Current scenario of quinolone hybrids with potential antibacterial activity against ESKAPE pathogens
J Gao, H Hou, F Gao - European Journal of Medicinal Chemistry, 2023 - Elsevier
Abstract The ESKAPE (Escherichia coli/E. coli, Staphylococcus aureus/S. aureus, Klebsiella
pneumonia/K. pneumoniae, Acinetobacter Baumannii/A. baumannii, Pseudomonas …
pneumonia/K. pneumoniae, Acinetobacter Baumannii/A. baumannii, Pseudomonas …
The antibacterial activity of fluoroquinolone derivatives: An update (2018–2021)
Y Jia, L Zhao - European journal of medicinal chemistry, 2021 - Elsevier
Bacterial infection is amongst the most common diseases in community and hospital
settings. Fluoroquinolones, exerting the antibacterial activity through binding to type II …
settings. Fluoroquinolones, exerting the antibacterial activity through binding to type II …
DNA Gyrase as a Target for Quinolones
AC Spencer, SS Panda - Biomedicines, 2023 - mdpi.com
Bacterial DNA gyrase is a type II topoisomerase that can introduce negative supercoils to
DNA substrates and is a clinically-relevant target for the development of new antibacterials …
DNA substrates and is a clinically-relevant target for the development of new antibacterials …
Antimicrobial activity of lactones
M Mazur, D Masłowiec - Antibiotics, 2022 - mdpi.com
The development of bacterial resistance to antibiotics and the consequent lack of effective
therapy is one of the biggest problems in modern medicine. A consequence of these …
therapy is one of the biggest problems in modern medicine. A consequence of these …
Recent insight into the biological activities and SAR of quinolone derivatives as multifunctional scaffold
Quinolones are a type of bicyclic privileged building block with immense therapeutic
potential. They are known for their crucial role in modulating numerous diseases conditions …
potential. They are known for their crucial role in modulating numerous diseases conditions …
Synthetic and Semisynthetic Compounds as Antibacterials Targeting Virulence Traits in Resistant Strains: A Narrative Updated Review
This narrative review paper provides an up-to-date overview of the potential of novel
synthetic and semisynthetic compounds as antibacterials that target virulence traits in …
synthetic and semisynthetic compounds as antibacterials that target virulence traits in …
Advanced methods for studying structure and interactions of macrolide antibiotics
T Jednačak, I Mikulandra, P Novak - International journal of molecular …, 2020 - mdpi.com
Macrolide antibiotics are macrocyclic compounds that are clinically used and prescribed for
the treatment of upper and lower respiratory tract infections. They inhibit the synthesis of …
the treatment of upper and lower respiratory tract infections. They inhibit the synthesis of …
Current insights and molecular docking studies of the drugs under clinical trial as RdRp inhibitors in COVID-19 treatment
I Pauly, A Kumar Singh, A Kumar… - Current …, 2022 - ingentaconnect.com
Study Background & Objective: After the influenza pandemic (1918), COVID-19 was
declared a Vth pandemic by the WHO in 2020. SARS-CoV-2 is an RNA-enveloped single …
declared a Vth pandemic by the WHO in 2020. SARS-CoV-2 is an RNA-enveloped single …
Organophotoredox-Catalyzed Reductive Tetrafluoroalkylation of Alkenes
VS Kostromitin, VV Levin… - The Journal of Organic …, 2022 - ACS Publications
A method for the hydroperfluoroalkylation of alkenes with 1, 2-dibromotetrafluoroethane
leading to tetrafluorinated bromides is described. The reaction is conveniently performed …
leading to tetrafluorinated bromides is described. The reaction is conveniently performed …
Enamines and Dimethylamino Imines as Building Blocks in Heterocyclic Synthesis: Reactions of DMF‐DMA Reagent with Different Functional Groups
N, N‐Dimethylformamide dimethyl acetal (DMF‐DMA) reagent can react with different
functional groups of organic compounds. Enamines and dimethylamino imines are obtained …
functional groups of organic compounds. Enamines and dimethylamino imines are obtained …