Secondary Sulfonamides as Effective Lactoperoxidase Inhibitors
Özet
Secondary sulfonamides (4a-8h) incorporating acetoxybenzamide, triacetoxybenzamide, hydroxybenzamide, and trihydroxybenzamide and possessing thiazole, pyrimidine, pyridine, isoxazole and thiadiazole groups were synthesized. Lactoperoxidase (LPO, E.C.1.11.1.7), as a natural antibacterial agent, is a peroxidase enzyme secreted from salivary, mammary, and other mucosal glands. In the present study, the in vitro inhibitory effects of some secondary sulfonamide derivatives (4a-8h) were examined against LPO. The obtained results reveal that secondary sulfonamide derivatives (4a-8h) are effective LPO inhibitors. The K-i values of secondary sulfonamide derivatives (4a-8h) were found in the range of 1.096 x 10(-3) to 1203.83 mu M against LPO. However, the most effective inhibition was found for N-(sulfathiazole)-3,4,5-triacetoxybenzamide (6a), with K-i values of 1.096 x 10(-3) +/- 0.471 x 10(-3) mu M as non-competitive inhibition.
Anahtar kelimeler
Atıf için künye
KÖKSAL, Z., KALIN, R., Camadan, Y., Usanmaz, H., Almaz, Z., Gülçin, İ., GOKCEN, T., GOREN, A. C., & Özdemir, H. (2017). Secondary Sulfonamides as Effective Lactoperoxidase Inhibitors. MOLECULES, 22(6). https://doi.org/10.3390/molecules22060793
BibTeX
@article{koksal2017-67354,
author = {KÖKSAL, ZEYNEP and KALIN, Ramazan and Camadan, Yasemin and Usanmaz, Hande and Almaz, Zuleyha and Gülçin, İlhami and GOKCEN, Taner and GOREN, Ahmet Ceyhan and Özdemir, Hasan},
title = {Secondary Sulfonamides as Effective Lactoperoxidase Inhibitors},
journal = {MOLECULES},
year = {2017},
volume = {22},
number = {6},
issn = {1420-3049},
doi = {10.3390/molecules22060793},
url = {https://akademik.atauni.edu.tr/yayinlar/67354-secondary-sulfonamides-as-effective-lactoperoxidase-inhibitors}
}