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Histone Methyltransferase


Histone methyltransferases (HMT) are histone-modifying enzymes), that catalyze the transfer of one, two, or three methyl groups to lysine and arginine residues of histone proteins. Methylation of histones is important biologically because it is the principal epigenetic modification of chromatin that determines gene expression, genomic stability, stem cell maturation, cell lineage development, genetic imprinting, DNA methylation, and cell mitosis.
  • Ralometostat EY8034

    Ralometostat (TNG908) is a potent, selective, and brain-penetrant PRMT5 inhibitor with an IC50 of 4 μM, exerting its effect through an MTA synergistic mechanism. It also demonstrates antitumor activity in xenograft models.

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  • Navlimetostat EY8033

    MRTX1719 is a potent and selective inhibitor of the protein arginine methyltransferase 5·methylthioadenosine phosphorylase complex (PRMT5·MTA), which serves as a potential selective therapeutic target for tumor intervention.

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  • Onametostat EY8032

    Onametostat (JNJ-64619178)是PRMT5抑制剂,具有较高的选择性和效力(PRMT5-MEP-50, IC50=0.14 nM)、良好的药代动力学特性以及安全性

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  • GSK126 EY1820

    GSK126是一种高活性,S-腺苷-蛋氨酸竞争性EZH2甲基转移酶抑制剂,Ki为0.5 nM。

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  • MM-102 EY1623

    MM-102是一种有效的WDR5/MLL相互作用抑制剂, WDR5结合检测中, IC50 =2.4 nM, Ki < 1nM。

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