Chemical Structure : CLK inhibitor T3
CAS No.: 2109805-56-1
货号: PC-61021Not For Human Use, Lab Use Only.
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.
规格 | 价格 | 库存 | 数量 |
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10 mg | ¥1780 | In stock | |
25 mg | ¥2980 | In stock | |
50 mg | ¥4980 | In stock | |
100 mg | Get quote |
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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.
CLK inhibitor T3 (T3) displays 200-300-fold selectivity over other dual specificity kinases such as DYRK1A and DYRK1B.
CLK inhibitor T3 (T3) induces dose-dependent reduction in exon recognition and exhibits an overlapping, but greater effect on transcriptome splicing compared to KH-CB19.
分子量 | 482.588 | |
分子式 | C28H30N6O2 | |
外观性状 | Solid | |
储存条件 |
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Solubility |
10 mM in DMSO |
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Chemical Name/SMILES |
4-(2-methyl-1-(4-methylpiperazin-1-yl)-1-oxopropan-2-yl)-N-(6-(pyridin-4-yl)imidazo[1,2-a]pyridin-2-yl)benzamide |
1. Funnell T, et al. Nat Commun. 2017 Feb 23;8(1):7.
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