Sulfonamide derivatives with benzothiazole scaffold: Synthesis and carbonic anhydrase I–II inhibition properties
   
Yazarlar (7)
Doç. Dr. Erbay KALAY Kafkas Üniversitesi, Türkiye
Serpil Gerni
Doç. Dr. Feyzi Sinan TOKALI Kafkas Üniversitesi, Türkiye
Osman Nuri Aslan Atatürk Üniversitesi, Türkiye
Makale Türü Özgün Makale (SSCI, AHCI, SCI, SCI-Exp dergilerinde yayınlanan tam makale)
Dergi Adı BIOTECHNOLOGY AND APPLIED BIOCHEMISTRY (Q3)
Dergi ISSN 0885-4513 Wos Dergi Scopus Dergi
Dergi Tarandığı Indeksler SCI-Expanded
Makale Dili İngilizce Basım Tarihi 02-2024
Cilt / Sayı / Sayfa 71 / 1 / 223–231 DOI 10.1002/bab.2534
Makale Linki https://iubmb.onlinelibrary.wiley.com/doi/full/10.1002/bab.2534
Özet
The secondary sulfonamide derivatives containing benzothiazole scaffold (1-10) were synthesized to determine their inhibition properties on two physiologically essential human carbonic anhydrases isoforms (hCAs, EC, 4.2.1.1), hCA I, and hCA II. The inhibitory effects of the compounds on hCA I and hCA II isoenzymes were investigated by comparing their IC and K values. The K values of compounds (1-10) against hCA I and hCA II are in the range of 0.052 ± 0.022-0.971 ± 0.280 and 0.025 ± 0.010-0.682 ± 0.335, respectively. Some of these inhibited the enzyme more effectively than the standard drug, acetazolamide. In particular, compounds 5 and 4 were found to be most effective on hCA I and hCA II.
Anahtar Kelimeler
benzothiazole moiety | human carbonic anhydrase I | human carbonic anhydrase II | inhibition | secondary sulfonamide derivatives