Cargando…
Ligand Selectivity in the Recognition of Protoberberine Alkaloids by Hybrid-2 Human Telomeric G-Quadruplex: Binding Free Energy Calculation, Fluorescence Binding, and NMR Experiments
The human telomeric G-quadruplex (G4) is an attractive target for developing anticancer drugs. Natural products protoberberine alkaloids are known to bind human telomeric G4 and inhibit telomerase. Among several structurally similar protoberberine alkaloids, epiberberine (EPI) shows the greatest spe...
Autores principales: | Deng, Nanjie, Xia, Junchao, Wickstrom, Lauren, Lin, Clement, Wang, Kaibo, He, Peng, Yin, Yunting, Yang, Danzhou |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6515380/ https://www.ncbi.nlm.nih.gov/pubmed/31010072 http://dx.doi.org/10.3390/molecules24081574 |
Ejemplares similares
-
Evaluating Molecular Docking Software for Small Molecule Binding to G-Quadruplex DNA
por: Dickerhoff, Jonathan, et al.
Publicado: (2021) -
Protoberberine Isoquinoline Alkaloids from Arcangelisia gusanlung
por: Yu, Ling-Ling, et al.
Publicado: (2014) -
Optimization of yeast-based production of medicinal protoberberine alkaloids
por: Galanie, Stephanie, et al.
Publicado: (2015) -
Thermodynamic fingerprints of ligand binding to human telomeric G-quadruplexes
por: Bončina, Matjaž, et al.
Publicado: (2015) -
Binding Study of the Fluorescent Carbazole Derivative with Human Telomeric G-Quadruplexes
por: Głuszyńska, Agata, et al.
Publicado: (2018)