Promegestone

Modify Date: 2026-07-03 08:23:59

Promegestone Structure
Promegestone structure
Common Name Promegestone
CAS Number 34184-77-5 Molecular Weight 326.47200
Density 1.09 g/cm3 Boiling Point 486.8ºC at 760 mmHg
Molecular Formula C22H30O2 Melting Point 152°
MSDS N/A Flash Point 180.4ºC

 Use of Promegestone


Promegestone (R-5020), a progestin, is a potent progesterone receptor (PR) agonist. Promegestone has the potential for endocrine regulation and cancer research[1].

 Names

Name promegestone
Synonym More Synonyms

 Promegestone Biological Activity

Description Promegestone (R-5020), a progestin, is a potent progesterone receptor (PR) agonist. Promegestone has the potential for endocrine regulation and cancer research[1].
Related Catalog
In Vitro Promegestone (R-5020; 1 nM) is efficient ligand with a full agonist response profile and a low EC50 of 0.33 nM) in HELN-hPR while it only partially induced luciferase activity in U2OS-zfPR (EC50=1.93 nM)[1]. Promegestone is inactive in HELN cells that express luciferase but no functional receptor[1]. Promegestone (10 nM) robustly stimulates SLC37A2 expression in cells expressing SUMO-deficient PR, but not in cells expressing WT PR in T47D cell models[3].
In Vivo Promegestone (R-5020; 8 mg/kg; intramuscularly)-treated pregnant mice on day 18 postbreeding has the least deterioration in extracellular collagen (lowest OD) and highest cell density compared to other groups on the day before birth[2].
References

[1]. Clémentine Garoche, et al. Human and Zebrafish Nuclear Progesterone Receptors Are Differently Activated by Manifold Progestins. Environ Sci Technol. 2020 Aug 4;54(15):9510-9518.

[2]. Michael A Kirby, et al. Progesterone Receptor-Mediated Actions Regulate Remodeling of the Cervix in Preparation for Preterm Parturition. Reprod Sci. 2016 Nov;23(11):1473-1483.

[3]. Todd P Knutson, et al. Posttranslationally modified progesterone receptors direct ligand-specific expression of breast cancer stem cell-associated gene programs. J Hematol Oncol. 2017 Apr 17;10(1):89.

 Chemical & Physical Properties

Density 1.09 g/cm3
Boiling Point 486.8ºC at 760 mmHg
Melting Point 152°
Molecular Formula C22H30O2
Molecular Weight 326.47200
Flash Point 180.4ºC
Exact Mass 326.22500
PSA 34.14000
LogP 5.17780
Index of Refraction 1.553
InChIKey QFFCYTLOTYIJMR-XMGTWHOFSA-N
SMILES CCC(=O)C1(C)CCC2C3CCC4=CC(=O)CCC4=C3CCC21C

 Toxicological Information

CHEMICAL IDENTIFICATION

RTECS NUMBER :
KG2965000
CHEMICAL NAME :
Estra-4,9-dien-3-one, 17-alpha-methyl-17-propionyl-
CAS REGISTRY NUMBER :
34184-77-5
LAST UPDATED :
199209
DATA ITEMS CITED :
1
MOLECULAR FORMULA :
C22-H30-O2
MOLECULAR WEIGHT :
326.52

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

MUTATION DATA

TYPE OF TEST :
Unscheduled DNA synthesis
TEST SYSTEM :
Rodent - rat Liver
DOSE/DURATION :
20 umol/L
REFERENCE :
CRNGDP Carcinogenesis (London). (Oxford Univ. Press, Pinkhill House, Southfield Road, Eynsham, Oxford OX8 1JJ, UK) V.1- 1980- Volume(issue)/page/year: 13,373,1992

 PromegestoneBioassay

View more

Name: Relative binding affinity (RBA) for glucocorticoid receptor compared to RU-28362
Source: ChEMBL
Target: Glucocorticoid receptor
External Id: CHEMBL686327
Name: Relative binding affinity to glucocorticoid receptor on cytosol from hepatoma tissue ...
Source: ChEMBL
Target: Glucocorticoid receptor
External Id: CHEMBL686331
Name: Relative binding affinity to glucocorticoid receptor on cytosol from liver at 24 hr
Source: ChEMBL
Target: Glucocorticoid receptor
External Id: CHEMBL686333
Name: Relative binding affinity to glucocorticoid receptor on cytosol from hepatoma tissue ...
Source: ChEMBL
Target: Glucocorticoid receptor
External Id: CHEMBL686332
Name: Relative binding affinity to glucocorticoid receptor on cytosol from thymus at 24 hr
Source: ChEMBL
Target: Glucocorticoid receptor
External Id: CHEMBL878587
Name: Relative binding affinity to glucocorticoid receptor on cytosol from liver at 4 hr
Source: ChEMBL
Target: Glucocorticoid receptor
External Id: CHEMBL686334
Name: Relative binding affinity to glucocorticoid receptor on cytosol from thymus at 4 hr
Source: ChEMBL
Target: Glucocorticoid receptor
External Id: CHEMBL686335
Name: Choleostatic liver toxicity, either proven histopathologically or where the ratio of ...
Source: ChEMBL
Target: N/A
External Id: CHEMBL3137727
Name: Severe hepatitis, defined as possibly life-threatening liver failure or through clini...
Source: ChEMBL
Target: N/A
External Id: CHEMBL3137728
Name: Chronic liver disease either proven histopathologically, or through a chonic elevatio...
Source: ChEMBL
Target: N/A
External Id: CHEMBL3137729
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 Synonyms

R5020
(8S,13S,14S,17S)-13,17-dimethyl-17-propanoyl-1,2,6,7,8,11,12,14,15,16-decahydrocyclopenta[a]phenanthren-3-one
Promegestona
Promegestone
17,21-dimethyl-19-nor-4,9-pregnadiene-3,20-dione
RU5020
Promegestonum
promegestrone
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