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)
- GC13014AZD 5153CAS: 1869912-39-9Purity: >98%
AZD 5153 is a bivalent BET/BRD4 bromodomain inhibitor with an IC₅₀ of 5nM for BRD4, which simultaneously binds to both bromodomains of BRD4, significantly modulates MYC, E2F, and mTOR transcriptional programs, and inhibits the expression of NSD3 target genes.
- GC16299BET bromodomain inhibitorCAS: 1380087-89-7Purity: >99.50%
Potent and selective inhibitor for BRD4
- GC16531Bromodomain Inhibitor, (+)-JQ1CAS: 1268524-70-4Purity: >99.50%
A selective inhibitor of BET bromodomains
| Catalog No. | Product Name | CAS No. | Purity | Structure |
|---|---|---|---|---|
| GC10382 | CPI-637 | 1884712-47-3 | >99.50% | |
CBP/EP300 bromodomain inhibitor | ||||
| GC10402 | Bromosporine | 1619994-69-2 | >99.50% | |
A non-specific bromodomain inhibitor | ||||
| GC10524 | GSK 525768A | 1260530-25-3 | >99.00% | |
| GC10727 | Ischemin sodium salt | - | >98% | |
CBP bromodomain inhibitor | ||||
| GC10979 | PFI 4 | 900305-37-5 | >98.00% | |
Potent and selective BRPF1 Bromodomain inhibitor | ||||
| GC12440 | GSK 5959 | 901245-65-6 | >98.00% | |
BRPF1 bromodomain inhibitor | ||||
| GC12588 | I-BRD9 | 1714146-59-4 | >99.50% | |
BRD9 inhibitor | ||||
| GC13014 | AZD 5153 | 1869912-39-9 | >98% | |
AZD 5153 is a bivalent BET/BRD4 bromodomain inhibitor with an IC₅₀ of 5nM for BRD4, which simultaneously binds to both bromodomains of BRD4, significantly modulates MYC, E2F, and mTOR transcriptional programs, and inhibits the expression of NSD3 target genes. | ||||
| GC13025 | GSK6853 | 1910124-24-1 | >99.00% | |
BRPF1 inhibitor | ||||
| GC13187 | I-BET 151 hydrochloride | - | >98% | |
BET bromodomain inhibitor | ||||
| GC13822 | (-)-JQ1 | 1268524-71-5 | >99.50% | |
A selective inhibitor of BET bromodomains | ||||
| GC14168 | UMB-32 | 1635437-39-6 | >98% | |
inhibitor of the BET bromodomain BRD4 and the bromodomain-containing transcription factor TAF1 and TAF1L | ||||
| GC14361 | PFI 3 | 1819363-80-8 | >98.00% | |
inhibitor of polybromo 1 and SMARCA4 | ||||
| GC14655 | OXF BD 02 | 1429129-68-9 | >98% | |
Selective inhibitor of the first bromodomain of BRD4 | ||||
| GC15152 | PF-CBP1 | 1962928-21-7 | >98% | |
CBP/p300 bromodomain inhibitor | ||||
| GC15175 | BAZ2-ICR | 1665195-94-7 | >98.50% | |
Selective BAZ2 bromodomain inhibitor | ||||
| GC15375 | PFI-1 (PF-6405761) | 1403764-72-6 | >99.50% | |
A BET bromodomain inhibitor | ||||
| GC15789 | GSK2801 | 1619994-68-1 | >99.50% | |
inhibitor of BAZ2A and BAZ2B bromodomains | ||||
| GC16299 | BET bromodomain inhibitor | 1380087-89-7 | >99.50% | |
Potent and selective inhibitor for BRD4 | ||||
| GC16531 | Bromodomain Inhibitor, (+)-JQ1 | 1268524-70-4 | >99.50% | |
A selective inhibitor of BET bromodomains | ||||
| GC16611 | GW841819X | - | >98% | |
BET bromodomain inhibitor | ||||
| GC16726 | BI-7273 | 1883429-21-7 | >99.50% | |
BRD9 bromodomain inhibitor | ||||
| GC16763 | NI-57 | 1883548-89-7 | >99.50% | |
bromodomains of BRPF proteins inhibitor | ||||
| GC16794 | UNC1215 | 1415800-43-9 | >98.00% | |
Potent L3MBTL3 domain inhibitor | ||||
