Movatterモバイル変換


[0]ホーム

URL:


Jump to content
WikipediaThe Free Encyclopedia
Search

5α-Dihydroaldosterone

From Wikipedia, the free encyclopedia
5α-Dihydroaldosterone
Names
IUPAC name
11β,21-Dihydroxy-3,20-dioxo-5α-pregnan-18-al
Preferred IUPAC name
(1S,3aS,3bS,5aS,9aS,9bS,10S,11aR)-10-Hydroxy-1-(hydroxyacetyl)-9a-methyl-7-oxohexadecahydro-11aH-cyclopenta[a]phenanthrene-11a-carbaldehyde
Identifiers
3D model (JSmol)
ChemSpider
UNII
  • InChI=1S/C21H30O5/c1-20-7-6-13(24)8-12(20)2-3-14-15-4-5-16(18(26)10-22)21(15,11-23)9-17(25)19(14)20/h11-12,14-17,19,22,25H,2-10H2,1H3/t12-,14-,15-,16+,17-,19+,20-,21+/m0/s1
    Key: IIBOWSHDTFRYKU-WHIQTFJJSA-N
  • C[C@]12CCC(=O)C[C@@H]1CC[C@@H]3[C@@H]2[C@H](C[C@]4([C@H]3CC[C@@H]4C(=O)CO)C=O)O
Properties
C21H30O5
Molar mass362.466 g/mol
Except where otherwise noted, data are given for materials in theirstandard state (at 25 °C [77 °F], 100 kPa).
Chemical compound

5α-Dihydroaldosterone is ametabolite ofaldosterone that is formed by5α-reductase.[1] It is apotentantinatriuretic agent similarly to but somewhat different from aldosterone.[1] It is produced in thekidneys.[1]

References

[edit]
  1. ^abcAzzouni F, Godoy A, Li Y, Mohler J (2012)."The 5 alpha-reductase isozyme family: a review of basic biology and their role in human diseases".Adv Urol.2012 530121.doi:10.1155/2012/530121.PMC 3253436.PMID 22235201.


Precursors
Corticosteroids
Glucocorticoids
Mineralocorticoids
Sex steroids
Androgens
Estrogens
Progestogens
Neurosteroids
Others
MRTooltip Mineralocorticoid receptor
Agonists
Antagonists


This article about apregnanes is astub. You can help Wikipedia byexpanding it.

Retrieved from "https://en.wikipedia.org/w/index.php?title=5α-Dihydroaldosterone&oldid=1313723892"
Categories:
Hidden categories:

[8]ページ先頭

©2009-2025 Movatter.jp