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Succinimide hydroxamic acids as potent inhibitors of histone deacetylase (HDAC)
Authors:Curtin Michael L  Garland Robert B  Heyman H Robin  Frey Robin R  Michaelides Michael R  Li Junling  Pease Lori J  Glaser Keith B  Marcotte Patrick A  Davidsen Steven K
Affiliation:Cancer Research Area, Abbott Laboratories, Dept. 47J, Bldg. AP10, 100 Abbott Park Road, Abbott Park, IL 60064, USA. mike.curtin@abbott.com
Abstract:A series of succinimide hydroxamic acids was prepared and evaluated in vitro for HDAC inhibition and tumor cell antiproliferation. While the original macrocyclic analogue 6 was quite potent in both assays, several appropriately substituted non-macrocyclic succinimides, such as 23, were equipotent.
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