Fluoroquinolones hybrid molecules as promising antibacterial agents in the fight against antibacterial resistance

IA Lungu, OL Moldovan, V Biriș, A Rusu - Pharmaceutics, 2022 - mdpi.com
The emergence of bacterial resistance has motivated researchers to discover new
antibacterial agents. Nowadays, fluoroquinolones keep their status as one of the essential …

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 …

1, 2, 3-Triazole-containing hybrids with potential antibacterial activity against ESKAPE pathogens

C Deng, H Yan, J Wang, K Liu, B Liu, Y Shi - European Journal of …, 2022 - Elsevier
ESKAPE pathogens, as priority 1 and 2 pathogens, are prevalent infectious agents
associated with high morbidity and mortality. ESKAPE can cause broad-spectrum diseases …

Discovery of indolylacryloyl-derived oxacins as novel potential broad-spectrum antibacterial candidates

YG Hu, N Battini, B Fang, CH Zhou - European Journal of Medicinal …, 2024 - Elsevier
The emergence of serious bacterial resistance towards clinical oxacins poses a
considerable threat to global public health, necessitating the development of novel structural …

Synthesis of new imidazole-triazole-glycoside hybrids as anti-breast cancer candidates

WI El-Sofany, WA El-sayed, AA Abd-Rabou… - Journal of Molecular …, 2022 - Elsevier
One of the leading causes of death worldwide among women is breast cancer. Thus,
discovering new multi-target anti-breast cancer drugs is mandatory to stimulate nitric oxide …

Synthesis and biological evaluation of ciprofloxacin–1, 2, 3-triazole hybrids as antitumor, antibacterial, and antioxidant agents

S Al-Taweel, Y Al-Saraireh, S Al-Trawneh… - Heliyon, 2023 - cell.com
Abstract Six novel ciprofloxacin-1, 2, 3-triazole hybrids (6a-f) were synthesized via click
reaction, by reacting of methyl 1-cyclopropyl-6-fluoro-4-oxo-7-(4-(3-oxobutanoyl) piperazin-1 …

Hybrid azine derivatives: a useful approach for antimicrobial therapy

D Amariucai-Mantu, V Mangalagiu, I Bejan, A Aricu… - Pharmaceutics, 2022 - mdpi.com
Nowadays, infectious diseases caused by microorganisms are a major threat to human
health, mostly because of drug resistance, multi-drug resistance and extensive-drug …

A Comprehensive Review on Chemical Synthesis and Chemotherapeutic Potential of 3-Heteroaryl Fluoroquinolone Hybrids

H Hryhoriv, SM Kovalenko, M Georgiyants, L Sidorenko… - Antibiotics, 2023 - mdpi.com
Fluoroquinolones have been studied for more than half a century. Since the 1960s, four
generations of these synthetic antibiotics have been created and successfully introduced …

Design, synthesis, and Anticancer and Antibacterial activities of Quinoline-5-Sulfonamides

A Zieba, D Pindjakova, M Latocha… - …, 2024 - pmc.ncbi.nlm.nih.gov
A series of new unique acetylene derivatives of 8-hydroxy-and 8-methoxyquinoline-5-
sulfonamide 3a–f and 6a–f were prepared by reactions of 8-hydroxy-and 8 …

Cyanomethylquinolones as a New Class of Potential Multitargeting Broad-Spectrum Antibacterial Agents

YM Tan, J Zhang, YJ Wei, YG Hu, SR Li… - Journal of Medicinal …, 2024 - ACS Publications
This work identified a class of cyanomethylquinolones (CQs) and their carboxyl analogues
as potential multitargeting antibacterial candidates. Most of the prepared compounds …