| 产品详情 |
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| Product Name | GSK J1 |
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| Description | Potent inhibitor of the H3K27 histone demethylases JMJD3 (KDM6B) and UTX (KDM6A) (IC50 values are 28 and 53 nM respectively). Also inhibits KDM5B, KDM5C and KDM5A (IC50 values are 170, 550 and 6,800 nM respectively). Exhibits no activity against a panel of other histone demethylases (IC50 >20 μM), and displays no significant inhibitory activity against 100 protein kinases at a concentration of 30 μM. Ethyl ester derivative and Negative Control also available.. Purity 99%. MW (observed): 389.45 |
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| Size | 50 mg |
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| Concentration | n/a |
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| Applications | n/a |
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| Other Names | N-[2-(2-Pyridinyl)-6-(1,2,4,5-tetrahydro-3H-3-benzazepin-3-yl)-4-pyrimidinyl]-β-alanine |
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| Gene, Accession, CAS # | CAS: 1373422-53-7 |
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| Catalog # | 4593/50 |
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| Price | |
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| Order / More Info | GSK J1 from TOCRIS BIOSCIENCE
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| Product Specific References | PubMed: 25671108, 27080563 |
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| 产品资料 |
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