CLK-IN-T3

  Cat. No.:  DC21722   Featured
Chemical Structure
2109805-56-1
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More than 5000 active chemicals with high quality for research!
Field of application
CLK inhibitor T3 (T3) is a highly potent, selective, and cell-based stable CDC-like kinase (CLK) inhibitor with 0.67, 15 and 110 nM for CLK1,2 and 3, respectively.
Cas No.: 2109805-56-1
Chemical Name: CLK-IN-T3
Synonyms: Clk Inhibitor T3;4-[2-Methyl-1-(4-methylpiperazin-1-yl)-1-oxopropan-2-yl]-N-(6-pyridin-4-ylimidazo[1,2-a]pyridin-2-yl)benzamide;CLK-IN-T3
SMILES: O=C(C(C)(C)C1C=CC(C(NC2=CN3C=C(C4C=CN=CC=4)C=CC3=N2)=O)=CC=1)N1CCN(C)CC1
Formula: C28H30N6O2
M.Wt: 482.588
Purity: >98%
Sotrage: 2 years -20°C Powder, 2 weeks 4°C in DMSO, 6 months -80°C in DMSO
Description: CLK inhibitor T3 (T3) is a highly potent, selective, and cell-based stable CDC-like kinase (CLK) inhibitor with 0.67, 15 and 110 nM for CLK1,2 and 3, respectively; displays 200-300-fold selectivity over other dual specificity kinases such as DYRK1A and DYRK1B; induces dose-dependent reduction in exon recognition and exhibits an overlapping, but greater effect on transcriptome splicing compared to KH-CB19.
References: References 1. Funnell T, et al. Nat Commun. 2017 Feb 23;8(1):7. View Related Products by Target Cdc2-like Kinase (CLK)
MSDS
COA
LOT NO. DOWNLOAD
2018-0101
2018-0101
2018-0101
2018-0101
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