Chemical Structure : BPTF inhibitor BZ1
CAS No.: 2766623-38-3
货号: PC-72758Not For Human Use, Lab Use Only.
BPTF inhibitor BZ1 is a potent, selective, cell-active inhibitor of bromodomain PHD finger transcription factor (BPTF) with Kd of 6.3 nM, >350-fold selectivity over BET bromodomains.
| 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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BPTF inhibitor BZ1 is a potent, selective, cell-active inhibitor of bromodomain PHD finger transcription factor (BPTF) with Kd of 6.3 nM, >350-fold selectivity over BET bromodomains.
BPTF inhibitor BZ1 sensitizes 4T1 breast cancer cells to doxorubicin but not BPTF knockdown cells, suggesting a specificity to BPTF.
| 分子量 | 278.74 | |
| 分子式 | C13H15ClN4O | |
| 外观性状 | Solid | |
| 储存条件 |
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| Solubility |
10 mM in DMSO |
|
| Chemical Name/SMILES |
5-((4-(2-Aminoethyl)phenyl)amino)-4-chloro-2-methylpyridazin-3(2H)-one |
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1. Huda Zahid, et al. J Med Chem. 2021 Sep 23;64(18):13902-13917.
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