产品描述
| 溶解性 |
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| 存贮条件 | 储存温度-20°C |
| 应用 | An inhibitor of JAK2, Flt-3, Ret, and JAK3 |
| 产品介绍 | TG101209是JAK2选择性抑制剂，IC50为6 nM，对Flt3和RET的IC50为25 nM和17 nM，比对JAK3的抑制性高30倍，对JAK2V617F和MPLW515L/K突变型敏感，还能抑制BRD4，IC50为130 nM。 |
| 备注 | TG101209 is a selective JAK2 inhibitor with IC50 of 6 nM, less potent to Flt3 and RET with IC50 of 25 nM and 17 nM, ~30-fold selective for JAK2 than JAK3, sensitive to JAK2V617F and MPLW515L/K mutations. |
| 生化机理 |
TG101209 is a potent and small molecule JAK2-selective kinase inhibitor with IC50 of 6, 25, 17 and 169 nM for JAK2, FLT3, RET and JAK3, respectively.TG101209 is useful for myeloproliferative disorder |
| 别名 | TG 101209;TG-101209;N-(1,1-二甲基乙基)-3-[[5-甲基-2-[[4-(4-甲基-1-哌嗪基)苯基]氨基]-4-嘧啶基]氨基]苯磺酰胺;TG 101209;TG-101209;N-tert-butyl-3-(5-methyl-2-(4-(4-methylpiperazin-1-yl)phenylamino)pyrimidin-4-ylamino)benzenesulfonamide |
