Chimerically designed HDAC- and tyrosine kinase inhibitors. A series of erlotinib hybrids as dual-selective inhibitors of EGFR, HER2 and histone deacetylases

标题
Chimerically designed HDAC- and tyrosine kinase inhibitors. A series of erlotinib hybrids as dual-selective inhibitors of EGFR, HER2 and histone deacetylases
作者
关键词
-
出版物
MedChemComm
Volume 3, Issue 7, Pages 829
出版商
Royal Society of Chemistry (RSC)
发表日期
2012-05-09
DOI
10.1039/c2md00317a

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