Centrinone
CAS No. 1798871-30-3
Centrinone ( LCR-263 )
产品货号. M23809 CAS No. 1798871-30-3
Centrinone (LCR-263) 是一种 polo 样激酶 4 (PLK4;Ki:0.16 nM) 的可逆抑制剂。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 2MG | ¥752 | 有现货 |
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| 5MG | ¥1137 | 有现货 |
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| 10MG | ¥1897 | 有现货 |
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| 50MG | ¥4176 | 有现货 |
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| 100MG | ¥5769 | 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 | ¥1609 | 有现货 |
|
生物学信息
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产品名称Centrinone
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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Centrinone (LCR-263) 是一种 polo 样激酶 4 (PLK4;Ki:0.16 nM) 的可逆抑制剂。
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产品描述Centrinone (LCR-263) is a reversible inhibitor of polo-like kinase 4 (PLK4; Ki:0.16 nM). (In Vitro):Centrinone (LCR-263) exhibits more than 1000-fold selectivity for Plk4 over Aurora A/B and does not affect cellular Aurora A or B substrate phosphorylation at concentrations that deplete centrosomes. Centrinone (LCR-263) treatment of HeLa human cervical carcinoma cells leads to a progressive reduction in foci containing centriolar and pericentriolar material markers at each round of cell division, until most cells lack centrioles and centrosomes. Treatment with Centrinone (LCR-263) reduces centriole number in multiciliated Xenopus epithelial cells, which indicates that Plk4 also controls centriole amplification in differentiated cells. Centrinone (LCR-263) treatment causes centrosome depletion in human and other vertebrate cells. Centrosome loss irreversibly arrests normal cells in a senescence-like G1 state by a p53-dependent mechanism that is independent of DNA damage, stress, Hippo signaling, extends mitotic duration, or segregation errors.
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体外实验——
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体内实验——
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同义词LCR-263
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通路Cell Cycle/DNA Damage
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靶点Aurora Kinase
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受体Aurora A|Aurora B|PLK4|PLK4 G95L
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研究领域——
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适应症——
化学信息
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CAS Number1798871-30-3
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分子量633.65
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分子式C26H25F2N7O6S2
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纯度>98% (HPLC)
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溶解度DMSO:31 mg/mL (48.92 mM)
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SMILESCC1=CC(NC2=NC(SC3=CC=C(S(=O)(CC4=CC=CC([N+]([O-])=O)=C4F)=O)C=C3F)=NC(N5CCOCC5)=C2OC)=NN1
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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.Wong YL. et al. Cell biology. Reversible centriole depletion with an inhibitor of Polo-like kinase 4. Science. 2015 Jun 5;348(6239):1155-60.
产品手册
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