Chemical Structure : SGC-STK17B-1
CAS No.: 2650530-00-8
货号: PC-38222Not For Human Use, Lab Use Only.
SGC-STK17B-1 is a potent, selective, ATP-competitive inhibitor of death-associated protein kinase family member STK17B (DRAK2) with IC50 of 34 nM, >100-fold selectivity over STK17A.
| 规格 | 价格 | 库存 | 数量 |
|---|---|---|---|
| 5 mg | ¥1580 | In stock | |
| 10 mg | ¥2480 | In stock | |
| 25 mg | ¥4280 | In stock | |
| 50 mg | Get quote | ||
| 100 mg | Get quote |
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SGC-STK17B-1 is a potent, selective, ATP-competitive inhibitor of death-associated protein kinase family member STK17B (DRAK2) with IC50 of 34 nM, >100-fold selectivity over STK17A.
SGC-STK17B-1 is also >100-fold selective over all of the other kinases tested, with only STK17A, CAMKK1, and AURKB (IC50s=5-9 uM) in panel of 403 wild type human kinase assays.
SGC-STK17B-1 demonstrated the highest cell potency in the NanoBRET target engagement assay (IC50=190 nM).
SGC-STK17B-1 is the first truly potent and selective chemical probe of STK17B.
| 分子量 | 358.448 | |
| 分子式 | C16H10N2O2S3 | |
| 外观性状 | Solid | |
| 储存条件 |
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| Solubility |
10 mM in DMSO |
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| Chemical Name/SMILES |
2-((6-(Benzo[b]thiophen-2-yl)thieno[3,2-d]pyrimidin-4-yl)thio)acetic acid |
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1. Alfredo Picado, et al. J Med Chem. 2020 Dec 10;63(23):14626-14646.
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