Microwave-Assisted Synthesis of (Piperidin-1-yl) quinolin-3-yl) methylene) hydrazinecarbothioamides as Potent Inhibitors of Cholinesterases: A Biochemical and In …
Alzheimer's disease (AD), a progressive neurodegenerative disorder, characterized by
central cognitive dysfunction, memory loss, and intellectual decline poses a major public …
central cognitive dysfunction, memory loss, and intellectual decline poses a major public …
Iodine-imine synergistic promoted povarov-type multicomponent reaction for the synthesis of 2, 2′-biquinolines and their application to a copper/ligand catalytic …
QQ Hu, YT Gao, JC Sun, JJ Gao, HX Mu, YM Li… - Organic …, 2021 - ACS Publications
An efficient iodine-imine synergistic promoted Povarov-type multicomponent reaction was
reported for the synthesis of a practical 2, 2′-biquinoline scaffold. The tandem annulation …
reported for the synthesis of a practical 2, 2′-biquinoline scaffold. The tandem annulation …
[HTML][HTML] Synthesis and biological activity of novel 4-aminoquinoline/1, 2, 3-triazole hybrids against Leishmania amazonensis
N Glanzmann, LMR Antinarelli… - Biomedicine & …, 2021 - Elsevier
Abstract Quinoline and 1, 2, 3-triazoles are well-known nitrogen-based heterocycles
presenting diverse pharmacological properties, although their antileishmanial activity is still …
presenting diverse pharmacological properties, although their antileishmanial activity is still …
Synthesis, spectroscopic characterization, DFT, molecular docking and in vitro antibacterial potential of novel quinoline derivatives
Y Bouzian, Y Sert, K Khalid, L Van Meervelt… - Journal of Molecular …, 2021 - Elsevier
In this work, three new quinolone derivatives were prepared by alkylation of 2-oxo-1, 2-
dihydroquinoline-4-carboxylic acid with ethyl 2-bromoacetate. The synthesized compounds …
dihydroquinoline-4-carboxylic acid with ethyl 2-bromoacetate. The synthesized compounds …
[HTML][HTML] Green synthesis of 2-trifluoromethyl quinoline derivatives under metal-free conditions and their antifungal properties
L Fan, F He, L Shi, G Yang, Z Pan, M Wang… - Journal of Saudi …, 2023 - Elsevier
The skeleton of 2-trifluoromethyl quinoline is the core structure of many natural products and
pharmaceutical molecules. The synthesis of this scaffold is limited by metal catalysis, harsh …
pharmaceutical molecules. The synthesis of this scaffold is limited by metal catalysis, harsh …
Facile Synthesis of 2-Acylthieno[2,3-b]quinolines via Cu-TEMPO-Catalyzed Dehydrogenation, sp2-C–H Functionalization (Nucleophilic Thiolation by S8) of 2 …
C Teja, FR Nawaz Khan - Organic letters, 2020 - ACS Publications
An efficient, solvent-free synthesis of 2-acylthieno [2, 3-b] quinolines is reported from 2-halo-
quinolinyl ketones through Cu-TEMPO catalyzed dehydrogenation, sp2-C–H …
quinolinyl ketones through Cu-TEMPO catalyzed dehydrogenation, sp2-C–H …
Antitumor activities for two Pt (II) complexes of tropolone and 8-hydroxyquinoline derivative
X Mo, K Chen, Z Chen, B Chu, D Liu, Y Liang… - Inorganic …, 2021 - ACS Publications
The reactions of cis-Pt (DMSO) 2Cl2 and tropolone (HL) with 8-hydroxyquinoline (HQ) or 2-
methyl-8-hydroxyquinoline (HMQ) gave [Pt (Q)(L)](1) and [Pt (MQ)(L)](2), which present …
methyl-8-hydroxyquinoline (HMQ) gave [Pt (Q)(L)](1) and [Pt (MQ)(L)](2), which present …
New quinoline/1, 2, 4-triazole hybrids as dual inhibitors of COX-2/5-LOX and inflammatory cytokines: Design, synthesis, and docking study
A novel series of 19 quinoline/1, 2, 4-triazole hybrid 6a-i and 7a-j was synthesized and
evaluated in vitro as dual COX-2/5-LOX inhibitors. Compounds 6e, 6i, and 7e displayed the …
evaluated in vitro as dual COX-2/5-LOX inhibitors. Compounds 6e, 6i, and 7e displayed the …
Recent contributions of quinolines to antimalarial and anticancer drug discovery research
T Van de Walle, L Cools, S Mangelinckx… - European Journal of …, 2021 - Elsevier
Quinoline, a privileged scaffold in medicinal chemistry, has always been associated with a
multitude of biological activities. Especially in antimalarial and anticancer research …
multitude of biological activities. Especially in antimalarial and anticancer research …
Discovery of novel quinolin-2-one derivatives as potential GSK-3β inhibitors for treatment of Alzheimer's disease: Pharmacophore-based design, preliminary SAR, in …
Recently, glycogen synthase kinase-3β (GSK-3β) has been considered as a critical factor
implicated in Alzheimer's disease (AD). In a previous work, a 3D pharmacophore model for …
implicated in Alzheimer's disease (AD). In a previous work, a 3D pharmacophore model for …