Please use this identifier to cite or link to this item: http://hdl.handle.net/20.500.12779/5148
Title: A combination of docking/dynamics simulations and pharmacophoric modeling to discover new dual c-Src/Abl kinase inhibitors
Authors: Manetti, Fabrizio 
Locatelli, G. A.
Maga, G.
Schenone, S.
Modugno, M.
Forli, S.
Corelli, Federico 
Botta, Maurizio 
Issue Date: 2006
Project: None 
Journal: JOURNAL OF MEDICINAL CHEMISTRY
Abstract: 
A computational protocol was applied to identify molecular scaffolds untested toward the c-Src tyrosine kinase. A combination of docking and dynamics calculations allowed us to build three-dimensional models of the complexes between Src and several of its known inhibitors. Interactions most contributing to activity of the inhibitors, in terms of hydrogen bonds and hydrophobic contacts, were codified into pharmacophoric models that were in turn applied to perform a search of commercially available compounds within the Asinex database. As a result, we identified 1,3,4-thiadiazoles and pyrazolydine-3,5-diones showing inhibitory activity in the submicromolar range in a cell-free assay toward Src. Moreover, since several of the compounds used to generate pharmacophores were also known as Abl inhibitors, we tested the identified hits toward Abl tyrosine kinase, finding activity in the submicromolar range. Such biological data suggested that the computational protocol is an efficient tool for identifying new hits toward both Src and Abl.
Description: 
36420
URI: http://hdl.handle.net/20.500.12779/5148
ISSN: 0022-2623
DOI: 10.1021/jm060236z
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