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Trimegestone

CAS No.
74513-62-5
Chemical Name:
Trimegestone
Synonyms
TRIMEBUTINEMALEATE;RU 27987;TRIMEGESTONE;Trimegestone-C13-D3;Trimegestone USP/EP/BP;74513-62-5 Trimegestone;17β-[(S)-2-Hydroxy-1-oxopropyl]-17α-methylestra-4,9-dien-3-one;Estra-4,9-dien-3-one,17-[(2S)-2-hydroxy-1-oxopropyl]-17-Methyl-, (17b)-;Estra-4,9-dien-3-one, 17-[(2S)-2-hydroxy-1-oxopropyl]-17-methyl-, (17β)-;8S,13S,14S,17S)-17-[(2S)-2-Hydroxypropanoyl]-13,17-diMethyl-1,2,6,7,8,11,12,14,15,16-decahydrocyclop
CBNumber:
CB1463057
Molecular Formula:
C22H30O3
Molecular Weight:
342.48
MDL Number:
MFCD00866261
MOL File:
74513-62-5.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-07-27 17:00:41

Trimegestone Properties

Boiling point 522.6±50.0 °C(Predicted)
Density 1.16±0.1 g/cm3(Predicted)
pka 13.04±0.20(Predicted)
form Solid
CAS DataBase Reference 74513-62-5
FDA UNII 4658K0H08W

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)
GHS07
Signal word  Warning
Hazard statements  H319
Precautionary statements  P264-P280-P305+P351+P338-P337+P313P

Trimegestone price More Price(8)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Biosynth FT39363 Trimegestone 74513-62-5 1mg $278.42 2026-06-04 Buy
Biosynth FT39363 Trimegestone 74513-62-5 5mg $1183.3 2026-06-04 Buy
Biosynth FT39363 Trimegestone 74513-62-5 10mg $1893.3 2026-06-04 Buy
aablocks AA005JLC (17β)-17-[(2S)-2-Hydroxy-1-oxopropyl]-17-methylestra-4,9-dien-3-one 99% 74513-62-5 10mg $1300 2026-05-28 Buy
AHH MT-59931 Trimegestone 97% 0.1g $410 2026-05-26 Buy
Product number Packaging Price Buy
FT39363 1mg $278.42 Buy
FT39363 5mg $1183.3 Buy
FT39363 10mg $1893.3 Buy
AA005JLC 10mg $1300 Buy
MT-59931 0.1g $410 Buy

Trimegestone Chemical Properties, Uses, Production

Description

Trimegestone was launched in Sweden in combination with 17 beta-estradiol as hormone replacement therapy (HRT) for the oral treatment of menopausal vasomotor symptoms and the prevention of osteoporosis. Trimegestone can be synthesized in a multistep process starting with 3,3-(ethylenedioxy)estra-5(10),9(11)-dien-17-one and involving a final key regio- and enantioselective reduction of the 17beta-2-oxopropionyl side chain with Saccharomyces cerevisiae in sodium acetate buffer. The norpregnane progestin, trimegestone, exhibited high specificity and affinity for the progesterone receptor, no affinity for the estrogen receptor, and weak affinity for androgen, glucocorticoid and mineralcorticoid receptors. The relative binding affinity of trimegestone for the progestin receptor was 7 times that of progesterone, 4.5 and 1.5 times greater than norethindrone and medroxyprogesterone acetate, respectively. The decrease in circulating estrogen associated with menopause is thought to contribute to a variety of diseases in women, including osteoporosis, cancers, cardiovascular disease, stroke and cognitive dectine. Estrogen conserves bone mass by reducing bone turnover. Estrogen replacement therapy (ERT) is recommended for all women at high risk for osteoporosis. However, estrogen therapy alone has been linked to an increase risk of endometrial cancer; thus progestin (such as trimegestone) is often prescribed in combination with estrogen for women who have not had a hysterectomy. The progestin blocks the estrogenic activity in the endometrium, thereby reducing the potential unwanted cell proliferation in response to estrogen administration. This action of progestin occurs without compromising the beneficial effects of estrogen on hot flashes and bone loss. A study in rats with osteopenia showed that treatment with trimegestone in combination with 17beta-estradiol for 2 months was superior to norethisterone in preventing bone loss. Treatment with trimegestone also more effectively prevented estradiol-induced uterine atrophy as compared to norethisterone. In clinical trials, trimegestone was found to be a highly effective oral progestone for endometrial protection and beneficial effects have been observed on anxiety, depression, somatic, and vasomotor menopausal symptoms. The combination provides improved and predictable cycle control and a better lipid profile in comparison with existing products. Minimal progestogenic adverse events (i.e. mastalgia, acne, nausea, leg cramps, seborrhea and bloatedness) were reported. Totelle Sekvens employs a cyclic regimen of 14 days of 2mg of 17beta--estradiol alone and 14 days in combination with 500 μg of trimegestone.

Originator

Aventis (France)

Uses

Trimegestone causes an increased risk for uterine sarcomas and endometrial cancers with prolonged use. Used in hormone replacement therapies and the treatment of post-menopausal diseases.

Definition

ChEBI: Trimegestone is a 20-oxo steroid.

brand name

Totelle Sekvens, Ondeva

General Description

Trimegestone, 17β-(S)-lactoyl-17-methyl-estra-4,9-dien-3-one, is a highly modified norprogesteronederivative. The key structural differences are a17β-lactoyl group in place of the typical acetyl group, a17α-methyl, and a C9-C10 double bond. Trimegestonelacks androgenic action and has little to no affinity for theER and GR. Although already approved for treating HRTin Sweden in combination with estradiol, it is still in developmentin the United States for its use in HRT and as a componentof oral contraceptives.

Trimegestone Preparation Products And Raw materials

Raw materials

Preparation Products

Global Suppliers ( 75)
Supplier Tel Email Country ProdList Advantage
J & K SCIENTIFIC LTD. 18210857532 18210857532 jkinfo@jkchemical.com China 96815 76
Chengdu Ai Keda Chemical Technology Co., Ltd. 4008-755-333 18080918076 800078821@qq.com China 9706 55
Shanghai T&W Pharmaceutical Co., Ltd. +86 21 61551611 China 9874 58
Chengdu HuaXia Chemical Reagent Co. Ltd 400-1166-196 13458535857 cdhxsj@163.com China 13323 58
Shenzhen Nexconn Pharmatechs Ltd. 0755-89396905 admin@nexconn.com China 299 55
Chizhou Kailong Import and Export Trade Co., Ltd. xg01_gj@163.com China 9413 50
BOC Sciences 16314854226 info@bocsci.com United States 9909 65
Raw material medicin reagent co.,Ltd sales@njromanme.com China 4511 58
Amadis Chemical Company Limited 571-89925085 sales@amadischem.com China 131885 58
Zhengzhou Acme Chemical Co., Ltd. 037163312495 13303845143 1416159398@qq.com China 10150 58

Related articles

View Latest Price from Trimegestone manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Trimegestone pictures 2026-07-27 Trimegestone
74513-62-5
$1820.00-3100.00 10g TargetMol Chemicals Inc.
Trimegestone pictures 2025-06-25 Trimegestone
74513-62-5
$1.10 1g 99.0% min 100 tons min Shaanxi Dideu Medichem Co. Ltd
Trimegestone pictures 2020-01-03 Trimegestone
74513-62-5
$7.00 1KG 99% 100kg Career Henan Chemical Co
  • Trimegestone pictures
  • Trimegestone
    74513-62-5
  • $1820.00-3100.00
  • TargetMol Chemicals Inc.
  • Trimegestone pictures
  • Trimegestone
    74513-62-5
  • $1.10
  • 99.0% min
  • Shaanxi Dideu Medichem Co. Ltd
(8s,13s,14s,17s)-17-[(2s)-2-hydroxypropanoyl]-13,17-dimethyl-1,2,6,7,8,11,12,14,15,16-decahydrocyclopenta[a]phenanthren-3-one TRIMEGESTONE RU 27987 TRIMEBUTINEMALEATE 17β-[(S)-2-Hydroxy-1-oxopropyl]-17α-methylestra-4,9-dien-3-one 8S,13S,14S,17S)-17-[(2S)-2-Hydroxypropanoyl]-13,17-diMethyl-1,2,6,7,8,11,12,14,15,16-decahydrocyclop Estra-4,9-dien-3-one,17-[(2S)-2-hydroxy-1-oxopropyl]-17-Methyl-, (17b)- 17-(2-hydroxy-1-oxopropyl)-13,17-dimethyl-1,2,6,7,8,11,12,14,15,16-decahydrocyclopenta[a]phenanthren-3-one Estra-4,9-dien-3-one, 17-[(2S)-2-hydroxy-1-oxopropyl]-17-methyl-, (17β)- Trimegestone USP/EP/BP Trimegestone-C13-D3 74513-62-5 Trimegestone 74513-62-5 C22H30O3