| Title: |
Design, Synthesis, Antiproliferative Potency and In Silico Studies of Novel Alkynyl Quinazolines as Potential EGFR Inhibitors |
| Authors: |
Apostolia Gkoutzivelaki; Sotiria-Iro Triantopoulou; Lykourgos Chiniadis; Alexandros Komiotis; Charalampos Triantis; Dimitri Komiotis; Athanasios Papakyriakou; Harris Pratsinis; Stella Manta |
| Source: |
International Journal of Molecular Sciences ; Volume 27 ; Issue 4 ; Pages: 1738 |
| Publisher Information: |
Multidisciplinary Digital Publishing Institute |
| Publication Year: |
2026 |
| Collection: |
MDPI Open Access Publishing |
| Subject Terms: |
Sonogashira reaction; alkynyl quinazolines; docking studies; EGFR inhibitors; cell cycle |
| Description: |
The epidermal growth factor receptor (EGFR) is a highly attractive and promising target for novel anticancer agents, particularly for non-small-cell lung cancer (NSCLC), due to its crucial role in regulating cell survival and proliferation. Despite the development of first-generation reversible inhibitors like Gefitinib and Erlotinib, acquired resistance necessitated the discovery of highly potent irreversible inhibitors effective against drug-resistant mutants. Molecular docking calculations utilizing both EGFR conformations identified five top-ranked compounds (QN012, QN017, QN019, QN022, and QN023) proposed for synthesis and biological evaluation. These in silico studies predicted high inhibitory activity against the active and inactive state of EGFR. Herein, we report the design, synthesis and biological evaluation of novel 4-anilino quinazoline derivatives, bearing various alkynyl substituents at position 6, expected to bind to the hinge Met793 residue of EGFR. The effects of the derivatives on various cancer cell lines in terms of cytotoxic/cytostatic activity, interference with cell cycle phase distribution, and suppression of EGFR phosphorylation set the basis for the design of more potent derivatives. |
| Document Type: |
text |
| File Description: |
application/pdf |
| Language: |
English |
| Relation: |
Biochemistry; https://dx.doi.org/10.3390/ijms27041738 |
| DOI: |
10.3390/ijms27041738 |
| Availability: |
https://doi.org/10.3390/ijms27041738 |
| Rights: |
https://creativecommons.org/licenses/by/4.0/ |
| Accession Number: |
edsbas.EA073B8 |
| Database: |
BASE |