- 全部删除
您的购物车当前为空
TL12-186 是一种依赖于 Cereblon 的激酶降解剂,可降解 CDK,BTK,FLT3,Aurora 等激酶。TL12-186 对 CDK2/cyclin A 和 CDK9/cyclin T1 有抑制作用,IC50 分别为 73 和 55 nM。


为众多的药物研发团队赋能,
让新药发现更简单!
TL12-186 是一种依赖于 Cereblon 的激酶降解剂,可降解 CDK,BTK,FLT3,Aurora 等激酶。TL12-186 对 CDK2/cyclin A 和 CDK9/cyclin T1 有抑制作用,IC50 分别为 73 和 55 nM。
| 规格 | 价格 | 库存 | 数量 |
|---|---|---|---|
| 1 mg | ¥ 346 | In stock | |
| 5 mg | ¥ 823 | In stock | |
| 10 mg | ¥ 1,290 | In stock | |
| 25 mg | ¥ 1,980 | In stock | |
| 50 mg | ¥ 3,360 | In stock | |
| 100 mg | ¥ 4,780 | In stock | |
| 200 mg | ¥ 6,660 | In stock | |
| 1 mL x 10 mM (in DMSO) | ¥ 1,390 | In stock |
TL12-186 相关产品
| 产品描述 | TL12-186 is a Cereblon-dependent kinase degrader that degrades CDK, BTK, FLT3, Aurora and other kinases.TL12-186 inhibits CDK2/cyclin A and CDK9/cyclin T1 with IC50s of 73 and 55 nM, respectively. |
| 靶点活性 | CRBN:12nM, CDK9-CyclinT1:55 nM (IC50), CDK2-CyclinA:73 nM (IC50) |
| 体外活性 | TL12-186在1μM筛选浓度下对193个激酶展示出90%以上的抑制效果[1]。通过AlphaScreen结合测定,它对CRBN显示出强大的结合能力,IC50为12nM[1]。TL12-186(1-10000 nM;2天)依赖CRBN的药理作用表现出,在WT细胞中相比CRBN-/-细胞抑制细胞存活的能力强13至15倍[1]。此外,在10到10000 nM浓度范围内,经过4小时处理,TL12-186选择性地抑制STAT1的磷酸化,而不诱导JAK1/2的降解[1]。 |
| 别名 | TL12186, TL12 186 |
| 分子量 | 931.46 |
| 分子式 | C44H51ClN10O9S |
| CAS No. | 2250025-88-6 |
| Smiles | O=C1NC(=O)C(N2C(=O)C=3C=CC=C(NCC(=O)NCCOCCOCCN4CCN(C5=CC=C(C=C5)NC6=NC=C(Cl)C(=N6)NC=7C=CC=CC7S(=O)(=O)C(C)C)CC4)C3C2=O)CC1 |
| 密度 | no data available |
| 颜色 | Yellow |
| 物理性状 | Solid |
| 存储 | keep away from direct sunlight | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. | |||||||||||||||||||||||||||||||||||
| 溶解度信息 | DMSO: 200 mg/mL (214.72 mM), Sonication is recommended. | |||||||||||||||||||||||||||||||||||
溶液配制表 | ||||||||||||||||||||||||||||||||||||
DMSO
| ||||||||||||||||||||||||||||||||||||
评论内容