Inhibitory effects of benzimidazole containing new phenolic Mannich bases on human carbonic anhydrase isoforms hCA I and II
Özet
New phenolic mono and bis Mannich bases incorporating benzimidazole, such as 2-(aminomethyl)-4-(1H-benzimidazol-2-yl)phenol and 2,6-bis(aminomethyl)-4-(1H-benzimidazol-2-yl)phenol were synthesized starting from 4-(1H-benzimidazol-2-yl)phenol. Amines used for the synthesis included dimethylamine, pyrrolidine, piperidine, N-methylpiperazine and morpholine. The CA inhibitory properties of these compounds were tested on the human carbonic anhydrase (CA, EC 4.2.1.1) isoforms hCA I and hCA II. These new compounds, as many phenols show moderate CA inhibitory properties.
Anahtar kelimeler
Atıf için künye
Gül, H. İ., Yazici, Z., Tanc, M., & Supuran, C. T. (2016). Inhibitory effects of benzimidazole containing new phenolic Mannich bases on human carbonic anhydrase isoforms hCA I and II. JOURNAL OF ENZYME INHIBITION AND MEDICINAL CHEMISTRY, 31(6), 1540–1544. https://doi.org/10.3109/14756366.2016.1156675
BibTeX
@article{gul2016-19982,
author = {Gül, Halise İnci and Yazici, Zehra and Tanc, Muhammet and Supuran, Claudiu T.},
title = {Inhibitory effects of benzimidazole containing new phenolic Mannich bases on human carbonic anhydrase isoforms hCA I and II},
journal = {JOURNAL OF ENZYME INHIBITION AND MEDICINAL CHEMISTRY},
year = {2016},
volume = {31},
number = {6},
pages = {1540--1544},
issn = {1475-6366},
doi = {10.3109/14756366.2016.1156675},
url = {https://akademik.atauni.edu.tr/yayinlar/19982-inhibitory-effects-of-benzimidazole-containing-new-phenolic-mannich-bases-on}
}