A review on progression of epidermal growth factor receptor (EGFR) inhibitors as an efficient approach in cancer targeted therapy

A Ayati, S Moghimi, S Salarinejad, M Safavi… - Bioorganic …, 2020 - Elsevier
The identification of molecular agents inhibiting specific functions in cancer cells
progression is considered as one of the most successful plans in cancer treatment. The …

Molecular targets and anticancer activity of quinoline–chalcone hybrids: Literature review

MFA Mohamed, GEDA Abuo-Rahma - RSC advances, 2020 - pubs.rsc.org
α, β-Unsaturated chalcone moieties and quinoline scaffolds play an important role in
medicinal chemistry, especially in the identification and development of potential anticancer …

[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 …

Insights into fourth generation selective inhibitors of (C797S) EGFR mutation combating non-small cell lung cancer resistance: a critical review

MA Mansour, AM AboulMagd, SH Abbas… - RSC …, 2023 - pubs.rsc.org
Lung cancer is the second most common cause of morbidity and mortality among cancer
types worldwide, with non-small cell lung cancer (NSCLC) representing the majority of most …

Synthesis and biological evaluation of novel [1, 2, 3] triazolo-pyrrolo [1, 2-a] pyrido [4, 3-d] pyrimidines as EGFR targeting anticancer agents

SR Bandi, N Kavitha, SK Nukala… - Journal of Molecular …, 2023 - Elsevier
Herein, we synthesized some new fused [1, 2, 3] triazolo-pyrrolo [1, 2-a] pyrido [4, 3-d]
pyrimidines via click chemistry followed by carbon-carbon bond coupling as key approach …

Quinoline-based molecules targeting c-Met, EGF, and VEGF receptors and the proteins involved in related carcinogenic pathways

A Martorana, G La Monica, A Lauria - Molecules, 2020 - mdpi.com
The quinoline ring system has long been known as a versatile nucleus in the design and
synthesis of biologically active compounds. Currently, more than one hundred quinoline …

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 …

Recruitment of hexahydroquinoline as anticancer scaffold targeting inhibition of wild and mutants EGFR (EGFRWT, EGFRT790M, and EGFRL858R)

MG Abo Al-Hamd, HO Tawfik, O Abdullah… - Journal of Enzyme …, 2023 - Taylor & Francis
Hexahydroquinoline (HHQ) scaffold was constructed and recruited for development of new
series of anticancer agents. Thirty-two new compounds were synthesised where x-ray …

Quinoline: an attractive scaffold in drug design

LFE Moor, TRA Vasconcelos… - Mini Reviews in …, 2021 - ingentaconnect.com
Quinoline and its derivatives comprise an important group of heterocyclic compounds that
exhibits a wide range of pharmacological properties such as antibacterial, antiviral …

Discovery of novel thienoquinoline-2-carboxamide chalcone derivatives as antiproliferative EGFR tyrosine kinase inhibitors

MS Abdelbaset, M Abdel-Aziz, M Ramadan… - Bioorganic & Medicinal …, 2019 - Elsevier
Novel thienoquinoline carboxamide-chalcone derivatives were prepared via the cyclization
of acylated chalcones and 2-mercaptoquinoline-3-carbaldehyde in DMF with K 2 CO 3 …