Description
An HDAC inhibitor that has an optimal effective concentration of 6-8 μM in a cell-based assay, is less toxic than trichostatin A, and works in a wide variety of biological systems; induces cell cycle arrest in cancer cells in vitro and in vivo; facilitates the cloning of inbred mouse strains produced by somatic cell nuclear transfer
Formal name: N-hydroxy-1,3-dioxo-1H-benz[de]isoquinoline-2(3H)-hexananmide
Synonyms: GCK 1026
Molecular weight: 326.4
CAS: 287383-59-9
Purity: ≥98%
Formulation: A crystalline solid
Product Type|Biochemicals|Small Molecule Inhibitors|Deacetylases||Research Area|Epigenetics, Transcription, & Translation|Erasers|Histone Deacetylation