Novel rhodanine-thiazole hybrids as potential antidiabetic agents: A structure-based drug design approach DOI
Shankar Gharge, Shankar G. Alegaon, Shriram D. Ranade

et al.

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

Expression of PPAR-γ TF by newly synthesized thiazolidine-2,4-diones to manage glycemic control: Insights from in silico, in vitro and experimental pharmacology in wistar rats DOI
Shankar Gharge, Shankar G. Alegaon, Shriram D. Ranade

et al.

Bioorganic Chemistry, Journal Year: 2024, Volume and Issue: 153, P. 107966 - 107966

Published: Nov. 17, 2024

Language: Английский

Citations

6

PPARγ modulator predictor (PGMP_v1): chemical space exploration and computational insights for enhanced type 2 diabetes mellitus management DOI
Sk. Abdul Amin, Lucia Sessa, Shovanlal Gayen

et al.

Molecular Diversity, Journal Year: 2025, Volume and Issue: unknown

Published: Feb. 1, 2025

Language: Английский

Citations

0

Design, synthesis and molecular dynamics simulations of thiazole-based hydrazones targeting MDA-MB-231 breast cancer cells DOI
Shankar G. Alegaon, Shankar Gharge,

Sunidhi Patil

et al.

Bioorganic Chemistry, Journal Year: 2025, Volume and Issue: 157, P. 108306 - 108306

Published: Feb. 23, 2025

Language: Английский

Citations

0

Novel quinoline–imidazole derivatives as inhibitors of Mycobacterium tuberculosis : an integrated approach combining molecular dynamics and in-vitro studies DOI

Neha Khebude,

Shankar G. Alegaon, Shriram D. Ranade

et al.

Molecular 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

0

Pioglitazone with SGLT2 inhibitors or GLP-1 receptor agonists in patients with type 2 diabetes and non-alcoholic fatty liver disease: could the combinations of an old friend with new players yield better outcomes? DOI Open Access
Georgios S. Papaetis, Michalis Picolos, Anastasia Sacharidou

et al.

Archives 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

0

Structure-Based Insights into Fatty Acid Modulation of Lipid-Sensing Nuclear Receptors PPARδ/γ for Glycemic Regulation DOI Creative Commons
Shankar Gharge,

Charushila V. Balikai,

Sachin Gudasi

et al.

Aspects of Molecular Medicine, Journal Year: 2025, Volume and Issue: unknown, P. 100079 - 100079

Published: March 1, 2025

Language: Английский

Citations

0

Unleashing the potential of traditional Chinese medicine: a computational approach to discovering drug targets utilizing the CSLN and molecular dynamics DOI
Qi Geng, Pengcheng Zhao,

Zhiwen Cao

et al.

Molecular Diversity, Journal Year: 2025, Volume and Issue: unknown

Published: May 3, 2025

Language: Английский

Citations

0

Comprehensive Review on Anti-Obesity Effects of Plant-Derived Compounds: Evidence from 3T3-L1 Adipocytes and High-Fat Diet Models DOI Creative Commons
Sachin Gudasi, M. B. Patil

Aspects of Molecular Medicine, Journal Year: 2025, Volume and Issue: unknown, P. 100089 - 100089

Published: May 1, 2025

Language: Английский

Citations

0

Novel rhodanine-thiazole hybrids as potential antidiabetic agents: A structure-based drug design approach DOI
Shankar Gharge, Shankar G. Alegaon, Shriram D. Ranade

et al.

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

Citations

2