A small-molecular inhibitor against Proteus mirabilis urease to treat catheter-associated urinary tract infections
Infection and blockage of indwelling urinary catheters is significant owing to its high
incidence rate and severe medical consequences. Bacterial enzymes are employed as …
incidence rate and severe medical consequences. Bacterial enzymes are employed as …
Semi-quantitative assay to measure urease activity by urinary catheter-associated Uropathogens
JM Duran Ramirez, J Gomez… - Frontiers in cellular …, 2022 - frontiersin.org
Catheter-associated urinary tract infections (CAUTIs) are one of the most common
healthcare-associated infections in the US, accounting for over 1 million cases annually and …
healthcare-associated infections in the US, accounting for over 1 million cases annually and …
N-acetylcysteine prevents catheter occlusion and inflammation in catheter associated-urinary tract infections by suppressing urease activity
A Manoharan, J Farrell, VR Aldilla… - Frontiers in Cellular …, 2023 - frontiersin.org
Introduction Proteus mirabilis is a key pathobiont in catheter-associated urinary tract
infections (CA-UTIs), which is well known to form crystalline biofilms that occlude catheters …
infections (CA-UTIs), which is well known to form crystalline biofilms that occlude catheters …
Metallochaperone UreG serves as a new target for design of urease inhibitor: a novel strategy for development of antimicrobials
Urease as a potential target of antimicrobial drugs has received considerable attention given
its versatile roles in microbial infection. Development of effective urease inhibitors, however …
its versatile roles in microbial infection. Development of effective urease inhibitors, however …
Identification of novel urease inhibitors by high-throughput virtual and in vitro screening
OR Abid, TM Babar, FI Ali, S Ahmed… - ACS Medicinal …, 2010 - ACS Publications
Ureases are important in both agriculture and human health. Bacterial ureases are directly
involved in many farm-field problems and pathological conditions. Here, we report a …
involved in many farm-field problems and pathological conditions. Here, we report a …
Arylmethylene hydrazine derivatives containing 1, 3-dimethylbarbituric moiety as novel urease inhibitors
A new series of arylmethylene hydrazine derivatives bearing 1, 3-dimethylbarbituric moiety
7a–o were designed, synthesized, and evaluated for their in vitro urease inhibitory activity …
7a–o were designed, synthesized, and evaluated for their in vitro urease inhibitory activity …
Design, synthesis, in vitro evaluation and docking studies on dihydropyrimidine-based urease inhibitors
In our previous report, we have identified 3, 4-dihydropyrimidine scaffold as promising class
of urease inhibitor in a structure based virtual screen (SBVS) experiment. In present study …
of urease inhibitor in a structure based virtual screen (SBVS) experiment. In present study …
Identification of novel bacterial urease inhibitors through molecular shape and structure based virtual screening approaches
The enzyme urease is an essential colonizing factor of the notorious carcinogenic pathogen
Helicobacter pylori (H. pylori), conferring acid resistance to the bacterium. Recently …
Helicobacter pylori (H. pylori), conferring acid resistance to the bacterium. Recently …
Exploration of thiourea-based scaffolds for the construction of bacterial ureases inhibitors
W Tabor, A Katsogiannou, D Karta… - ACS …, 2023 - ACS Publications
A series of 32 thiourea-based urease inhibitors were synthesized and evaluated against
native bacterial enzyme and whole cells of Sporosarcina pasteurii and Proteus mirabilis …
native bacterial enzyme and whole cells of Sporosarcina pasteurii and Proteus mirabilis …
Novel phenylurea-pyridinium derivatives as potent urease inhibitors: Synthesis, in vitro, and in silico studies
SE Sadat-Ebrahimi, A Bigdelou, RH Sooreshjani… - Journal of Molecular …, 2022 - Elsevier
Urease is known as a virulence factor of some pathogen in the living organism. In this study,
a novel series of phenylurea conjugated to different alkyl pyridinium were designed …
a novel series of phenylurea conjugated to different alkyl pyridinium were designed …
相关搜索
- proteus mirabilis tract infection
- tract infections urease activity
- molecular shape urease inhibitors
- tract infections catheter occlusion
- catheter occlusion urease activity
- high throughput urease inhibitors
- scaffolds for the construction ureases inhibitors
- proteus mirabilis pathogenic potential
- tract infection pathogenic potential