Chemical Structure : YKL-06-061
CAS No.: 2172617-15-9
货号: PC-63122Not For Human Use, Lab Use Only.
YKL-06-061 is a potent, selective, second-generation salt-inducible kinase (SIK) inhibitor with IC50 of 6.56/1.77/20.5 nM for SIK1/2/3, respectively.
规格 | 价格 | 库存 | 数量 |
---|---|---|---|
5 mg | ¥880 | In stock | |
10 mg | ¥1380 | In stock | |
25 mg | ¥2180 | In stock | |
50 mg | ¥3480 | In stock | |
100 mg | Get quote |
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YKL-06-061 is a potent, selective, second-generation salt-inducible kinase (SIK) inhibitor with IC50 of 6.56/1.77/20.5 nM for SIK1/2/3, respectively.
YKL-06-061 inhibits only one kinase FRK (IC50=1.1 nM), more strongly than SIKs, in a panel of 468 human kinases.
YKL-06-061 dose-dependently increases MITF mRNA expression in human melanoma cells.
YKL-06-061 induces significant pigmentation in Mc1r-deficient mice and normal human skin.
分子量 | 527.673 | |
分子式 | C30H37N7O2 | |
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 |
Pyrimido[4,5-d]pyrimidin-2(1H)-one,1-cyclobutyl-3-(2,6-dimethylphenyl)-3,4-dihydro-7-[[2-methoxy-4-(4-methyl-1-piperazinyl)phenyl]amino]- |
1. Mujahid N, et al. Cell Rep. 2017 Jun 13;19(11):2177-2184.
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