Synthesis and carbonic anhydrase inhibitory activities of new thienyl-substituted pyrazoline benzenesulfonamides

Ebru MeteDepartment of Chemistry, Faculty of Science, Ataturk University, Erzurum, Turkey, Correspondence[email protected]

Birnur ComezDepartment of Pharmaceutical Chemistry, Faculty of Pharmacy, Ataturk University, Erzurum, Turkey,

Halise Inci GulDepartment of Pharmaceutical Chemistry, Faculty of Pharmacy, Ataturk University, Erzurum, Turkey,

Ilhami GulcinDepartment of Chemistry, Faculty of Science, Ataturk University, Erzurum, Turkey, ;Department of Zoology, College of Science, King Saud University, Riyadh, Saudi Arabia, and

Claudiu T. SupuranNeurofarba Department and Laboratorio di Chimica Bioinorganica, Polo Scientifico, Universita' degli Studi di Firenze, Sesto Fiorentino (Firenze), Italy

Figures & data

Scheme 1. Synthesis of 1,3,5-trisubstituted pyrazoline-bearing benzenesulfonamides, 9–16.

Table 1. Human CA isoenzymes (hCA I and II) inhibition value of the compounds (9–16) by the esterase method with 4-nitrophenyl acetate as substrate.

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Synthesis and carbonic anhydrase inhibitory activities of new thienyl-substituted pyrazoline benzenesulfonamides

Table 1. Human CA isoenzymes (hCA I and II) inhibition value of the compounds (9–16) by the esterase method with 4-nitrophenyl acetate as substrate.

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Synthesis and carbonic anhydrase inhibitory activities of new thienyl-substituted pyrazoline benzenesulfonamides

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Table 1. Human CA isoenzymes (hCA I and II) inhibition value of the compounds (9–16) by the esterase method with 4-nitrophenyl acetate as substrate.

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