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Finerenone

Chemical Structure : Finerenone

CAS No.: 1050477-31-0

Finerenone (BAY 94-8862, BAY 948862)

Catalog No.: PC-63433Not For Human Use, Lab Use Only.

Finerenone (BAY 94-8862) is a potent, selective, orally available mineralocorticoid receptor (MR) antagonist with IC50 of 18 nM.

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Purity & Documentation Purity: >98% (HPLC) Select Batch:

Biological Activity

Finerenone (BAY 94-8862) is a potent, selective, orally available mineralocorticoid receptor (MR) antagonist with IC50 of 18 nM.
Finerenone (BAY 94-8862) displays excellent selectivity (>500-fold) versus GR, AR, and PR, also shows no L type Ca2+ channel activity.
Finerenone (BAY 94-8862) elicits a significant and dose-dependent increase in the urinary sodium/potassium ratio in vivo, with a MED of 0.3 mg kg1 p.o.
Finerenone (BAY 94-8862) exhibits three- to tenfold greater potency and higher efficacy in acute rat natriuresis model compared with eplerenone, demonstrates potential for the treatment of chronic heart failure (CHF).

Physicochemical Properties

M.Wt 378.432
Formula C21H22N4O3
Appearance Solid
CAS No.
Storage
Solide Powder
-20 °C 12 Months; 4°C 6 Months
In Solvent
-80 °C 6 Months; -20°C 6 Months
Shipping
Solubility

10 mM in DMSO

Chemical Name/SMILES

(4S)-4-(4-Cyano-2-methoxyphenyl)-5-ethoxy-2,8-dimethyl-1,4-dihydro-1,6-naphthyridine-3-carboxamide

References

1. Bärfacker L, et al. ChemMedChem. 2012 Aug;7(8):1385-403.

2. Kolkhof P, et al. J Cardiovasc Pharmacol. 2014 Jul;64(1):69-78.

3. Filippatos G, et al. Eur Heart J. 2016 Jul 14;37(27):2105-14.

4. Amazit L, et al. J Biol Chem. 2015 Sep 4;290(36):21876-89.

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