Sakowski Jacek, Sattler Isabel, Schlitzer Martin
Institut für Pharmazeutische Chemie, Philipps-Universität Marburg, Marbacher Weg 6, D-35032, Marburg, Germany.
Bioorg Med Chem. 2002 Feb;10(2):233-9. doi: 10.1016/s0968-0896(01)00274-7.
We have developed the 4-nitrocinnamoyl substituted benzophenone 4a as a novel non-thiol farnesyltransferase inhibitor. Replacement of the p-tolyl moiety of our initial lead structure 4a by different para and ortho substituted phenyl residues as well as by 1-naphthyl resulted in derivatives with considerably enhanced activity displaying IC(50) values between 42 and 52 nM. These compounds represent novel, readily accessible non-thiol farnesyltransferase inhibitors being more active than the corresponding thiol-containing analogues.
我们已开发出4-硝基肉桂酰取代的二苯甲酮4a作为一种新型非硫醇法尼基转移酶抑制剂。用不同的对位和邻位取代苯基残基以及1-萘基取代我们最初的先导结构4a的对甲苯基部分,得到了活性显著增强的衍生物,其IC(50)值在42至52 nM之间。这些化合物代表了新型的、易于获得的非硫醇法尼基转移酶抑制剂,其活性比相应的含硫醇类似物更高。