| 溶解性 | DMSO 22 mg/mL Water <1 mg/mL Ethanol <1 mg/mL |
| 存贮条件 | 储存温度-20°C |
| 备注 | BML-190 is a selective cannabinoid CB2 receptor inverse agonist with Ki of 435 nM, with 50-fold selectivity over CB1 receptor. |
| 生化机理 | BML-190 is a potent and selective CB2 receptor ligand (Ki values are 435 nM and > 2 μM for CB2 and CB1 respectively). Studies involving HEK-293 cells indicate that BML-190 increases the accumulation of cAMP, via forskolin-stimulated mechanism. Alternate studies suggest that BML-190 reduces the toxicity of culture supernatants to SH-SY5Y human neutroblastoma cells. Various research suggests that BML-190 is an essential tool in studying the proliferation of neuroblastoma. |
| 别名 | Indomethacin Morpholinylamide;Ethanone, 2-[1-(4-chlorobenzoyl)-5-methoxy-2-methyl-1H-indol-3-yl]-1-(4-morpholinyl)-;Indomethacin Morpholinylamide;Ethanone, 2-[1-(4-chlorobenzoyl)-5-methoxy-2-methyl-1H-indol-3-yl]-1-(4-morpholinyl)- |
BML-190,CB 2受体反向激动剂
BML-190 （订货以英文为准）
编号：B126713
CAS号：2854-32-2
分子式：C23H23N2O4CL
分子量：426.89
| 产品名称 | BML-190 |
| 中文名称 | BML-190,CB 2受体反向激动剂 |
| CAS号 | 2854-32-2 |
| 分子式（M.F.） | C23H23N2O4CL |
| 分子量（M.W.） | 426.89 |
| 储存条件 | -20°C储存 |
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