[HTML][HTML] Thiazole ring-the antimicrobial, anti-inflammatory, and anticancer active scaffold

S Hosseininezhad, A Ramazani - Arabian Journal of Chemistry, 2023 - Elsevier
Background Thiazole ring is one of the most important heterocycle scaffolds in organic and
medicinal chemistry due to this scaffold being the backbone of numerous drugs and their …

A comprehensive review of recent advances in the biological activities of quinazolines

HAM Gomaa - Chemical Biology & Drug Design, 2022 - Wiley Online Library
Quinazoline heterocycles are critical in the development of medications. Quinazoline
derivatives have been intensively researched, providing a wide range of compounds with …

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 …

Schiff base derivatives against monkeypox virus: Synthesis, in silico, MM-GBSA and SAR properties

H Karataş, HK Kiliç, B Tüzün, Z Kökbudak - Journal of Molecular Structure, 2024 - Elsevier
Schiff base-bearing molecules have been reported to exhibit potent biological activities;
Therefore, the synthesis and applications of these molecules are of great importance. In this …

[HTML][HTML] A review on progress of thiazole derivatives as potential anti-inflammatory agents

KH Narasimhamurthy, TR Swaroop… - European Journal of …, 2024 - Elsevier
Inflammation is a body response against infection that activates other biological components
that include various cytokines, chemokines and other biological compounds that trigger …

New Diaryl-1,2,4-triazolo[3,4-a]pyrimidine Hybrids as Selective COX-2/sEH Dual Inhibitors with Potent Analgesic/Anti-inflammatory and Cardioprotective Properties

LH Al-Wahaibi, MH Abdel-Rahman, K El-Adl… - ACS …, 2024 - ACS Publications
COX-2-selective drugs were withdrawn from the market just a few years after their
development due to cardiovascular side effects. As a result, developing a selective COX-2 …

Design, Synthesis and Cytotoxicity Screening of New Thiazole Derivatives as Potential Anticancer Agents through VEGFR-2 Inhibition

T Al-Warhi, M Abualnaja, OA Abu Ali, NM Alyamani… - Symmetry, 2022 - mdpi.com
Z-configurated isomers are kinetically preferred molecules. Compounds with Z-configuration
are contained in many natural products, biologically active compounds and as synthons for …

Small Molecules as Anti‐inflammatory Agents: Molecular Mechanisms and Heterocycles as Inhibitors of Signaling Pathways

NJ Basha - ChemistrySelect, 2023 - Wiley Online Library
Cancer and inflammation interlink with many pathways. Millions of people died because of
these two disorders. Major pathways that cause both inflammation and cancer are STAT3 …

Design and synthesis of new dihydropyrimidine/sulphonamide hybrids as promising anti-inflammatory agents via dual mPGES-1/5-LOX inhibition

LH Al-Wahaibi, AM Elshamsy, TFS Ali… - Frontiers in …, 2024 - frontiersin.org
A novel series of dihydropyrimidine/sulphonamide hybrids 3a–j with anti-inflammatory
properties have been developed and tested as dual mPGES-1/5-LOX inhibitors. In vitro …

Utilization of 2-cyano-N-(2, 5-dioxopyrrolidin-1-yl) acetamide for the synthesis of thiazole, pyrazole and pyridene derivatives with a biological evaluation

MAMA Reheim, ISA Hafiz, RM Darweesh… - Journal of the Iranian …, 2024 - Springer
A range of fused heterocyclic compounds are generated utilizing the crucial intermediary 2-
cyano-N-(2, 5-dioxopyrrolidin-1-yl) acetamide 4. Spectral analysis was executed to support …