Información del producto
- 5-Pyrimidinecarboxamide, N-hydroxy-2-[4-[[[(1-methyl-1H-indol-3-yl)methyl]amino]methyl]-1-piperidinyl]-
- Jnj 26481585
- N-Hydroxy-2-[4-[[[(1-methyl-1H-indol-3-yl)methyl]amino]methyl]-1-piperidinyl]-5-pyrimidinecarboxamide
- N1-(2-(1h-indol-3-yl)ethyl)-n4-(pyridin-4-yl)benzene-1,4-diamine
- Quisinostat
JNJ-26481585-d3 is a potent and selective histone deacetylase inhibitor that has been shown to inhibit the growth of tumor cells by inducing apoptosis. JNJ-26481585-d3 selectively inhibits the activity of histone deacetylases, which are enzymes that remove acetyl groups from lysine residues in histones. The inhibition of these enzymes leads to transcriptional silencing of genes, which is an important step in cancer development. The minimal toxicity of this drug makes it suitable for long-term treatment with low doses.
Propiedades químicas
Consulta técnica sobre: 3D-AKB32029 JNJ-26481585-d3
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