A series of secondary and tertiary aryl sulfonamides were synthesized under flow conditions and evaluated for their ability to selectively inhibit tumor-associated carbonic anhydrase isoforms IX and XII. The tested compounds revealed to be highly potent CA IX inhibitors in nanomolar range, and to inhibit CA XII activity with different ranks of potencies. Remarkably, 4-methyl-N-phenylbenzenesulfonamide was a selective nanomolar CA IX inhibitor with an IC50 of 90 nM.
Flow Synthesis and Biological Activity of Aryl Sulfonamides as Selective Carbonic Anhydrase IX and XII Inhibitors
CAROTTI, Andrea;GIOIELLO, ANTIMO
2014
Abstract
A series of secondary and tertiary aryl sulfonamides were synthesized under flow conditions and evaluated for their ability to selectively inhibit tumor-associated carbonic anhydrase isoforms IX and XII. The tested compounds revealed to be highly potent CA IX inhibitors in nanomolar range, and to inhibit CA XII activity with different ranks of potencies. Remarkably, 4-methyl-N-phenylbenzenesulfonamide was a selective nanomolar CA IX inhibitor with an IC50 of 90 nM.File in questo prodotto:
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