Epiandrosterone

Modify Date: 2024-01-02 18:57:49

Epiandrosterone Structure
Epiandrosterone structure
Common Name Epiandrosterone
CAS Number 481-29-8 Molecular Weight 290.440
Density 1.1±0.1 g/cm3 Boiling Point 413.1±45.0 °C at 760 mmHg
Molecular Formula C19H30O2 Melting Point 172-174 °C
MSDS USA Flash Point 176.4±21.3 °C

 Use of Epiandrosterone


Epiandrosterone is a steroid hormone with weak androgenic activity. Epiandrosterone is naturally produced by the enzyme 5α-reductase from the adrenal hormone DHEA.

 Names

Name epiandrosterone
Synonym More Synonyms

 Epiandrosterone Biological Activity

Description Epiandrosterone is a steroid hormone with weak androgenic activity. Epiandrosterone is naturally produced by the enzyme 5α-reductase from the adrenal hormone DHEA.
Related Catalog
Target

Human Endogenous Metabolite

References

[1]. Mitamura K, et al. Determination of sulfates of androsterone and epiandrosterone in human serum using isotope diluted liquid chromatography-electrospray ionization-mass spectrometry. Biomed Chromatogr. 2005 Dec;19(10):796-801.

 Chemical & Physical Properties

Density 1.1±0.1 g/cm3
Boiling Point 413.1±45.0 °C at 760 mmHg
Melting Point 172-174 °C
Molecular Formula C19H30O2
Molecular Weight 290.440
Flash Point 176.4±21.3 °C
Exact Mass 290.224579
PSA 37.30000
LogP 3.75
Vapour Pressure 0.0±2.2 mmHg at 25°C
Index of Refraction 1.536
Water Solubility practically insoluble

 Safety Information

Personal Protective Equipment Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
Safety Phrases S22-S24/25
RIDADR NONH for all modes of transport
WGK Germany 3
HS Code 2937290090

 Synthetic Route

 Customs

HS Code 2937290090

 Articles6

More Articles
Novel potent and selective bile acid derivatives as TGR5 agonists: biological screening, structure-activity relationships, and molecular modeling studies.

J. Med. Chem. 51 , 1831-41, (2008)

TGR5, a metabotropic receptor that is G-protein-coupled to the induction of adenylate cyclase, has been recognized as the molecular link connecting bile acids to the control of energy and glucose home...

Potent and selective steroidal inhibitors of 17beta-hydroxysteroid dehydrogenase type 7, an enzyme that catalyzes the reduction of the key hormones estrone and dihydrotestosterone.

J. Med. Chem. 52 , 7488-502, (2009)

17beta-Hydroxysteroid dehydrogenase type 7 (17beta-HSD7) catalyzes the reduction of estrone (E(1)) into estradiol (E(2)) and of dihydrotestosterone (DHT) into 5alpha-androstane-3beta,17beta-diol (3bet...

A simple method for the small scale synthesis and solid-phase extraction purification of steroid sulfates.

Steroids 92 , 74-80, (2014)

Steroid sulfates are a major class of steroid metabolite that are of growing importance in fields such as anti-doping analysis, the detection of residues in agricultural produce or medicine. Despite t...

 Synonyms

UNII:8TR252Z538
D-epiandrosterone
3β-Hydroxyetioallocholan-17-one
3b-Hydroxy-5a-androstane-17-one
3β-Hydroxy-5α-androstan-17-one
3BETA-HYDROXY-5ALPHA-ANDROSTAN-17-ONE
3b-Androsterone
3b-Androstanol-17-one
EINECS 207-563-3
Epi-androsterone
3β-hydroxy-androstan-17-one
ISOANDROSTERONE
MFCD00064134
5α-Androstan-17-one, 3β-hydroxy-
epiandrosteron
3b-Hydroxy-17-oxo-5a-androstane
trans-Androsterone
Epiandrosterone
3β-Androsterone
(3β,5α)-3-Hydroxyandrostan-17-one
3B-HYDROXY-5A-ANDROSTAN-17-ONE
Androstan-17-one, 3-hydroxy-, (3β,5α)-
(3b,5a)-3-Hydroxyandrostan-17-one
(3S,5S,8R,9S,10S,13S,14S)-3-Hydroxy-10,13-dimethylhexadecahydro-17H-cyclopenta[a]phenanthren-17-one
Androsterone, (3β)-
3b-Hydroxyetioallocholan-17-one
3beta-Androsterone
EPLANDROSTERONE
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