A series of potent and selective, triazolylphenyl-based histone deacetylases inhibitors with activity against pancreatic cancer cells and Plasmodium falciparum
作者:
Chen Y [1]
;
Lopez-Sanchez M [2]
;
Savoy DN [3]
;
Billadeau DD ;
Dow GS ;
Kozikowski AP
作者单位:
Walter Reed Army Inst Res, Div Expt Therapeut, Silver Spring, MD 20910 USA
[1]
Univ Illinois, Dept Med Chem & Pharmacognosy, Drug Discovery Program, Chicago, IL 60612 USA
[2]
Mayo Clin Coll Med, Div Oncol Res, Dept Immunol, Rochester, MN 55905 USA
[3]
期刊:
《Journal of Medicinal Chemistry》
2008年51卷12期3437-3448页
关键词:
HDAC INHIBITORS;CRYSTAL-STRUCTURE;TERMINAL ALKYNES;CLASS-I;CYCLOADDITION;HOMOLOG;AZIDES;YEAST;SAHA;ACTIVATION
发布时间:
2013-11-21
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