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Bioorg Med Chem Lett ; 19(6): 1715-7, 2009 Mar 15.
Article in English | MEDLINE | ID: mdl-19243939

ABSTRACT

A quinazoline that decreases polyglutamine aggregate burden in a cell-based assay was identified from a high-throughput screen of a chemical-compound library, provided by the NIH Molecular Libraries Small Molecule Repository (MLSMR). A structure and activity study yielded leads with submicromolar potency.


Subject(s)
Chemistry, Pharmaceutical/methods , Nerve Tissue Proteins/antagonists & inhibitors , Nuclear Proteins/antagonists & inhibitors , Quinazolines/chemistry , Combinatorial Chemistry Techniques , Drug Design , Drug Discovery , Drug Evaluation, Preclinical , Humans , Huntingtin Protein , Inhibitory Concentration 50 , Models, Chemical , Molecular Structure , Peptides/chemistry , Structure-Activity Relationship
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