Chemical Structure : GPR183 antagonist SAE-14
CAS No.: 1241280-25-0
货号: PC-72117Not For Human Use, Lab Use Only.
GPR183 antagonist SAE-14 is a potent, selective GPR183 antagonist with IC50 of 28.5 nM, inhibits GPR183-dependent 7α,25-dihydroxycholesterol-induced calcium signaling in HL-60 cells.
规格 | 价格 | 库存 | 数量 |
---|---|---|---|
5 mg | ¥1480 | In stock | |
10 mg | ¥2280 | In stock | |
25 mg | ¥3980 | In stock | |
50 mg | ¥5980 | In stock | |
100 mg | Get quote |
大包装,大折扣!
E-mail: sales@probechem.com
Tech Support: tech@probechem.com
GPR183 antagonist SAE-14 is a potent, selective GPR183 antagonist with IC50 of 28.5 nM, inhibits GPR183-dependent 7α,25-dihydroxycholesterol-induced calcium signaling in HL-60 cells.
GPR183 antagonist SAE-14 inhibits calcium mobilization induced by 7α,25-OHC (EC80 209 nM).
GPR183 antagonist SAE-14 reversed CCI-induced mechanical allodynia in a time-dependent manner when administered in vivo to mice.
7α,25-dihydroxycholesterol induced allodynia in mice, SAE-14 blocked the effects of 7α,25-OHC in a dose-dependent manner.
分子量 | 364.368 | |
分子式 | C19H19F3N2O2 | |
外观性状 | Solid | |
储存条件 |
|
|
Solubility |
10 mM in DMSO |
|
Chemical Name/SMILES |
3-(3,4-difluorophenyl)-N-(3-fluoro-5-morpholinophenyl)propanamide |
1. Kathryn Braden, et al. J Pharmacol Exp Ther. 2020 Nov;375(2):367-375.
备案号:沪ICP备16042516号-1 Copyright © 2022 probechem.com. All Rights Reserved. probechem Copyright