名称:
Synthesis of 2-quinolinecarboxamide derivatives as potential HDAC inhibitors
摘要:
Inhibition of histone deacetylase activity appears as an original and effective approach for the treatment of cancer. A series of novel quinoline-containing derivatives has been synthesized and found that some of these compounds possess nanomolar histone deacetylase inhibitory activity.
DOI:
10.1007/s10593-011-0825-x