Design Synthesis and Biological Evaluation of 123-Triazole-linked triazino56-bindole-benzene sulfonamide Conjugates as Potent Carbonic Anhydrase I II IX and XIII Inhibitors

摘要

A series of 1,2,3-triazole-linked triazino[5,6-b]indole-benzene sulfonamide hybrids ( ) was synthesized and evaluated for carbonic anhydrase (CA, EC 4.2.1.1) inhibitory activity against the human (h) isoforms hCA I, II, XIII (cytosolic isoforms), and hCA IX (transmembrane tumor-associated isoform). The results revealed that the compounds exhibited K values in the low to medium nanomolar range against hCA II and hCA IX (K s ranging from 7.7 nM to 41.3 nM) and higher K values against hCA I and hCA XIII. Compound showed potent inhibition of hCA II (K = 7.7nM), being more effective compared to the standard inhibitor acetazolamide (AAZ) (K = 12.1 nM). Compounds and showed moderate activity against hCA XIII (K = 69.8 and 65.8 nM). Hence, compound could be consider as potential lead candidate for the design of potent and selective hCA II inhibitors.