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Mps1-IN-2

    98%

Mps1-IN-2

源葉(MedMol)
S82470
1228817-38-6
C26H36N6O3
480.6024
Mps1-IN-2
品牌 貨號 產(chǎn)品規(guī)格 價格(RMB) 庫存(上海) 北京 武漢 南京 購買數(shù)量
源葉(MedMol) S82470-5mg 98% ¥640.00元 預(yù)計交期:2-3天 - - -
源葉(MedMol) S82470-10mg 98% ¥980.00元 預(yù)計交期:2-3天 - - -
源葉(MedMol) S82470-50mg 98% ¥3100.00元 預(yù)計交期:2-3天 - - -
產(chǎn)品介紹 參考文獻 質(zhì)檢證書(COA) 摩爾濃度計算器 相關(guān)產(chǎn)品

產(chǎn)品介紹

Mps1-IN-2 is a potent, selective and ATP-competitive dual Mps1/Plk1 inhibitor, with an IC50 and a Kd of 145 nM and 12 nM for Mps1 and a Kd of 61 nM for Plk1.
產(chǎn)品描述: Mps1-IN-2 is a potent, selective and ATP-competitive dual Mps1/Plk1 inhibitor, with an IC50 and a Kd of 145 nM and 12 nM for Mps1 and a Kd of 61 nM for Plk1.
靶點: Mps1:12 nM (Kd);GAK:140 nM (Kd);PLK1:61 nM (Kd);PLK3:1600 nM (Kd);PLK4:'3100 nM (Kd);STK33:5000 nM (Kd);Kinesin;?PLK
體外研究: Mps1-IN-2 is a potent, selective and ATP-competitive Mps1 kinase inhibitor, with an IC50 and a Kd of 145 nM and 12 nM. Mps1-IN-2 also shows high affinity for PLK1 and GAK with Kds of 61 and 140 nM, respectively, but shows little or no inhibition on other 352 member kinases. Mps1-IN-2 can induces bypass of a checkpoint-mediated mitotic arrest in U2OS cells
參考文獻: 1. Kwiatkowski N, et al. Small-molecule kinase inhibitors provide insight into Mps1 cell cycle function. Nat Chem Biol. 2010 May;6(5):359-68.
溶解性: soluble  in  DMSO
保存條件: -20℃
配置溶液濃度參考:
1mg 5mg 10mg
1 mM 2.081 ml 10.404 ml 20.807 ml
5 mM 0.416 ml 2.081 ml 4.161 ml
10 mM 0.208 ml 1.04 ml 2.081 ml
50 mM 0.042 ml 0.208 ml 0.416 ml
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參考文獻

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摩爾濃度計算器

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