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别名 Ec2la
CB2R PAM 是一种口服活性大麻素 2 型受体(CB2Rs)阳性突变调节剂,它能增强 CP 55940 和 2-Arachidonylglycerol 刺激的 [35S]GTPγS 与 CB2 受体的结合,但在没有激动剂的情况下没有作用。CB2R PAM 在神经病理性疼痛小鼠模型中显示出抗损伤活性。


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CB2R PAM 是一种口服活性大麻素 2 型受体(CB2Rs)阳性突变调节剂,它能增强 CP 55940 和 2-Arachidonylglycerol 刺激的 [35S]GTPγS 与 CB2 受体的结合,但在没有激动剂的情况下没有作用。CB2R PAM 在神经病理性疼痛小鼠模型中显示出抗损伤活性。
| 规格 | 价格 | 库存 | 数量 |
|---|---|---|---|
| 1 mg | ¥ 532 | In stock | |
| 5 mg | ¥ 1,230 | In stock | |
| 10 mg | ¥ 1,950 | In stock | |
| 25 mg | ¥ 3,290 | In stock | |
| 50 mg | ¥ 4,780 | In stock | |
| 100 mg | ¥ 6,850 | In stock | |
| 500 mg | ¥ 13,700 | In stock |
CB2R PAM 相关产品
| 产品描述 | CB2R PAM is an orally active cannabinoid type 2 receptor (CB2Rs) positive mutational modulator that enhances CP 55940 and 2-Arachidonylglycerol-stimulated [35S]GTPγS binding to CB2 receptors, but has no effect in the absence of agonists. ...CB2R PAM shows anti-injury activity in a mouse model of neuropathic pain. |
| 体外活性 | CB2R PAM (100 nM) 显著增强了 CP55940 和 2-AG 对 CB2Rs 的 [35S]GTPγS 结合能力的促进作用,但 AEA 则不受影响。[1] |
| 体内活性 | CB2R PAM (1-20 mg/kg; p.o.) 表现出抗痛觉活性。[1] |
| 别名 | Ec2la |
| 分子量 | 435.33 |
| 分子式 | C21H24BrFN2O2 |
| CAS No. | 2244579-87-9 |
| Smiles | N(C(=O)C1CCCCCC1)C=2C(=O)N(CC3=CC=C(F)C=C3)C=C(Br)C2C |
| 颜色 | Green |
| 物理性状 | Solid |
| 存储 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. | |||||||||||||||||||||||||||||||||||
| 溶解度信息 | DMSO: 45.0 mg/mL (103.4 mM), Sonication is recommended. | |||||||||||||||||||||||||||||||||||
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