Otrubova Katerina, Lushington Gerald, Vander Velde David, McGuire Kathleen L, McAlpine Shelli R
Department of Medicinal Chemistry, The University of Kansas, Lawrence, KS 66045-7582, USA.
J Med Chem. 2008 Feb 14;51(3):530-44. doi: 10.1021/jm070731a. Epub 2008 Jan 11.
We report an extensive structure-activity relationship (SAR) of 62 compounds active against two drug-resistant colon cancer cell lines. Our comprehensive evaluation of two generations of compounds utilizes SAR, NMR, and molecular modeling to evaluate the key 3D features of potent compounds. Of the seven most potent compounds reported here, five are second-generation, emphasizing our ability to incorporate potent features found in the first generation and utilize their structures to design potency into the second generation. These analogs share no structural homology to current colon cancer drugs, are cytotoxic at levels on par with existing drugs treating other cancers, and demonstrate selectivity for drug-resistant colon cancer cell lines over noncancerous cell lines. Thus, we have established sansalvamide A as an excellent lead for treating multiple drug-resistant colon cancers.
我们报告了62种对两种耐药结肠癌细胞系具有活性的化合物的广泛构效关系(SAR)。我们对两代化合物的综合评估利用SAR、核磁共振(NMR)和分子建模来评估强效化合物的关键三维特征。本文报道的七种最强效化合物中,有五种是第二代化合物,这突出了我们整合第一代化合物中发现的强效特征并利用其结构在第二代化合物中设计出高活性的能力。这些类似物与目前的结肠癌药物没有结构同源性,其细胞毒性水平与治疗其他癌症的现有药物相当,并且对耐药结肠癌细胞系显示出比对非癌细胞系更高的选择性。因此,我们已将sansalvamide A确立为治疗多重耐药结肠癌的优秀先导化合物。