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Details

Stereochemistry RACEMIC
Molecular Formula C30H35NO3.ClH
Molecular Weight 494.065
Optical Activity ( + / - )
Defined Stereocenters 2 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ORMELOXIFENE HYDROCHLORIDE

SMILES

Cl.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=ZRGUGBSQWQXLHB-XZVFQGBBSA-N
InChI=1S/C30H35NO3.ClH/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;1H/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
Centchroman, a selective estrogen receptor modulator, as a contraceptive and for the management of hormone-related clinical disorders.
2001 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
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.
Name Type Language
ORMELOXIFENE HYDROCHLORIDE
USP-RS  
Common Name English
CENTCHROMAN HYDROCHLORIDE
MI  
Common Name English
6720 CDRI
Code English
PYRROLIDINE, 1-(2-(4-((3R,4R)-3,4-DIHYDRO-7-METHOXY-2,2-DIMETHYL-3-PHENYL-2H-1-BENZOPYRAN-4-YL)PHENOXY)ETHYL)-, HYDROCHLORIDE (1:1), REL-
Systematic Name English
CENTCHROMAN HYDROCHLORIDE [MI]
Common Name English
CDRI-67/20
Code English
TRANS-2,2-DIMETHYL-3-PHENYL-4-P-(.BETA.-PYRROLIDINOETHOXY)PHENYL-7-METHOXYCHROMAN HYDROCHLORIDE
Systematic Name English
67/20-CDRI
Code English
Code System Code Type Description
CAS
51023-56-4
Created by admin on Sat Dec 16 08:58:10 GMT 2023 , Edited by admin on Sat Dec 16 08:58:10 GMT 2023
PRIMARY
FDA UNII
GL3LAI70F3
Created by admin on Sat Dec 16 08:58:10 GMT 2023 , Edited by admin on Sat Dec 16 08:58:10 GMT 2023
PRIMARY
MERCK INDEX
m3242
Created by admin on Sat Dec 16 08:58:10 GMT 2023 , Edited by admin on Sat Dec 16 08:58:10 GMT 2023
PRIMARY Merck Index
SMS_ID
300000041211
Created by admin on Sat Dec 16 08:58:10 GMT 2023 , Edited by admin on Sat Dec 16 08:58:10 GMT 2023
PRIMARY
EPA CompTox
DTXSID40965301
Created by admin on Sat Dec 16 08:58:10 GMT 2023 , Edited by admin on Sat Dec 16 08:58:10 GMT 2023
PRIMARY
PUBCHEM
3039688
Created by admin on Sat Dec 16 08:58:10 GMT 2023 , Edited by admin on Sat Dec 16 08:58:10 GMT 2023
PRIMARY