The present invention pertains to the use of certain 3,4-diarylpyazoles of formula (I), both
in vitro and
in vivo, to inhibit
heat shock protein 90 (HSP90), and in the treatment of conditions mediated by HSP90, including, for example,
cancer; wherein: Ar3 is independently: a C5-20
aryl group, and is optionally substituted; Ar4 is independently: a C5-20
aryl group, and is optionally substituted; R5 is independently:
hydrogen; halo; hydroxyl;
ether; formyl; acyl; carboxy; ester; acyloxy; oxycarbonyloxy; amido; acylamido; aminocarbonyloxy; tetrazolyl; amino; nitro; cyano; azido; sulfhydryl;
thioether; sulfonamide; C1-7
alkyl; C3-20heterocycyl; or C5-20
aryl; R<SP>N< / SP> is independently: —H; C1-7
alkyl; C3-20heterocycyl; or, C5-20aryl; and pharmaceutically acceptable salts, solvates, amides, esters, ethers, chemically protected forms, and prodrugs thereof. The present invention also pertains to such compounds, pharmaceutical compositions comprising such compounds, such compounds for medical use, such compounds use in the treatment of conditions mediated by HSP90, including, for example,
cancer, and use of such compounds in the preparation of medicaments for such treatments.