Structure–activity relationships of aryloxyalkanoic acid hydroxyamides as potent inhibitors of histone deacetylase
作者:Charles M. Marson、Thevaki Mahadevan、Jon Dines、Stéphane Sengmany、James M. Morrell、John P. Alao、Simon P. Joel、David M. Vigushin、R. Charles Coombes
DOI:10.1016/j.bmcl.2006.09.085
日期:2007.1
Syntheses of aryloxyalkanoic acid hydroxyamides are described, all of which are potent inhibitors of histone deacetylase, some being more potent in vitro than trichostatin A (IC(50)=3 nM). Variation of the substituents on the benzene ring as well as fusion of a second ring have marked effects on potency, in vitro IC(50) values down to 1 nM being obtained.
描述了芳氧基链烷酸羟酰胺的合成,所有这些都是组蛋白脱乙酰基酶的有效抑制剂,有些在体外比曲古抑菌素A更有效(IC(50)= 3 nM)。苯环上取代基的变化以及第二个环的融合对效能都有显着影响,体外IC(50)值低至1 nM。