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 …

[HTML][HTML] Review on recent development of quinoline for anticancer activities

M Ilakiyalakshmi, AA Napoleon - Arabian Journal of Chemistry, 2022 - Elsevier
Quinoline is an efficient scaffold for anticancer drug development as its derivatives have
shown potent results through several mechanisms like growth regulators through “apoptosis …

Recent advances in the development of pyrazole derivatives as anticancer agents

Y Zhang, C Wu, N Zhang, R Fan, Y Ye, J Xu - International Journal of …, 2023 - mdpi.com
Pyrazole derivatives, as a class of heterocyclic compounds, possess unique chemical
structures that confer them with a broad spectrum of pharmacological activities. They have …

Chemodynamic therapy agents Cu (II) complexes of quinoline derivatives induced ER stress and mitochondria-mediated apoptosis in SK-OV-3 cells

WY Shen, CP Jia, AN Mo, H Liang, ZF Chen - European Journal of …, 2021 - Elsevier
Three Cu (II) complexes of quinoline derivatives as cancer chemodynamic therapy agents
were synthesized and characterized. These complexes were heavily taken up by cells and …

Design, synthesis and biological evaluation of novel benzo-and tetrahydrobenzo-[h] quinoline derivatives as potential DNA-intercalating antitumor agents

F Jafari, H Baghayi, P Lavaee, F Hadizadeh… - European journal of …, 2019 - Elsevier
A new series of benzo-and tetrahydro benzo-[h] quinoline bearing a flexible (dimethylamino)
ethylcarboxamide side chain was designed and synthesized as DNA-intercalating antitumor …

[HTML][HTML] Synthesis and evaluation of novel N1-acylated 5-(4-pyridinyl) indazole derivatives as potent and selective haspin inhibitors

MM Shawky, M Abdallah, H Khalifa, Y Aboushady… - Bioorganic …, 2024 - Elsevier
Protein kinase dysregulation was strongly linked to cancer pathogenesis. Moreover, histone
alterations were found to be among of the most important post-translational modifications …

Novel anthraquinone compounds inhibit colon cancer cell proliferation via the reactive oxygen species/JNK pathway

Y Li, F Guo, Y Guan, T Chen, K Ma, L Zhang, Z Wang… - Molecules, 2020 - mdpi.com
A series of amide anthraquinone derivatives, an important component of some traditional
Chinese medicines, were structurally modified and the resulting antitumor activities were …

Induction of Paraptotic Cell Death in Breast Cancer Cells by a Novel Pyrazolo[3,4-h]quinoline Derivative through ROS Production and Endoplasmic Reticulum Stress

PL Nguyen, CH Lee, H Lee, J Cho - Antioxidants, 2022 - mdpi.com
Chemotherapy has been a standard intervention for a variety of cancers to impede tumor
growth, mainly by inducing apoptosis. However, development of resistance to this regimen …

[HTML][HTML] Roles and regulation of Haspin kinase and its impact on carcinogenesis

R Quadri, S Sertic, M Muzi-Falconi - Cellular signalling, 2022 - Elsevier
Cancer therapy is based on the selective clearance of malignant cells without severely
damaging healthy tissues, and current clinical practice is constantly in need for new …

Potently inhibiting cancer cell migration with novel 3H-pyrazolo [4, 3-f] quinoline boronic acid ROCK inhibitors

N Dayal, CG Mikek, D Hernandez, GA Naclerio… - European journal of …, 2019 - Elsevier
Rho-associated protein kinases (ROCKs) are ubiquitously expressed in most adult tissues,
and are involved in modulating the cytoskeleton, protein synthesis and degradation …