UNC3866
UNC3866 性质
沸点 | 1034.5±65.0 °C(Predicted) |
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密度 | 1.129±0.06 g/cm3(Predicted) |
储存条件 | Sealed in dry,Store in freezer, under -20°C |
溶解度 | 溶于二甲基亚砜 |
形态 | 结晶固体 |
酸度系数(pKa) | 13.39±0.46(Predicted) |
颜色 | 白色至米白色 |
UNC3866 用途与合成方法
IC50: 66±1.2 nM (CBX7)
UNC3866, a potent antagonist of the methyl-lysine (Kme) reading function of the Polycomb CBX and CDY families of chromodomains. UNC3866 binds the chromodomains of CBX4 and CBX7 most potently with a K d of 100 nM for each, and is 6- to 18-fold selective versus seven other CBX and CDY chromodomains while being highly selective versus >250 other protein targets. UNC3866 inhibits PC3 cell proliferation, a known CBX7 phenotype, while UNC4219, a methylated negative control compound, has negligible effects. UNC3866 is a potent and cellularly active antagonist of PRC1 chromodomains. UNC3866 is the most potent ligand reported for CBX7 with a K d of 97±2.4 nM. UNC3866 is equipotent for CBX4, which is most similar to CBX7, while it is 18-, 6- and 12-fold selective for CBX4/7 over CBX2, -6 and -8, respectively. Additionally, UNC3866 is 65-fold selective for CBX4/7 over CDY1 and 9-fold selective for CBX4/7 over CDYL1b and CDYL2.
UNC3866 价格(试剂级)
更新日期 | 产品编号 | 产品名称 | CAS号 | 包装 | 价格 |
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2024-11-08 | HY-100832 | UNC3866 | 1872382-47-2 | 2mg | 800 |
2024-11-08 | HY-100832 | UNC3866 | 1872382-47-2 | 5mg | 1000 |