Epigenetic Reader Domain

Epigenetic Reader Domain(表观识别蛋白结构域)

Epigenetic regulators of gene expression and chromatin state include so-called writers, erasers, and readers of chromatin modifications.Well-characterized examples of reader domains include bromodomains typically binding acetyllysine and chromatin organization modifier (chromo), malignant brain tumor (MBT), plant homeodomain (PHD), and Tudor domains generally associating with methyllysine. Research on epigenetic readers has been tremendously influenced by the discovery of selective inhibitors targeting the bromodomain and extraterminal motif (BET) family of acetyl-lysine readers. The human genome encodes 46 proteins containing 61 bromodomains clustered into eight families. Distinct experimental approaches are used to identify the first BET inhibitors, GSK 525762A and (+)-JQ-1.

The Polycomb group (PcG) protein, enhancer of zeste homologue 2 (EZH2), has an essential role in promoting histone H3 lysine 27 trimethylation (H3K27me3) and epigenetic gene silencing. This function of EZH2 is important for cell proliferation and inhibition of cell differentiation, and is implicated in cancer progression. Cyclin-dependent kinases regulate epigenetic gene silencing through phosphorylation of EZH2. In many types of cancers including lymphomas and leukemia, EZH2 is postulated to exert its oncogenic effects via aberrant histone and DNA methylation, causing silencing of tumor suppressor genes.

p300/CBP is not only a transcriptional adaptor but also a histone acetyltransferase.

Epigenetic Reader Domain 相关产品(242)

  • GC10174 structure
    GC10174SGC-CBP30
    CAS: 1613695-14-9
    纯度: >99.50%

    A potent inhibitor of CREBBP/EP300 bromodomains

  • GC10382 structure
    GC10382CPI-637
    CAS: 1884712-47-3
    纯度: >99.50%

    An inhibitor of CBP/EP300 bromodomains

  • GC10402 structure
    GC10402Bromosporine
    CAS: 1619994-69-2
    纯度: >99.50%

    A non-specific bromodomain inhibitor

  • GC10979 structure
    GC10979PFI 4
    CAS: 900305-37-5
    纯度: >98.00%

    A chemical probe for BRPF1

  • GC11418 structure
    GC11418MI-2
    CAS: 1271738-62-5
    纯度: >99.00%

    An inhibitor of menin-MLL fusion protein interactions

  • GC11439 structure
    GC11439MG 149
    CAS: 1243583-85-8
    纯度: >99.50% / >98.00%

    MG 149是一种组蛋白乙酰转移酶(HAT)抑制剂,对Tip60和MOF的IC 50 值分别为74μM和47μM。

  • GC12199 structure
    GC12199MI-3
    CAS: 1271738-59-0
    纯度: >98.00%

    An inhibitor of menin-MLL fusion protein interactions

  • GC12419 structure
    GC12419UNC 926 hydrochloride
    CAS: 1184136-10-4
    纯度: >98.00%

    An antagonist of L3MBTL1, L3MBTL3, and L3MBTL4

  • GC12440 structure
    GC12440GSK 5959
    CAS: 901245-65-6
    纯度: >98.00%

    An inhibitor of the BRPF1 bromodomain

  • GC12450 structure
    GC12450BI 2536
    CAS: 755038-02-9
    纯度: >99.50% / >98.00%

    BI 2536是一种双重Polo样激酶(PLK)/溴结构域抑制剂,在无细胞激酶实验中,BI 2536 对PLK1、PLK2和PLK3的半数抑制浓度(IC 50 )值分别为0.83nM、3.5nM和9.0nM。

  • GC12588 structure
    GC12588I-BRD9
    CAS: 1714146-59-4
    纯度: >99.50%

    A BRD9 bromodomain inhibitor

  • GC12733 structure
    GC12733C646
    CAS: 328968-36-1
    纯度: >98.00%

    C646是一种有效的选择性p300/CBP组蛋白乙酰转移酶抑制剂(Ki 400 nM),已被证明具有多效性,包括神经保护、抗癌和抗上皮间质转化(anti-EMT)作用。

  • GC13025 structure
    GC13025GSK6853
    CAS: 1910124-24-1
    纯度: >99.00%

    A selective chemical probe for the bromodomain of BRPF1

  • GC13148 structure
    GC13148MS436
    CAS: 1395084-25-9
    纯度: >99.00%

    MS436 是一类新的溴结构域抑制剂,对 BRD4 BrD1 具有估计的 Ki=30-50 nM 的强亲和力,对 BrD2 的选择性是 10 倍。

  • GC13822 structure
    GC13822(-)-JQ1
    CAS: 1268524-71-5
    纯度: >99.50%

    A selective inhibitor of BET bromodomains

  • GC14063 structure
    GC14063GSK1324726A
    CAS: 1300031-52-0
    纯度: >98.00%

    A selective inhibitor of BET family proteins

  • GC14103 structure
    GC14103NSC228155
    CAS: 113104-25-9
    纯度: >98.00%

    An EGFR activator and inhibitor of KID-KIX interactions

  • GC14199 structure
    GC14199RVX-208
    CAS: 1044870-39-4
    纯度: >99.00%

    A selective BET bromodomain antagonist

  • GC14361 structure
    GC14361PFI 3
    CAS: 1819363-80-8
    纯度: >98.00%

    Probe for bromodomains of SMARCA2/4 and PB1(bromodomain 5)

  • GC14699 structure
    GC14699CPI-203
    CAS: 1446144-04-2
    纯度: >99.00%

    A bioavailable inhibitor of BET bromodomains

  • GC14787 structure
    GC14787Curcumin
    CAS: 458-37-7
    纯度: >98.00%

    A yellow pigment with diverse biological activities

  • GC15175 structure
    GC15175BAZ2-ICR
    CAS: 1665195-94-7
    纯度: >98.50%

    A BAZ2A/B bromodomain inhibitor

  • GC15375 structure
    GC15375PFI-1 (PF-6405761)
    CAS: 1403764-72-6
    纯度: >99.50%

    A BET bromodomain inhibitor

  • GC15747 structure
    GC15747I-BET151 (GSK1210151A)
    CAS: 1300031-49-5
    纯度: >99.50%

    A BRD2, BRD3, and BRD4 inhibitor