GLPBio

Bromodomain

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Bromodomains are a family of evolutionarily conserved protein modules of approximately 110 amino acids that have been found in chromatin-associated proteins as well as nuclear histone acetyltransferases (HATs). Besides its role in chromatin remodeling, recent studies have identified that bromodomains, as acetyl-lysine binding domains, are able to recognize and bind ε–N-acetylated lysine residues in histone and non-histone proteins. The nuclear magnetic resonance (NMR) spectroscopic analysis reveals that the chemical structure of bromodomains, consisting of four left-handed α-helices (including αZ, αA, αB and αC) connected by two loops (ZA and BC loops), forms a deep hydrophobic cavity serving as the acetyl-lysine recognition site.

Products Related to Bromodomain(44)

  • GC16817 structure
    GC16817BI-9564
    CAS: 1883429-22-8
    Purity: >99.50%

    BRD9/7 specific inhibitor

  • GC17482 structure
    GC17482OF-1
    CAS: 919973-83-4
    Purity: >98.00%

    BRPF1B and BRPF2 bromodomain inhibitor

  • GC17973 structure
    GC17973OTX-015
    CAS: 202590-98-5
    Purity: >99.50%

    OTX-015 inhibits the binding of BRD2, BRD3, and BRD4 to acetylated histone 4 in a concentration-dependent manner, with IC 50 values from 92-112nM.

  • GC18750 structure
    GC18750NEO2734
    CAS: 2081072-29-7
    Purity: >99.50%

    An orally active dual p300/CBP and BET bromodomain selective inhibitor

  • GC43320 structure
    GC43320CPI-268456
    CAS: 1380087-86-4
    Purity: >98.00%

    CPI-268456 (compound 141) is a potent BRD4 inhibitor with an IC50 of <0.5 μM.

  • GC43889 structure
    GC43889I-CBP112 (hydrochloride)
    CAS: 2147701-33-3
    Purity: >90.00%

    cAMP-responsive element-binding protein binding protein (CREBBP) and E1A-associated protein p300 (EP300) are transcriptional co-activators that modulate DNA replication, DNA repair, cell growth, transformation, and development.

  • GC45503 structure
  • GC45640 structure
    GC45640TP-238 (hydrochloride)
    CAS: 2415263-05-5
    Purity: >99.00%

    A neuropeptide with diverse biological activities

  • GC46675 structure
    GC466754-Phenyl-2-pyrrolidinone
    CAS: 1198-97-6
    Purity: >98.00%

    A precursor and synthetic intermediate

  • GC48408 structure
    GC48408TW9
    CAS: 2614417-90-0
    Purity: >98.00%

    A dual inhibitor of BRD4 and HDAC1

  • GC49029 structure
    GC49029CAY17c
    CAS: 2414373-11-6
    Purity: >98.00%

    An inhibitor of BRD4 and class I and class IIb HDACs

  • GC50070 structure
    GC50070I-BET 151 dihydrochloride
    CAS: 1883545-47-8
    Purity: >98%

    BET bromodomain inhibitor; also promotes differentiation of hiPSCs into megakaryocytes

  • GC60182 structure
    GC60182GSK046
    CAS: 2474876-09-8
    Purity: >98.00%

    GSK046 (iBET-BD2) is a potent, selective and orally active BD2 bromodomain inhibitor of the BET proteins, with IC50s of 264 nM (BRD2 BD2), 98 nM (BRD3 BD2), 49 nM (BRD4 BD2) and 214 nM (BRDT BD2), respectively.

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

    RVX-208 (RVX-208) is an inhibitor of BET transcriptional regulators with selectivity for the second bromodomain. The IC50s are 87 μM and 0.51 μM for BD1 and BD2, respectively.

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

    I-BET151 (GSK1210151A) (GSK1210151A) is a BET bromodomain inhibitor which inhibits BRD4, BRD2, and BRD3 with pIC50 of 6.1, 6.3, and 6.6, respectively.

  • GC17073 structure
    GC17073I-BET-762
    CAS: 1260907-17-2
    Purity: >99.00%

    I-BET-762 (I-BET762; GSK525762) is a BET bromodomain inhibitor with IC50 of 32.5-42.5 nM.

  • GC18096 structure
    GC18096UNC669
    CAS: 1314241-44-5
    Purity: >98.50%

    L3MBTL antagonist,potent and selective

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

    BRD4 inhibitor

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

    BET proteins inhibitor

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

    BET bromodomain inhibitor