Design, synthesis, and evaluation of cyclic amide/imide-bearing hydroxamic acid derivatives as class-selective histone deacetylase (HDAC) inhibitors.
Shinji, Chihiro
Design, synthesis, and evaluation of cyclic amide/imide-bearing hydroxamic acid derivatives as class-selective histone deacetylase (HDAC) inhibitors. [electronic resource] - Bioorganic & medicinal chemistry Nov 2006 - 7625-51 p. digital
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
0968-0896
10.1016/j.bmc.2006.07.008 doi
Amides--chemistry
Cell Line, Tumor
Cell Proliferation--drug effects
Drug Design
Enzyme Inhibitors--chemical synthesis
Heterocyclic Compounds--chemical synthesis
Histone Deacetylase Inhibitors
Histone Deacetylases--chemistry
Humans
Hydroxamic Acids--chemistry
Imides--chemistry
Models, Molecular
Molecular Structure
Structure-Activity Relationship
Design, synthesis, and evaluation of cyclic amide/imide-bearing hydroxamic acid derivatives as class-selective histone deacetylase (HDAC) inhibitors. [electronic resource] - Bioorganic & medicinal chemistry Nov 2006 - 7625-51 p. digital
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
0968-0896
10.1016/j.bmc.2006.07.008 doi
Amides--chemistry
Cell Line, Tumor
Cell Proliferation--drug effects
Drug Design
Enzyme Inhibitors--chemical synthesis
Heterocyclic Compounds--chemical synthesis
Histone Deacetylase Inhibitors
Histone Deacetylases--chemistry
Humans
Hydroxamic Acids--chemistry
Imides--chemistry
Models, Molecular
Molecular Structure
Structure-Activity Relationship