Tetrahydrocorticosterone

In today's world, Tetrahydrocorticosterone has become a topic of great relevance and interest to a wide spectrum of society. From its impact on the global economy to its influence on people's daily lives, Tetrahydrocorticosterone has sparked debates and discussions in different areas. In order to understand this phenomenon more deeply, it is essential to analyze its different dimensions and repercussions. In this article, we will explore the many facets of Tetrahydrocorticosterone and its relevance today, as well as the future perspectives it raises.

Tetrahydrocorticosterone
Names
IUPAC name
3α,11β,21-Trihydroxy-5β-pregnan-20-one
Systematic IUPAC name
1-phenanthren-1-yl]-2-hydroxyethan-1-one
Other names
3α,5α-Tetrahydrocorticosterone; 5β-Pregnane-3α,11β,21-triol-20-one
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.000.627 Edit this at Wikidata
UNII
  • InChI=1S/C21H34O4/c1-20-8-7-13(23)9-12(20)3-4-14-15-5-6-16(18(25)11-22)21(15,2)10-17(24)19(14)20/h12-17,19,22-24H,3-11H2,1-2H3/t12-,13-,14+,15+,16-,17+,19-,20+,21+/m1/s1
    Key: RHQQHZQUAMFINJ-DTDWNVJFSA-N
  • C12C(O)3(CC4C(O)CC43C)1CC2C(=O)CO
Properties
C21H34O4
Molar mass 350.499 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa).

3α,5α-Tetrahydrocorticosterone (3α,5α-THB), or simply tetrahydrocorticosterone (THB or THCC), is an endogenous glucocorticoid hormone.[1]

See also

References

  1. ^ McInnes KJ, Kenyon CJ, Chapman KE, et al. (May 2004). "5alpha-reduced glucocorticoids, novel endogenous activators of the glucocorticoid receptor". The Journal of Biological Chemistry. 279 (22): 22908–12. doi:10.1074/jbc.M402822200. PMID 15044432.


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