| Literature DB >> 28390994 |
Sarosh Iqbal1, Muhammad Saleem2, M Kamran Azim3, Muhammad Taha4, Uzma Salar3, Khalid Mohammed Khan5, Shahnaz Perveen6, M Iqbal Choudhary7.
Abstract
Discovery and development of carbonic anhydrase inhibitors is crucial for their clinical use as antiepileptic, diurectic and antiglaucoma agents. Keeping this in mind, we have synthesized carbohydrazones 1-27 and evaluated them for their in vitro carbonic anhydrase inhibitory potential. Out of twenty-seven compounds, compounds 1 (IC50=1.33±0.01µM), 2 (IC50=1.85±0.24µM), 3 (IC50=1.37±0.06µM), and 9 (IC50=1.46±0.12µM) have showed carbonic anhydrase inhibition better than the standard drug zonisamide (IC50=1.86±0.03µM). Moreover, compounds 4 (IC50=2.32±0.04µM), 5 (IC50=3.96±0.35µM), 7 (IC50=2.33±0.02µM), and 8 (IC50=2.67±0.01µM) showed good inhibitory activity. Cheminformatic analysis has shown that compounds 1 and 2 possess lead-like properties. In addition, kinetic and molecular docking studies were also performed to investigate the binding interaction between carbohydrazones and carbonic anhydrase enzyme. This study has identified a novel and potent class of carbonic anhydrase inhibitors with the potential to be investigated further.Entities:
Keywords: Carbohydrazones; Carbonic anhydrase II inhibitors; Cheminformatic analysis; Kinetic studies; Ligand docking; bis-Schiff bases
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Year: 2017 PMID: 28390994 DOI: 10.1016/j.bioorg.2017.03.014
Source DB: PubMed Journal: Bioorg Chem ISSN: 0045-2068 Impact factor: 5.275