Thalidomide-NH-PEG7 是用于合成 ADC 的 E3 连接酶配体-接头共轭物。Thalidomide-NH-PEG7 可以通过 linker 与蛋白质的配体连接，形成 PROTAC iRucaparib-AP6 (一种高度特异性的 PARP1 降解物)。
| Cas No. | 2641838-98-2 |
| 分子式 | C27H39N3O11 |
| 分子量 | 581.61 |
| 储存条件 | Store at -20°C |
| General tips | For obtaining a higher solubility , please warm the tube at 37 ℃ and shake it in the ultrasonic bath for a while. |
| Shipping Condition | Evaluation sample solution : ship with blue ice
All other available size: ship with RT , or blue ice upon request |
| 产品描述 | Thalidomide-NH-PEG7 is a synthesized E3 ligase ligand-linker conjugate forADC. Thalidomide-NH-PEG7 can be connected to the ligand for protein by a linker to form PROTAC iRucaparib-AP6, a highly specific PARP1 degrader[1]. [1]. Wang S, et al. Uncoupling of PARP1 trapping and inhibition using selective PARP1 degradation.Nat Chem Biol. 2019 Dec;15(12):1223-1231. |
