Anticancer therapeutic potential of benzofuran scaffolds

AA Abbas, KM Dawood - RSC advances, 2023 - pubs.rsc.org
Benzofuran moiety is the main component of many biologically active natural and synthetic
heterocycles. These heterocycles have unique therapeutic potentials and are involved in …

Exploration of novel VEGFR2 tyrosine kinase inhibitors via design and synthesis of new alkylated indolyl-triazole Schiff bases for targeting breast cancer

MS Nafie, ATA Boraei - Bioorganic Chemistry, 2022 - Elsevier
Abstract According to the World Health Organization (WHO) statistics: In 2020, there were
2.3 million women diagnosed with breast cancer and 685,000 deaths globally. Therefore …

Current scenario of 1, 3-oxazole derivatives for anticancer activity

X Yan, J Wen, L Zhou, L Fan… - Current Topics in …, 2020 - ingentaconnect.com
Cancer, which has been cursed for human beings for long time is considered as one of the
leading causes of morbidity and mortality across the world. In spite of different types of …

Discovery of novel pyrazolo [3, 4-b] pyridine scaffold-based derivatives as potential PIM-1 kinase inhibitors in breast cancer MCF-7 cells

MS Nafie, AM Amer, AK Mohamed… - Bioorganic & Medicinal …, 2020 - Elsevier
Pim-1 kinase targeted recently has proved an essential goal of breast cancer therapy. We
report the design, synthesis with full characterization analysis of pyrazolo [3, 4-b] pyridine …

Synthesis and molecular docking of some novel 3-thiazolyl-coumarins as inhibitors of VEGFR-2 kinase

TZ Abolibda, M Fathalla, B Farag, MEA Zaki… - Molecules, 2023 - mdpi.com
One crucial strategy for the treatment of breast cancer involves focusing on the Vascular
Endothelial Growth Factor Receptor (VEGFR-2) signaling system. Consequently, the …

[HTML][HTML] Green synthesis and molecular docking study of some new thiazoles using terephthalohydrazide chitosan hydrogel as ecofriendly biopolymeric catalyst

JY Al-Humaidi, SM Gomha, NAA El-Ghany, B Farag… - Catalysts, 2023 - mdpi.com
Terephthalohydrazide chitosan hydrogel (TCs) was prepared and investigated as an
ecofriendly biopolymeric catalyst for synthesis of some novel thiazole and thiadiazole …

Synthesis of new substituted pyridine derivatives as potent anti-liver cancer agents through apoptosis induction: In vitro, in vivo, and in silico integrated approaches

ATA Boraei, EH Eltamany, IAI Ali, SM Gebriel… - Bioorganic …, 2021 - Elsevier
Liver cancer is the most common type of cancer in many countries. New studies and
statistics show rising liver cancer worldwide, so it is essential to seek new agents for this …

Discovery of New Apoptosis-Inducing Agents for Breast Cancer Based on Ethyl 2-Amino-4,5,6,7-Tetra Hydrobenzo[b]Thiophene-3-Carboxylate: Synthesis, In Vitro …

EM Gad, MS Nafie, EH Eltamany, MSAG Hammad… - Molecules, 2020 - mdpi.com
A multicomponent synthesis was empolyed for the synthesis of ethyl 2-amino-4, 5, 6, 7-
tetrahydrobenzo [b] thiophene-3-carboxylate 1. An interesting cyclization was obtained …

Synthesis, characterization of some pyrazine derivatives as anti-cancer agents: In vitro and in Silico approaches

ES Tantawy, AM Amer, EK Mohamed… - Journal of Molecular …, 2020 - Elsevier
In continuation of our interest on the synthesis of fused quinoxalines and pyrazines
derivatives and due to the resultant pharmacological interest in compounds which belong to …

Molecular docking, anti-proliferative activity and induction of apoptosis in human liver cancer cells treated with androstane derivatives: Implication of PI3K/AKT/mTOR …

SW Kattan, MS Nafie, GA Elmgeed, W Alelwani… - The Journal of Steroid …, 2020 - Elsevier
Worldwide, cancer is still an area with high unmet medical need. Lead optimization efforts
towards structure-based drug design were employed to discover newly synthesized hetero …