20 articles for thisTarget
The following articles (labelled with PubMed ID or TBD) are for your review
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Design, synthesis and biological evaluation of metronidazole-thiazole derivatives as antibacterial inhibitors.
School of Life Science Nanjing University
Design, synthesis and antibacterial activities of 5-(pyrazin-2-yl)-4H-1,2,4-triazole-3-thiol derivatives containing Schiff base formation as FabH inhibitory.
Nanjing University
QSAR studies on benzoylaminobenzoic acid derivatives as inhibitors of beta-ketoacyl-acyl carrier protein synthase III.
Shri G.S. Institute of Technology and Science
Synthesis and biological evaluation of novel sulfonyl-naphthalene-1,4-diols as FabH inhibitors.
Portland State University
Synthesis and biological evaluation of a C5-biphenyl thiolactomycin library.
University of Birmingham
Structure-activity relationships at the 5-position of thiolactomycin: an intact (5R)-isoprene unit is required for activity against the condensing enzymes from Mycobacterium tuberculosis and Escherichia coli.
National Institute of Allergy and Infectious Diseases
Discovery of vinylogous carbamates as a novel class ofß-ketoacyl-acyl carrier protein synthase III (FabH) inhibitors.
Soochow University
Synthesis, molecular modeling and biological evaluation ofß-ketoacyl-acyl carrier protein synthase III (FabH) as novel antibacterial agents.
Nanjing University
Design, synthesis, and structure-activity relationships of pyrazole derivatives as potential FabH inhibitors.
Nanjing University
Design, synthesis and biological evaluation of novel thiazole derivatives as potent FabH inhibitors.
Nanjing University
Novel E. coli beta-ketoacyl-acyl carrier protein synthase III inhibitors as targeted antibiotics.
Konkuk University
Synthesis and biological evaluation of thiazolidine-2-one 1,1-dioxide as inhibitors of Escherichia coli beta-ketoacyl-ACP-synthase III (FabH).
Portland State University
Biphenyl-based analogues of thiolactomycin, active against Mycobacterium tuberculosis mtFabH fatty acid condensing enzyme.
The University of Birmingham
Discovery and development of novel rhodanine derivatives targeting enoyl-acyl carrier protein reductase.
Nanjing University
Discovery of novel bacterial FabH inhibitors (Pyrazol-Benzimidazole amide derivatives): Design, synthesis, bioassay, molecular docking and crystal structure determination.
Fudan University
Synthesis, molecular modeling and biological evaluation of PSB as targeted antibiotics.
Nanjing University
Synthesis, antibacterial activities and molecular docking studies of peptide and Schiff bases as targeted antibiotics.
Nanjing University
Biological and structural evaluation of 10R- and 10S-methylthio-DDACTHF reveals a new role for sulfur in inhibition of glycinamide ribonucleotide transformylase.
The Scripps Research Institute