-)-

SMILES

CC1(C)OC2=C(C=CC(O)=C2)[C@H]([C@@H]1C3=CC=CC=C3)C4=CC=C(OCCN5CCCC5)C=C4

InChI

InChIKey=PAIABUZDHNKOIL-IZLXSDGUSA-N
InChI=1S/C29H33NO3/c1-29(2)28(22-8-4-3-5-9-22)27(25-15-12-23(31)20-26(25)33-29)21-10-13-24(14-11-21)32-19-18-30-16-6-7-17-30/h3-5,8-15,20,27-28,31H,6-7,16-19H2,1-2H3/t27-,28+/m1/s1

HIDE SMILES / InChI

Molecular Formula C29H33NO3
Molecular Weight 443.5772
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 2 / 2
E/Z Centers 0
Optical Activity UNSPECIFIED

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
Centchroman, a selective estrogen receptor modulator, as a contraceptive and for the management of hormone-related clinical disorders.
2001 Jul
Modulation of estrogen action during preimplantation period and in immature estradiol-primed rat uterus by anti-implantation agent, ormeloxifene.
2005 Jun
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
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
Clinical pharmacokinetics and interaction of centchroman--a mini review.
2010 Apr
Long-term progestin contraceptives (LTPOC) induce aberrant angiogenesis, oxidative stress and apoptosis in the guinea pig uterus: A model for abnormal uterine bleeding in humans.
2010 Apr 27
Effects of estrogen, raloxifene, and levormeloxifene on the expression of Rho-kinase signaling molecules in urethral smooth muscle cells.
2010 Dec
The effect of long-term hormonal treatment on voiding patterns during filling cystometry and on urethral histology in a postpartum, ovariectomized female rat.
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.
Substance Class Chemical
Created
by admin
on Sat Dec 16 02:18:34 GMT 2023
Edited
by admin
on Sat Dec 16 02:18:34 GMT 2023
Record UNII
3JG8WB8GBG
Record Status Validated (UNII)
Record Version
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Name Type Language
7-DESMETHYLORMELOXIFENE, (-)-
Common Name English
2H-1-BENZOPYRAN-7-OL, 3,4-DIHYDRO-2,2-DIMETHYL-3-PHENYL-4-(4-(2-(1-PYRROLIDINYL)ETHOXY)PHENYL)-, (3R,4R)-REL-(-)-
Systematic Name English
7-DESMETHYL LEVORMELOXIFENE
Common Name English
7-DESMETHYLCENTCHROMAN, (-)-
Common Name English
2H-1-BENZOPYRAN-7-OL, 3,4-DIHYDRO-2,2-DIMETHYL-3-PHENYL-4-(4-(2-(1-PYRROLIDINYL)ETHOXY)PHENYL)-, TRANS-(-)-
Systematic Name English
(3R,4R)-3,4-DIHYDRO-2,2-DIMETHYL-3-PHENYL-4-(4-(2-(1-PYRROLIDINYL)ETHOXY)PHENYL)-2H-1-BENZOPYRAN-7-OL
Common Name English
(-)-7-DES-METHYL-ORMELOXIFENE
Common Name English
2H-1-BENZOPYRAN-7-OL, 3,4-DIHYDRO-2,2-DIMETHYL-3-PHENYL-4-(4-(2-(1-PYRROLIDINYL)ETHOXY)PHENYL)-, (3R,4R)-
Systematic Name English
Code System Code Type Description
PUBCHEM
3069190
Created by admin on Sat Dec 16 02:18:34 GMT 2023 , Edited by admin on Sat Dec 16 02:18:34 GMT 2023
PRIMARY
FDA UNII
3JG8WB8GBG
Created by admin on Sat Dec 16 02:18:34 GMT 2023 , Edited by admin on Sat Dec 16 02:18:34 GMT 2023
PRIMARY
CAS
193331-65-6
Created by admin on Sat Dec 16 02:18:34 GMT 2023 , Edited by admin on Sat Dec 16 02:18:34 GMT 2023
ALTERNATIVE
CAS
285130-93-0
Created by admin on Sat Dec 16 02:18:34 GMT 2023 , Edited by admin on Sat Dec 16 02:18:34 GMT 2023
PRIMARY
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TARGET->MODULATOR
ENANTIOMER -> ENANTIOMER
RACEMATE -> ENANTIOMER
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PRODRUG -> METABOLITE ACTIVE
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ACTIVE MOIETY