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Submit ReviewMU 1742 is a potent and selective casein kinase 1α (CK1α), CK1δ and CK1ε inhibitor (IC50 values are 6, 7 and 28 nM for CK1δ, CK1α and CK1ε respectively). In vivo, MU 1742 inhibits CK1δ/ε-dependent DVL3 phosphorylation in mouse lung tissue. MU 1742 is orally bioavailable.
This compound is supplied in conjunction with the Structural Genomics Consortium. For further characterization details, please visit the MU 1742 probe summary on the SGC website.
分子量 | 408.46 |
公式 | C22H22F2N6 |
储存 | Store at -20°C |
纯度 | ≥98% (HPLC) |
PubChem ID | 167312208 |
InChI Key | SWOIFXHMBKFCRM-UHFFFAOYSA-N |
Smiles | FC1=CN=C(C=C1)C2=C(C3=CC=NC4=C3C=CN4)N(CC5(F)CCN(C)CC5)C=N2 |
上方提供的技术数据仅供参考。批次相关数据请参见分析证书。
Tocris products are intended for laboratory research use only, unless stated otherwise.
溶剂 | 最高浓度 mg/mL | 最高浓度 mM | |
---|---|---|---|
溶解性 | |||
DMSO | 40.85 | 100 | |
ethanol | 40.85 | 100 |
以下数据基于产品分子量 408.46。 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.
浓度/溶剂体积/质量 | 1 mg | 5 mg | 10 mg |
---|---|---|---|
1 mM | 2.45 mL | 12.24 mL | 24.48 mL |
5 mM | 0.49 mL | 2.45 mL | 4.9 mL |
10 mM | 0.24 mL | 1.22 mL | 2.45 mL |
50 mM | 0.05 mL | 0.24 mL | 0.49 mL |
参考文献是支持产品生物活性的出版物。
Němec et al (2023) Discovery of potent and exquisitely selective inhibitors of kinase CK1 with tunable isoform selectivity. Angew.Chem.Int.Ed.Engl. 62 e202217532 PMID: 36625768
If you know of a relevant reference for MU 1742, please let us know.
关键词: MU 1742, MU 1742 supplier, MU1742, casein, kinases, inhibitors, inhibits, CK1epsilon, CK1delta, CK1alpha, selective, potent, SGC, in, vivo, orally, bioavailable, CK1α, CK1δ, CK1ε, Casein, Kinase, 1, 7979, Tocris Bioscience
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