SR 144528
| 规格 | 价格 | 货期 | 数量 |
|---|---|---|---|
| 5mg | ¥940.00 | 10-15工作日发货 | |
| 10mg | ¥1662.00 | 10-15工作日发货 | |
| 25mg | ¥3705.00 | 10-15工作日发货 | |
| 50mg | ¥6351.00 | 10-15工作日发货 |
特色产品
- 用于免疫印迹和质谱分析等后续操作
- 适用于30 KDa-130 KDa大小的蛋白
- 可将信号灵敏度提高100倍
- 同时保持稳定的特异性和分辨率
- 提供更高的转录效率并抑制免疫激活
- 使用5-moUTP和Cy5-utp修饰
产品描述
Ki= 0.6 nM
SR 144528 is a CB2 receptor inverse agonist.
The CB2 receptor is principally expressed in immune tissue where it is involved in cannabinoid-mediated immune responses, but CB2 mRNA has been detected in mouse cerebellar cells and cerebellum and in rat microglial cells.
In vitro: SR 144528 displayed subnanomolar affinity for both the rat spleen and cloned human CB2 receptors and had a 700-fold lower affinity for both the rat brain and cloned human CB1 receptors. Moreover, SR 144528 showed no affinity for more than 70 receptors, ion channels or enzymes tested. SR 144528 could antagonize the inhibitory effects of the cannabinoid receptor agonist CP 55,940 on forskolin-stimulated adenylyl cyclase activity in cell lines expressing the human CB2 receptor but not in cells expressing the human CB1. In addition, SR 144528 could selectively block the mitogen-activated protein kinase activity that was induced by CP 55,940 in cell lines expressing human CB2 while an IC50 value of more than 1 μM was observed in cells expressing human CB1 [1].
In vivo: Animal study showed that oral administration of SR 144528 could totally displace the ex vivo [3H]-CP 55,940 binding to mouse spleen membranes with a long action duration. Whereas, after the oral route SR 144528 did not interact with the cannabinoid receptor expressed in the mouse brain CB1 [1].
Clinical trial: Up to now, SR 144528 is still in the preclinical development stage.
Reference:
[1] Rinaldi-Carmona M et al. SR 144528, the first potent and selective antagonist of the CB2 cannabinoid receptor. J Pharmacol Exp Ther. 1998 Feb;284(2):644-50.
产品性质
| 物理外观 | A crystalline solid |
| CAS号 | 192703-06-3 |
| 分子式 | C29H34ClN3O |
| 分子量 | 475.2 |
| 小分子别名 | SR144528 |
| 化学名称 | 5-(4-chloro-3-methylphenyl)-1-[(4-methylphenyl)methyl]-N-[(1S,2S,4R)-1,3,3-trimethylbicyclo[2.2.1]hept-2-yl]-1H-pyrazole-3-carboxamide |
| 溶解度 | ≤30mg/ml in ethanol;20mg/ml in DMSO;30mg/ml in dimethyl formamide |
| SMILES | CC(C)([C@H]1C[C@]2(C)CC1)[C@H]2NC(c1n[n](Cc2ccc(C)cc2)c(-c(cc2)cc(C)c2Cl)c1)=O |
| 存储条件 | -20°C |
| 运输条件 | 蓝冰 |
产品应用 (实验数据来自文献,APExBIO并未验证,仅供参考)
IC50和靶点
| 生物活性描述 | SR144528 是一种强效的选择性 CB2 受体拮抗剂,其 Ki 值为 0.6 nM。 |



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