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GSK-J4?HCl

    
98.8%

GSK-J4 Hydrochloride

源葉(MedMol)
S29703 一鍵復制產品信息
1797983-09-5
C24H28ClN5O2
453.96
MFCD26142638
GSK-J4 鹽酸鹽;GSK-J4 HCl; GSK J4 HCl; GSK-J4 hydrochloride
貨號 規格 價格 上海 北京 武漢 南京 購買數量
S29703-10mg
98.8% ¥190.00 7 - - -
S29703-25mg
98.8% ¥380.00 6 - - -
S29703-100mg
≥98% ¥1020.00 貨期:2-3天 - - -
產品介紹 參考文獻 質檢證書(COA) 摩爾濃度計算器 相關產品

產品介紹

GSK J4 HCl是一種細胞滲透性的GSK J1前體藥物,是第一個選擇性H3K27組蛋白去甲基化酶JMJD3和UTX抑制劑,無細胞試驗中IC50為60 nM,抑制JMJ家族的去甲基化酶活性

產品描述: GSK J4 HCl是一種細胞滲透性的GSK J1前體藥物,是第一個選擇性H3K27組蛋白去甲基化酶JMJD3和UTX抑制劑,無細胞試驗中IC50為60 nM,抑制JMJ家族的去甲基化酶活性
靶點: JMJD3 (Cell-free assay):60 nM;HistoneDemethylase
體外研究: GSK-J4 Hydrochloride has cellular activity in Flag-JMJD3-transfected HeLa cells, in which GSK-J4 prevents the JMJD3-induced loss of nuclear H3K27me3 immunostaining. Administration of GSK-J4 increases total nuclear H3K27me3 levels in untransfected cells. GSK-J4 significantly reduces the expression of 16 of 34 LPS-driven cytokines, including tumour-necrosis factor-α (TNF-α).
GSK-J4 Hydrochloride (5 μM; 48 hours) causes a more than 3-fold increase in mouse podocyte H3K27me3 content. H3K27me3 levels in cultured podocytes, GSK-J4 reduces Jagged-1 mRNA and Jagged-1 protein levels. Correspondingly, when exposed podocytes to the inducer of dedifferentiation TGF-β1, pretreatment with GSK-J4 preventes both the increase in intracellular N1-ICD levels and the increase in α-SMA and the decrease in podocin mRNA levels.
GSK-J4 Hydrochloride (10, 25 nM) acts upon DCs promoting the differentiation of Treg cells, improving Treg stability and suppressive capacities, without affecting the differentiation of Th1 and Th17 cells.
GSK-J4 Hydrochloride inhibits JMJD3 expression that is induced by TGF-β1.
GSK-J4 Hydrochloride inhibits H3K4 demethylation at Xist, Nodal, and HoxC13 in female embryonic stem cells.
體內研究: GSK-J4 hydrochloride is a potent dual inhibitor of H3K27me3/me2-demethylases JMJD3/KDM6B and UTX/KDM6A. It inhibits LPS-induced TNF-α production in human primary macrophages. GSK-J4 hydrochloride is a cell permeable prodrug of GSK-J1.
細胞實驗: Cell lines: Mouse podocytes Concentrations: 5 μM Incubation Time: 48 h Method: Cells were serum starved for 4 hours, followed by treatment with EPZ-6438 (10 μM) or GSK-J4 (5 μM) for 48 hours.
動物實驗: Animal Models: BALB/c mice Dosages: 10 mg/kg Administration: i.p.
參考文獻: 1. Kruidenier L, et al. Nature, 2012, 488(7411), 404-408. 2. Majumder S, et al. J Clin Invest. 2018 Jan 2;128(1):483-499.
溶解性: Soluble  in  DMSO、Ethanol、H2O
保存條件: -20℃
配置溶液濃度參考:
1mg 5mg 10mg
1 mM 2.203 ml 11.014 ml 22.028 ml
5 mM 0.441 ml 2.203 ml 4.406 ml
10 mM 0.22 ml 1.101 ml 2.203 ml
50 mM 0.044 ml 0.22 ml 0.441 ml
注意: 部分產品我司僅能提供部分信息,我司不保證所提供信息的權威性,僅供客戶參考交流研究之用。

參考文獻

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摩爾濃度計算器

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