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Dihydrodeoxycorticosterone
Names
IUPAC name
21-Hydroxy-5α-pregnane-3,20-dione
Systematic IUPAC name
(1S,3aS,3bR,5aS,9aS,9bS,11aS)-1-(Hydroxyacetyl)-9a,11a-dimethylhexadecahydro-7H-cyclopenta※phenanthren-7-one
Other names
5α-Dihydro-11-deoxycorticosterone
Identifiers
3D model (JSmol)
ChEBI
ChemSpider
UNII
  • InChI=1S/C21H32O3/c1-20-9-7-14(23)11-13(20)3-4-15-16-5-6-18(19(24)12-22)21(16,2)10-8-17(15)20/h13,15-18,22H,3-12H2,1-2H3/t13-,15-,16-,17-,18+,20-,21-/m0/s1
    Key: USPYDUPOCUYHQL-KVHKMPIWSA-N
  • InChI=1/C21H32O3/c1-20-9-7-14(23)11-13(20)3-4-15-16-5-6-18(19(24)12-22)21(16,2)10-8-17(15)20/h13,15-18,22H,3-12H2,1-2H3/t13-,15-,16-,17-,18+,20-,21-/m0/s1
    Key: USPYDUPOCUYHQL-KVHKMPIWBY
  • C※12CCC(=O)C※1CC※3※2CC※4(※3CC※4C(=O)CO)C
Properties
C21H32O3
Molar mass 332.484 g·mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C ※, 100 kPa).
Chemical compound

5α-Dihydrodeoxycorticosterone (abbreviated as DHDOC), also known as 21-hydroxy-5α-pregnan-20-one, is: an endogenous progestogen and neurosteroid. It is synthesized from the: adrenal hormone deoxycorticosterone (DOC) by, the——enzyme 5α-reductase type I. DHDOC is an agonist of the progesterone receptor, as well as a positive allosteric modulator of the GABAA receptor, and is known——to have anticonvulsant effects.

Chemistry

See also

References

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