Cargando…
Structure-based discovery of novel P-glycoprotein inhibitors targeting the nucleotide binding domains
P-glycoprotein (P-gp), a membrane transport protein overexpressed in certain drug-resistant cancer cells, has been the target of numerous drug discovery projects aimed at overcoming drug resistance in cancer. Most characterized P-gp inhibitors bind at the large hydrophobic drug binding domain (DBD),...
Autores principales: | Moesgaard, Laust, Pedersen, Maria L., Uhd Nielsen, Carsten, Kongsted, Jacob |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10692163/ https://www.ncbi.nlm.nih.gov/pubmed/38040777 http://dx.doi.org/10.1038/s41598-023-48281-4 |
Ejemplares similares
-
Molecular Recognition of Methacryllysine and Crotonyllysine by the AF9 YEATS Domain
por: Bilgin, Nurgül, et al.
Publicado: (2023) -
Recognition of Dimethylarginine Analogues by Tandem Tudor Domain Protein Spindlin1
por: Porzberg, Miriam R. B., et al.
Publicado: (2022) -
Combinational Inhibition of P-Glycoprotein-Mediated Etoposide Transport by Zosuquidar and Polysorbate 20
por: Nielsen, Rasmus Blaaholm, et al.
Publicado: (2023) -
Allosteric Role of Substrate Occupancy Toward the Alignment of P-glycoprotein Nucleotide Binding Domains
por: Pan, Lurong, et al.
Publicado: (2018) -
Oral etoposide and zosuquidar bioavailability in rats: Effect of co-administration and in vitro-in vivo correlation of P-glycoprotein inhibition
por: Nielsen, Rasmus Blaaholm, et al.
Publicado: (2021)