CARBONIC-ANHYDRASE INHIBITORS .36. INHIBITION OF ISOZYME-I AND ISOZYME-II WITH SCHIFF-BASES DERIVED FROM CHALKONES AND AROMATIC HETEROCYCLIC SULFONAMIDES/
Ct. Supuran et al., CARBONIC-ANHYDRASE INHIBITORS .36. INHIBITION OF ISOZYME-I AND ISOZYME-II WITH SCHIFF-BASES DERIVED FROM CHALKONES AND AROMATIC HETEROCYCLIC SULFONAMIDES/, European journal of medicinal chemistry, 31(6), 1996, pp. 439-447
A series of 27 Schiff bases was prepared by reaction of chalkones with
sulfanilamide and 5-amino-1,3,4-thiadiazole-2-sulfonamide. The new co
mpounds were characterized by analysis and standard physico-chemical m
ethods. They possess good inhibitory properties towards isozymes I and
II of carbonic anhydrase. Structure-activity effects in this series o
f inhibitors are also discussed.