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Medicinal Chemistry

Green Synthesis of New Peptide Triazoles with Potential Activity Against Protease-Activated Receptor 2 (PAR2)

Protease-activated receptor 2 (PAR2) is a G-protein-coupled receptor critical in regulating inflammation, pain, and physiological functions such as wound healing and epithelial barrier integrity. Chronic PAR2 activation contributes to numerous inflammatory and immune diseases, including inflammatory bowel disease (IBD), asthma, and arthritis, and plays a role in tumor progression by promoting proliferation, angiogenesis, and metastasis.

Urea-Hydrogen Peroxide-Mediated C(sp2 )-H Bond Selenylation of Imidazoheteroarenes and Simple Activated Arenes

In recent decades there has been uprising interest in the medicinal properties of organoselenides. These ubiquitous structural have their wide applications in material sciences, in catalysis and modern organic transformations. Research studies have led to important discoveries regarding selective C–Se bond formation and in this context a notable approach is direct selenylation. In this regard, nitrogen- or oxygen-containing arenes with organoselenides have appeared as a very important class of molecules, with diverse applications in the biological sciences.

Synthesis of Minor Cannabinoid Analogues Related to Antiproliferative Natural Products

Throughout history, natural products have consistently proven to be invaluable sources of solutions for humanity, particularly regarding the development of treatments for diseases. If only small molecules are taken into consideration, almost half of the approved anti-cancer drugs since mid-last century are either natural products or compounds related to them in some way. Among the natural products that have gained increasing interest in recent decades are cannabinoids and related meroterpenoids. 

Bioguided Fractionation of Modified Plant Extract: An Efficient Approach for Discovering Bioactive Compounds and Identifying Biological Targets

This study presents a methodology for bioactivity-guided fractionation of chemically modified Ambrosia tenuifolia extracts using mild derivatization conditions at room temperature. New trypanocidal compounds less toxic than the starting materials were obtained in a single reaction step. In addition, bioinformatics tools were used to identify potential biological targets for Trypanosoma cruzi, reducing the need for extensive biological testing.

Progress Towards the Synthesis of Quinone-based Cathode Materials for New Rechargeable Battery Architectures

Our growing population, development, and increasing energy demands will strain the environment in the coming decades, necessitating breakthroughs in sustainable energy generation and storage. State-of-the-art lithium-ion batteries face significant challenges, including limited lithium resources, safety issues, and electrochemical performance nearing theoretical limits. Novel rechargeable batteries, such as magnesium-ion batteries, present promising alternatives due to their material abundance and improved safety.

Sustainable Heterocycle Synthesis via Gold Catalysis: Exploring Amino Acids and Water-Soluble Catalysts

Heterocyclic ring systems are essential in drug design, serving as core structures in many approved drugs. Nitrogen- and oxygen-containing heterocycles, in particular, have become increasingly significant in recent years. Despite the availability of efficient synthetic methods, there is an ongoing need for new approaches that offer higher molecular complexity, better functional group compatibility, and atom economy, using readily available starting materials under mild conditions.