CAS NO: | 105431-72-9 |
包装 | 价格(元) |
10 mM * 1 mL in DMSO | 电议 |
5mg | 电议 |
10mg | 电议 |
50mg | 电议 |
100mg | 电议 |
200mg | 电议 |
生物活性 | Linopirdine (DuP 996) is an orally active, selectiveM-type K+current (IM; Kv7; KCNQ Channels)inhibitor with anIC50of 2.4 μM. Linopirdine is aTRPV1agonist. Linopirdine, a putative cognition enhancing drug, increases acetylcholine release in rat brain tissue[1][2][3]. | ||||||||||||||||
IC50& Target | IC50: 2.4 μM (M-type K+current)[1] | ||||||||||||||||
体外研究 (In Vitro) | Linopirdine (DuP 996) inhibits IC (measured as a medium afterhyperpolarization tail current, ImAHP) with an IC50of 16.3 μM. Linopirdine (100 μM) weakly inhibits the K+leak current, IL, the transient outward current, IA, the delayed rectifier, IK, and the slow component of IAHP, by 28, 37, 36 and 52 percent, respectively. The mixed Na+/K+inward rectifying current, IQ, is essentially unaffected by Linopirdine (IC50>300 μM)[1]. | ||||||||||||||||
体内研究 (In Vivo) | Linopirdine (DuP 996; i.v.; 0.1-6 mg/kg; increasing doses) transiently (10-15 min) and dose-dependently increases MAP by up to 15%[2].
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分子量 | 391.46 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C26H21N3O | ||||||||||||||||
CAS 号 | 105431-72-9 | ||||||||||||||||
中文名称 | 利诺吡啶 | ||||||||||||||||
运输条件 | Room temperature in continental US; may vary elsewhere. | ||||||||||||||||
储存方式 |
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溶解性数据 | In Vitro: DMSO : 125 mg/mL(319.32 mM;Need ultrasonic) 配制储备液
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以下溶剂前显示的百
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