- 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
(3)
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BRPF1
(9)
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BRPF2
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BRPF3
(2)
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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
(4)
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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 (902)
Related Products (902)
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Antibodies (109)
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Epigenetic Reader Domain Isoform Comparison
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Menin-MLL-IN-35
0 ImagesCat. No.: HY-186043CAS No.: 2654080-48-3Menin-MLL-IN-35 (compound 286) is an inhibitor of menin/MLL protein/protein interaction with an IC50 value of 0.096 μM in MEIS1 mRNA expression. Menin-MLL-IN-35 can be used in the research of cancer, myelodysplastic syndrome (MDS), myeloproliferative neoplasms (MPN), and diabetes. -
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BI 2536 (Standard)
0 ImagesCat. No.: HY-50698RCAS No.: 755038-02-9 -
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GSK778 hydrochloride
0 ImagesCat. No.: HY-136570ACAS No.: 2863657-79-6Synonyms: iBET-BD1 hydrochloride -
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GSK4028 (Standard)
0 ImagesCat. No.: HY-101027ARCAS No.: 2079886-19-2GSK4028 (Standard) is the analytical standard of GSK4028 (HY-101027A). This product is intended for research and analytical applications. GSK4028 is the enantiomeric negative control of GSK4027, which is a PCAF/GCN5 bromodomain chemical probe, the pIC50 of GSK4028 is 4.9 in a time-resolved fluorescence resonance energy transfer (TR-FRET) assay. -
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FL-411 (Standard)
0 ImagesCat. No.: HY-111102RCAS No.: 2118944-88-8Synonyms: BRD4-IN-1 (Standard) -
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SB-699551 (Standard)
0 ImagesCat. No.: HY-103100RCAS No.: 864741-95-7SB-699551 (Standard) is the analytical standard of SB-699551 (HY-103100). This product is intended for research and analytical applications. SB-699551 is a potent and selective 5-HT5A antagonist with a Ki value of 5.1 μM. SB-699551 increases the phosphorylation levels of CREB and ATF1, and decreases the phosphorylation levels of AKT, PRAS40, P70S6K, FOXO1, and S6RP. SB-699551 improves drug-induced cognitive deficits. SB-699551 improves social withdrawal and forgetfulness. SB-699551 inhibits breast cancer. -
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I-CBP112 hydrochloride
0 ImagesCat. No.: HY-19541ACAS No.: 2147701-33-3I-CBP112 hydrochloride is a selective inhibitor of CBP/P300 that directly binds their bromodomains (Kds = 142 and 625 nM, respectively). I-CBP112 significantly reduces the leukemia-initiating potential of MLL-AF9(+) acute myeloid leukemia cells in a dose-dependent manner in vitro and in vivo. I-CBP112 increases the cytotoxic activity of BET bromodomain inhibitor JQ1 as well as doxorubicin. -
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SGC-CBP30 (Standard)
0 ImagesCat. No.: HY-15826RCAS No.: 1613695-14-9SGC-CBP30 (Standard) is the analytical standard of SGC-CBP30 (HY-15826). This product is intended for research and analytical applications. SGC-CBP30, a chemical probe, is a potent and highly selective CBP/p300 bromodomain (Kds of 21 nM and 32 nM for CBP and p300, respectively) inhibitor, displaying 40-fold selectivity over the first bromodomain of BRD4 [BRD4(1)] bound. SGC-CBP30 strongly reduces secretion of IL-17A in Th17 cells and has anti-inflammatory effects. -
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BRD4 Inhibitor-32
0 ImagesCat. No.: HY-160636CAS No.: 1445992-86-8BRD4 Inhibitor-32 (example 15) is a BRD4 inhibitor that can be used in acute kidney disease and chronic kidney disease research. -
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ENL/AF9 YEATS-IN-1
0 ImagesCat. No.: HY-188074CAS No.: 2657651-10-8ENL/AF9 YEATS-IN-1 is a ENL/AF9 YEATS domain inhibitor. ENL/AF9 YEATS-IN-1 suppresses oncogene expression in cells by inhibiting the ENL/AF9 YEATS domain. ENL/AF9 YEATS-IN-1 can be used in leukemia research. -
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Revumenib (Standard)
0 ImagesCat. No.: HY-136175RCAS No.: 2169919-21-3Synonyms: SNDX-5613 (Standard)Revumenib (Standard) is the analytical standard of Revumenib (HY-136175). This product is intended for research and analytical applications. Revumenib (SNDX-5613) is a potent and specific Menin-MLL inhibitor with a binding Ki of 0.149 nM and a cell based IC50 of 10-20 nM. Revumenib can be used for the research of MLL-rearranged (MLL-r) acute leukemias, including acute lymphoblastic leukemia (ALL) and acute myeloid leukemia (AML). -
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Y06036 (Standard)
0 ImagesCat. No.: HY-111502RCAS No.: 1832671-96-1 -
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BRD4 ligand 13
0 ImagesCat. No.: HY-178094CAS No.: 1101702-81-1BRD4 ligand 13 is a BRD4 ligand that can be used for the synthesis of PROTACs, such as Cath-L-dBET1 (HY-173257). BRD4 ligand 13 is a target protein ligand-conjugate that can be used for the synthesis of PROTACs, such as SJH1-51B (HY-162240). -
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Naphthol AS-E (Standard)
0 ImagesCat. No.: HY-104068RCAS No.: 92-78-4Naphthol AS-E (Standard) is the analytical standard of Naphthol AS-E (HY-104068). This product is intended for research and analytical applications. Naphthol AS-E is a potent and cell-permeable inhibitor of KIX-KID interaction. Naphthol AS-E directly binds to the KIX domain of CBP (Kd:8.6 μM), blocks the interaction between the KIX domain and the KID domain of CREB with IC50 of 2.26 μM. Naphthol AS-E can be used for cancer research. -
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MZ 1 (Standard)
0 ImagesCat. No.: HY-107425RCAS No.: 1797406-69-9MZ 1 (Standard) is the analytical standard of MZ 1 (HY-107425). This product is intended for research and analytical applications. MZ 1 is a PROTAC connected by ligands for von Hippel-Lindau and BRD4. MZ 1 potently and rapidly induces reversible, long-lasting, and selective removal of BRD4 over BRD2 and BRD3. Kds of 382/120, 119/115, and 307/228 nM for BRD4 BD1/2, BRD3 BD1/2, and BRD2 BD1/2, respectively. -
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Menin-MLL-IN-36
0 ImagesCat. No.: HY-186044CAS No.: 2654078-52-9Menin-MLL-IN-36 (compound 398) is an inhibitor of menin/MLL protein/protein interaction with an IC50 value of 0.043 μM in MEIS1 mRNA expression. Menin-MLL-IN-36 can be used in the research of cancer, myelodysplastic syndrome (MDS), myeloproliferative neoplasms (MPN), and diabetes. -
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BET-IN-24
0 ImagesCat. No.: HY-160446CAS No.: 2407658-21-1Bet-in-24 (example 2) is a bromodomain and extra-terminal (BET) inhibitor. BET-IN-24 can be used in the study of virology, heart failure, inflammation, central nervous system (CNS) diseases and many cancers -
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E-7386 (Standard)
0 ImagesCat. No.: HY-111386RCAS No.: 1799824-08-0 -
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BI-7273 (Standard)
0 ImagesCat. No.: HY-100351RCAS No.: 1883429-21-7BI-7273 (Standard) is the analytical standard of BI-7273 (HY-100351). This product is intended for research and analytical applications. BI-7273 is a selective, and cell-permeable BRD9 inhibitor, with an IC50 and a Kd of 19 and 0.75 nM; also shows high effect on BRD7, with an IC50 and a Kd of 117 nM and 0.3 nM. -
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