GO289
CAS No. 694522-87-7
GO289 ( GO-289 | GO 289 )
产品货号. M15657 CAS No. 694522-87-7
GO289 (GO-289, GO 289) 是一种有效的选择性酪蛋白激酶 2 (CK2) 抑制剂,体外激酶测定中的 IC50 为 7 nM。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 5MG | ¥311 | 有现货 |
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| 10MG | ¥511 | 有现货 |
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| 25MG | ¥977 | 有现货 |
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| 50MG | ¥1488 | 有现货 |
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| 100MG | ¥2070 | 有现货 |
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| 200MG | ¥2889 | 有现货 |
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| 500MG | 获取报价 | 有现货 |
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| 1G | 获取报价 | 有现货 |
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| 1 mL x 10 mM in DMSO | ¥343 | 有现货 |
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生物学信息
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产品名称GO289
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注意事项本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
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产品简述GO289 (GO-289, GO 289) 是一种有效的选择性酪蛋白激酶 2 (CK2) 抑制剂,体外激酶测定中的 IC50 为 7 nM。
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产品描述GO289 (GO-289, GO 289) is a potent and selective inhibitor of casein kinase 2 (CK2) with IC50 of 7 nM in in vitro kinase assays, shows minor effects on CKIδ and CKIα activity in vitro; GO289 showed only a moderate or minor effect on the activity of 59 kinases from a variety of classes, the second most affected kinase was PIM2 with an IC50 of 13 nM; caused dose-dependent lengthening of circadian period not only in Bmal1-dLuc reporter cells but also in Per2-dLuc reporter cells with a phase opposite to that of Bmal1-dLuc, inhibits phosphorylation of clock protein PER2 S693 in cells; strongly inhibits Caki-2, A498, and 769-P cancer cells, significantly reduces growth of mouse MLL-AF9 leukemia cells without effect on hematopoietic progenitor cells; shows effectivity on circadian period and reporter signal intensity in spleen explants of MLL-AF9 mice.
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体外实验——
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体内实验——
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同义词GO-289 | GO 289
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通路Metabolic Enzyme/Protease
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靶点Casein Kinase
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受体Casein Kinase
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研究领域——
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适应症——
化学信息
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CAS Number694522-87-7
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分子量419.297
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分子式C17H15BrN4O2S
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纯度>98% (HPLC)
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溶解度In Vitro:?DMSO : 16.67 mg/mL (39.76 mM)
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SMILES——
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化学全称5-bromo-2-methoxy-4-(((3-(methylthio)-5-phenyl-4H-1,2,4-triazol-4-yl)imino)methyl)phenol
运输与储存
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储存条件(-20℃)
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运输条件With Ice Pack
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稳定性≥ 2 years
参考文献
1. Tsuyoshi Oshima, et al. Science Advances 23 Jan 2019: Vol. 5, no. 1, eaau9060. DOI: 10.1126/sciadv.aau9060.
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