49 articles for thisTarget
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Discovery of a novel covalent non-ß-lactam inhibitor of the metallo-ß-lactamase NDM-1.

Uit The Arctic University of Norway
Triazolylthioacetamide: A Valid Scaffold for the Development of New Delhi Metallo-ß-Lactmase-1 (NDM-1) Inhibitors.

North-West University
Fragment-based discovery of inhibitor scaffolds targeting the metallo-ß-lactamases NDM-1 and VIM-2.

Uit The Arctic University of Norway
Amino Acid Thioester Derivatives: A Highly Promising Scaffold for the Development of Metallo-ß-lactamase L1 Inhibitors.

North-West University
The applications of binuclear metallohydrolases in medicine: recent advances in the design and development of novel drug leads for purple acid phosphatases, metallo-ß-lactamases and arginases.

The University of Queensland
Design, synthesis, and evaluation of 2 beta-alkenyl penam sulfone acids as inhibitors of beta-lactamases.

F. Hoffmann-La Roche
Mercaptophosphonate compounds as broad-spectrum inhibitors of the metallo-beta-lactamases.

University of Li£Ge
Design, synthesis and antibacterial activity evaluation of ebselen derivatives in NDM-1 producing bacteria.

Ocean University of China
Exploiting the Carboxylate-Binding Pocket of β-Lactamase Enzymes Using a Focused DNA-Encoded Chemical Library.

Baylor College of Medicine
Rational Design of Benzobisheterocycle Metallo-β-Lactamase Inhibitors: A Tricyclic Scaffold Enhances Potency against Target Enzymes.

University of the Republic (UdelaR)
Discovery of hydroxamate as a promising scaffold dually inhibiting metallo- and serine-β-lactamases.

Northwest University
Fluorinated captopril analogues inhibit metallo-β-lactamases and facilitate structure determination of NDM-1 binding pose.

UiT The Arctic University of Norway
The activity and mechanism of vidofludimus as a potent enzyme inhibitor against NDM-1-positive E. coli.

Northeast Agricultural University
Kinetics, Thermodynamics, and Structural Effects of Quinoline-2-Carboxylates, Zinc-Binding Inhibitors of New Delhi Metallo-β-lactamase-1 Re-sensitizing Multidrug-Resistant Bacteria for Carbapenems.

Freie University Berlin
Inhibitors for metallo-β-lactamases from the B1 and B3 subgroups provide an avenue to combat a major mechanism of antibiotic resistance.

The University of Queensland
Design, Synthesis, and Biological Evaluation of New 1H-Imidazole-2-Carboxylic Acid Derivatives as Metallo-β-Lactamase Inhibitors.

Xihua University
Aurones and derivatives as promising New Delhi metallo-β-lactamase (NDM-1) inhibitors.

Univ. Grenoble Alpes
Small-molecule inhibitors of bacterial-producing metallo-β-lactamases: insights into their resistance mechanisms and biochemical analyses of their activities.

University Sains Malaysia
Recent advances in β-lactamase inhibitor chemotypes and inhibition modes.

Xihua University
α-Aminophosphonate inhibitors of metallo-β-lactamases NDM-1 and VIM-2.

Uppsala University
1,2,4-Triazole-3-thione analogues with an arylakyl group at position 4 as metallo-β-lactamase inhibitors.

Cnrs
Optimized Ebselen-Based Inhibitors of Bacterial Ureases with Nontypical Mode of Action.

Wroclaw University
Synthesis of novel ciprofloxacin-avibactam conjugates for the development of second-generation non-β-lactam-β-lactamase inhibitors.

CSIR-Institute of Himalayan Bioresource Technology
Crystal Structures of Metallo-β-Lactamase (IMP-1) and Its D120E Mutant in Complexes with Citrate and the Inhibitory Effect of the Benzyl Group in Citrate Monobenzyl Ester.

Kumamoto University
Structure-activity relationship of 6-methylidene penems bearing 6,5 bicyclic heterocycles as broad-spectrum beta-lactamase inhibitors: evidence for 1,4-thiazepine intermediates with C7 R stereochemistry by computational methods.

Wyeth Research
Structure-activity relationship of 6-methylidene penems bearing tricyclic heterocycles as broad-spectrum beta-lactamase inhibitors: crystallographic structures show unexpected binding of 1,4-thiazepine intermediates.

Wyeth Research
Mechanism of inactivation of beta-lactamases by novel 6-methylidene penems elucidated using electrospray ionization mass spectrometry.

Wyeth Research
Penicillin-derived inhibitors that simultaneously target both metallo- and serine-beta-lactamases.

Southern Methodist University
Dipyridyl-substituted thiosemicarbazone as a potent broad-spectrum inhibitor of metallo-β-lactamases.

Northwest University
Investigation of synergistic antimicrobial effects of the drug combinations of meropenem and 1,2-benzisoselenazol-3(2H)-one derivatives on carbapenem-resistant Enterobacteriaceae producing NDM-1.

The Hong Kong Polytechnic University
Allyl and propargyl substituted penam sulfones as versatile intermediates toward the syntheses of new beta-lactamase inhibitors.

Wyeth-Ayerst Research
Structure-activity relationships of biphenyl tetrazoles as metallo-beta-lactamase inhibitors.

Merck Research Laboratories
3-mercapto-1,2,4-triazoles and N-acylated thiosemicarbazides as metallo-β-lactamase inhibitors.

The University of Queensland
Synthesis and kinetic testing of new inhibitors for a metallo-β-lactamase from Klebsiella pneumonia and Pseudomonas aeruginosa.

Helwan University
NOTA analogue: A first dithiocarbamate inhibitor of metallo-β-lactamases.

Zhengzhou University
Structure activity relationship studies on rhodanines and derived enethiol inhibitors of metallo-β-lactamases.

University of Oxford
Structure-activity relationship study and optimisation of 2-aminopyrrole-1-benzyl-4,5-diphenyl-1H-pyrrole-3-carbonitrile as a broad spectrum metallo-β-lactamase inhibitor.

The University of Queensland
Dipicolinic Acid Derivatives as Inhibitors of New Delhi Metallo-β-lactamase-1.

University of California San Diego
ACSS2 inhibitors and methods of use thereof

Epivario
Macrocyclic chlorine substituted indole derivatives

Bayer Aktiengesellschaft
Compounds targeting PRMT5

Aligos Therapeutics
JAK kinase inhibitor compounds for treatment of respiratory disease

Theravance Biopharma R&D Ip
Flavanone derivatives, and preparation method and use thereof

Xuanwu Hospital of Capital Medical University
Glutathione transferase from Plasmodium falciparum--interaction with malagashanine and selected plant natural products.

University of Zimbabwe
Tyrosinase inhibitory effect of benzoic acid derivatives and their structure-activity relationships.

Yonsei University
Aromatic heterocyclic derivative having TRPV4-inhibiting activity

Shionogi
Alicyclic[c] benzopyrone derivatives and uses thereof

Huazhong University of Science & Technology