| 英文名称 | Thailanstatin A |
|---|---|
| 中文名称 | 泰兰斯他汀A |
| CAS号 | 1426953-21-0 |
| 分子式 | C28H41NO9 |
| 分子量 | 535.63 |
| 英文名称 | Thailanstatin A |
|---|---|
| 中文名称 | 泰兰斯他汀A |
| CAS号 | 1426953-21-0 |
| 分子式 | C28H41NO9 |
| 分子量 | 535.63 |
Thailanstatin A is an ultra-potent inhibitor of eukaryotic RNA splicing (IC50=650 nM). Thailanstatin A exerts effects via non-covalent binding to the SF3b subunit of the U2 snRNA subcomplex of the spliceosome and shows low-nM to sub-nM IC50s against multiple cancer cell lines. Thailanstatin A, a payload for ADCs, is conjugated to the lysines on trastuzumab yielding “linker-less” ADC.