RSC Medicinal Chemistry, Journal Year: 2024, Volume and Issue: unknown
Published: Nov. 21, 2024
New rhodanine–thiazole clubbed compounds (7a–7l) were synthesised and characterised with various spectroscopy methods.
Language: Английский
RSC Medicinal Chemistry, Journal Year: 2024, Volume and Issue: unknown
Published: Nov. 21, 2024
New rhodanine–thiazole clubbed compounds (7a–7l) were synthesised and characterised with various spectroscopy methods.
Language: Английский
Bioorganic Chemistry, Journal Year: 2024, Volume and Issue: 153, P. 107966 - 107966
Published: Nov. 17, 2024
Language: Английский
Citations
6Molecular Diversity, Journal Year: 2025, Volume and Issue: unknown
Published: Feb. 1, 2025
Language: Английский
Citations
0Bioorganic Chemistry, Journal Year: 2025, Volume and Issue: 157, P. 108306 - 108306
Published: Feb. 23, 2025
Language: Английский
Citations
0Molecular Simulation, Journal Year: 2025, Volume and Issue: unknown, P. 1 - 19
Published: March 14, 2025
The rationale for designing and synthesising quinoline–imidazole hybrids as antitubercular cytotoxic agents stems from the strategic combination of two bioactive structural motifs to create compounds with enhanced efficacy, dual targeting, potential overcome drug resistance challenges in tuberculosis treatment. Herein, we report design synthesis hybrids. FTIR, Mass, 1H-NMR 13C-NMR spectral data characterised synthesised compounds. These were evaluated their activity against Mycobacterium (MTB) H37Rv Hep G2, normal mouse fibroblast L929 cell lines. evaluation revealed that compound 6 g exhibited promising activities a MIC value 6.26 µg/ml, while, 6d, h 6i showed moderate MTB inhibition. Additionally, 6d demonstrated cytotoxicity HepG2 lines an IC50 46.74 ± 1.209 μg/ml. Further selected underwent theoretical investigation via molecular docking, stability assessment MD trajectories quantum computations justify experimental results. obtained predicted silico indicate act effective inhibitors.
Language: Английский
Citations
0Archives of Medical Science - Atherosclerotic Diseases, Journal Year: 2025, Volume and Issue: 10(1), P. 1 - 15
Published: March 14, 2025
More than 25% of the adult population worldwide and approximately 50–75% patients with type 2 diabetes are diagnosed non-alcoholic fatty liver disease. Insulin resistance is one most crucial factors underlying its pathogenesis a significant determinant progression to steatohepatitis. The complex pathophysiology disease emphasizes need for combination treatment strategies drug classes that target different cellular pathways, since no single agent can control all mechanisms contributing development evolution. Pioglitazone, main thiazolidinedione in clinical practice, only true insulin sensitizing antidiabetic our therapeutic armamentarium diabetes. Current international practice guidelines recommend PIO as promising therapy who experience NASH GLP-1 receptor agonists SGLT2 inhibitors have shown salutary cardiometabolic renal effects diabetes, well beneficial activities those This review discusses pathophysiological background use these three categories It also explores thoroughly combinations pioglitazone either or inhibitors, their future role this setting.
Language: Английский
Citations
0Aspects of Molecular Medicine, Journal Year: 2025, Volume and Issue: unknown, P. 100079 - 100079
Published: March 1, 2025
Language: Английский
Citations
0Molecular Diversity, Journal Year: 2025, Volume and Issue: unknown
Published: May 3, 2025
Language: Английский
Citations
0Aspects of Molecular Medicine, Journal Year: 2025, Volume and Issue: unknown, P. 100089 - 100089
Published: May 1, 2025
Language: Английский
Citations
0RSC Medicinal Chemistry, Journal Year: 2024, Volume and Issue: unknown
Published: Nov. 21, 2024
New rhodanine–thiazole clubbed compounds (7a–7l) were synthesised and characterised with various spectroscopy methods.
Language: Английский
Citations
2