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)
- GC12419UNC 926 hydrochlorideCAS: 1184136-10-4纯度: >98.00%
An antagonist of L3MBTL1, L3MBTL3, and L3MBTL4
| 货号 | 产品名称 | CAS号 | 纯度 | 结构 |
|---|---|---|---|---|
| GC10174 | SGC-CBP30 | 1613695-14-9 | >99.50% | |
A potent inhibitor of CREBBP/EP300 bromodomains | ||||
| GC10382 | CPI-637 | 1884712-47-3 | >99.50% | |
An inhibitor of CBP/EP300 bromodomains | ||||
| GC10402 | Bromosporine | 1619994-69-2 | >99.50% | |
A non-specific bromodomain inhibitor | ||||
| GC10979 | PFI 4 | 900305-37-5 | >98.00% | |
A chemical probe for BRPF1 | ||||
| GC11418 | MI-2 | 1271738-62-5 | >99.00% | |
An inhibitor of menin-MLL fusion protein interactions | ||||
| GC11439 | MG 149 | 1243583-85-8 | >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 | MI-3 | 1271738-59-0 | >98.00% | |
An inhibitor of menin-MLL fusion protein interactions | ||||
| GC12419 | UNC 926 hydrochloride | 1184136-10-4 | >98.00% | |
An antagonist of L3MBTL1, L3MBTL3, and L3MBTL4 | ||||
| GC12440 | GSK 5959 | 901245-65-6 | >98.00% | |
An inhibitor of the BRPF1 bromodomain | ||||
| GC12450 | BI 2536 | 755038-02-9 | >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 | I-BRD9 | 1714146-59-4 | >99.50% | |
A BRD9 bromodomain inhibitor | ||||
| GC12733 | C646 | 328968-36-1 | >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 | GSK6853 | 1910124-24-1 | >99.00% | |
A selective chemical probe for the bromodomain of BRPF1 | ||||
| GC13148 | MS436 | 1395084-25-9 | >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 | (-)-JQ1 | 1268524-71-5 | >99.50% | |
A selective inhibitor of BET bromodomains | ||||
| GC14063 | GSK1324726A | 1300031-52-0 | >98.00% | |
A selective inhibitor of BET family proteins | ||||
| GC14103 | NSC228155 | 113104-25-9 | >98.00% | |
An EGFR activator and inhibitor of KID-KIX interactions | ||||
| GC14199 | RVX-208 | 1044870-39-4 | >99.00% | |
A selective BET bromodomain antagonist | ||||
| GC14361 | PFI 3 | 1819363-80-8 | >98.00% | |
Probe for bromodomains of SMARCA2/4 and PB1(bromodomain 5) | ||||
| GC14699 | CPI-203 | 1446144-04-2 | >99.00% | |
A bioavailable inhibitor of BET bromodomains | ||||
| GC14787 | Curcumin | 458-37-7 | >98.00% | |
A yellow pigment with diverse biological activities | ||||
| GC15175 | BAZ2-ICR | 1665195-94-7 | >98.50% | |
A BAZ2A/B bromodomain inhibitor | ||||
| GC15375 | PFI-1 (PF-6405761) | 1403764-72-6 | >99.50% | |
A BET bromodomain inhibitor | ||||
| GC15747 | I-BET151 (GSK1210151A) | 1300031-49-5 | >99.50% | |
A BRD2, BRD3, and BRD4 inhibitor | ||||
