Aldosterone, 98%
Aldosterone, 98%
Aldosterone, 98%
Thermo Scientific Chemicals

Aldosterone, 98%

Aldosterone, CAS # 52-39-1, is a hormone secreted by the adrenal cortex, which regulates electrolyte and water balance by increasing the renal retention of sodium and potassium excretion.
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Catalog number 215360050
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Chemical Identifiers
CAS52-39-1
IUPAC Name(1S,3aS,3bS,9aR,9bS,10S,11aR)-10-hydroxy-1-(2-hydroxyacetyl)-9a-methyl-7-oxo-1H,2H,3H,3aH,3bH,4H,5H,7H,8H,9H,9aH,9bH,10H,11H,11aH-cyclopenta[a]phenanthrene-11a-carbaldehyde
Molecular FormulaC21H28O5
InChI KeyPQSUYGKTWSAVDQ-ZVIOFETBSA-N
SMILESC[C@]12CCC(=O)C=C1CC[C@H]1[C@@H]3CC[C@H](C(=O)CO)[C@]3(C[C@H](O)[C@H]21)C=O
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SpecificationsSpecification SheetSpecification Sheet
Specific optical rotation+150° to +162° (20°C, 589 nm) (c=0.1, CHCl3)
Appearance (Color)White to light yellow
HPLC>=97.5 %
Appearance (Form)Powder
Infrared spectrumConforms
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General Description
Aldosterone is a pregnane-based steroidal hormone produced by the outer-section (zona glomerulosa) of the adrenal cortex in the adrenal gland by the action of aldosterone synthase (CYP11B2)
It modulates electrolyte and water balance by increasing the renal retention of sodium and potassium excretion.
Applications
Aldosterone binds to mineralocorticoid receptors (MR; NR3C2) and MR-aldosterone complexes regulating the expression of genes involved in the retention of sodium, secretion of potassium, and water reabsorption, resulting in an increase in the blood pressure
In vitro, it has been involved with the pathogenesis of obesity-related glomerulopathy through activation of Wnt/β-catenin signaling in podocytes
Aldosterone has been used in combination with salt to induce renal injury in mice
It is used to stimulate primary liver sinusoidal endothelial cells
RUO – Research Use Only
Literature References
Zhu, J.J.; Chen, Y.P.; Yang, M., Liu, B.L.; Dong, J.; Dong, H.R.; Rui, H.L.; Cheng, H. Aldosterone is involved in the pathogenesis of obesity-related glomerulopathy through activation of Wnt/β-catenin signaling in podocytes. Mol Med Rep. 2018, 17, (3), 4589-4598.
Luo, X.; Dan, W.; Luo, X.; Zhu, X.; Wang, G.; Ning, Z., Li, Y.; Ma, X., Yang, R.; Jin, S.; Huang, Y.; Meng, Y.; Li, X. Caveolin 1-related autophagy initiated by aldosterone-induced oxidation promotes liver sinusoidal endothelial cells defenestration. Redox Biol. 2017, 13, 508-521.
Briet, M.; Schiffrin, E. Aldosterone: effects on the kidney and cardiovascular system. Nature Reviews Nephrology. 2010, 6, 261–273.