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N-piperidine Ibrutinib hydrochloride 是一种强效的 BTK 抑制剂,是BTK 配体,抑制 WT BTK 和 C481S BTK ,可用于合成一系列 PROTAC 分子。N-piperidine Ibrutinib hydrochloride具有潜在的抗癌活性,可抑制癌细胞的生长和增殖。

N-piperidine Ibrutinib hydrochloride 是一种强效的 BTK 抑制剂,是BTK 配体,抑制 WT BTK 和 C481S BTK ,可用于合成一系列 PROTAC 分子。N-piperidine Ibrutinib hydrochloride具有潜在的抗癌活性,可抑制癌细胞的生长和增殖。
| 规格 | 价格 | 库存 | 数量 |
|---|---|---|---|
| 1 mg | ¥ 526 | In Stock | |
| 5 mg | ¥ 1,160 | In Stock | |
| 10 mg | ¥ 1,850 | In Stock | |
| 25 mg | ¥ 3,690 | In Stock | |
| 50 mg | ¥ 5,290 | In Stock | |
| 100 mg | ¥ 7,250 | In Stock | |
| 200 mg | ¥ 9,770 | In Stock | |
| 1 mL x 10 mM (in DMSO) | ¥ 1,270 | In Stock |
N-piperidine Ibrutinib hydrochloride 相关产品
| 产品描述 | N-piperidine Ibrutinib hydrochloride is a potent BTK inhibitor, a BTK ligand, inhibits WT BTK and C481S BTK, which can be used to synthesize a range of PROTAC molecules.N-piperidine Ibrutinib hydrochloride has potential anticancer N-piperidine Ibrutinib hydrochloride has potential anticancer activity, inhibiting the growth and proliferation of cancer cells. |
| 靶点活性 | BTK (C481S):30.7 nM, BTK (WT):51.0 nM |
| 体外活性 | N-piperidine Ibrutinib hydrochloride 可用于合成有效的 PROTAC BTK 降解剂,如 SJF638、SJF678 和 SJF608 等[2]。 |
| 分子量 | 422.91 |
| 分子式 | C22H23ClN6O |
| CAS No. | 2231747-18-3 |
| Smiles | Cl.Nc1ncnc2n(nc(-c3ccc(Oc4ccccc4)cc3)c12)C1CCNCC1 |
| 密度 | no data available |
| 存储 | keep away from direct sunlight,keep away from moisture | 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: 80 mg/mL (189.16 mM), Sonication is recommended. H2O: 30 mg/mL (70.94 mM), Sonication is recommended. | ||||||||||||||||||||||||||||||||||||||||
| 体内实验配方 | 10% DMSO+40% PEG300+5% Tween 80+45% Saline: 3.3 mg/mL (7.8 mM), Sonication is recommended. 请按顺序添加溶剂,在添加下一种溶剂之前,尽可能使溶液澄清。如有必要,可通过加热、超声、涡旋处理进行溶解。工作液建议现配现用。以上配方仅供参考,体内配方并不是绝对的,请根据不同情况进行调整。 | ||||||||||||||||||||||||||||||||||||||||
溶液配制表 | |||||||||||||||||||||||||||||||||||||||||
H2O/DMSO
DMSO
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