CAS: | 327033-36-3 | |
分子式: | C11H6F3NO2S | |
分子量: | 273.23 | |
中文名称: |
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英文名称: |
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用途: | TCS-PIM-1-4a是Pim抑制剂,能通过AMPK的活化阻断 mTORC1活性,对各种骨髓和淋巴细胞株有杀伤活性,IC50从0.8到40 μM。 |
货号 | 品牌 | 产品名称 | 规格 | 包装、参考价格 | 详情 | ||||||||
T879581 | MACKLIN | TCS-PIM-1-4a | ≥99% | 452元/5mg; 700元/10mg; 2705元/50mg; | 展开 | ||||||||
储存:2-8℃ | |||||||||||||
1811725 | J&K | TCS-PIM-1-4a | 99%, 是Pim抑制剂, 能通过AMPK的活化阻断 mTORC1活性, 对各种骨髓和淋巴细胞株有杀伤活性, IC50从0.8到40 μM | 570元/5MG; 770元/10MG; | 展开 | ||||||||
基本信息
产品描述 TCS-PIM-1-4a is a Pim inhibitor that blocks mTORC1 activity via activation of AMPK; kills a wide range of both myeloid and lymphoid cell lines (with IC50 values ranging from 0.8 to 40 μM). IC50 value: Target: Pim SMI-4a a novel benzylidene-thiazolidine-2, 4-dione small molecule inhibitor of the Pim kinases, kills a wide range of both myeloid and lymphoid cell lines with precursor T-cell lymphoblastic leukemia/lymphoma (pre-T-LBL/T-ALL) being highly sensitive. Incubation of pre-T-LBL cells with SMI-4a induced G1 phase cell-cycle arrest secondary to a dose-dependent induction of p27(Kip1), apoptosis through the mitochondrial pathway, and inhibition of the mammalian target of rapamycin C1 (mTORC1) pathway based on decreases in phospho-p70 S6K and phospho-4E-BP1, 2 substrates of this enzyme. In addition, treatment of these cells with SMI-4a was found to induce phosphorylation of extracellular signal-related kinase1/2 (ERK1/2), and the combination of SMI-4a and a mitogen-activated protein kinase kinase 1/2 (MEK1/2) inhibitor was highly synergistic in killing pre-T-LBL cells. SMI-4a blocked the rapamycin-sensitive mTORC1 activity by stimulating the phosphorylation and thus activating the mTORC1 negative regulator AMP-dependent protein kinase (AMPK). 靶点(IC50 & Targe) Pim 1,24nM Pim 2,100nM Pim 1/2 参考文献 [1]. Lin YW, Beharry ZM, Hill EG, et al. A small molecule inhibitor of Pim protein kinases blocks the growth of precursor T-cell lymphoblastic leukemia/lymphoma. Blood. 2010 ;115(4):824-33. [2]. Beharry Z, Mahajan S, Zemskova M,et al. The Pim protein kinases regulate energy metabolism and cell growth. Proc Natl Acad Sci U S A. 2011;108(2):528-33. [3]. Benoit SR, Ji M, Fleming R,et al . Predictors of dropouts from a San Diego diabetes program: a case control study. Prev Chronic Dis. 2004:1(4):A10. [4]. Zuping Xia, Christian Knaak, Jian Ma et al. Synthesis and Evaluation of Novel Inhibitors of Pim-1 and Pim-2 Protein Kinases. J. Med. Chem., 2009, 52 (1), pp 74-86 |