- Signaling Pathways
- Epigenetics
- Epigenetic Reader Domain
Epigenetic Reader Domain
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 Isoform Specific Products
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Epigenetic Reader Domain
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Brd
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BRPF1
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BRPF2
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BRPF3
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BRD2
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BRD3
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BRD4
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BRDT
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CECR2
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BD1
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BD2
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BRD7
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BRD9
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BET
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BAZ
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Epigenetic Reader Domain Inhibitors
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Epigenetic Reader Domain Agonists
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Epigenetic Reader Domain Antagonists
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Epigenetic Reader Domain Activators
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Epigenetic Reader Domain Modulators
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Epigenetic Reader Domain Chemicals
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Epigenetic Reader Domain Inducer
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Epigenetic Reader Domain Degraders
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Epigenetic Reader Domain Controls
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Epigenetic Reader Domain Substrate
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Epigenetic Reader Domain Ligands
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Epigenetic Reader Domain Related Products (905)
Related Products (905)
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Antibodies (109)
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Epigenetic Reader Domain Isoform Comparison
- BRD4 Inhibitor-13
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(2R,3R)-GSK973
0 ImagesCat. No.: HY-138563A(2R,3R)-GSK973 is an isomer of GSK973. GSK973 is a highly selective, orally bioavailable inhibitor of the BD2s (second bromodomains) of the BET family. -
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- PLK1/BRD4-IN-2
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- FT001
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A-485 (Standard)
0 ImagesA-485 (Standard) is the analytical standard of A-485 (HY-107455). This product is intended for research and analytical applications. A-485, a chemical probe, is a potent and selective catalytic inhibitor of p300/CBP with IC50s of 9.8 nM and 2.6 nM for p300 and CBP histone acetyltransferase (HAT), respectively. -
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- MMH1-NR
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IACS-9571 TFA
0 ImagesCat. No.: HY-102000ACAS No.: 1883598-69-3Synonyms: ASIS-P040 TFA -
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NVS-BET-1
0 ImagesCat. No.: HY-142265CAS No.: 1639115-52-8NVS-BET-1 is a BET bromodomain inhibitor that regulates keratinocyte plasticity. -
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CBP/p300-IN-2
0 ImagesCat. No.: HY-128761CAS No.: 2158265-96-2CBP/EP300-IN-2 is an inhibitor of CBP/EP300 with IC50 values of 1.07 nM and 5.96 nM for CBP/HTRF and Myc, respectively. CBP/EP300-IN-2, example 25, is extracted from patent WO2017205538A1. -
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XYD270
0 ImagesCat. No.: HY-182082XYD270 is an orally active BRD9 PROTAC degrader. XYD270 inhibits the proliferation of cancer cells. XYD270 suppresses tumor growth in a mouse model of acute myeloid leukemia. XYD270 can be used in research related to synovial sarcoma and acute myeloid leukemia. -
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CZL-105
0 ImagesCat. No.: HY-187436CAS No.: 3094841-98-9CZL-105 is a highly potent, selective, and orally active p300/CBP inhibitor, with IC50 values of 0.09 μM and 0.08 μM against p300 and CBP bromodomains, respectively. CZL-105 inhibits the proliferation of OPM-2 multiple myeloma cells with an IC50 of 57 nM, and induces G0/G1 cell cycle arrest and apoptosis. CZL-105 is applicable for research related to multiple myeloma. -
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AMX-883
0 ImagesCat. No.: HY-182766CAS No.: 3102636-19-8AMX-883 a selective and orally active BRD9 molecular glue degrader that drives differentiation in acute myeloid leukaemia. AMX-883 shows selectivity over all other bromodomain containing proteins and proteome wide. AMX-883 does not employ the commonly used E3 ligases (cereblon, VHL) but instead drives degradation via DCAF16 as a targeted glue. AMX-883 can be used for the study of acute myeloid leukaemia (AML). -
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BRD7-IN-1 free base
0 ImagesCat. No.: HY-111905ACAS No.: 2305379-66-0BRD7-IN-1 free base, a modified derivative of BI7273 (BRD7/9 inhibitor), binds to a VHL ligand via a linker to form a PROTAC VZ185 (VZ185 against BRD7/9 with DC50s of 4.5 and 1.8 nM, respectively). -
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CD235
0 ImagesCat. No.: HY-128977CAS No.: 1627716-57-7CD235 is a structurally similar analogue of CD161. CD161 is a potent and orally bioavailable BET bromodomain inhibitor. -
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- PROTAC BRD4 Degrader linker conjugate-2
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- I-BET282E
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PROTAC BRD9 Degrader-5
0 ImagesCat. No.: HY-145947CAS No.: 2704616-86-2PROTAC BRD9 Degrader-5 is a BRD9 PROTAC degrader. PROTAC BRD9 Degrader-5 is used in research on acute myeloid leukemia, rhabdoid tumor, synovial sarcoma, and multiple myeloma. -
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- GSK040
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GSK9311 hydrochloride
0 ImagesCat. No.: HY-100729ACAS No.: 2253733-09-2 -
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UNC926 hydrochloride
0 ImagesCat. No.: HY-16510ACAS No.: 1782573-49-2UNC926 hydrochloride is a methyl-lysine (Kme) reader domain inhibitor that inhibits L3MBTL1 with an IC50 of 3.9 μM. -
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