Hsp90 C-terminal inhibitors are advantageous for the development of new cancer chemotherapeutics due to their ability to segregate client protein degradation from induction of the prosurvival heat shock response, which is a major detriment associated with Hsp90 N-terminal inhibitors under clinical investigation. Based upon prior SAR trends, a 1,2,3-triazole side chain was placed in lieu of the aryl side chain and attached to both the coumarin and biphenyl scaffold. Antiproliferative studies against SKBr3 and MCF-7 breast cancer cell lines demonstrated these triazole-containing compounds to exhibit improved activity. These compounds were shown to manifest Hsp90 inhibitory activity through Western blot analysis and represent a new scaffold up...
Novobiocin, a known DNA gyrase inhibitor, binds to a nucleotide-binding site located on the Hsp90 C-...
La résistance aux traitements actuels du cancer (polychimiothérapie) incite à trouver de nouvelles c...
As C−terminal inhibitors of a 90−kDa heat shock protein (Hsp90), novobiocin and its deri...
Hsp90 C-terminal inhibitors are advantageous for the development of new cancer chemotherapeutics due...
A series of triazole-containing novobiocin analogues has been designed, synthesized and their inhibi...
Modulation of Hsp90 C-terminal function represents a promising therapeutic approach for the treatmen...
Dissertation (Ph.D.)--University of Kansas, Medicinal Chemistry, 2007.The 90 kDa heat shock proteins...
Development of heat shock protein 90 (Hsp90) C‐terminal inhibitors has emerged as an exciting strate...
The heat shock protein 90 (Hsp90) folding machinery is essential for the maturation of nascent polyp...
Hsp90 is a promising therapeutic target for the treatment of cancer. Novobiocin is the first Hsp90 C...
Since Hsp90 modulates all six hallmarks of cancer simultaneously, it has become an attractive target...
This document is the Accepted Manuscript version of a Published Work that appeared in final form in ...
Inhibition of Hsp90 C-terminal function is an advantageous therapeutic paradigm for the treatment of...
Modulation of Hsp90 C-terminal function represents a promising therapeutic approach for the treatme...
The research described in this thesis focuses on heat shock protein 90 kDa (Hsp90), which is a molec...
Novobiocin, a known DNA gyrase inhibitor, binds to a nucleotide-binding site located on the Hsp90 C-...
La résistance aux traitements actuels du cancer (polychimiothérapie) incite à trouver de nouvelles c...
As C−terminal inhibitors of a 90−kDa heat shock protein (Hsp90), novobiocin and its deri...
Hsp90 C-terminal inhibitors are advantageous for the development of new cancer chemotherapeutics due...
A series of triazole-containing novobiocin analogues has been designed, synthesized and their inhibi...
Modulation of Hsp90 C-terminal function represents a promising therapeutic approach for the treatmen...
Dissertation (Ph.D.)--University of Kansas, Medicinal Chemistry, 2007.The 90 kDa heat shock proteins...
Development of heat shock protein 90 (Hsp90) C‐terminal inhibitors has emerged as an exciting strate...
The heat shock protein 90 (Hsp90) folding machinery is essential for the maturation of nascent polyp...
Hsp90 is a promising therapeutic target for the treatment of cancer. Novobiocin is the first Hsp90 C...
Since Hsp90 modulates all six hallmarks of cancer simultaneously, it has become an attractive target...
This document is the Accepted Manuscript version of a Published Work that appeared in final form in ...
Inhibition of Hsp90 C-terminal function is an advantageous therapeutic paradigm for the treatment of...
Modulation of Hsp90 C-terminal function represents a promising therapeutic approach for the treatme...
The research described in this thesis focuses on heat shock protein 90 kDa (Hsp90), which is a molec...
Novobiocin, a known DNA gyrase inhibitor, binds to a nucleotide-binding site located on the Hsp90 C-...
La résistance aux traitements actuels du cancer (polychimiothérapie) incite à trouver de nouvelles c...
As C−terminal inhibitors of a 90−kDa heat shock protein (Hsp90), novobiocin and its deri...