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Merck
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Key Documents

218705

Sigma-Aldrich

Casein Kinase I Inhibitor, D4476

InSolution, ≥95%

同義詞:

InSolution Casein Kinase I Inhibitor, D4476

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About This Item

經驗公式(希爾表示法):
C23H18N4O3
分子量::
398.41
分類程式碼代碼:
12352200

品質等級

化驗

≥95% (HPLC)

形狀

liquid

製造商/商標名

Calbiochem®

儲存條件

OK to freeze
desiccated (hygroscopic)
protect from light

運輸包裝

wet ice

儲存溫度

−20°C

一般說明

A cell-permeable, potent, and relatively specific ATP-competitive inhibitor of CK1 (IC50 = 200 nM from S. pombe; 0.3 µM for CK1δ) and ALK5 (IC50 = 500 nM). A weak inhibitor of p38α MAP kinase (IC50 = 12 µM) and several other kinases tested, including PKB, SGK, and GSK-3β. Suppresses the site-specific phosphorylation (Ser322 and Ser325) and nuclear exclusion of FOXO1A in H4IIE hepatoma cells. Shown to be ~10-fold more potent than IC261 (Cat. No. 400090; IC50 = 2.5 µM for CK1).

生化/生理作用

Cell permeable: yes
Primary Target
CK1, CK1d
Product competes with ATP.
Reversible: no
Target IC50: 0.2 µM, 0.3 µM against CK1, CK1d, respectively

包裝

Packaged under inert gas
Please refer to vial label for lot-specific concentration.

警告

Toxicity: Irritant (B)

外觀

A 10 mM (1 mg/251 µl) solution of Casein Kinase I Inhibitor, D4476 (Cat. No. 218696) in DMSO

重構

Following initial use, aliquot and refrigerate (4°C).

其他說明

Rena, G., et al. 2004. EMBO Reports5, 60.

法律資訊

CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany

分析證明 (COA)

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