Biological activity of oxadiazole and thiadiazole derivatives

UA Atmaram, SM Roopan - Applied Microbiology and Biotechnology, 2022 - Springer
The 5-membered oxadiazole and thiadiazole scaffolds are the most privileged and well-
known heterocycles, being a common and essential feature of a variety of natural products …

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 …

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 …

Topoisomerase II inhibitors design: Early studies and new perspectives

HK Swedan, AE Kassab, EM Gedawy, SE Elmeligie - Bioorganic Chemistry, 2023 - Elsevier
The DNA topoisomerase enzymes are widely distributed throughout all spheres of life and
are necessary for cell function. Numerous antibacterial and cancer chemotherapeutic drugs …

Design, synthesis, and anticancer activity of novel 4-thiazolidinone-phenylaminopyrimidine hybrids

A Türe, M Ergül, M Ergül, A Altun, İ Küçükgüzel - Molecular Diversity, 2021 - Springer
Thiazolidinones and phenylaminopyrimidines are known as anticancer agents. Imatinib is
the pioneer phenylaminopyrimidine derivative kinase inhibitor, which is used for the …

Insights on fluoroquinolones in cancer therapy: Chemistry and recent developments

PC Sharma, R Goyal, A Sharma, D Sharma… - Materials Today …, 2020 - Elsevier
Cancer is a very risky life-threatening disease having most formidable afflictions in the world.
Several anticancer agents are commercially accessible, however, the emergence of …

Modification of 7-piperazinylquinolone antibacterials to promising anticancer lead compounds: Synthesis and in vitro studies

H Ahadi, S Emami - European Journal of Medicinal Chemistry, 2020 - Elsevier
Amongst the fluoroquinolone antibacterials, the 7-piperazinyl containing chemotypes such
as norfloxacin, enoxacin, ciprofloxacin, pefloxacin, lomefloxacin, enrofloxacin, ofloxacin …

The search for new antibacterial agents among 1, 2, 3-triazole functionalized ciprofloxacin and Norfloxacin hybrids: synthesis, docking studies, and biological activity …

H Hryhoriv, I Mariutsa, SM Kovalenko… - Scientia …, 2021 - mdpi.com
Among all modern antibiotics, fluoroquinolones are well known for their broad spectrums of
activity and efficiency toward microorganisms and viruses. However, antibiotic resistance is …

Novel fluoroquinolones containing 2‐arylamino‐2‐oxoethyl fragment: Design, synthesis, evaluation of antibacterial and antituberculosis activities and molecular …

N Kulabaş, A Türe, A Bozdeveci… - Journal of …, 2022 - Wiley Online Library
Novel substituted fluoroquinolone derivatives, compounds 6–20 were designed,
synthesized, and evaluated for antituberculosis and antibacterial activity. Antibacterial …

Thiadiazole and thiazole derivatives as potential antimicrobial agents

Ц Khamitova, D Berillo, A Lozynskyi… - Mini Reviews in …, 2024 - benthamdirect.com
Background: This review summarizes data on heterocyclic systems with thiadiazole and
thiazole fragments in molecules as promising antimicrobial agents. Introduction: Thiadiazole …