SML3759
MU1742
≥95% (HPLC)
别名:
4-(1-((4-Fluoro-1-methylpiperidin-4-yl)methyl)-4-(5-fluoropyridin-2-yl)-1H-imidazol-5-yl)-1H-pyrrolo[2,3-b]pyridine, MU 1742, MU-1742
SMILES string
FC5(CCN(CC5)C)C[n]1cnc(c1c3c4c([nH]cc4)ncc3)c2ncc(cc2)F
InChI key
SWOIFXHMBKFCRM-UHFFFAOYSA-N
assay
≥95% (HPLC)
form
powder
color
white to beige
solubility
DMSO: 2 mg/mL, clear
storage temp.
2-8°C
Quality Level
Biochem/physiol Actions
MU1742 is an orally active, potent and selective casein kinase 1 inhibitor (CK1α/δ/ε IC50 = 7/6/28 nM; p38α IC50 >3 μM) with high kinome-wide selectivity. MU1742 inhibits CLL19-induced chemotaxis (IC50 = 200 nM; MEC1 cells) and CK1δ/ε-dependent DVL3 phosphorylation (IC50 = 200 nM post 18h treatment; HL60 cells) in cultures and in lung tissue in mice in vivo (5h post 100 mg/kg p.o. using HCl salt form).
Orally active, potent and selective casein kinase 1 (CK1, CKI) inhibitor in vitro and in vivo.
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
法规信息
新产品
此项目有
Discovery of Potent and Exquisitely Selective Inhibitors of Kinase CK1 with Tunable Isoform Selectivity
Angewandte Chemie (International ed. in English), 62(11) (2023)
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