Novel 1, 3-thiazole analogues with potent activity against breast cancer: A design, synthesis, in vitro, and in silico study

MG Salem, DMA El-Maaty, YIM El-Deen, BH Elesawy… - Molecules, 2022 - mdpi.com
Breast cancer is the most common cancer in women, responsible for over half a million
deaths in 2020. Almost 75% of FDA-approved drugs are mainly nitrogen-and sulfur …

Design, synthesis and mechanistic study of new 1, 2, 4-triazole derivatives as antimicrobial agents

NH Amin, MT El-Saadi, AA Ibrahim… - Bioorganic …, 2021 - Elsevier
Abstract Novel 5-amino-1, 2, 4-triazole derivatives and their cyclized 1, 2, 4-triazolo [1, 5-a]
pyrimidine analogues were designed, synthesized and evaluated for their antimicrobial …

The anticancer therapeutic potential of pyrimidine–sulfonamide hybrids

P Zhang, C Shi, T Dong, J Song… - Future Medicinal Chemistry, 2024 - Taylor & Francis
Cancer as a devastating malignancy, seriously threatens human life and health, but most
chemotherapeutics have long been criticized for unsatisfactory therapeutic efficacy due to …

[HTML][HTML] Design, synthesis and docking studies of new hydrazinyl-thiazole derivatives as anticancer and antimicrobial agents

AM El-Naggar, A Zidan, EB Elkaeed… - Journal of Saudi …, 2022 - Elsevier
Increase in the number of infections caused by pathogenic microbes in cancer patients has
prompted the searcher to invest in the development of agents having dual anticancer and …

Design, synthesis, antitumor, and VEGFR-2 inhibition activities of novel 4-anilino-2-vinyl-quinazolines: Molecular modeling studies

A Hamdi, HW El-Shafey, DIA Othman, AS El-Azab… - Bioorganic …, 2022 - Elsevier
The antitumor activity of newly synthesized 4-anilino-2-vinylquinazolines 8a-r was measured
comparable to sorafenib as a standard drug. The 2-vinylquinazolines 8a-r were evaluated …

Design, synthesis, molecular modeling, and anticancer evaluation of new VEGFR-2 inhibitors based on the indolin-2-One scaffold

MA Abdelgawad, AM Hayallah, SNA Bukhari, A Musa… - Pharmaceuticals, 2022 - mdpi.com
A new series of indoline-2-one derivatives was designed and synthesized based on the
essential pharmacophoric features of VEGFR-2 inhibitors. Anti-proliferative activities were …

New thieno [3, 2-d] pyrimidine-based derivatives: Design, synthesis and biological evaluation as antiproliferative agents, EGFR and ARO inhibitors inducing apoptosis …

AM Farghaly, OM AboulWafa, HH Baghdadi… - Bioorganic …, 2021 - Elsevier
An array of newly synthesized thieno [3, 2-d] pyrimidine-based derivatives and
thienotriazolopyrimidines hybridized with some pharmacophoric anticancer fragments were …

Structural Perspectives in the Development of Novel EGFR Inhibitors for the Treatment of NSCLC

R Makhija, A Sharma, R Dubey… - Mini Reviews in …, 2024 - benthamdirect.com
Non-small cell Lung cancer (NSCLC) is the most common type of lung cancer, which is
caused by high consumption of tobacco and smoking. It is an epithelial lung cancer that …

Anticancer Studies of Newly Synthesized Thiazole Derivatives: Synthesis, Characterization, Biological Activity, and Molecular Docking

FA Al-Salmi, AH Alrohaimi, ME Behery, W Megahed… - Crystals, 2023 - mdpi.com
Thiazole and its derivatives have received a lot of attention from researchers due to its wide
biological, pharmacological, and anticancer properties. A novel series of 2-[2-[4-Hydroxy-3 …

Development of certain aminoquinazoline scaffolds as potential multitarget anticancer agents with apoptotic and anti-proliferative effects: Design, synthesis and …

NH Amin, MT El-Saadi, MM Abdel-Fattah… - Bioorganic …, 2023 - Elsevier
Abstract Newly designed 4-aminoquinazoline derivatives (5a-f, 6a, b, 7, 8, 9, 10a-c, 11a, b,
12a, b and 13a, b) have been synthesized and evaluated for their potential multitarget …