1675821-32-5
1675821-32-5 結(jié)構(gòu)式
基本信息
5-[(4-Hydroxy-2,6-dimethylphenyl)methylene]-1,3-bis(phenylmethyl)-2,4,6(1H,3H,5H)-pyrimidinetrione
2,4,6(1H,3H,5H)-Pyrimidinetrione, 5-[(4-hydroxy-2,6-dimethylphenyl)methylene]-1,3-bis(phenylmethyl)-
物理化學(xué)性質(zhì)
| 報(bào)價日期 | 產(chǎn)品編號 | 產(chǎn)品名稱 | CAS號 | 包裝 | 價格 |
| 2026/06/05 | HY-110263 | 1675821-32-5 EML 425 | 1675821-32-5 | 5mg | 1100元 |
| 2026/06/05 | HY-110263 | 1675821-32-5 EML 425 | 1675821-32-5 | 10mM * 1mLin DMSO | 1210元 |
| 2026/06/05 | HY-110263 | 1675821-32-5 EML 425 | 1675821-32-5 | 10mg | 1900元 |
常見問題列表
|
p300 1.1 μM (IC 50 ) |
CBP 2.9 μM (IC 50 ) |
EML 425 (EML425, Compound 7h) is a potent and selective reversible inhibitor of CBP/p300, noncompetitive versus both acetyl-CoA and a histone H3 peptide, and endows with good cell permeability. EML 425 inhibits both p300 and CBP (IC 50 values of 2.9 and 1.1 μM, respectively) while being practically inactive against the enzymes general control non derepressible-5 (GCN5) and p300/CBP-associated factor (PCAF). EML 425 induces a marked and time-dependent reduction in the acetylation of lysine H4K5 and H3K9 in U937 cells. EML 425 is shown to be a reversible inhibitor, noncompetitive versus both acetyl-CoA and a histone H3 peptide, and able to bind both the free enzyme and the enzyme-substrate complex, even with unequal affinity constants. The best scoring docking poses suggest that the binding site for EML 425 is an alternative pocket lying near the substrate lysine binding groove and close to the acetylation site.