2bt0: Difference between revisions

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{{STRUCTURE_2bt0|  PDB=2bt0  |  SCENE=  }}  
{{STRUCTURE_2bt0|  PDB=2bt0  |  SCENE=  }}  


'''NOVEL, POTENT SMALL MOLECULE INHIBITORS OF THE MOLECULAR CHAPERONE HSP90 DISCOVERED THROUGH STRUCTURE-BASED DESIGN'''
===NOVEL, POTENT SMALL MOLECULE INHIBITORS OF THE MOLECULAR CHAPERONE HSP90 DISCOVERED THROUGH STRUCTURE-BASED DESIGN===




==Overview==
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The crystal structure of a previously reported screening hit 1 (CCT018159) bound to the N terminal domain of molecular chaperone Hsp90 has been used to design 5-amide analogues. These exhibit enhanced potency against the target in binding and functional assays with accompanying appropriate cellular pharmacodynamic changes. Compound 11 (VER-49009) compares favorably with the clinically evaluated 17-AAG.
The line below this paragraph, {{ABSTRACT_PUBMED_15974572}}, adds the Publication Abstract to the page
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{{ABSTRACT_PUBMED_15974572}}


==About this Structure==
==About this Structure==
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[[Category: Heat shock]]
[[Category: Heat shock]]
[[Category: Phosphorylation]]
[[Category: Phosphorylation]]
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