Novel N-hydroxyfurylacrylamide-based histone deacetylase (HDAC) inhibitors with branched CAP group (Part 2). [electronic resource]
Producer: 20140318Description: 5339-54 p. digitalISSN:- 1464-3391
- Acrylamide -- chemical synthesis
- Binding Sites
- Catalytic Domain
- Cell Line, Tumor
- Cell Proliferation -- drug effects
- Crystallography, X-Ray
- HCT116 Cells
- Hep G2 Cells
- Histone Deacetylase 1 -- antagonists & inhibitors
- Histone Deacetylase 6
- Histone Deacetylase Inhibitors -- chemical synthesis
- Histone Deacetylases -- chemistry
- Humans
- Molecular Docking Simulation
- Recombinant Proteins -- biosynthesis
- Repressor Proteins -- antagonists & inhibitors
- Structure-Activity Relationship
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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