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 …
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 …
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 …
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 …
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
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 …
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 …
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 …
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 …
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) …
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 …
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
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 …
explored. Three cancer cell lines, MCF-7, HepG2, and A548, as well as the normal Vero cell …