CDC-like Kinase Inhibitor, Cpd-2,5MG,5343500001,Sigma

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订货号 0BW1842
品牌型号 Sigma 5343500001
货期 询货期
最小订货量 1件
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产品介绍 Product Description

General description

A cell-permeable imidazo[1,2-b]pyrazol derived compound that acts as a highly potent and specific inhibitor of CDC-like kinases (CLK; IC50 = 1.1 and 2.4 nM for CLK1 and CLK2, respectively). Exhibits only trivial activity against serine-arginine protein kinases (SRPK) 1, 2, and 3 (IC50 = 200, 310, and 230 nM, respectively). Induces pre-mRNA splicing alteration of multiple genes involved in growth and survival pathways resulting in the depletion of respective proteins. Causes a significance decrease in endogenous phosphorylated serine-arginine proteins and enlarges nuclear speckles in MDA-MB-468 cells. Induces apoptosis and Inhibits the growth of multiple cancer cell lines (GI50 = 3.0, 1.9, 1.7, 2.2, 1.4, 2.0, and 0.6 µM for MDA-MB-468, A549, COLO205, HCT116, NCIH23, SW620, and COLO320 DM cells, respectively).


Biochem/physiol Actions

Cell permeable: yes
Primary Target
CLK1
Reversible: yes


Packaging

Packaged under inert gas


Preparation Note

Following reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 3 months at -20°C.


Other Notes

Araki, S., et al. 2015. Plos One.10, e0116929.


Legal Information

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


Disclaimer

Toxicity: Standard Handling (A)


技术参数 Specifications
assay≥98% (HPLC)
Quality Segment100
formsolid
manufacturer/tradenameCalbiochem®
storage conditionOK to freeze,protect from light
colorlight pink
solubilityDMSO: 100 mg/mL
storage temp.2-8°C
长度(mm)
宽度(mm)
高度(mm)
重量(kg)
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