CAS NO: | 1426953-21-0 |
包装 | 价格(元) |
1mg | 电议 |
5mg | 电议 |
10mg | 电议 |
50mg | 电议 |
生物活性 | Thailanstatin A is an ultra-potent inhibitor of eukaryoticRNA 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 multiplecancercell lines. Thailanstatin A, a payload for ADCs, is conjugated to the lysines on trastuzumab yielding “linker-less” ADC[1][2][3]. | ||||||||||||||||
体外研究 (In Vitro) | Thailanstatin A (TST-A) is a potent antiproliferative natural product discovered by our group fromBurkholderia thailandensisMSMB43[2]. | ||||||||||||||||
分子量 | 535.63 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C28H41NO9 | ||||||||||||||||
CAS 号 | 1426953-21-0 | ||||||||||||||||
中文名称 | 泰兰斯他汀A | ||||||||||||||||
运输条件 | Room temperature in continental US; may vary elsewhere. | ||||||||||||||||
储存方式 |
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溶解性数据 | In Vitro: DMSO : 250 mg/mL(466.74 mM;Need ultrasonic) 配制储备液
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以下溶剂前显示的百
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