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Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 21:324-328
A series of novel hydroxamic acid based histone deacetylases (HDAC) inhibitors with aryl ether and aryl sulfone residues at the terminus of a substituted, unsaturated 5-carbon spacer moiety have been synthesized for the first time and evaluated. Comp
Autor:
Paul Zhichkin, Edward Kesicki, Jennifer Treiberg, Lisa Bourdon, Matthew Ronsheim, Hua Chee Ooi, Stephen White, Angela Judkins, David Fairfax
Publikováno v:
Organic Letters; Mar2007, Vol. 9 Issue 7, p1415-1418, 4p