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ChemMedChem ; 4(6): 963-6, 2009 Jun.
Article in English | MEDLINE | ID: mdl-19301319

ABSTRACT

Heat shock protein 90 (Hsp90) plays a key role in stress response and protection of the cell against the effects of mutation. Herein we report the identification of an Hsp90 inhibitor identified by fragment screening using a high-concentration biochemical assay, as well as its optimisation by in silico searching coupled with a structure-based drug design (SBDD) approach.


Subject(s)
HSP90 Heat-Shock Proteins/antagonists & inhibitors , Oximes/chemistry , Pyrimidines/chemistry , Binding Sites , Cell Line, Tumor , Computer Simulation , Crystallography, X-Ray , Drug Design , HSP90 Heat-Shock Proteins/metabolism , Humans , Oximes/chemical synthesis , Oximes/pharmacology , Pyrimidines/chemical synthesis , Pyrimidines/pharmacology , Structure-Activity Relationship
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