Chemical Structure : R121919
CAS No.: 195055-03-9
货号: PC-21280Not For Human Use, Lab Use Only.
R121919 (NBI30775) is a highly potent, selective and nonpeptide antagonist of corticotropin-releasing factor 1 (CRF1) receptor with binding Ki of 3 nM (human and rat CRHR1), inhibits CRHR1-mediated signal transduction in transfected cells with IC50 of 60 nM.
| 规格 | 价格 | 库存 | 数量 |
|---|---|---|---|
| 25 mg | ¥1780 | In stock | |
| 50 mg | ¥2880 | In stock | |
| 100 mg | ¥4580 | In stock | |
| 200 mg | Get quote | ||
| 1 g | Get quote |
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R121919 (NBI30775) is a highly potent, selective and nonpeptide antagonist of corticotropin-releasing factor 1 (CRF1) receptor with binding Ki of 3 nM (human and rat CRHR1), inhibits CRHR1-mediated signal transduction in transfected cells with IC50 of 60 nM.
R121919 has a 1000-fold lower affinity to 70 other central receptors tested.
R121919 dose-dependently suppresses CRH-induced ACTH secretion in rat corticotrope cells.
R121919 attenuates the behavioral and endocrine responses to stress in rats.
| 分子量 | 380.54 | |
| 分子式 | C22H32N6 | |
| 外观性状 | Solid | |
| 储存条件 |
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| Solubility |
10 mM in DMSO |
|
| Chemical Name/SMILES |
3-[6-(dimethylamino)-4-methyl-pyrid-3-yl]-2,5-dimethyl-N,N-dipropyl-pyrazolo[2,3-a]pyrimidin-7-amine |
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1. Gutman DA, et al. J Pharmacol Exp Ther. 2003 Feb;304(2):874-80.
2. Lancel M, et al. J Psychiatr Res. 2002 Jul-Aug;36(4):197-208.
3. M E Keck, et al. Eur J Neurosci. 2001 Jan;13(2):373-80.
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