Medina Jesus R, Grant Seth W, Axten Jeffrey M, Miller William H, Donatelli Carla A, Hardwicke Mary Ann, Oleykowski Catherine A, Liao Qiaoyin, Plant Ramona, Xiang Hong
Oncology Research, GlaxoSmithKline, Collegeville, PA 19426, USA.
Bioorg Med Chem Lett. 2010 Apr 15;20(8):2552-5. doi: 10.1016/j.bmcl.2010.02.091. Epub 2010 Mar 1.
Novel Aurora inhibitors were identified truncating clinical candidate GSK1070916. Many of these truncated compounds retained potent activity against Aurora B with good antiproliferative activity. Mechanistic studies suggested that these compounds, depending on the substitution pattern, may or may not exert their antiproliferative effects via inhibition of Aurora B. The SAR results from this investigation will be presented with an emphasis on the impact structural changes have on the cellular phenotype.
新型极光激酶抑制剂是通过截断临床候选药物GSK1070916而鉴定出来的。这些截断的化合物中有许多对极光激酶B仍具有强效活性,并具有良好的抗增殖活性。机制研究表明,这些化合物根据取代模式的不同,可能会也可能不会通过抑制极光激酶B发挥其抗增殖作用。本次研究的构效关系结果将着重阐述结构变化对细胞表型的影响。