Synthesis and evaluation of n-heteroarylsubstituted triazolosulfonamides as carbonic anhydrase inhibitors

Abstract

A new series of N-heteroarylsubstituted triazolosulfonamide compounds were synthesized and their inhibitory effects on the activity of purified human carbonic anhydrase (hCA) I and II were evaluated. Compounds (3 a-k) were prepared by propargylation of N-heteroaryl compounds. Compound 5 was obtained from sulfanilamide and sodium nitrite followed by addition of sodium azide. The products (6 a-k) were synthesized from compounds 3 and 5. The results showed that all the synthesized compounds were inhibited the CA isoenzymes activity. Figure 6a (IC50 = 0.52 mu M for hCA I and 0.34 mu M for hCA II) has the most inhibitory effect among the synthesized compounds.