23 articles for thisTarget
The following articles (labelled with PubMed ID or TBD) are for your review
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Article Title
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Recent advances in the discovery and development of antibacterial agents targeting the cell-division protein FtsZ.
Stony Brook University
Synthesis and Evaluation of Quinazolines as Inhibitors of the Bacterial Cell Division Protein FtsZ.
University of California Davis
Design, synthesis and antibacterial activity of cinnamaldehyde derivatives as inhibitors of the bacterial cell division protein FtsZ.
Shandong University
Advances in the discovery of novel antimicrobials targeting the assembly of bacterial cell division protein FtsZ.
Shandong University
Chrysophaentins are competitive inhibitors of FtsZ and inhibit Z-ring formation in live bacteria.
National Institute of Diabetes and Digestive and Kidney Diseases
3-Phenyl substituted 6,7-dimethoxyisoquinoline derivatives as FtsZ-targeting antibacterial agents.
The State University of New Jersey
A bactericidal guanidinomethyl biaryl that alters the dynamics of bacterial FtsZ polymerization.
University of Medicine and Dentistry of New Jersey
Novel trisubstituted benzimidazoles, targeting Mtb FtsZ, as a new class of antitubercular agents.
State University of New York
Parallel solid synthesis of inhibitors of the essential cell division FtsZ enzyme as a new potential class of antibacterials.
Laval University
Novel pyridopyrazine and pyrimidothiazine derivatives as FtsZ inhibitors.
Southern Research Institute
Probing the binding site of curcumin in Escherichia coli and Bacillus subtilis FtsZ--a structural insight to unveil antibacterial activity of curcumin.
National Institute of Pharmaceutical Education and Research
Bacterial GTPases as druggable targets to tackle antimicrobial resistance.
Indian Institute of Science Education and Research Bhopal
The cell division protein FtsZ as a cellular target to hit cystic fibrosis pathogens.
University of Pavia
The natural anthraquinone dye purpurin exerts antibacterial activity by perturbing the FtsZ assembly.
National Institute of Technology Calicut
Design and synthesis of quinolinium-based derivatives targeting FtsZ for antibacterial evaluation and mechanistic study.
Guangdong University of Technology
Discovery of FtsZ inhibitors by virtual screening as antibacterial agents and study of the inhibition mechanism.
The Hong Kong Polytechnic University
Targeting the FtsZ Allosteric Binding Site with a Novel Fluorescence Polarization Screen, Cytological and Structural Approaches for Antibacterial Discovery.
Csic
Design, synthesis and evaluation of novel 9-arylalkyl-10-methylacridinium derivatives as highly potent FtsZ-targeting antibacterial agents.
Shandong University
[125I]A-312110, a novel high-affinity 1,4-dihydropyridine ATP-sensitive K+ channel opener: characterization and pharmacology of binding.
Abbott Laboratories