[HTML][HTML] Proteus mirabilis biofilm: development and therapeutic strategies

R Wasfi, SM Hamed, MA Amer… - Frontiers in cellular and …, 2020 - frontiersin.org
Proteus mirabilis is a Gram negative bacterium that is a frequent cause of catheter-
associated urinary tract infections (CAUTIs). Its ability to cause such infections is mostly …

[HTML][HTML] Recent advances in design of new urease inhibitors: A review

P Kafarski, M Talma - Journal of advanced research, 2018 - Elsevier
Urease is a nickel-dependent metalloenzyme found in plants, some bacteria, and fungi.
Bacterial enzyme is of special importance since it has been demonstrated as a potent …

Recent updates of fluoroquinolones as antibacterial agents

HAA Ezelarab, SH Abbas, HA Hassan… - Archiv der …, 2018 - Wiley Online Library
Fluoroquinolones remain one of the most important kind of antibacterial agents used
nowadays. The emergence of more virulent and resistant strains of bacteria by the …

Optimized ebselen-based inhibitors of bacterial ureases with nontypical mode of action

K Macegoniuk, W Tabor, L Mazzei… - Journal of Medicinal …, 2023 - ACS Publications
Screening of 25 analogs of Ebselen, diversified at the N-aromatic residue, led to the
identification of the most potent inhibitors of Sporosarcina pasteurii urease reported to date …

Unraveling the anti-biofilm potential of green algal sulfated polysaccharides against Salmonella enterica and Vibrio harveyi

J Vishwakarma, S VL - Applied Microbiology and Biotechnology, 2020 - Springer
One of the main reasons for the bacterial resistance to antibiotics is caused by biofilm
formation of microbial pathogens during bacterial infections. Salmonella enterica and Vibrio …

Design, synthesis, molecular docking, anti-Proteus mirabilis and urease inhibition of new fluoroquinolone carboxylic acid derivatives

MAA Abdullah, GEDAA Abuo-Rahma… - Bioorganic …, 2017 - Elsevier
New hydroxamic acid, hydrazide and amide derivatives of ciprofloxacin in addition to their
analogues of levofloxacin were prepared and identified by different spectroscopic …

Levofloxacin and sulfa drugs linked via Schiff bases: Exploring their urease inhibition, enzyme kinetics and in silico studies

SAAS Tirmazi, MA Qadir, M Ahmed, M Imran… - Journal of Molecular …, 2021 - Elsevier
Involvement of urease in various pathological conditions specifically in gastric and peptic
ulcers make it an important therapeutic target. In the present study urease inhibition was …

Identification and molecular modeling of new quinolin-2-one thiosemicarbazide scaffold with antimicrobial urease inhibitory activity

MAI Elbastawesy, YAMM El-Shaier, M Ramadan… - Molecular Diversity, 2021 - Springer
A new series of 6-substituted quinolin-2-one thiosemicarbazides 6a–j has been synthesized.
The structure of the target compounds was proved by different spectroscopic and elemental …

Design, synthesis and molecular docking of new N-4-piperazinyl ciprofloxacin-triazole hybrids with potential antimicrobial activity

HHH Mohammed, ESMN Abdelhafez, SH Abbas… - Bioorganic …, 2019 - Elsevier
Abstract New N-4-piperazinyl ciprofloxacin-triazole hybrids 6a-o were prepared and
characterized. The in vitro antimycobacterial activity revealed that compound 6a …

Potential antivirulence activity of sub-inhibitory concentrations of ciprofloxacin against Proteus mirabilis isolates: an in-vitro and in-vivo study

MA Elhosseini, TE El-Banna, FI Sonbol… - Annals of Clinical …, 2024 - Springer
Background Proteus mirabilis is a significant nosocomial pathogen that is frequently
associated with a wide range of infections, necessitating heightened attention to mitigate …