GSK-J4 (Free base)
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Catalog number2762-1
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PricePlease ask
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Size1 mg
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Alternative_nameN-[2-(2-Pyridinyl)-6-(1,2,4,5-tetrahydro-3H-3-benzazepin-3-yl)-4-pyrimidinyl]-β-alanine ethyl ester
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DescriptionGSK- J4 is cell-permeable ethyl ester of GSK-J1 (Cat. Nos. 2260 & 2761). Acts as a histone demethylase JMJD3/UTX inhibitor. Inhibits demethylation of histone H3K27. Reduces LPS-induced proinflammatory cytokine production in primary human macrophages (IC₅₀ = 9 μM for the inhibition of TNFα release). Rescues newborn pups from embryonic lethality in BRAF knockin mice which recapitulate major features of RASopathies.
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CAS Number1373423-53-0
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Structure AvailableY
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Salt FormNo
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Molecular FormulaC₂₄H₂₇N₅O₂
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Molecular Weight417.5
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Cell PermeableY
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Purity≥99% by TLC
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SolubilitiesDMSO (~ 40 mg/ml) or EtOH (~ 40 mg/ml)
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HandlingProtect from light and moisture
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Tag LineA histone demethylase JMJD3/UTX inhibitor
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Storage Condition-20°C
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Shipping ConditionGel Pack
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Shelf Life36 months
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MDL NumberMFCD22683852
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PubChem CID71729975
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SMILESCCOC(=O)CCNC1=NC(=NC(=C1)N2CCC3=CC=CC=C3CC2)C4=CC=CC=N4
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InChiInChI=1S/C24H27N5O2/c1-2-31-23(30)10-14-26-21-17-22(28-24(27-21)20-9-5-6-13-25-20)29-15-11-18-7-3-4-8-19(18)12-16-29/h3-9,13,17H,2,10-12,14-16H2,1H3,(H,26,27,28)
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InChi KeyWBKCKEHGXNWYMO-UHFFFAOYSA-N
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MSDS AvailableYes
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Gene target
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Short nameGSK-J4 (Free base)
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Alternative nameGSK-J4 (Free base)
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