N-piperidine Ibrutinib hydrochloride

CAS: 2231747-18-3 货号: N654912 分子式: C22H23ClN6O 分子量: 422.91 PubChem CID: 139465991
有货
级别和纯度: 10mM in DMSO
别名
N-哌啶盐酸伊布替尼
储存条件
避光,干燥,-80℃储存
运输条件
特低温运输
★
规格
库存
价格
数量
1ml
N654912-1ml
期货 Stock Image
¥1,540.90
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概述


N-piperidine Ibrutinib hydrochloride (Compound 1) is a reversible Ibrutinib derivative. N-piperidine Ibrutinib hydrochloride is a potent BTK inhibitor with IC 50 s of 51.0 and 30.7 nM for WT BTK and C481S BTK , respectively N-piperidine Ibrutinib hydrochloride can be used as a BTK ligand in the synthesis of a series of PROTACs , such as SJF620 . SJF620 is a potent PROTAC BTK degrader with a DC 50 of 7.9 nM .

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 DC 50 s of 374, 162, and 8.3 nM, respectively. MCE has not independently confirmed the accuracy of these methods. They are for reference only.

IC50& Target:IC50: 51.0 nM (WT BTK), 30.7 nM (C481S BTK)

规格

别名
N-哌啶盐酸伊布替尼
规格或纯度
10mM in DMSO
英文名称
N-piperidine Ibrutinib hydrochloride
生化机理
N-piperidine Ibrutinib 盐酸盐(化合物 1)是一种可逆的 Ibrutinib 衍生物。N-piperidine Ibrutinib 盐酸盐是一种强效的 BTK 抑制剂,对 WT BTK 和 C481S BTK 的 IC 50 s 分别为 51.0 和 30.7 nM。N-piperidine Ibrutinib hy
储存条件
避光,干燥,-80℃储存
运输条件
特低温运输
名称和识别符
分子类型
小分子
PubChem CID
分子量
422.91

高级数据

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