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http://hdl.handle.net/10553/35747
| Título: | 5-Ethynylarylnaphthalimides as antitumor agents: synthesis and biological evaluation | Autores/as: | Quintana-Espinoza, Patricia Martín-Acosta, Pedro Amesty, Ángel Martín Rodríguez, Patricia Lorenzo-Castrillejo, Isabel Fernández Pérez, Leandro Fco Machín, Félix Estévez-Braun, Ana |
Clasificación UNESCO: | 32 Ciencias médicas | Palabras clave: | Naphthalimides Antiproliferative activity Topoisomerase II DNA damage Saccaromyces cereviciae |
Fecha de publicación: | 2017 | Proyectos: | "Evaluación Preclinica de Nuevas Estructuras Quimicas Diseñadas Para Inhibir la Ruta Oncogenica Jak-Stat O Como Moduladores Selectivos de Los Receptores Estrógenos" Desarrollo Preclínico de Nuevas Estructuras Bioactivas Moduladoras de Las Actividades Oncogénicas de Stat3/5 O de Los Receptores de Estrógenos |
Publicación seriada: | Bioorganic and Medicinal Chemistry | Resumen: | A set of 5-ethynylarylnaphthalimides was synthesized by Sonogashira cross-coupling reactions and evaluated for antiproliferative and antitopoisomerase II in vitro activities. Furthermore docking studies of these molecules as DNA-intercalators were carried out and the in vivo DNA-damaging activity was also determined with the model organism Saccharomyces cerevisiae. From the obtained results three naphthalimides 6, 13 and 14 showed strong topoisomerase II inhibitory activity. These three molecules also presented good docking scores as DNA-intercalators using a self-complementary oligodeoxynucleotide d (ATGCAT)(2) as a model, and compounds 13 and 14 were among the most cytotoxic in the in vivo DNA-damaging activity. | URI: | http://hdl.handle.net/10553/35747 | ISSN: | 0968-0896 | DOI: | 10.1016/j.bmc.2017.02.024 | Fuente: | Bioorganic and Medicinal Chemistry[ISSN 0968-0896],v. 25, p. 1976-1983 |
| Colección: | Artículos |
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