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Details

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

SHOW SMILES / InChI
Structure of ORMELOXIFENE

SMILES

COC1=CC2=C(C=C1)[C@H]([C@H](C3=CC=CC=C3)C(C)(C)O2)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
Effect of centchroman on cellular and humoral immunity.
2007 Oct-Dec
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
ORMELOXIFENE
INN   MART.   WHO-DD  
INN  
Official Name English
ormeloxifene [INN]
Common Name English
ORMELOXIFENE [MART.]
Common Name English
CENTCHROMAN
MI  
Common Name English
CENTRON
Brand Name English
(±)-1-(2-(P-(TRANS-7-METHOXY-2,2-DIMETHYL-3-PHENYL-4-CHROMANYL)PHENOXY)ETHYL)PYRROLIDINE
Common Name English
CENTCHROMAN [MI]
Common Name English
TRANS-CENTCHROMAN
Common Name English
Ormeloxifene [WHO-DD]
Common Name English
SAHELI
Brand Name English
Classification Tree Code System Code
WHO-VATC QG03XC04
Created by admin on Sat Dec 16 18:04:56 GMT 2023 , Edited by admin on Sat Dec 16 18:04:56 GMT 2023
WHO-ATC G03XC04
Created by admin on Sat Dec 16 18:04:56 GMT 2023 , Edited by admin on Sat Dec 16 18:04:56 GMT 2023
NCI_THESAURUS C481
Created by admin on Sat Dec 16 18:04:56 GMT 2023 , Edited by admin on Sat Dec 16 18:04:56 GMT 2023
Code System Code Type Description
MERCK INDEX
m3242
Created by admin on Sat Dec 16 18:04:56 GMT 2023 , Edited by admin on Sat Dec 16 18:04:56 GMT 2023
PRIMARY Merck Index
MESH
C508548
Created by admin on Sat Dec 16 18:04:56 GMT 2023 , Edited by admin on Sat Dec 16 18:04:56 GMT 2023
PRIMARY
PUBCHEM
35805
Created by admin on Sat Dec 16 18:04:56 GMT 2023 , Edited by admin on Sat Dec 16 18:04:56 GMT 2023
PRIMARY
WIKIPEDIA
ORMELOXIFENE
Created by admin on Sat Dec 16 18:04:56 GMT 2023 , Edited by admin on Sat Dec 16 18:04:56 GMT 2023
PRIMARY
FDA UNII
44AXY5VE90
Created by admin on Sat Dec 16 18:04:56 GMT 2023 , Edited by admin on Sat Dec 16 18:04:56 GMT 2023
PRIMARY
CAS
31477-60-8
Created by admin on Sat Dec 16 18:04:56 GMT 2023 , Edited by admin on Sat Dec 16 18:04:56 GMT 2023
PRIMARY
DRUG CENTRAL
570
Created by admin on Sat Dec 16 18:04:56 GMT 2023 , Edited by admin on Sat Dec 16 18:04:56 GMT 2023
PRIMARY
EVMPD
SUB09462MIG
Created by admin on Sat Dec 16 18:04:56 GMT 2023 , Edited by admin on Sat Dec 16 18:04:56 GMT 2023
PRIMARY
DRUG BANK
DB13310
Created by admin on Sat Dec 16 18:04:56 GMT 2023 , Edited by admin on Sat Dec 16 18:04:56 GMT 2023
PRIMARY
NCI_THESAURUS
C90722
Created by admin on Sat Dec 16 18:04:56 GMT 2023 , Edited by admin on Sat Dec 16 18:04:56 GMT 2023
PRIMARY
ChEMBL
CHEMBL154126
Created by admin on Sat Dec 16 18:04:56 GMT 2023 , Edited by admin on Sat Dec 16 18:04:56 GMT 2023
PRIMARY
CAS
78994-24-8
Created by admin on Sat Dec 16 18:04:56 GMT 2023 , Edited by admin on Sat Dec 16 18:04:56 GMT 2023
SUPERSEDED
EPA CompTox
DTXSID6046844
Created by admin on Sat Dec 16 18:04:56 GMT 2023 , Edited by admin on Sat Dec 16 18:04:56 GMT 2023
PRIMARY
INN
7100
Created by admin on Sat Dec 16 18:04:56 GMT 2023 , Edited by admin on Sat Dec 16 18:04:56 GMT 2023
PRIMARY
SMS_ID
100000083347
Created by admin on Sat Dec 16 18:04:56 GMT 2023 , Edited by admin on Sat Dec 16 18:04:56 GMT 2023
PRIMARY