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Finerenone
CAS No. 1050477-31-0
Finerenone ( BAY 94-8862;BAY 948862 )
Catalog No. M10243 CAS No. 1050477-31-0
Finerenone (BAY 94-8862) is a potent, selective, orally available mineralocorticoid receptor (MR) antagonist with IC50 of 18 nM.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 5MG | 67 | In Stock |
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| 10MG | 104 | In Stock |
|
| 25MG | 209 | In Stock |
|
| 50MG | 337 | In Stock |
|
| 100MG | 537 | In Stock |
|
| 200MG | 610 | In Stock |
|
| 500MG | 896 | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
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Product NameFinerenone
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NoteResearch use only, not for human use.
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Brief DescriptionFinerenone (BAY 94-8862) is a potent, selective, orally available mineralocorticoid receptor (MR) antagonist with IC50 of 18 nM.
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DescriptionFinerenone (BAY 94-8862) is a potent, selective, orally available mineralocorticoid receptor (MR) antagonist with IC50 of 18 nM; displays excellent selectivity (>500-fold) versus GR, AR, and PR, also shows no L type Ca2+ channel activity; 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.; 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).Heart FailurePhase 3 Clinical
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SynonymsBAY 94-8862;BAY 948862
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PathwayNuclear Receptor/Transcription Factor
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TargetMLR
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RecptorMLR
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Research Area——
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Indication——
Chemical Information
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CAS Number1050477-31-0
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Formula Weight378.43
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Molecular FormulaC21H22N4O3
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Purity>98% (HPLC)
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Solubility——
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SMILESO=C(C1=C(C)NC2=C(C(OCC)=NC=C2C)[C@@H]1C3=CC=C(C#N)C=C3OC)N
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Chemical Name(4S)-4-(4-Cyano-2-methoxyphenyl)-5-ethoxy-2,8-dimethyl-1,4-dihydro-1,6-naphthyridine-3-carboxamide
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
1. Brfacker 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.
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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