Synthesis and anticancer activity evaluation of naphthalene-substituted triazole spirodienones

L Luo, JJ Jia, Q Zhong, X Zhong, S Zheng… - European journal of …, 2021 - Elsevier
Building on our previous work that discovered 1, 2, 4-triazole–spirodienone as a promising
pharmacophore for anticancer activity, we have further diversified 1, 2, 4–triazole …

[HTML][HTML] Novel 4-thiophenyl-pyrazole, pyridine, and pyrimidine derivatives as potential antitumor candidates targeting both EGFR and VEGFR-2; design, synthesis …

SM Al-Muntaser, AA Al-Karmalawy, AM El-Naggar… - RSC …, 2023 - pubs.rsc.org
In this article, we continued our previous effort to develop new selective anticancer
candidates based on the basic pharmacophoric requirements of both EGFR and VEGFR-2 …

[HTML][HTML] Cell cycle arrest and apoptosis-inducing ability of benzimidazole derivatives: design, synthesis, docking, and biological evaluation

S Nazreen, ASA Almalki, SEI Elbehairi, AA Shati… - Molecules, 2022 - mdpi.com
In the current study, new benzimidazole-based 1, 3, 4-oxadiazole derivatives have been
synthesized and characterized by NMR, IR, MS, and elemental analysis. The final …

Synthesis and biological evaluation of novel tricyclic oxazine and oxazepine fused quinazolines. Part 2: Gefitinib analogs

M Sun, J Zhao, X Chen, Z Zong, J Han, Y Du… - Bioorganic & Medicinal …, 2016 - Elsevier
Two series of novel tricyclic oxazine and oxazepine fused quinazolines have been designed
and synthesized. The in vitro antitumor effect of the title compounds was screened on N87 …

Design, synthesis, and antiproliferative activity of new indole/1, 2, 4‐triazole/chalcone hybrids as EGFR and/or c‐MET inhibitors

E Mahmoud, D Abdelhamid, BGM Youssif… - Archiv der …, 2024 - Wiley Online Library
A novel group of indolyl‐1, 2, 4‐triazole‐chalcone hybrids was designed, synthesized, and
assessed for their anticancer activity. The synthesized compounds exhibited significant …

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 …

Ramachary-Bressy-Wang [3+ 2] cycloaddition reaction: Synthesis of fully decorated 1, 2, 3-triazoles as potent anticancer and EGFR inhibitors

M Kumar, SK Nukala, NS Thirukovela… - Journal of Molecular …, 2022 - Elsevier
A general strategy was developed for the synthesis of new fully decorated 1, 2, 3-triazoles
(5a-m & 6a-e) containing coumarine and sulfonyl-benzimidazole from 3-(2-((1-methyl-1H …

Design and synthesis of novel quinoline/chalcone/1, 2, 4-triazole hybrids as potent antiproliferative agent targeting EGFR and BRAFV600E kinases

AM Mohassab, HA Hassan, D Abdelhamid… - Bioorganic …, 2021 - Elsevier
New quinoline/chalcone hybrids containing 1, 2, 4-triazole moiety have been designed,
synthesized and their structures elucidated and confirmed by various spectroscopic …

New series of isoxazole derivatives targeting EGFR-TK: Synthesis, molecular modeling and antitumor evaluation

ET Warda, IA Shehata, MB El-Ashmawy… - Bioorganic & Medicinal …, 2020 - Elsevier
New series of isoxazole derivatives were synthesized and evaluated for in vitro antitumor
activity against HepG2, MCF-7 and HCT-116 cancer cells. Results showed that 4b and 25a …

Design, synthesis and anticervical cancer activity of new benzofuran–pyrazol-hydrazono-thiazolidin-4-one hybrids as potential EGFR inhibitors and apoptosis …

HAS Abbas, SS Abd El-Karim - Bioorganic chemistry, 2019 - Elsevier
This study represents the synthetic approaches of a new set of 2-(((3-(benzofuran-2-yl)-1-
phenyl-1H-pyrazol-4-yl) methylene) hydrazono)-5-(aryl) thiazolidin-4-one derivatives 4–22 …