5-Aryl-4-(5-substituted-2,4-dihydroxyphenyl)-1,2,3-thiadiazoles as inhibitors of Hsp90 chaperone
The synthesis and in vitro binding of the thiadiazole inhibitors of Hsp90 with K ds up to 5 nM. A series of 5-aryl-4-(5-substituted-2,4-dihydroxyphenyl)-1,2,3-thiadiazoles were synthesized and their binding to several constructs of human Hsp90 chaperone measured by isothermal titration calorimetry (...
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Veröffentlicht in: | Bioorganic & medicinal chemistry letters 2009-02, Vol.19 (4), p.1089-1092 |
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Format: | Artikel |
Sprache: | eng |
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