Heat shock protein 90 (Hsp90) is a molecular chaperone that is responsible for activating many signaling proteins and is a promising target in tumor biology. We have identified small-molecule benzisoxazole derivatives as Hsp90 inhibitors. Crystallographic studies show that these compounds bind in the ATP binding pocket interacting with the Asp93. Structure based optimization led to the identification of potent analogues, such as 13, with good biochemical profiles
Heat shock protein 90 (Hsp90) is a chaperone responsible for the maturation of many cancer-related p...
AbstractHeat shock protein 90 (Hsp90) is a highly conserved molecular chaperone that plays a vital r...
Heat shock protein 90 (Hsp90) is a chaperone responsible for the maturation of many cancer-related p...
Heat shock protein 90 (Hsp90) is a molecular chaperone that is responsible for activating many signa...
A structural investigation on the isoxazole scaffold led to the discovery of 3,4-isoxazolediamide co...
A structural investigation on the isoxazole scaffold led to the discovery of 3,4-isoxazolediamide co...
none21noA structural investigation on the isoxazole scaffold led to the discovery of 3,4-isoxazoledi...
We describe the development of a novel series of N-aryl-benzimidazolone HSP90 inhibitors (9) targeti...
The molecular chaperone heat shock protein 90 (HSP90) is essential for the folding stability, intrac...
Although the heat shock protein 90 (HSP90) inhibitor 17-allylamino-17-demethoxygeldanamycin (17-AAG)...
The last decade has seen the molecular chaperone heat shock protein 90 (HSP90) emerge as an exciting...
A potential therapeutic strategy for targeting cancer that has gained much interest is the inhibitio...
The molecular chaperone HSP90 is currently under investigation as a promising target for anticancer ...
A potential therapeutic strategy for targeting cancer that has gained much interest is the inhibitio...
Heat shock protein 90 (Hsp90) is an essential molecular chaperone that performs vital stress-related...
Heat shock protein 90 (Hsp90) is a chaperone responsible for the maturation of many cancer-related p...
AbstractHeat shock protein 90 (Hsp90) is a highly conserved molecular chaperone that plays a vital r...
Heat shock protein 90 (Hsp90) is a chaperone responsible for the maturation of many cancer-related p...
Heat shock protein 90 (Hsp90) is a molecular chaperone that is responsible for activating many signa...
A structural investigation on the isoxazole scaffold led to the discovery of 3,4-isoxazolediamide co...
A structural investigation on the isoxazole scaffold led to the discovery of 3,4-isoxazolediamide co...
none21noA structural investigation on the isoxazole scaffold led to the discovery of 3,4-isoxazoledi...
We describe the development of a novel series of N-aryl-benzimidazolone HSP90 inhibitors (9) targeti...
The molecular chaperone heat shock protein 90 (HSP90) is essential for the folding stability, intrac...
Although the heat shock protein 90 (HSP90) inhibitor 17-allylamino-17-demethoxygeldanamycin (17-AAG)...
The last decade has seen the molecular chaperone heat shock protein 90 (HSP90) emerge as an exciting...
A potential therapeutic strategy for targeting cancer that has gained much interest is the inhibitio...
The molecular chaperone HSP90 is currently under investigation as a promising target for anticancer ...
A potential therapeutic strategy for targeting cancer that has gained much interest is the inhibitio...
Heat shock protein 90 (Hsp90) is an essential molecular chaperone that performs vital stress-related...
Heat shock protein 90 (Hsp90) is a chaperone responsible for the maturation of many cancer-related p...
AbstractHeat shock protein 90 (Hsp90) is a highly conserved molecular chaperone that plays a vital r...
Heat shock protein 90 (Hsp90) is a chaperone responsible for the maturation of many cancer-related p...