Quinolines, a perpetual, multipurpose scaffold in medicinal chemistry

P Yadav, K Shah - Bioorganic Chemistry, 2021 - Elsevier
Quinoline is a versatile pharmacophore, a privileged scaffold and an outstanding fused
heterocyclic compound with a wide range of pharmacological prospective such as …

Quinolone hybrids and their anti-cancer activities: An overview

F Gao, X Zhang, T Wang, J **ao - European journal of medicinal chemistry, 2019 - Elsevier
The global pandemic of drug-sensitive cancers and the increasing threat from drug-resistant
cancers make an urgent need to develop more effective anti-cancer candidates. Quinolone …

Studies on the interactions of theaflavin-3, 3′-digallate with bovine serum albumin: Multi-spectroscopic analysis and molecular docking

X Yu, X Cai, S Li, L Luo, J Wang, M Wang, L Zeng - Food Chemistry, 2022 - Elsevier
Tea cream, produced by interactions among tea ingredients, is undesirable in tea beverage
industry. The interaction between bovine serum albumin (BSA) and theaflavin-3, 3 …

[HTML][HTML] Imidazole-pyridine hybrids as potent anti-cancer agents

B Aruchamy, C Drago, V Russo, GM Pitari… - European Journal of …, 2023 - Elsevier
In the current investigation, fifteen novel imidazole-pyridine-based molecules were
synthesized and tested against cell lines of the lung (H1299) and colon (HCT116) …

Cytotoxic properties of 1, 3, 4-thiadiazole derivatives—A review

S Janowska, A Paneth, M Wujec - Molecules, 2020 - mdpi.com
During recent years, small molecules containing five-member heterocyclic moieties have
become the subject of considerable growing interest for designing new antitumor agents …

Thiadiazole derivatives as anticancer agents

M Szeliga - Pharmacological Reports, 2020 - Springer
In spite of substantial progress made toward understanding cancer pathogenesis, this
disease remains one of the leading causes of mortality. Thus, there is an urgent need to …

Development of adamantane scaffold containing 1, 3, 4-thiadiazole derivatives: Design, synthesis, anti-proliferative activity and molecular docking study targeting …

MMS Wassel, YA Ammar, GAME Ali, A Belal… - Bioorganic …, 2021 - Elsevier
Abstract A new series of 1, 3, 4-thiadiazolo-adamantane derivatives were synthesized
through molecular hybridization approach, then used as starting material to synthesize …

Azoimine quinoline derivatives: Synthesis, classical and electrochemical evaluation of antioxidant, anti-inflammatory, antimicrobial activities and the DNA/BSA binding

K Douadi, S Chafaa, T Douadi, M Al-Noaimi… - Journal of Molecular …, 2020 - Elsevier
Four azoimine quinoline derivatives namely (1Z)-N'-(4-fluorophenyl)-2-oxo-N-quinolin-8-
ylpropanehydrazonamide (H 2 LF),(1Z)-2-oxo-N′-phenyl-N-quinolin-8-ylpropane …

Synthesis and antibacterial medicinal evaluation of carbothioamido hydrazonyl thiazolylquinolone with multitargeting antimicrobial potential to combat increasingly …

ZL Zang, YX Wang, N Battini, WW Gao… - European Journal of …, 2024 - Elsevier
The global microbial resistance is a serious threat to human health, and multitargeting
compounds are considered to be promising to combat microbial resistance. In this work, a …

Design, synthesis, in-silico and biological evaluation of novel 2-Amino-1, 3, 4-thiadiazole based hydrides as B-cell lymphoma-2 inhibitors with potential anticancer …

SA Ibrahim, MM Salem, HA Abd Elsalam… - Journal of Molecular …, 2022 - Elsevier
Abstract In the current study, 5-(pyridin-2-yl)-1, 3, 4-thiadiazol-2-amine (1) was synthesized
via one step reaction of picolinic acid with thiosemicarbazide in the presence of POCl 3 …