Gududuru Veeresa, Hurh Eunju, Sullivan Joshua, Dalton James T, Miller Duane D
Department of Pharmaceutical Sciences, College of Pharmacy, University of Tennessee Health Science Center, Memphis, TN 38163, USA.
Bioorg Med Chem Lett. 2005 Sep 15;15(18):4010-3. doi: 10.1016/j.bmcl.2005.06.032.
In our continuing efforts to develop novel chemotherapeutic agents for prostate cancer, recently we reported the discovery of 2-arylthiazolidine-4-carboxylic acid amides (ATCAAs) as a new class of cytotoxic agents. Several of them were very effective in killing specific human prostate cancer cell lines with low/sub-micromolar cytotoxicity and high selectivity against control cells in our sulforhodamine B assay. Encouraged with these preliminary results, we decided to further optimize this new scaffold to enhance the potency and selectivity. Current work describes the synthesis, SAR, and biological evaluation of new compounds for their ability to inhibit the growth of five human prostate cancer cell lines. The cytotoxicity data demonstrated that ATCAAs are sensitive to simple modifications or changes, which allowed us to understand the minimum structural requirements of this class of compounds to exhibit potent and selective anticancer activity against prostate cancer cells.
在我们持续致力于开发新型前列腺癌化疗药物的过程中,最近我们报道了发现2-芳基噻唑烷-4-羧酸酰胺(ATCAA)作为一类新的细胞毒性药物。在我们的磺基罗丹明B试验中,其中几种对特定的人前列腺癌细胞系具有非常有效的杀伤作用,细胞毒性低/亚微摩尔,且对对照细胞具有高选择性。受这些初步结果的鼓舞,我们决定进一步优化这个新的骨架结构以提高效力和选择性。当前的工作描述了新化合物的合成、构效关系(SAR)以及它们抑制五种人前列腺癌细胞系生长能力的生物学评价。细胞毒性数据表明,ATCAA对简单的修饰或改变很敏感,这使我们能够了解这类化合物对前列腺癌细胞表现出强效和选择性抗癌活性的最低结构要求。