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Details

Stereochemistry ABSOLUTE
Molecular Formula C30H35NO3.C4H4O4
Molecular Weight 573.676
Optical Activity UNSPECIFIED
Defined Stereocenters 2 / 2
E/Z Centers 1
Charge 0

SHOW SMILES / InChI
Structure of LEVORMELOXIFENE FUMARATE

SMILES

OC(=O)\C=C\C(O)=O.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=CKDZFQCZLXNLRD-JJGRXVLVSA-N
InChI=1S/C30H35NO3.C4H4O4/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;5-3(6)1-2-4(7)8/h4-6,9-16,21,28-29H,7-8,17-20H2,1-3H3;1-2H,(H,5,6)(H,7,8)/b;2-1+/t28-,29+;/m1./s1

HIDE SMILES / InChI

Molecular Formula C30H35NO3
Molecular Weight 457.6038
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 2 / 2
E/Z Centers 0
Optical Activity UNSPECIFIED

Molecular Formula C4H4O4
Molecular Weight 116.0722
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 1
Optical Activity NONE

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

6.9422403E11
Preventing
SEVISTA

Approved Use

Contraceptive

Launch Date

6.9422403E11
Primary
Unknown

Approved Use

Unknown
PubMed

PubMed

TitleDatePubMed
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
Antioxidant defense system during endometrial receptivity in the guinea pig: effect of ormeloxifene, a selective estrogen receptor modulator.
2006 Jan
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
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 Fri Dec 15 19:19:40 UTC 2023
Edited
by admin
on Fri Dec 15 19:19:40 UTC 2023
Record UNII
2XFK7X56Q3
Record Status Validated (UNII)
Record Version
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Name Type Language
LEVORMELOXIFENE FUMARATE
Common Name English
PYRROLIDINE, 1-(2-(4-((3R,4R)-3,4-DIHYDRO-7-METHOXY-2,2-DIMETHYL-3-PHENYL-2H-1-BENZOPYRAN-4-YL)PHENOXY)ETHYL)-, (2E)-2-BUTENEDIOATE (1:1)
Systematic Name English
LEVORMELOXIFENE FUMARATE [JAN]
Common Name English
Code System Code Type Description
PUBCHEM
9938031
Created by admin on Fri Dec 15 19:19:40 UTC 2023 , Edited by admin on Fri Dec 15 19:19:40 UTC 2023
PRIMARY
FDA UNII
2XFK7X56Q3
Created by admin on Fri Dec 15 19:19:40 UTC 2023 , Edited by admin on Fri Dec 15 19:19:40 UTC 2023
PRIMARY
CAS
199583-01-2
Created by admin on Fri Dec 15 19:19:40 UTC 2023 , Edited by admin on Fri Dec 15 19:19:40 UTC 2023
PRIMARY
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