CAS NO: | 2231747-18-3 |
生物活性 | N-piperidine Ibrutinib hydrochloride (Compound 1) is a reversible Ibrutinib derivative. N-piperidine Ibrutinib hydrochloride is a potentBTKinhibitor withIC50s of 51.0 and 30.7 nM for WTBTKand C481SBTK, respectively[1]. N-piperidine Ibrutinib hydrochloride can be used as aBTKligand in the synthesis of a series ofPROTACs, such as SJF620 (HY-133137). SJF620 is a potentPROTACBTK degrader with a DC50of 7.9 nM[2]. | ||||||||||||||||
IC50& Target | IC50: 51.0 nM (WT BTK), 30.7 nM (C481S BTK)[1] | ||||||||||||||||
体外研究 (In Vitro) | N-piperidine Ibrutinib hydrochloride can be used as a BTK ligand in the synthesis of a series of PROTACs. SJF638, SJF678, and SJF608 are potent PROTAC BTK degraders with DC50s of 374, 162, and 8.3 nM, respectively[2]. | ||||||||||||||||
分子量 | 422.91 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C22H23ClN6O | ||||||||||||||||
CAS 号 | 2231747-18-3 | ||||||||||||||||
运输条件 | Room temperature in continental US; may vary elsewhere. | ||||||||||||||||
储存方式 | -20°C, sealed storage, away from moisture and light *In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture and light) | ||||||||||||||||
溶解性数据 | In Vitro: DMSO : 100 mg/mL(236.46 mM;Need ultrasonic) H2O : 50 mg/mL(118.23 mM;Need ultrasonic) 配制储备液
* 请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效。 In Vivo: 请根据您的实验动物和给药方式选择适当的溶解方案。以下溶解方案都请先按照In Vitro方式配制澄清的储备液,再依次添加助溶剂: ——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议您现用现配,当天使用;
以下溶剂前显示的百
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