Synthesis of some coumarinyl chalcones of pharmacological interest

INIS

• synthesis 100%
• analgesics 100%
• antioxidants 66%
• comparative evaluations 66%
• inhibition 66%
• pneumonia 66%
• aromatics 66%
• aldehydes 66%
• india 33%
• zones 33%
• sodium 33%
• metabolites 33%
• hydrogen 1 33%
• nmr 33%
• streptomycin 33%
• thin-layer chromatography 33%
• melting points 33%
• coumarins 33%
• coumarin 33%
• halogens 33%
• chemistry 33%

Chemistry

• Chalcone 100%
• Synthesis (Chemical) 100%
• Antibacterial 60%
• Antiinflammatory 60%
• Aldehyde 40%
• Coumarin 40%
• % Inhibition 40%
• Bioactivity 20%
• Antioxidant Agent 20%
• Chemical Reaction 20%
• Substitution Reaction 20%
• 1H NMR Spectroscopy 20%
• Melting Point 20%
• Thin Layer Chromatography 20%
• Group 20%
• Chemistry 20%
• Diclofenac Sodium 20%
• Halogen 20%
• Plant Metabolite 20%
• Novobiocin 20%
• Streptomycin 20%

Pharmacology, Toxicology and Pharmaceutical Science

• Chalcone Derivative 100%
• Antibacterial Activity 60%
• Antiinflammatory Activity 60%
• Analgesic Agent 60%
• Antioxidant Capacity 40%
• Pneumonia 40%
• Aldehyde 40%
• Pharmacological Activity 40%
• Plant 20%
• Dihydrotachysterol 20%
• Biological Activity 20%
• Diclofenac 20%
• Streptomycin 20%
• Gram Positive Bacterium 20%
• Coumarin Derivative 20%
• Halogen 20%
• Coumarin 20%
• Novobiocin 20%