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Chelation-Mediated Palladium(II)-Catalyzed Domino Heck−Mizoroki/Suzuki−Miyaura Reactions Using Arylboronic Acids: Increasing Scope and Mechanistic Understanding

Journal of organic chemistry, 2011-04, Vol.76 (8), p.2433-2438

2011

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Multitarget Therapeutic Strategies for Alzheimer’s Disease: Review on Emerging Target Combinations

BioMed research international, 2020, Vol.2020 (2020), p.1-27

2020

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Identification of Xanthones as Selective Killers of Cancer Cells Overexpressing the ABC Transporter MRP1

ChemMedChem, 2011-08, Vol.6 (8), p.1478-1484

2011

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Hydrogeochemical and isotopic assessment for characterizing groundwater quality in the Mitidja plain (northern Algeria)

Environmental science and pollution research international, 2023-07, Vol.30 (33), p.80029-80054

2023

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Multitarget Therapeutics for Neurodegenerative Diseases

BioMed research international, 2020, Vol.2020, p.6532827-2

2020

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Dual inhibitors of Pseudomonas aeruginosa virulence factors LecA and LasB

Chemical science (Cambridge), 2024-08, Vol.15 (33), p.13333-13342

2024

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Minimally Invasive Mutagenesis Gives Rise to a Biosynthetic Polyketide Library

Angewandte Chemie (International ed.), 2012-10, Vol.51 (42), p.10664-10669

International ed. in English, 2012

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Substrate‐Inspired Fragment Merging and Growing Affords Efficacious LasB Inhibitors

Angewandte Chemie International Edition, 2022-01, Vol.61 (5), p.e202112295-n/a

International ed. in English, 2022

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N‑Aryl-3-mercaptosuccinimides as Antivirulence Agents Targeting Pseudomonas aeruginosa Elastase and Clostridium Collagenases

Journal of medicinal chemistry, 2020-08, Vol.63 (15), p.8359-8368

2020

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N -Aryl Mercaptopropionamides as Broad-Spectrum Inhibitors of Metallo-β-Lactamases

Journal of medicinal chemistry, 2022-03, Vol.65 (5), p.3913-3922

2022

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Discovery of a Potent Inhibitor Class with High Selectivity toward Clostridial Collagenases

Journal of the American Chemical Society, 2017-09, Vol.139 (36), p.12696-12703

2017

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Tackling Pseudomonas aeruginosa Virulence by a Hydroxamic Acid-Based LasB Inhibitor

ACS chemical biology, 2018-09, Vol.13 (9), p.2449-2455

2018

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Trisubstituted Imidazoles as Mycobacterium tuberculosis Glutamine Synthetase Inhibitors

Journal of medicinal chemistry, 2012-03, Vol.55 (6), p.2894-2898

2012

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High affinity rigidified AT2 receptor ligands with indane scaffolds

MedChemComm, 2019-12, Vol.10 (12), p.2146-2160

2019

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High affinity rigidified AT 2 receptor ligands with indane scaffolds

MedChemComm, 2019-12, Vol.10 (12), p.2146-2160

2019

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High affinity rigidified AT2 receptor ligands with indane scaffolds† †Electronic supplementary information (ESI) available: Chiral GC-MS chromatograms of compound 15 and 16, HPLC purity of the test compounds and computational details. See DOI: 10.1039/c9md00402e

MedChemComm, 2019-11, Vol.10 (12), p.2146-2160

2019

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N -Aryl mercaptoacetamides as potential multi-target inhibitors of metallo-β-lactamases (MBLs) and the virulence factor LasB from Pseudomonas aeruginosa

RSC medicinal chemistry, 2021-10, Vol.12 (10), p.1698-1708

2021

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Disruption of Fibers from the Tau Model AcPHF6 by Naturally Occurring Aurones and Synthetic Analogues

ACS chemical neuroscience, 2016-07, Vol.7 (7), p.995-1003

2016

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Binding Mode Characterization and Early in Vivo Evaluation of Fragment-Like Thiols as Inhibitors of the Virulence Factor LasB from Pseudomonas aeruginosa

ACS infectious diseases, 2018-06, Vol.4 (6), p.988-997

2018

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High affinity rigidified AT(2) receptor ligands with indane scaffolds

MedChemComm, 2019, Vol.10 (12), p.2146

2019

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Aryl mercaptoacetamides as potential multi-target inhibitors of metallo-β-lactamases (MBLs) and the virulence factor LasB from

RSC medicinal chemistry, 2021-10, Vol.12 (1), p.1698-178

2021

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DXR Inhibition by Potent Mono- and Disubstituted Fosmidomycin Analogues

Journal of medicinal chemistry, 2013-08, Vol.56 (15), p.6190-6199

2013

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Substratinspirierte Fragment‐Fusion und ‐Erweiterung führt zu wirksamen LasB‐Inhibitoren

Angewandte Chemie, 2022-01, Vol.134 (5), p.n/a

2022

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Chelation-Mediated Palladium(II)-Catalyzed Domino Heck−Mizoroki/Suzuki−Miyaura Reactions Using Arylboronic Acids: Increasing Scope and Mechanistic Understanding

A New PqsR Inverse Agonist Potentiates Tobramycin Efficacy to Eradicate Pseudomonas aeruginosa Biofilms

Multitarget Therapeutic Strategies for Alzheimer’s Disease: Review on Emerging Target Combinations

Identification of Xanthones as Selective Killers of Cancer Cells Overexpressing the ABC Transporter MRP1

Hydrogeochemical and isotopic assessment for characterizing groundwater quality in the Mitidja plain (northern Algeria)

Multitarget Therapeutics for Neurodegenerative Diseases

Dual inhibitors of Pseudomonas aeruginosa virulence factors LecA and LasB

Minimally Invasive Mutagenesis Gives Rise to a Biosynthetic Polyketide Library

Substrate‐Inspired Fragment Merging and Growing Affords Efficacious LasB Inhibitors

Novel Multitarget-Directed Ligands (MTDLs) with Acetylcholinesterase (AChE) Inhibitory and Serotonergic Subtype 4 Receptor (5-HT4R) Agonist Activities As Potential Agents against Alzheimer’s Disease: The Design of Donecopride

N‑Aryl-3-mercaptosuccinimides as Antivirulence Agents Targeting Pseudomonas aeruginosa Elastase and Clostridium Collagenases

N -Aryl Mercaptopropionamides as Broad-Spectrum Inhibitors of Metallo-β-Lactamases

Discovery of a Potent Inhibitor Class with High Selectivity toward Clostridial Collagenases

Tackling Pseudomonas aeruginosa Virulence by a Hydroxamic Acid-Based LasB Inhibitor

Trisubstituted Imidazoles as Mycobacterium tuberculosis Glutamine Synthetase Inhibitors

High affinity rigidified AT2 receptor ligands with indane scaffolds

High affinity rigidified AT 2 receptor ligands with indane scaffolds

High affinity rigidified AT2 receptor ligands with indane scaffolds† †Electronic supplementary information (ESI) available: Chiral GC-MS chromatograms of compound 15 and 16, HPLC purity of the test compounds and computational details. See DOI: 10.1039/c9md00402e

N -Aryl mercaptoacetamides as potential multi-target inhibitors of metallo-β-lactamases (MBLs) and the virulence factor LasB from Pseudomonas aeruginosa

Disruption of Fibers from the Tau Model AcPHF6 by Naturally Occurring Aurones and Synthetic Analogues

Binding Mode Characterization and Early in Vivo Evaluation of Fragment-Like Thiols as Inhibitors of the Virulence Factor LasB from Pseudomonas aeruginosa

High affinity rigidified AT(2) receptor ligands with indane scaffolds

Aryl mercaptoacetamides as potential multi-target inhibitors of metallo-β-lactamases (MBLs) and the virulence factor LasB from

DXR Inhibition by Potent Mono- and Disubstituted Fosmidomycin Analogues

Substratinspirierte Fragment‐Fusion und ‐Erweiterung führt zu wirksamen LasB‐Inhibitoren

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