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)
- GC73357Menin-MLL inhibitor-22CAS: 2851841-61-5纯度: >99.00%
Menin-MLL inhibitor-22(化合物C20)是美宁与混合谱系白血病(MLL)之间相互作用的口服活性抑制剂(IC50=7nM)。
- GC73365CBP/p300-IN-20CAS: 2999742-92-4纯度: >98.00%
CBP/p300-IN-20是一种强效且选择性的p300/CBP抑制剂,p300的pIC50为10.1。
- GC73448PROTAC BRD4 Degrader-19CAS: 2684292-71-3纯度: >98.00%
PROTAC BRD4 Degrader-19(化合物176)是一种靶向BRD4蛋白进行降解的PROTAC。
- GC73466PROTAC BRD9 Degrader-6CAS: 2676211-62-2纯度: >98.00%
PROTAC BRD9 Degrader-6是BRD9的有效降解剂(IC50=0.13 nM),可用于BAF复合物相关疾病的研究。
- GC73627HDAC/JAK/BRD4-IN-1CAS: 2755325-84-7纯度: >95.00%
HDAC/JAK/BRD4-IN-1(化合物25ap)是一种强效的HDAC/JAK/BRD4三重抑制剂。
- GC73742BET bromodomain inhibitor 4CAS: 2407658-41-5纯度: >99.00%
BET bromodomain inhibitor 4(实施例7)是BET溴结构域的抑制剂。
- GC73819PROTAC BET Degrader-12纯度: >98.00%
PROTAC BET Degrader-12(化合物8b)是含溴结构域和末端外结构域(BET)的蛋白质的PROTAC降解剂,其以DCAF11依赖的方式降解BRD3和BRD4。
- GC73884PLK1/BRD4-IN-2CAS: 2251709-89-2纯度: 不显示
PLK1/BRD4-IN-2(化合物15)是一种BI-2536类似物和双重抑制剂,靶向pol -like kinase 1 (PLK1)和BRD4bromodomain (BRD4-BD1 IC50=28 nM, PLK1 IC50=40 nM)。
- GC73885PLK1/BRD4-IN-3CAS: 2251709-91-6纯度: >99.00%
PLK1/BRD4-IN-3(化合物21)是溴结构域4 (BRD4)和polo样激酶1 (PLK1)的选择性双重抑制剂。
- GC73953BRD4/NAMPT-IN-1CAS: 3049218-28-9纯度: >99.00%
BRD4/NAMPT-IN-1(化合物A2)对NAMPT和BRD4显示出强烈的抑制作用(IC50=35nM(NAMPT)和58nM(BRD4))。
| 货号 | 产品名称 | CAS号 | 纯度 | 结构 |
|---|---|---|---|---|
| GC73357 | Menin-MLL inhibitor-22 | 2851841-61-5 | >99.00% | |
Menin-MLL inhibitor-22(化合物C20)是美宁与混合谱系白血病(MLL)之间相互作用的口服活性抑制剂(IC50=7nM)。 | ||||
| GC73359 | ACBI2 | 2913161-19-8 | >99.00% | |
ACBI2是一种高效且口服活性的VHL-PROTAC SMARCA2降解剂(EC50:7 nM),在RKO细胞中以1 nM的DC50值选择性降解SMARCA2。 | ||||
| GC73365 | CBP/p300-IN-20 | 2999742-92-4 | >98.00% | |
CBP/p300-IN-20是一种强效且选择性的p300/CBP抑制剂,p300的pIC50为10.1。 | ||||
| GC73423 | BET-IN-14 | 2243669-93-2 | >99.00% | |
BET-IN-14是一种口服活性的pan BET抑制剂(IC50: 5.35 nM)。 | ||||
| GC73425 | GSK737 | 2748687-95-6 | >99.00% | |
GSK737是一种BRD4 BD1和BD2抑制剂,pIC50值分别为5.3和7.3。 | ||||
| GC73448 | PROTAC BRD4 Degrader-19 | 2684292-71-3 | >98.00% | |
PROTAC BRD4 Degrader-19(化合物176)是一种靶向BRD4蛋白进行降解的PROTAC。 | ||||
| GC73466 | PROTAC BRD9 Degrader-6 | 2676211-62-2 | >98.00% | |
PROTAC BRD9 Degrader-6是BRD9的有效降解剂(IC50=0.13 nM),可用于BAF复合物相关疾病的研究。 | ||||
| GC73504 | SRX3177 | 2241237-51-2 | >99.00% | |
SRX3177是CDK4/6、PI3K和BRD4的三重抑制剂,IC50分别为33 nM(BRD4 BD1)、89 nM(BR D4 BD2)、79 nM(PI3Kα)、83 nM(PI 3Kδ)、3.18μM(PI3Kγ)、<2.5 nM(CDK4)、3.3 nM(CDK6)。 | ||||
| GC73598 | IV-255 | - | >98.00% | |
IV-255是BRG1溴结构域的选择性小分子抑制剂。 | ||||
| GC73627 | HDAC/JAK/BRD4-IN-1 | 2755325-84-7 | >95.00% | |
HDAC/JAK/BRD4-IN-1(化合物25ap)是一种强效的HDAC/JAK/BRD4三重抑制剂。 | ||||
| GC73660 | SMD-3040 | 3033109-92-8 | >99.00% | |
SMD-3040是一种强效且选择性的SMARCA2 PROTAC降解剂(DC50:12nM)。 | ||||
| GC73661 | SMD-3040 TFA | - | >99.00% | |
SMD-3040 TFA是SMARCA2的选择性降解剂。 | ||||
| GC73742 | BET bromodomain inhibitor 4 | 2407658-41-5 | >99.00% | |
BET bromodomain inhibitor 4(实施例7)是BET溴结构域的抑制剂。 | ||||
| GC73756 | MMH2-NR | - | >98.00% | |
MMH2-NRMMH2的负控制。 | ||||
| GC73773 | PLK1/BRD4-IN-5 | - | >99.00% | |
PLK1/BRD4-IN-5(化合物SC10)是一种口服活性PLK1和BRD4抑制剂,IC50值分别为0.3 nM和60.8 nM。 | ||||
| GC73819 | PROTAC BET Degrader-12 | - | >98.00% | |
PROTAC BET Degrader-12(化合物8b)是含溴结构域和末端外结构域(BET)的蛋白质的PROTAC降解剂,其以DCAF11依赖的方式降解BRD3和BRD4。 | ||||
| GC73879 | BRD4 Inhibitor-30 | 1789731-20-9 | >99.00% | |
BRD4 Inhibitor-30(化合物1)是一种BRD4抑制剂,IC50值为415 nM。 | ||||
| GC73884 | PLK1/BRD4-IN-2 | 2251709-89-2 | 不显示 | |
PLK1/BRD4-IN-2(化合物15)是一种BI-2536类似物和双重抑制剂,靶向pol -like kinase 1 (PLK1)和BRD4bromodomain (BRD4-BD1 IC50=28 nM, PLK1 IC50=40 nM)。 | ||||
| GC73885 | PLK1/BRD4-IN-3 | 2251709-91-6 | >99.00% | |
PLK1/BRD4-IN-3(化合物21)是溴结构域4 (BRD4)和polo样激酶1 (PLK1)的选择性双重抑制剂。 | ||||
| GC73953 | BRD4/NAMPT-IN-1 | 3049218-28-9 | >99.00% | |
BRD4/NAMPT-IN-1(化合物A2)对NAMPT和BRD4显示出强烈的抑制作用(IC50=35nM(NAMPT)和58nM(BRD4))。 | ||||
| GC73958 | BRD4 ligand 6 TFA | 2763548-61-2 | >99.00% | |
BRD4 ligand 6 TFA是BRD4配体6的TFA盐形式。 | ||||
| GC73990 | SDU-071 | - | >98.00% | |
SDU-071是BRD4-p53抑制剂的强效口服活性抑制剂。 | ||||
| GC74003 | BBC0403 | 2644662-83-7 | >98.00% | |
BBC0403是一种选择性BRD2抑制剂,对BRD2 (BD2)和BRD2 (BD1)的Kds分别为7.64 μM和41.37 μM。 | ||||
| GC74035 | AU-24118 | - | >98.00% | |
AU-24118是mSWI/SNF ATP酶(SMARCA2和SMARCA4)和PBRM1的口服生物可利用蛋白水解靶向嵌合体(PROTAC)降解剂。 | ||||
