Cargando…
Structure-dependent inhibition of the ETS-family transcription factor PU.1 by novel heterocyclic diamidines
ETS transcription factors mediate a wide array of cellular functions and are attractive targets for pharmacological control of gene regulation. We report the inhibition of the ETS-family member PU.1 with a panel of novel heterocyclic diamidines. These diamidines are derivatives of furamidine (DB75)...
Autores principales: | Munde, Manoj, Wang, Shuo, Kumar, Arvind, Stephens, Chad E., Farahat, Abdelbasset A., Boykin, David W., Wilson, W. David, Poon, Gregory M. K. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3902942/ https://www.ncbi.nlm.nih.gov/pubmed/24157839 http://dx.doi.org/10.1093/nar/gkt955 |
Ejemplares similares
-
Targeting the DNA-binding activity of the human ERG transcription factor using new heterocyclic dithiophene diamidines
por: Nhili, Raja, et al.
Publicado: (2013) -
The Unusual Monomer Recognition of Guanine-Containing
Mixed Sequence DNA by a Dithiophene Heterocyclic Diamidine
por: Munde, Manoj, et al.
Publicado: (2014) -
Pharmacologic efficacy of PU.1 inhibition by heterocyclic dications: a mechanistic analysis
por: Stephens, Dominique C., et al.
Publicado: (2016) -
Engineered modular heterocyclic-diamidines for sequence-specific recognition of mixed AT/GC base pairs at the DNA minor groove
por: Guo, Pu, et al.
Publicado: (2021) -
Green Fluorescent Diamidines as Diagnostic Probes for Trypanosomes
por: Giordani, Federica, et al.
Publicado: (2014)