Cargando…
A Chemocentric Approach to the Identification of Cancer Targets
A novel chemocentric approach to identifying cancer-relevant targets is introduced. Starting with a large chemical collection, the strategy uses the list of small molecule hits arising from a differential cytotoxicity screening on tumor HCT116 and normal MRC-5 cell lines to identify proteins associa...
Autores principales: | Flachner, Beáta, Lörincz, Zsolt, Carotti, Angelo, Nicolotti, Orazio, Kuchipudi, Praveena, Remez, Nikita, Sanz, Ferran, Tóvári, József, Szabó, Miklós J., Bertók, Béla, Cseh, Sándor, Mestres, Jordi, Dormán, György |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2012
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3338416/ https://www.ncbi.nlm.nih.gov/pubmed/22558171 http://dx.doi.org/10.1371/journal.pone.0035582 |
Ejemplares similares
-
Dual Inhibitors of AChE and BACE-1 for Reducing Aβ in Alzheimer’s Disease: From In Silico to In Vivo
por: Stern, Noa, et al.
Publicado: (2022) -
Rapid Identification of Potential Drug Candidates from Multi-Million Compounds’ Repositories. Combination of 2D Similarity Search with 3D Ligand/Structure Based Methods and In Vitro Screening
por: Szilágyi, Katalin, et al.
Publicado: (2021) -
Robust Recombinant Expression of Human Placental Ribonuclease Inhibitor in Insect Cells
por: Flachner, Beáta, et al.
Publicado: (2022) -
Combination of 2D/3D Ligand-Based Similarity Search in Rapid Virtual Screening from Multimillion Compound Repositories. Selection and Biological Evaluation of Potential PDE4 and PDE5 Inhibitors
por: Dobi, Krisztina, et al.
Publicado: (2014) -
Design and Selection of Novel C1s Inhibitors by In Silico and In Vitro Approaches
por: Szilágyi, Katalin, et al.
Publicado: (2019)