Design, Synthesis, and Evaluation of Novel Modular Bisubstrate Analogue Inhibitors of Farnesyltransferase
作者:Martin Schlitzer、Isabel Sattler
DOI:10.1002/(sici)1521-3773(19990712)38:13/14<2032::aid-anie2032>3.0.co;2-d
日期:1999.7.12
Promising potential chemotherapeutics for the treatment of cancer can be developed from farnesyltransferase inhibitors. A novel class of modular bisubstrate farnesyltransferase inhibitors is presented that can be synthesized in a straightforward manner. An example of such an inhibitor is compound 1, which has an IC50 value of 3.7 μM.
可以从法呢基转移酶抑制剂开发用于治疗癌症的有前景的潜在化学疗法。提出了一类新的模块化双底物法呢基转移酶抑制剂,可以直接合成。这种抑制剂的一个例子是化合物 1,其 IC50 值为 3.7 μM。