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RTICBM-189 是可透过血脑屏障的大麻素 1 型受体变构调节剂,在 Ca2+动员试验中pIC50为 7.54,对 hCB1和 mCB1的 pIC50分别为 5.29 和 6.25。
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RTICBM-189 是可透过血脑屏障的大麻素 1 型受体变构调节剂,在 Ca2+动员试验中pIC50为 7.54,对 hCB1和 mCB1的 pIC50分别为 5.29 和 6.25。
规格 | 价格 | 库存 | 数量 |
---|---|---|---|
1 mg | ¥ 197 | In stock | |
5 mg | ¥ 473 | In stock | |
10 mg | ¥ 822 | In stock | |
25 mg | ¥ 1,730 | In stock | |
50 mg | ¥ 2,610 | In stock | |
100 mg | ¥ 3,710 | In stock | |
200 mg | ¥ 4,970 | In stock | |
1 mL x 10 mM (in DMSO) | ¥ 637 | In stock |
产品描述 | RTICBM-189 is a potent, brain-penetrant allosteric modulator of the cannabinoid type-1 (CB1) receptor with a pIC50 of 7.54 in Ca2+ mobilization assay. RTICBM-189 has pIC50s of 5.29 and 6.25 for hCB1 and mCB1, respectively. |
靶点活性 | CB1 (human):5.29 (pIC50), CB1:7.54 (pIC50), CB1 (mouse):6.25 (pIC50) |
分子量 | 309.19 |
分子式 | C15H14Cl2N2O |
CAS No. | 551909-15-0 |
Smiles | Clc1ccc(NC(=O)NCCc2cccc(Cl)c2)cc1 |
密度 | 1.330 g/cm3 (Predicted) |
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: 100 mg/mL (323.43 mM), Sonication is recommended. | |||||||||||||||||||||||||||||||||||
溶液配制表 | ||||||||||||||||||||||||||||||||||||
DMSO
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以上为“体内实验配液计算器”的使用方法举例,并不是具体某个化合物的推荐配制方式,请根据您的实验动物和给药方式选择适当的溶解方案。
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