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Merck

A9477

Sigma-Aldrich

Aldosterone

≥95% (HPLC), powder

Sinónimos:

11β,21-Dihydroxy-3,20-dioxo-4-pregnen-18-al, 11β,21-Dihydroxypregn-4-ene-3,18,20-trione, 18-Aldocorticosterone, Reichstein X

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5 MG
$86.300
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$389.000
100 MG
$879.000

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5 MG
$86.300
25 MG
$389.000
100 MG
$879.000

About This Item

Fórmula empírica (notación de Hill):
C21H28O5
Número de CAS:
Peso molecular:
360.44
Beilstein:
3224996
Número CE:
Número MDL:
Código UNSPSC:
51111800
ID de la sustancia en PubChem:
NACRES:
NA.77

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Nombre del producto

Aldosterone, ≥95% (HPLC)

origen biológico

synthetic (organic)

esterilidad

non-sterile

Ensayo

≥95% (HPLC)

Formulario

powder

técnicas

cell culture | mammalian: suitable

solubilidad

chloroform: 20 mg/mL, clear to slightly hazy, colorless to light yellow

Condiciones de envío

ambient

temp. de almacenamiento

room temp

cadena SMILES

C[C@]12CCC(=O)C=C1CC[C@H]3[C@@H]4CC[C@H](C(=O)CO)[C@]4(C[C@H](O)[C@H]23)C=O

InChI

1S/C21H28O5/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/h8,11,14-17,19,22,25H,2-7,9-10H2,1H3/t14-,15-,16+,17-,19+,20-,21+/m0/s1

Clave InChI

PQSUYGKTWSAVDQ-ZVIOFETBSA-N

Información sobre el gen

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Descripción general

Aldosterone plays a significant role in the multi-factorial regulation of salt, potassium, blood pressure, and acid-base balance. It is also involved in maternal volume expansion during fetal development to support fetal perfusion and may contribute to the increased expression of placental growth factors. While its primary activity is associated with the kidney, aldosterone can also interact with mineralocorticoid receptors in other tissues such as the gastrointestinal tract, respiratory epithelium, myocardium, and vascular smooth muscle.[1] Aldosterone antagonists or mineralocorticoid receptor antagonists (MRAs) can be beneficial for patients with various clinical conditions, including primary aldosteronism (PA), primary and resistant hypertension, heart failure (HF), and chronic kidney disease (CKD).[2]

Aplicación

Aldosterone has been used:
  • as a RPMI-1640 medium supplement for podocyte culture to test its pathogenicity in obesity-related glomerulopathy (ORG)[3]
  • in combination with salt to induce renal injury in mice[4]
  • to stimulate primary liver sinusoidal endothelial cells (LSECs) and in the generation of hyperaldosteronism model in mice[5]

The d-isomer of aldosterone is considered to be the biologically active isomer.

Acciones bioquímicas o fisiológicas

Aldosterone is a biologically active aldosterone isomer; a mineralocorticoid produced by the adrenal cortex. It induces urinary excretion of K+ and renal reabsorption of Na+.[6] It is produced from adrenocorticotropic hormone (ACTH) and is essential for maintaining sodium homeostasis in the distal tubules.[7] Aldosterone binds to the mineralocorticoid receptor and may modulate vascular system and induce kidney damage.[8] It contributes to the progression of chronic kidney disease(CKD).[4] Aldosterone is part of the renin-angiotensin-aldosterone system (RAAS).[5]

Otras notas

Exists as an equilibrium mixture of the aldehyde and the hemiacetal.

Producto relacionado

Referencia del producto
Descripción
Precios

Código de clase de almacenamiento

11 - Combustible Solids

Clase de riesgo para el agua (WGK)

WGK 3

Punto de inflamabilidad (°F)

Not applicable

Punto de inflamabilidad (°C)

Not applicable

Equipo de protección personal

Eyeshields, Gloves, type N95 (US)


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Certificados de análisis (COA)

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Los clientes también vieron

Role of bardoxolone methyl, a nuclear factor erythroid 2-related factor 2 activator, in aldosterone-and salt-induced renal injury
Hisamichi M
Hypertension Research, 41(1), 8-8 (2018)
Aldosterone and Mineralocorticoid Receptor System in Cardiovascular Physiology and Pathophysiology
Cannavo A, et al.
Oxidative Medicine and Cellular Longevity, 2018 (2018)
Caveolin 1-related autophagy initiated by aldosterone-induced oxidation promotes liver sinusoidal endothelial cells defenestration
Luo X, et al.
Redox Biology, 13(5), 508-521 (2017)
Aldosterone and renin measurements
Cartledge S and Lawson N
Annals of Clinical Biochemistry, 37(3), 262-278 (2000)
Aldosterone: effects on the kidney and cardiovascular system
Briet M and Schiffrin EL
Nature Reviews. Nephrology, 6(5), 261-261 (2010)

Questions

1–5 of 5 Questions  
  1. What is the Department of Transportation shipping information for this product?

    1 answer
    1. Transportation information can be found in Section 14 of the product's (M)SDS.To access the shipping information for this material, use the link on the product detail page for the product.

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  2. How do I make a stock solution of Product A9477, Aldosterone?

    1 answer
    1. To prepare a 100 μg/ml stock solution, add 5 ml of absolute ethanol to 5 mg, gently swirl to dissolve, then add 45 ml sterile medium. Freeze the stock in working aliquots, but avoid repeated freeze/thaw cycles.

      Helpful?

  3. What is the difference between Aldosterone Products A9477 and 05521?

    1 answer
    1. The main differences between A9477 and 05521 are the assays performed on the products. The assay results are lot specific and can be viewed on the Certificate of Analysis.

      Helpful?

  4. Is Product A9477, Aldosterone, the d- or l- isomer?

    1 answer
    1. The A9477 is the d-Aldosterone (per our supplier), which is considered to be the biologically active isomer.

      Helpful?

  5. Is Product A9477, Aldosterone, tested for solubility?

    1 answer
    1. Yes, A9477 is tested for solubility using 20mg/ml in chloroform. For biological applications, you can solubilize aldosterone in ethanol to at least 1 mg/mL. Please refer to literature references for further solubility information.

      Helpful?

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