Chemical Structure : Spironolactone
CAS No.: 52-01-7
Catalog No.: PC-28336Not For Human Use, Lab Use Only.
Spironolactone is a potent aldosterone antagonist that acts on the aldosterone mineralocorticoid receptor (IC50=24 nM) and androgen receptor (IC50=77 nM), promotes podocyte autophagy and regulates pain.
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|---|---|---|---|
| 1 g | $48 | In stock | |
| 5 g | $98 | In stock | |
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Spironolactone is a potent aldosterone antagonist that acts on the aldosterone mineralocorticoid receptor (IC50=24 nM) and androgen receptor (IC50=77 nM), promotes podocyte autophagy and regulates pain.
Spironolactone improves hypertension-related vascular hypertrophy and remodeling by reducing angiotensin II (Ang II)-induced inflammation.
Spironolactone reduces aldosterone-induced vascular and soft tissue calcification through PIT1-dependent signaling, and alleviates vascular dysfunction in type II diabetic mice by reducing oxidative stress and restoring NO/GC signaling.
Spironolactone interferes with aldosterone biosynthesis in the adrenal cortex and inhibit voltage-dependent Ca2+ channels to exert antihypertensive effects.
| M.Wt | 416.58 | |
| Formula | C24H32O4S | |
| Appearance | Solid | |
| Storage |
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| Solubility |
10 mM in DMSO |
|
| Chemical Name/SMILES |
Pregn-4-ene-21-carboxylic acid, 7-(acetylthio)-17-hydroxy-3-oxo-, γ-lactone, (7α,17α)- |
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1. Sakurabayashi-Kitade S, et al. Atherosclerosis. 2009 Sep;206(1):54-60
2. Jakob Voelkl, et al. J Clin Invest. 2013 Feb;123(2):812-22.
3. Ryuzea Miura, et al. J Pharmacol Sci. 2006 Jul;101(3):256-9.

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