A 438079
CAS No. 899507-36-9
A 438079 ( —— )
产品货号. M26041 CAS No. 899507-36-9
A 438079 是一种有效的、选择性的 P2X7 受体拮抗剂 (pIC50: 6.9)。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 2MG | ¥335 | 有现货 |
|
| 5MG | ¥546 | 有现货 |
|
| 10MG | ¥881 | 有现货 |
|
| 25MG | ¥1562 | 有现货 |
|
| 50MG | ¥2688 | 有现货 |
|
| 100MG | ¥4113 | 有现货 |
|
| 500MG | 获取报价 | 有现货 |
|
| 1G | 获取报价 | 有现货 |
|
| 1 mL x 10 mM in DMSO | ¥740 | 有现货 |
|
生物学信息
-
产品名称A 438079
-
注意事项本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
-
产品简述A 438079 是一种有效的、选择性的 P2X7 受体拮抗剂 (pIC50: 6.9)。
-
产品描述A 438079 is a potent, and selective antagonist of P2X7 receptor (pIC50: 6.9).(In Vitro):A 438079 blocks BzATP-(10 μM) evoked changes in intracellular calcium concentrations with an IC50 of 321 nM in 1321N1 cells stably expressing rat P2X7 receptors. A 438079 is also selective for the P2X7 receptor, at concentrations up to 100 μM.(In Vivo):In neuropathic rats noxious and innocuous evoked activity of different classes of spinal neurons is reduced by A 438079 (80 μmol/kg, i.v.), and it significantly raises withdrawal thresh-olds in both the SNL and CCI models. A 438079 has superior neuroprotective effects compared with an equal dose of phenobarbital (25 mg/kg). A 438079 partially but significantly prevents the 6-OHDA-induced depletion of striatal DA stores. Pretreatment with A 438079 reduces nociceptive behavior scores in the HC model.
-
体外实验In 1321N1 cells stably expressing rat P2X7?receptors, A 438079 blocks BzATP-(10 μM) evoked changes in intracellular calcium concentrations with an IC50 of 321 nM. A 438079 is also selective for the P2X7 receptor, at concentrations up to 100 μM.
-
体内实验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. 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).?A 438079 partially but significantly prevents the 6-OHDA-induced depletion of striatal DA stores. Pretreatment with A 438079 reduces nociceptive behaviour scores in the HC model.
-
同义词——
-
通路Membrane Transporter/Ion Channel
-
靶点P2X Receptor
-
受体TRPM4
-
研究领域——
-
适应症——
化学信息
-
CAS Number899507-36-9
-
分子量306.15
-
分子式C13H9Cl2N5
-
纯度>98% (HPLC)
-
溶解度In Vitro:?DMSO : 100 mg/mL (326.64 mM)
-
SMILESClc1cccc(-c2nnnn2Cc2cccnc2)c1Cl
-
化学全称——
运输与储存
-
储存条件(-20℃)
-
运输条件With Ice Pack
-
稳定性≥ 2 years
参考文献
1.9-Phenanthrol inhibits human TRPM4 but not TRPM5 cationic channels[J]. British Journal of Pharmacology, 2010, 153(8):1697-1705.
021-51111890
购物车()
sales@molnova.cn

