Synthesis, α-Glucosidase Inhibitory Activity and Molecular Docking Study of Chalcone Derivatives Bearing a 1H-1,2,3-Triazole Unit

Keyphrases

• 1,2,3-Triazole Hybrids 33%
• 1H-1,2,3-triazole 100%
• Active Agent 33%
• Active Interaction 33%
• Active Sites 33%
• Antidiabetic 33%
• Antidiabetic Drugs 33%
• Cation-anion Interaction 33%
• Chalcone 66%
• Chalcone Derivatives 100%
• Drug Candidates 33%
• Glucosidase 100%
• Health Anxiety 33%
• Highly Active 33%
• Hybrid Compounds 66%
• Hydrogen Bonds (H-bonds) 33%
• IC50 66%
• Inhibitory Activity 100%
• Inhibitory Potential 33%
• Metabolic Conditions 33%
• Molecular Docking Studies 100%
• Pharmaceutical Sector 33%
• Quercetin 33%
• Saccharomyces Cerevisiae 33%
• Triazole Hybrids 33%
• Type 1 Diabetes Mellitus (T1DM) 33%

Pharmacology, Toxicology and Pharmaceutical Science

• Antidiabetic Agent 66%
• Chalcone 66%
• Chalcone Derivative 100%
• Diabetes Mellitus 33%
• Glucosidase 100%
• IC50 66%
• Quercetin 33%
• Saccharomyces cerevisiae 33%
• Triazole 100%