Title : Synthesis and biological evaluation of novel FK228 analogues as potential isoform selective HDAC inhibitors.

Pub. Date : 2016 Oct 4

PMID : 27318982






2 Functional Relationships(s)
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1 Synthesis and biological evaluation of novel FK228 analogues as potential isoform selective HDAC inhibitors. romidepsin histone deacetylase 9 Homo sapiens
2 This study demonstrated that simple modification at the C4 and C7 side chains in FK228 is effective for improving both HDAC inhibitory activity and isoform selectivity; moreover, potent and highly isoform-selective class I HDAC1 inhibitors were identified. romidepsin histone deacetylase 9 Homo sapiens