Structure activity relationships and the binding mode of quinolinone-pyrimidine hybrids as reversal agents of multidrug resistance mediated by P-gp
Abstract P-gp-associated multidrug resistance is a major impediment to the success of chemotherapy. With the aim of finding non-toxic and effective P-gp inhibitors, we investigated a panel of quinolin-2-one-pyrimidine hybrids. Among the active compounds, two of them significantly increased intracell...
Guardado en:
Autores principales: | Jerónimo Laiolo, Priscila Ailin Lanza, Oscar Parravicini, Cecilia Barbieri, Daniel Insuasty, Justo Cobo, D. Mariano Adolfo Vera, Ricardo Daniel Enriz, Maria Cecilia Carpinella |
---|---|
Formato: | article |
Lenguaje: | EN |
Publicado: |
Nature Portfolio
2021
|
Materias: | |
Acceso en línea: | https://doaj.org/article/98b225c1e09c43bfa1d0517e683523c4 |
Etiquetas: |
Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
|
Ejemplares similares
-
Cytotoxicity of Amino‐BODIPY Modulated via Conjugation with 2‐Phenyl‐3‐Hydroxy‐4(1H)‐Quinolinones
por: Martin Porubský, et al.
Publicado: (2021) -
New Therapeutic Strategy for Overcoming Multidrug Resistance in Cancer Cells with Pyrazolo[3,4-<i>d</i>]pyrimidine Tyrosine Kinase Inhibitors
por: Ana Podolski-Renić, et al.
Publicado: (2021) -
Synthesis, reactions, and applications of pyrimidine derivatives
por: Mahmoud S. Tolba, et al.
Publicado: (2022) -
Glycosaminoglycans are interactants of Langerin: comparison with gp120 highlights an unexpected calcium-independent binding mode.
por: Eric Chabrol, et al.
Publicado: (2012) -
Effects of 4(1H)-quinolinone derivative, a novel non-nucleotide allosteric purinergic P2Y 2 agonist, on cardiomyocytes in neonatal rats
por: Kensuke Sakuma, et al.
Publicado: (2017)