4-Dehydroepiandrosterone

Today we will talk about 4-Dehydroepiandrosterone, a topic that has captured the attention of millions of people around the world. 4-Dehydroepiandrosterone is a fascinating topic that has generated a great debate in today's society. From its impact on history to its relevance today, 4-Dehydroepiandrosterone has sparked endless questions and reflections. In this article, we will explore different aspects of 4-Dehydroepiandrosterone, from its origins to its possible implications in the future. Whether you are an expert in the field or are simply interested in learning more about it, this article is for you. So get ready to immerse yourself in the exciting world of 4-Dehydroepiandrosterone and discover everything this theme has to offer.

4-Dehydroepiandrosterone
Skeletal formula of 4-dehydroepiandrosterone
Ball-and-stick model of the 4-dehydroepiandrosterone molecule
Names
IUPAC name
3β-Hydroxyandrost-4-en-17-one
Systematic IUPAC name
(3aS,3bR,7S,9aR,9bS,11aS)-7-Hydroxy-9a,11a-dimethyl-2,3,3a,3b,4,5,7,8,9,9a,9b,10,11,11a-tetradecahydro-1H-cyclopentaphenanthren-1-one
Other names
Androst-4-en-3β-ol-17-one
Identifiers
3D model (JSmol)
ChEMBL
ChemSpider
UNII
  • InChI=1S/C19H28O2/c1-18-9-7-13(20)11-12(18)3-4-14-15-5-6-17(21)19(15,2)10-8-16(14)18/h11,13-16,20H,3-10H2,1-2H3/t13-,14-,15-,16-,18-,19-/m0/s1 checkY
    Key: VMYTXBKVYDESSJ-USOAJAOKSA-N checkY
  • O=C1CC2()3()CCC4=C(O)CC4(C)3()CC21C
  • O=C43(CC21(C(=C/(O)CC1)\CC23CC4)C)C
Properties
C19H28O2
Molar mass 288.431 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa).
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4-Dehydroepiandrosterone (4-DHEA) is a steroid that is an isomer of 5-dehydroepiandrosterone.

4-DHEA has been prepared by laboratory synthesis.[1][2]

Synonyms

Synonyms for 4-dehydroepiandrosterone are:

3β-Hydroxy-4-androsten-17-one, 3β-hydroxyandrost-4-en-17-one, 3β-hydroxy-D4-androsten-17-one, 3β-hydroxyandrost-4-en-17-one, 3β-hydroxy-etioallocholan-4-en-17-one, and 4-androsten-3β-ol-17-one.

References

  1. ^ Klimstra, Paul D.; Colton, F. B. Synthesis of 3β-hydroxyestr-4-en-17-one and 3β-hydroxyandrost-4-en-17-one. Steroids (1967), 10(4), 411-24.
  2. ^ Ward, Margaret G.; Orr, James C.; Engel, Lewis L. A convenient synthesis of 3β-hydroxyandrost-4-en-17-one. Journal of Organic Chemistry (1965), 30(5), 1421-3.



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