Design, synthesis, anticancer activity and molecular docking of novel 1H-benzo [d] imidazole derivatives as potential EGFR inhibitors

CE Theodore, G Sivaiah, SBB Prasad… - Journal of Molecular …, 2023 - Elsevier
Here, we present the design, synthesis, and evaluation of a new series of 1H-benzo [d]
imidazole derivatives (10a–j) to determine their anticancer efficacy. The MCF-7 and HCT116 …

Synthesis and Biological Evaluation of Novel Carbohydrate‐Derived Derivatives of Erlotinib

W Yu, L Jiang, C Shen, P Zhang - Drug Development Research, 2016 - Wiley Online Library
Preclinical Research A series of novel carbohydrate‐derived Erlotinib derivatives were
prepared by the copper‐catalyzed cycloaddition reaction of erlotinib with various azido …

Synthesis and antiproliferative activity of 1 H-1, 2, 3-triazole-4 H-chromene-d-glucose hybrid compounds with dual inhibitory activity against EGFR/VEGFR-2 and …

DT Nguyen, SH Do, TH Le, TH Nguyen… - New Journal of …, 2022 - pubs.rsc.org
A series of 1H-1, 2, 3-triazole-4H-chromene-D-glucose hybrid compounds 7a-o was
synthesized via click chemistry using 2-amino-7-propargyloxy-4H-chromene-3-carbonitriles …

Design, synthesis and biological evaluation of a new series of thiazolyl-pyrazolines as dual EGFR and HER2 inhibitors

B Sever, MD Altıntop, MO Radwan, A Özdemir… - European journal of …, 2019 - Elsevier
Epidermal growth factor receptor (EGFR, also known as HER1) and HER2, prominent
members of receptor tyrosine kinase (RTK) superfamily, have been reported as diagnostic or …

Synthesis of Indole-1, 3, 4-Oxadiazole Based Sulfonyl 1, 2, 3-Triazoles as Potent Anticancer and EGFR Inhibitors

JMR Velidandla, SK Koppula - Russian Journal of Bioorganic Chemistry, 2023 - Springer
Herein, we synthesized some new indole-1, 3, 4-oxadiazole based sulfonyl 1, 2, 3-triazoles
via a click chemistry approach and then characterized their structures by NMR, mass, and …

Synthesis, anticancer activity and molecular modeling studies of 1, 2, 4-triazole derivatives as EGFR inhibitors

HAM El-Sherief, BGM Youssif, SNA Bukhari… - European journal of …, 2018 - Elsevier
A series of novel compounds carrying 1, 2, 4-triazole scaffold were prepared and evaluated
for their antiproliferative activities against NCI 60 cell line. Compounds 10 (a, c), 11 (ad), and …

Design, synthesis and biological evaluation of thiazolidinone derivatives as potential EGFR and HER-2 kinase inhibitors

PC Lv, CF Zhou, J Chen, PG Liu, KR Wang… - Bioorganic & medicinal …, 2010 - Elsevier
Two series of thiazolidinone derivatives designing for potential EGFR and HER-2 kinase
inhibitors have been discovered. Some of them exhibited significant EGFR and HER-2 …

New pyrimidine and pyrazole-based compounds as potential EGFR inhibitors: Synthesis, anticancer, antimicrobial evaluation and computational studies

IMM Othman, ZM Alamshany, NY Tashkandi… - Bioorganic …, 2021 - Elsevier
This study was focused on the synthesis of new pyrimidines 4a, b, 5a, b and pyrazoles 6a, b
as ATP mimicking tyrosine kinase inhibitors of the epidermal growth factor receptor (EGFR) …

Anti-Proliferative, Anti-EGFR and In Silico Studies of a Series of New Imidazole Tethered 1, 2, 4-Oxadiazoles

S Lavunuri, RV Nadh, SK Rapeti - Polycyclic Aromatic Compounds, 2024 - Taylor & Francis
Herein, we prepared some new imidazole-1, 2, 4-oxadiazole hybrids (6a–6o) and
investigated their antiproliferative potential on three human cancer cell lines (HepG2, A549 …

Design, synthesis, anticancer activity and docking studies of novel quinazoline-based thiazole derivatives as EGFR kinase inhibitors

MS Raghu, HA Swarup, T Shamala, BS Prathibha… - Heliyon, 2023 - cell.com
The in vitro anticancer efficacy of a new series of quinazoline-based thiazole derivatives was
explored. Three cancer cell lines, MCF-7, HepG2, and A548, as well as the normal Vero cell …