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首页-小分子抑制剂&激动剂-Metabolic Enzyme/Protease-Cytochrome P450 (CYPs)-Dexfadrostat
Dexfadrostat

Chemical Structure : Dexfadrostat

CAS No.: 102676-87-9

Dexfadrostat ((R)-Fadrozole, (R)-CGS 16949A, FAD286)

货号: PC-73413Not For Human Use, Lab Use Only.

Dexfadrostat ((R)-Fadrozole, CGS 16949A, FAD286) is a potent nonsteroidal inhibitor of aldosterone synthase (CYP 11B2, steroid 18-hydroxylase), also inhibits human placental aromatase (pIC50=6.17).

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

生物&药学活性

Dexfadrostat ((R)-Fadrozole, CGS 16949A, FAD286) is a potent nonsteroidal inhibitor of aldosterone synthase (CYP 11B2, steroid 18-hydroxylase), also inhibits human placental aromatase (pIC50=6.17).
Dexfadrostat ((R)-Fadrozole, CGS 16949A, FAD286) inhibits aldosterone biosynthesis and reverses cardiac fibrosis in spontaneously hypertensive heart failure rats.

物理化学性质&存储条件

分子量 223.279
分子式 C14H13N3
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

Benzonitrile, 4-[(5R)-5,6,7,8-tetrahydroimidazo[1,5-a]pyridin-5-yl]-

参考文献

1. Furet P, et al. J Med Chem. 1993;36(10):1393-1400.

2. Minnaard-Huiban M, et al. Endocrinology. 2008;149(1):28-31.

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