Cargando…
Structure-Guided Development of Deoxycytidine Kinase Inhibitors with Nanomolar Affinity and Improved Metabolic Stability
[Image: see text] Recently, we have shown that small molecule dCK inhibitors in combination with pharmacological perturbations of de novo dNTP biosynthetic pathways could eliminate acute lymphoblastic leukemia cells in animal models. However, our previous lead compound had a short half-life in vivo....
Autores principales: | Nomme, Julian, Li, Zheng, Gipson, Raymond M., Wang, Jue, Armijo, Amanda L., Le, Thuc, Poddar, Soumya, Smith, Tony, Santarsiero, Bernard D., Nguyen, Hien-Anh, Czernin, Johannes, Alexandrova, Anastassia N., Jung, Michael E., Radu, Caius G., Lavie, Arnon |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical
Society
2014
|
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4255734/ https://www.ncbi.nlm.nih.gov/pubmed/25341194 http://dx.doi.org/10.1021/jm501124j |
Ejemplares similares
-
Targeting host deoxycytidine kinase attenuates Staphylococcus aureus virulence
por: Winstel, Volker, et al.
Publicado: (2023) -
Pulse dipolar EPR for determining nanomolar binding affinities
por: Ackermann, Katrin, et al.
Publicado: (2022) -
Targeted Delivery of Deoxycytidine Kinase to Her2-Positive Cells Enhances the Efficacy of the Nucleoside Analog Fludarabine
por: Koduvayur, Sujatha P., et al.
Publicado: (2016) -
Structural basis for activation of the therapeutic l-nucleoside analogs 3TC and troxacitabine by human deoxycytidine kinase
por: Sabini, Elisabetta, et al.
Publicado: (2007) -
Correction: Pulse dipolar EPR for determining nanomolar binding affinities
por: Ackermann, Katrin, et al.
Publicado: (2022)