Chemical Structure : FCPR03
CAS No.: 1917347-65-9
货号: PC-62973Not For Human Use, Lab Use Only.
FCPR03 is a novel potent, selective PDE4 inhibitor with IC50 of 60, 31 and 47 nM for PDE4CAT (PDE4 catalytic domain), PDE4B1 and PDE4D7, respectively.
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---|---|---|---|
2 mg | ¥1480 | In stock | |
5 mg | ¥2580 | In stock | |
10 mg | ¥3980 | In stock | |
25 mg | ¥5980 | In stock | |
100 mg | Get quote |
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FCPR03 is a novel potent, selective PDE4 inhibitor with IC50 of 60, 31 and 47 nM for PDE4CAT (PDE4 catalytic domain), PDE4B1 and PDE4D7, respectively.
FCPR03 displays >2,000-fold selectivity over other PDEs.
FCPR03 effectively increases the production of cAMP, promotes CREB phosphorylation, and inhibits NF-κB activation both in vitro and in vivo.
FCPR03 displays anti-neuroinflammation potential, promising antidepressant-like effects in vivo.
分子量 | 299.318 | |
分子式 | C15H19F2NO3 | |
外观性状 | Solid | |
储存条件 |
|
|
Solubility |
10 mM in DMSO |
|
Chemical Name/SMILES |
3-(cyclopropylmethoxy)-4-(difluoromethoxy)-N-isopropylbenzamide |
1. Zou ZQ, et al. J Pharmacol Exp Ther. 2017 Jul;362(1):67-77.
2. Zhou ZZ, et al. ACS Chem Neurosci. 2017 Jan 18;8(1):135-146.
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