Please use this identifier to cite or link to this item: http://nopr.niscair.res.in/handle/123456789/48234
Title: Inhibition of urease by some new synthesized 1,2,4-triazol derivatives: Inhibition mechanism and molecular docking
Authors: Kalfa, Aylin
Demir, Elif Ayazoglu
Colak, Ahmet
Yasar, Ahmet
Bekircan, Olcay
Keywords: Urease;Inhibition;Triazole;Noncompetitive;Docking
Issue Date: Jun-2019
Publisher: NISCAIR-CSIR, India
Abstract: Urease is a metalloenzyme that catalyzes the hydrolysis of urea to ammonia and carbon dioxide. This ammonia secretion may cause significant increase in pH and is responsible for negative effects of urease activity in human health and agriculture. So, jack bean urease inhibition potentials of a newly synthesized of 2-[3-(4-chlorophenyl)-5-(4-methoxybenzyl)-4H-1,2,4-triazol-4-l]acetohydrazide derivative compounds have been investigated in this study. Initially, IC50 values of six molecules (B16-B21) have been determined. According to this, it is seen that the B20 molecule is the most effective inhibitor. Docking studies also supported this end result. Urease inhibition type and Ki value are found to be noncompetitive and 32.01±0.25 µM, respectively, in the presence of compound B20. These results suggest that the B20 compound is a potential urease inhibitor.
Page(s): 720-726
URI: http://nopr.niscair.res.in/handle/123456789/48234
ISSN: 0975-0983(Online); 0376-4699(Print)
Appears in Collections:IJC-B Vol.58B(06) [June 2019]

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