Chemical synthesis and molecular docking study of new thiazole, thiophene, and thieno [2, 3-d] pyrimidine derivatives as potential antiproliferative and antimicrobial …

IMM Othman, ZM Alamshany, NY Tashkandi… - Journal of Molecular …, 2022 - Elsevier
This context deals with the design and synthesis of a new set of derivatives containing
thiazole, thiophene, and thieno [2, 3-d] pyrimidine motifs 3-13 starting with 2-((2 …

Ultrasound-assisted green synthesis of triazole-based azomethine/thiazolidin-4-one hybrid inhibitors for cancer therapy through targeting dysregulation signatures of …

AH Abdelmonsef, AM El-Saghier… - Green Chemistry Letters …, 2023 - Taylor & Francis
The overexpression of Rab proteins was linked to cancer development, making this family of
proteins an attractive drug target for the identification of novel inhibitors against tumor …

[HTML][HTML] 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] Synthesis, molecular docking, and dynamic simulation targeting main protease (Mpro) of new, thiazole clubbed pyridine scaffolds as potential COVID-19 …

A Alghamdi, AS Abouzied, A Alamri, S Anwar… - Current Issues in …, 2023 - mdpi.com
Many biological activities of pyridine and thiazole derivatives have been reported, including
antiviral activity and, more recently, as COVID-19 inhibitors. Thus, in this paper, we …

[HTML][HTML] Three-component synthesis of some new coumarin derivatives as anticancer agents

LA Alshabanah, LA Al-Mutabagani, SM Gomha… - Frontiers in …, 2022 - frontiersin.org
A three-component reaction for the synthesis of novel 3-heteroaryl-coumarin utilizing
acetylcoumarin synthon, under ultrasonic irradiation was developed using chitosan-grafted …

[HTML][HTML] New amino acid Schiff bases as anticancer agents via potential mitochondrial complex I-associated hexokinase inhibition and targeting AMP-protein kinases …

AA Noser, AH Abdelmonsef, M El-Naggar, MM Salem - Molecules, 2021 - mdpi.com
Two series of novel amino acid Schiff base ligands containing heterocyclic moieties, such as
quinazolinone 3–11 and indole 12–20 were successfully synthesized and confirmed by …

Design, synthesis and molecular docking of novel substituted azepines as inhibitors of PI3K/Akt/TSC2/mTOR signaling pathway in colorectal carcinoma

AA Noser, AH Abdelmonsef, MM Salem - Bioorganic Chemistry, 2023 - Elsevier
A series of novel substituted azepines (2–7) was synthesized using both traditional and
ultrasonic techniques. The efficiency of the reaction rate and yield was improved by …

Novel thiadiazole-thiazole hybrids: Synthesis, molecular docking, and cytotoxicity evaluation against liver cancer cell lines

GF Aljohani, TZ Abolibda, M Alhilal… - Journal of Taibah …, 2022 - Taylor & Francis
One of the worst diseases, cancer claims millions of lives each year throughout the world,
necessitating the creation of novel treatments. In this study, we designed a novel series of 1 …

[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 …

[HTML][HTML] Synthesis and biological evaluation of thiazolyl-ethylidene hydrazino-thiazole derivatives: a novel heterocyclic system

LA Al-Mutabagani, FM Abdelrazek, SM Gomha… - Applied Sciences, 2021 - mdpi.com
The reaction of 2-(1-(2-(2-(4-methoxybenzylidene) hydrazinyl)-4-methylthiazol-5-yl)
ethylidene) hydrazinecarbothioamide with a range of hydrazonoyl chlorides and α-halo …