The use of privileged scaffolds as a starting point for the construction of libraries of bioactive compounds is a widely used strategy in drug discovery and development. Scaffold decoration, morphing and hopping are additional techniques that enable the modification of the chosen privileged framework and better explore the chemical space around it. In this study, two series of highly functionalized pyrimidine and pyridine derivatives were synthesized using a scaffold morphing approach consisting of triazine compounds obtained previously as antiviral agents. Newly synthesized azines were evaluated against lymphoma, hepatocarcinoma, and colon epithelial carcinoma cells, showing in five cases acceptable to good anticancer activity associated with low cytotoxicity on healthy fibroblasts. Finally, ADME in vitro studies were conducted on the best derivatives of the two series showing good passive permeability and resistance to metabolic degradation.
Serendipitous Identification of Azine Anticancer Agents Using a Privileged Scaffold Morphing Strategy.
利用优势骨架变形策略意外发现嗪类抗癌药物
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作者:Cesarini Silvia, Vicenti Ilaria, Poggialini Federica, Filippi Silvia, Mancin Eleonora, Fiaschi Lia, De Marchi Elisa, Giammarino Federica, Vagaggini Chiara, Bizzarri Bruno Mattia, Saladino Raffaele, Dreassi Elena, Zazzi Maurizio, Botta Lorenzo
| 期刊: | Molecules | 影响因子: | 4.600 |
| 时间: | 2024 | 起止号: | 2024 Mar 24; 29(7):1452 |
| doi: | 10.3390/molecules29071452 | 研究方向: | 肿瘤 |
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