Powder: -20°C for 3 years | In solvent: -80°C for 1 year
Flumexadol is a selective and affinity 5-HT2C receptor agonist with a Ki of 25 nM for the (+)-enantiomer of Flumexadol, and is 40-fold selective over the 5-HT2A receptor. Flumexadol is an orally active non-narcotic analgesic.
説明 | Flumexadol is a selective and affinity 5-HT2C receptor agonist with a Ki of 25 nM for the (+)-enantiomer of Flumexadol, and is 40-fold selective over the 5-HT2A receptor. Flumexadol is an orally active non-narcotic analgesic. |
ターゲット&IC50 | 5-HT2C receptor:25 nM (ki) |
分子量 | 231.21 |
分子式 | C11H12F3NO |
CAS No. | 30914-89-7 |
Powder: -20°C for 3 years | In solvent: -80°C for 1 year
DMSO: 100 mg/mL (432.51 mM), Sonication is recommended.
You can also refer to dose conversion for different animals. 詳細
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Flumexadol 30914-89-7 GPCR/G Protein Neuroscience 5-HT Receptor Inhibitor inhibitor inhibit