STK16-IN-1
CAS No. 1223001-53-3
STK16-IN-1 ( —— )
产品货号. M23392 CAS No. 1223001-53-3
STK16-IN-1 是 STK16 激酶的抑制剂 (IC50: 295 nM)。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 2MG | ¥112 | 有现货 |
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| 5MG | ¥183 | 有现货 |
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| 10MG | ¥326 | 有现货 |
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| 25MG | ¥663 | 有现货 |
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| 50MG | ¥986 | 有现货 |
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| 100MG | ¥1377 | 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 |
|
| 1 mL x 10 mM in DMSO | ¥201 | 有现货 |
|
生物学信息
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产品名称STK16-IN-1
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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STK16-IN-1 是 STK16 激酶的抑制剂 (IC50: 295 nM)。
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产品描述STK16-IN-1 is an inhibitor of STK16 kinase (IC50: 295 nM).
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体外实验STK16-IN-1, which exhibits potent inhibitory activity against STK16 kinase (IC50=0.295 μM) with excellent selective across the kinome as assessed using the KinomeScanTM profiling assay. STK16-IN-1 inhibits mTOR kinase with an IC50 of 5.56 μM. In MCF-7 cells, treatment with STK16-IN-1 results in a reduction in cell number and accumulation of binucleated cells, which can be recapitulated by RNAi knockdown of STK16. Co-treatment of STK16-IN-1 with chemotherapeutics such as cisplatin, doxorubicin, colchicine and paclitaxel results in a slight potentiation of the anti-proliferative effects of the chemotherapeutics. STK16-IN-1 provides a useful tool compound for further elucidating the biological functions of STK16).
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体内实验——
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同义词——
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通路Others
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靶点Other Targets
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受体STK16
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研究领域——
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适应症——
化学信息
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CAS Number1223001-53-3
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分子量293.3
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分子式C17H12FN3O
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纯度>98% (HPLC)
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溶解度DMSO:15 mg/mL (51.14 mM; Need ultrasonic and warming)
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SMILESCC1=C(C=CC(=C1)N2C(=O)C=CC3=CN=C4C(=C32)C=CN4)F
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化学全称——
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.Liu F, et al. Discovery of a Highly Selective STK16 Kinase Inhibitor. ACS Chem Biol. 2016 Jun 17;11(6):1537-43.
产品手册
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