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首页-小分子抑制剂&激动剂-Epigenetics-Bromodomain-JQ1
JQ1

Chemical Structure : JQ1

CAS No.: 1268524-70-4

JQ1 (JQ-1, (+)-JQ-1)

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.

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纯度 & COA & 质检文件 纯度: >98% (HPLC) Select Batch:

生物&药学活性

(+)-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.
JQ1 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.

物理化学性质&存储条件

分子量 456.9882
分子式 C23H25ClN4O2S
外观性状 Solid
CAS No.
储存条件
固体粉末
-20 °C 12 个月; 4°C 6 个月
配置液
-80 °C 6 个月; -20°C 6 个月
Shipping
Solubility

DMSO: ≥ 45 mg/mL

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)-

参考文献

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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