Carbonic anhydrase inhibitory properties of novel sulfonamide derivatives of aminoindanes and aminotetralins
Özet
Six sulfonamides derived from indanes and tetralines were synthesized. The human carbonic anhydrase isozymes hCA I and hCA II inhibition effects of the synthesized sulfonamides were determined. From these compounds, while N-(5,6-dimethoxy-2,3-dihydro-1H-inden-2-yl) methane sulfonamide showed the most potent inhibitory effect against hCA I (K-i = 46 +/- 5.4 mu M, r(2) = 0.978), N-(1,2,3,4-tetrahydronaphthalene-2-yl) methanesulfonamide was found to have the best inhibitory effect against hCA II (K-i = 94 +/- 7.6 mu M, r(2) = 0.982).
Anahtar kelimeler
Atıf için künye
AKBABA, Y., AKINCIOGLU, A., GOCER, H., Göksu, S., Gülçin, İ., & Supuran, C. T. (2014). Carbonic anhydrase inhibitory properties of novel sulfonamide derivatives of aminoindanes and aminotetralins. JOURNAL OF ENZYME INHIBITION AND MEDICINAL CHEMISTRY, 29(1), 35–42. https://doi.org/10.3109/14756366.2012.750311
BibTeX
@article{akbaba2014-68001,
author = {AKBABA, Yusuf and AKINCIOGLU, Akin and GOCER, Hulya and Göksu, Süleyman and Gülçin, İlhami and Supuran, Claudiu T.},
title = {Carbonic anhydrase inhibitory properties of novel sulfonamide derivatives of aminoindanes and aminotetralins},
journal = {JOURNAL OF ENZYME INHIBITION AND MEDICINAL CHEMISTRY},
year = {2014},
volume = {29},
number = {1},
pages = {35--42},
issn = {1475-6366},
doi = {10.3109/14756366.2012.750311},
url = {https://akademik.atauni.edu.tr/yayinlar/68001-carbonic-anhydrase-inhibitory-properties-of-novel-sulfonamide-derivatives-of}
}