AM630
面议
- 阿拉丁
- 生产商
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分子式 C23H25IN2O3 分子量504.36 Beilstein号 EC号 MFCD01861183 MDL号 MFCD01861183 PubChem编号 属性 沸点 605.93 °C at 760 mmHg 折光率 1.65 溶
| 货号 | CAS号 | 操作 |
|---|---|---|
| A124994-100mg | 164178-33-0 | 询底价 |
| A124994-25mg | 164178-33-0 | 询底价 |
| A124994-5mg | 164178-33-0 | 询底价 |
耗材描述
- 分子式 C23H25IN2O3
- 分子量504.36
- Beilstein号
- EC号 MFCD01861183
- MDL号 MFCD01861183
- PubChem编号
属性
| 沸点 | 605.93 °C at 760 mmHg |
| 折光率 | 1.65 |
| 溶解性 | Soluble in DMSO, DMF, ethanol, water (0.2 mg/ml) at 25 °C, and 1:4 DMF:PBS(pH 7.2) (0.2 mg/ml). |
| 存贮条件 | 储存温度2-8℃ |
| 密度 | 1.5000 |
描述
| 应用 | A selective CB2 receptor antagonist that binds to CB1 and CB2 receptors |
| 产品介绍 | AM630是CB2拮抗剂，Ki为31.2 nM，比对CB1受体的抑制性高150倍以上。 |
| 生化机理 |
AM630 is a selectivity CB2 antagonist with Ki of 31.2 nM; > 150 fold selectivity over CB1 receptor. AM630 is a selective CB2 receptor antagonist that binds to CB1 and CB2 receptors with Ki values of 5.2 uM and 31.2 nM, respectively. AM630 has been shown to display 165-fold selectivity over CB1 receptors and behave as a weak partial/inverse agonist at CB1 receptors. AM630 acts as a cannabinoid receptor antagonist in mouse brain, vas deferens and guinea pig brain, but acts as an agonist in guinea pig leum. AM630 acts as an inverse agonist on cloned human CB1 receptors. |
| 别名 | AM 630;AM-630; [6-碘-2-甲基-1-[2-(4-吗啉基)乙基]-1H-吲哚-3-基](4-甲氧基苯基)甲酮;AM 630;AM-630; 6-Iodo-2-methyl-1-[2-(4-morpholinyl)ethyl]-1H-indol-3-yl](4-methoxyphenyl)methanone; Iodopravadoline |
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