Chemical Structure : JQ1
CAS No.: 1268524-70-4
货号: PC-43338Not For Human Use, Lab Use Only.
(+)-JQ-1 (JQ1) is a potent, selective, cell-permeable BET bromodomain inhibitor with IC50 of 77 nM/33 nM for BRD4 BD1 and BD2, respectively.
规格 | 价格 | 库存 | 数量 |
---|---|---|---|
25 mg | ¥1580 | In stock | |
100 mg | ¥3580 | In stock | |
500 mg | ¥10580 | In stock | |
1 g | ¥16800 | In stock |
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(+)-JQ-1 (JQ1) is a potent, selective, cell-permeable BET bromodomain inhibitor with IC50 of 77 nM/33 nM for BRD4 BD1 and BD2, respectively; induces rapid expression of keratin in treated NMC 797 cells, displaces the BRD4 fusion oncoprotein from chromatin, prompting squamous differentiation and specific antiproliferative effects in BRD4-dependent cell lines and patient-derived xenograft models.
分子量 | 456.9882 | |
分子式 | C23H25ClN4O2S | |
外观性状 | Solid | |
储存条件 |
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Solubility |
DMSO: ≥ 45 mg/mL |
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Chemical Name/SMILES |
6H-Thieno[3,2-f][1,2,4]triazolo[4,3-a][1,4]diazepine-6-acetic acid, 4-(4-chlorophenyl)-2,3,9-trimethyl-, 1,1-dimethylethyl ester, (6S)- |
1. Filippakopoulos P, et al. Nature. 2010 Dec 23;468(7327):1067-73.
2. Matzuk MM, et al. Cell. 2012 Aug 17;150(4):673-84.
3. Peirs S, et al. Leukemia. 2017 Oct;31(10):2037-2047.
4. Tögel L, et al. Mol Cancer Ther. 2016 Jun;15(6):1217-26.
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