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首页-小分子抑制剂&激动剂-Nuclear Receptor/Transcription Factor-Mineralocorticoid Receptor (MLR)-Finerenone
Finerenone

Chemical Structure : Finerenone

CAS No.: 1050477-31-0

Finerenone (BAY 94-8862, BAY 948862)

货号: 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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5 mg ¥880 In stock
10 mg ¥1280 In stock
25 mg ¥2180 In stock
50 mg ¥3680 In stock
100 mg ¥5680 In stock
250 mg Get quote

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纯度 & COA & 质检文件 纯度: >98% (HPLC) Select Batch:

生物&药学活性

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).

物理化学性质&存储条件

分子量 378.432
分子式 C21H22N4O3
外观性状 Solid
CAS No.
储存条件
固体粉末
-20 °C 12 个月; 4°C 6 个月
配置液
-80 °C 6 个月; -20°C 6 个月
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

参考文献

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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