CAS NO: | 23210-58-4 |
包装 | 价格(元) |
10 mM * 1 mL in DMSO | 电议 |
50mg | 电议 |
100mg | 电议 |
200mg | 电议 |
500mg | 电议 |
生物活性 | Ifenprodil tartrate is a typical noncompetitiveNMDAreceptor antagonist. Ifenprodil tartrate exerts high affinity at NR1A/NR2B receptors (IC50=0.34 μM) over 400-fold than at NR1A/NR2A receptors (IC50=146 μM)[1]. Ifenprodil tartrate inhibitsGIRK (Kir3), reduces inward currents through the basal GIRK activity. Ifenprodil tartrate has the potential to be a cerebral vasodilator[2]. | ||||||||||||||||
IC50& Target | IC50: 0.34 μM (NR1A/NR2B receptor); 146 μM (NR1A/NR2A receptor)[1] | ||||||||||||||||
体外研究 (In Vitro) | G protein-activated inwardly rectifying K+ channels (GIRK)[1]. | ||||||||||||||||
Clinical Trial | |||||||||||||||||
分子量 | 400.49 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C25H33NO8 | ||||||||||||||||
CAS 号 | 23210-58-4 | ||||||||||||||||
中文名称 | 酒石酸艾芬地尔;苄哌酚胺 | ||||||||||||||||
结构分类 |
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来源 |
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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 : ≥ 500 mg/mL(1248.47 mM) H2O : 5 mg/mL(12.48 mM;Need ultrasonic) *"≥" means soluble, but saturation unknown. 配制储备液
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以下溶剂前显示的百
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