CAS NO: | 130580-02-8 |
包装: | 5mg |
市场价: | 1200元 |
生物活性 | Eplivanserin (SR-46349) hemifumarate is a potent, selective and orally active5-HT2Areceptorantagonist, with anIC50of 5.8 nM in rat cortical membrane, and aKdof 1.14 nM. Eplivanserin hemifumarate displays >20-fold selectivity more selective for5-HT2Athan 5-HT2Band 5-HT2C[1][2]. | ||||||||||||||||
IC50& Target[1][2] |
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体外研究 (In Vitro) | Eplivanserin hemifumarate (SR 46349B) shows weak inhibition on other 5-HT kinases, with IC50s of 0.12 μM (Pig cortex 5-HT1C), 14 μM (Rat hippocampus 5-HT1A), and 16 μM (Rat stnatum 5-HT1B, Ox caudate nucleus 5-HT1D). Eplivanserin also has inhibitory effects on rat cortex adrenergic α1and α2, rat whole brain histammine H1, Na+channel, and rat striatum dopamine D1and D2, with IC50s of 3.4 μM, 1.0 μM, 5.0 μM, 39 μM, 9 μM and 28 μM, respectively[1]. | ||||||||||||||||
体内研究 (In Vivo) | Eplivanserin hemifumarate (SR 46349B) inhibits 5-HT2receptor binding of [3H]ketanserin with an ED50of 0.087 mg/kg after i.p. injection, and 0.097 mg/kg after p.o administration in mice[1]. | ||||||||||||||||
Clinical Trial | |||||||||||||||||
分子量 | 386.43 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C19H21FN2O2.1/2C4H4O4 | ||||||||||||||||
CAS 号 | 130580-02-8 | ||||||||||||||||
中文名称 | 富马酸依利色林 | ||||||||||||||||
运输条件 | Room temperature in continental US; may vary elsewhere. | ||||||||||||||||
储存方式 | 4°C, sealed storage, away from moisture *In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture) | ||||||||||||||||
溶解性数据 | In Vitro: DMSO : 25 mg/mL(64.69 mM;ultrasonic and warming and heat to 60℃) 配制储备液
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