Benzenesulfonohydrazides inhibiting urease: Design, synthesis, their in vitro and in silico studies-Reference-Cited by-同舟云学术

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Benzenesulfonohydrazides inhibiting urease: Design, synthesis, their in vitro and in silico studies

Published:2020-11 Issue: Volume:1220 Page:128740
ISSN:0022-2860
Container-title:Journal of Molecular Structure
language:en
Short-container-title:Journal of Molecular Structure

Author:

Ahmed Mahmood,Imran Muhammad,Muddassar Muhammad,Hussain Riaz,Khan Muhammad Usman,Ahmad Saghir,Mehboob Muhammad Yasir,Ashfaq Saira

Publisher

Elsevier BV

Subject

Inorganic Chemistry,Organic Chemistry,Spectroscopy,Analytical Chemistry

Reference38 articles.

1. 3-Arylpropionylhydroxamic acid derivatives as Helicobacter pylori urease inhibitors: synthesis, molecular docking and biological evaluation;Shi;Bioorg. Med. Chem.,2016

2. Synthesis, biological evaluation and molecular docking of N-phenyl thiosemicarbazones as urease inhibitors;Hameed;Bioorg. Chem.,2015

3. Ureases as a target for the treatment of gastric and urinary infections;Follmer;J. Clin. Pathol.,2010

4. Identification of novel bacterial urease inhibitors through molecular shape and structure based virtual screening approaches;Imran;RSC Adv.,2020

5. Essential role of urease in pathogenesis of gastritis induced by Helicobacter pylori in gnotobiotic piglets;Eaton;Infect. Immun.,1991

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