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首页-小分子抑制剂&激动剂-JAK/STAT Signaling-Pim-AZD1208
AZD1208

Chemical Structure : AZD1208

CAS No.: 1204144-28-4

AZD1208 (AZD-1208)

货号: PC-22796Not For Human Use, Lab Use Only.

AZD1208 is a potent and selective, ATP-competitive pan-Pim kinase inhibitor with IC50 of 0.4/5.0/1.9 nM for Pim-1/2/3, respectively.

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纯度 & COA & 质检文件 纯度: >98% (HPLC) Select Batch:

生物&药学活性

AZD1208 is a potent and selective, ATP-competitive pan-Pim kinase inhibitor with IC50 of 0.4/5.0/1.9 nM for Pim-1/2/3, respectively.
AZD1208 has Ki values of 0.1 nM for Pim-1, 1.92 nM for Pim-2, and 0.4 nM for Pim-3.
AZD1208 inhibits AML cell-line growth and can induce cell-cycle arrest and apoptosis, accompanied by a dose-dependent reduction in phosphorylation of Bcl-2 antagonist of cell death, 4EBP1, p70S6K, and S6.
AZD1208 potently inhibits the level of pBAD with IC50 of 10 nM for Pim-1, 151 nM for Pim-2, and 102 nM for Pim-3in U2-OS cells.
AZD1208 (10 mg/kg or 30 mg/kg) inhibits the growth of MOLM-16 and KG-1a xenograft tumors in vivo.

物理化学性质&存储条件

分子量 379.48
分子式 C21H21N3O2S
外观性状 Solid
CAS No.
储存条件
固体粉末
-20°C 12 个月; 4°C 6 个月
配置液
-80°C 6 个月; -20°C 6 个月
Shipping
Solubility

10 mM in DMSO

Chemical Name/SMILES

(R,Z)-5-((2-(3-Aminopiperidin-1-yl)-[1,1'-biphenyl]-3-yl)methylene)thiazolidine-2,4-dione

参考文献

1. Keeton EK,

2. Dakin LA, et al. Bioorg Med Chem Lett. 2012;22(14):4599–4604.

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