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Multicharged Phthalocyanines as Selective Ligands for G-Quadruplex DNA Structures

The stabilization of G-Quadruplex DNA structures by ligands is a promising strategy for telomerase inhibition in cancer therapy since this enzyme is responsible for the unlimited proliferation of cancer cells. To assess the potential of a compound as a telomerase inhibitor, selectivity for quadruple...

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Библиографические подробности
Опубликовано в: :Molecules
Главные авторы: Ramos, Catarina I. V., Almeida, Susana P., Lourenço, Leandro M. O., Pereira, Patrícia M. R., Fernandes, Rosa, Faustino, M. Amparo F., Tomé, João P. C., Carvalho, Josué, Cruz, Carla, Neves, M. Graça P. M. S.
Формат: Artigo
Язык:Inglês
Опубликовано: MDPI 2019
Предметы:
Online-ссылка:https://ncbi.nlm.nih.gov/pmc/articles/PMC6412362/
https://ncbi.nlm.nih.gov/pubmed/30781675
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/molecules24040733
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