کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
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1364881 | 981548 | 2007 | 9 صفحه PDF | دانلود رایگان |
![عکس صفحه اول مقاله: Methotrexate γ-hydroxamate derivatives as potential dual target antitumor drugs Methotrexate γ-hydroxamate derivatives as potential dual target antitumor drugs](/preview/png/1364881.png)
A series of new aminopteroyl-based hydroxamate derivatives were synthesized and tested in vitro in cell culture models as potential dual target drugs. These compounds were designed to target two families of enzymes, matrix metalloproteinases (MMP) and a folate enzyme, dihydrofolate reductase (DHFR). These enzymes are the components of two unrelated cellular pathways and they are often over-expressed in metastasizing tumors. In addition to the synthesis and full structural characterization of the hybrid molecules, we describe their inhibitory activities against a series of MMPs (MMP-2, MMP-7, MMP-9, MMP-14) and DHFR, as well as their antiproliferative activity in three cancer cell lines. The new hydroxamate derivatives of MTX proved to be effective inhibitors of MMPs and DHFR in the micromolar and nanomolar range, respectively. Furthermore, they showed strong antiproliferative activity against A549 cells (non-small cell lung carcinoma), and PPC-1 and Tsu-Pr1 prostate cancer cell lines. Therefore, based on the present results, these bi-functional drugs may be good candidates to target specific tumors in animal models due to potential combined effects on two pathways crucial for tumor development.
A series of new aminopteroyl-based hydroxamate derivatives was synthesized and tested in vitro in cell culture models and as inhibitors of two families of enzymes, matrix metalloproteinases (MMP) and dihydrofolate reductase (DHFR), which are the components of two unrelated cellular pathways in metastasizing tumors.Figure optionsDownload as PowerPoint slide
Journal: Bioorganic & Medicinal Chemistry - Volume 15, Issue 3, 1 February 2007, Pages 1266–1274