Universidad Autónoma de Nuevo León, UANL, Facultad de Ciencias Químicas, Av. Universidad s/n, Ciudad Universitaria, San Nicolás de los Garza, Nuevo Leon CP 66451, México.
Curr Med Chem. 2012;19(26):4377-98. doi: 10.2174/092986712803251593.
Eleven years after the start of a new millennium characterized by amazing scientific development, the cure for cancer remains a major challenge for humanity. In this regard, scientific efforts have focused on the search for new therapeutic targets that involve specific recognition and stop the spread of cancer cells, as well as the development of new therapeutic options that show greater specificity and better therapeutic efficacy. This review includes recent published literature about new anticancer drug design using scaffolds of β-lactams, sulfonamides, quinoline, quinoxaline and natural products, and focuses on the structure-activity relationships of scaffolds that have been reported to potently inhibit cell growth of human tumor cell lines. It describes not only those synthetic or natural compounds aimed at specific molecular targets of cancer cells in vitro, but also compounds currently in clinical trials.
新千年伊始,科学发展令人惊叹,然而 11 年过去了,癌症仍然是人类面临的重大挑战。在这方面,科学研究的重点是寻找新的治疗靶点,这些靶点涉及到特异性识别和阻止癌细胞扩散,以及开发具有更高特异性和更好治疗效果的新治疗选择。本综述包括最近发表的关于使用β-内酰胺、磺胺、喹啉、喹喔啉和天然产物支架设计新型抗癌药物的文献,重点介绍了已报道的能有效抑制人肿瘤细胞系细胞生长的支架的结构-活性关系。它不仅描述了那些旨在针对癌细胞特定分子靶点的合成或天然化合物,还描述了目前正在临床试验中的化合物。