CAS NO: | 899507-36-9 |
包装 | 价格(元) |
10 mM * 1 mL in DMSO | 电议 |
10mg | 电议 |
50mg | 电议 |
100mg | 电议 |
200mg | 电议 |
500mg | 电议 |
生物活性 | A 438079 is a potent, and selective P2X7receptor antagonist with pIC50 of 6.9. | ||||||||||||||||
IC50& Target | pIC50: 6.9 (P2X7receptor) | ||||||||||||||||
体外研究 (In Vitro) | In 1321N1 cells stably expressing rat P2X7 receptors, A 438079 blocks BzATP-(10 μM) evoked changes in intracellular calcium concentrations with an IC50of 321 nM. A 438079 is also selective for the P2X7receptor, at concentrations up to 100 μM[1]. | ||||||||||||||||
体内研究 (In Vivo) | A 438079 (80 μmol/kg, i.v.) reduces noxious and innocuous evoked activity of different classes of spinal neurons in neuropathic rats. A 438079 (100 and 300 μmol/kg, i.p.) significantly raises withdrawal thresh-olds in both the SNL and CCI models[1]. Intraperitoneal injection of A 438079 (5 and 15 mg/kg) 60 min after triggering seizures reduces seizure severity and neuronal death within the hippocampus. A 438079 has superior neuroprotective effects compared with an equally dose of phenobarbital (25 mg/kg)[2]. A 438079 partially but significantly prevents the 6-OHDA-induced depletion of striatal DA stores[3]. Pretreatment with A 438079 reduces nociceptive behaviour scores in the HC model[4]. | ||||||||||||||||
分子量 | 306.15 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C13H9Cl2N5 | ||||||||||||||||
CAS 号 | 899507-36-9 | ||||||||||||||||
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 : 100 mg/mL(326.64 mM;Need ultrasonic) H2O : 0.2 mg/mL(0.65 mM;Need ultrasonic) 配制储备液
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