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Development of novel Asf1-H3/H4 inhibitors.


ABSTRACT: The histone chaperone anti-silencing function 1 (Asf1) has emerged as a promising target for therapeutic intervention for multiple cancers (Cell2006, 127, 458). Asf1 is involved in the packaging of the eukaryotic genome into chromatin, which is essential for normal growth, development, and differentiation, as this regulates all nuclear processes that use DNA as a substrate. Starting from a collection of HTS leads, we identified a series of N-acyl hydrazones as novel inhibitors of the Asf-histone H3/H4 interaction. These compounds represent the first example of inhibitors capable of disrupting the Asf1-H3/H4 complex.

SUBMITTER: Miknis GF 

PROVIDER: S-EPMC4437580 | biostudies-literature | 2015 Feb

REPOSITORIES: biostudies-literature

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Development of novel Asf1-H3/H4 inhibitors.

Miknis Greg F GF   Stevens Sarah J SJ   Smith Luke E LE   Ostrov David A DA   Churchill Mair E A ME  

Bioorganic & medicinal chemistry letters 20141204 4


The histone chaperone anti-silencing function 1 (Asf1) has emerged as a promising target for therapeutic intervention for multiple cancers (Cell2006, 127, 458). Asf1 is involved in the packaging of the eukaryotic genome into chromatin, which is essential for normal growth, development, and differentiation, as this regulates all nuclear processes that use DNA as a substrate. Starting from a collection of HTS leads, we identified a series of N-acyl hydrazones as novel inhibitors of the Asf-histone  ...[more]

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