Ki20227 是一种高选择性 CSF1R (c-Fms 酪氨酸激酶)抑制剂,对 CSF1R,VEGFR2 (血管内皮生长因子受体 2),c-Kit (干细胞因子受体) 和 PDGFRβ (血小板衍生的生长因子受体 β) 的 IC50 分别为 2 nM,12 nM,451 nM 和 217 nM。Ki20227 可以抑制破骨细胞分化和溶骨性破坏。 Product description: Ki20227 is a highly selective c-Fms tyrosine kinase (CSF1R) inhibitor with IC50s of 2 nM, 12 nM, 451 and 217 nM for CSF1R, VEGFR2 (vascular endothelial growth factor receptor-2), c-Kit (stem cell factor receptor) and PDGFRβ (platelet-derived growth factor receptor β). Ki20227 suppresses osteoclast differentiation and osteolytic bone destruction.
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Ki20227
CAS number:623142-96-1 molecular formula:C24H24N4O5S
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| Chinese alias | - | ||
| English alias | 1-(4-(6,7-Dimethoxyquinolin-4-yl)oxy-2-methoxyphenyl)-3-(1-(1,3-thiazol-2-yl)ethyl)urea | AKOS015904288 | Urea, N-(4-((6,7-dimethoxy-4-quinolinyl)oxy)-2-methoxyphenyl)-N'-(1-(2-thiazolyl)ethyl)- | Ki20227 | Ki-20227 | 1-[4-(6,7-dimethoxyquinolin-4-yl)oxy- | ||
| CAS number | 623142-96-1 | molecular formula | C24H24N4O5S |
| molecular weight | 480.55 g/mol | Exact mass | - |
| PSA | 132.000 Ų | logp | 3.600 |
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