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Carbonic Anhydrase Inhibition Activities of Schiff's Bases Based on Quinazoline-Linked Benzenesulfonamide.

Adel S El-AzabAlaa A-M Abdel-AzizHazem A GhabbourSilvia BuaAlessio NocentiniHamad M Al KahtaniNawaf A AlsaifMohamed H M Al-AgamyClaudiu T Supuran
Published in: Molecules (Basel, Switzerland) (2022)
Human carbonic anhydrase (CA, EC 4.2.1.1) (hCA) isoforms I, II, IX, and XII were investigated for their inhibitory activity with a series of new Schiff's bases based on quinazoline scaffold 4 - 27 . The hCA I isoform was efficiently inhibited by Schiff's bases 4 - 6 , 10 - 19 , 22 - 27 and had an inhibition constant (Ki) value of 52.8-991.7 nM compared with AAZ (Ki, 250 nM). Amongst the quinazoline derivatives, the compounds 2 , 3 , 4 , 10 , 11 , 16 , 18 , 24 , 26 , and 27 were proven to be effective hCA II inhibitors, with Ki values of 10.8-52.6 nM, measuring up to AAZ (Ki, 12 nM). Compounds 2 - 27 revealed compelling hCA IX inhibitory interest with Ki values of 10.5-99.6 nM, rivaling AAZ (Ki, 25.0 nM). Quinazoline derivatives 3 , 10 , 11 , 13 , 15 - 19 , and 24 possessed potent hCA XII inhibitory activities with K I values of 5.4-25.5 nM vs. 5.7 nM of AAZ. Schiff's bases 7 , 8 , 9 , and 21 represented attractive antitumor hCA IX carbonic anhydrase inhibitors (CAIs) with K I rates (22.0, 34.8, 49.2, and 45.3 nM, respectively). Compounds 5 , 7 , 8 , 9 , 14 , 18 , 19 , and 21 showed hCA I inhibitors on hCA IX with a selectivity index of 22.46-107, while derivatives 12 , 14 , and 18 showed selective hCA I inhibitors on hCA XII with a selectivity profile of 45.04-58.58, in contrast to AAZ (SI, 10.0 and 43.86). Compounds 2 , 5 , 7 - 14 , 19 - 23 , and 25 showed a selectivity profile for hCA II inhibitors over hCA IX with a selectivity index of 2.02-19.67, whereas derivatives 5 , 7 , 8 , 13 , 14 , 15 , 17 , 20 , 21 , and 22 showed selective hCA II inhibitors on hCA XII with a selectivity profile of 4.84-26.60 balanced to AAZ (SI, 0.48 and 2.10).
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