Synthesis of novel Schiff base benzamides via ring opening of thienylidene azlactones for potential antimicrobial activities

INIS

• rings 100%
• synthesis 100%
• nmr 100%
• hydrogen 4 100%
• schiff bases 100%
• in vitro 50%
• enzymes 50%
• hydrates 50%
• phosphates 50%
• candida 50%
• receptors 50%
• hydrazine 50%
• hydrogen 1 50%
• carbon 13 50%
• growth inhibition 50%
• escherichia coli 50%
• capacity 50%
• aldehydes 50%
• pseudomonas 50%
• bonding 50%
• mass spectra 50%
• glucosamine 50%
• methionine 50%
• imines 50%

Chemistry

• Antimicrobial Agent 100%
• Benzamide 100%
• Ring Opening Reaction 100%
• Imine 100%
• Thiophene 100%
• Hydrazinyl 66%
• formation 66%
• 1H NMR Spectroscopy 33%
• 13C NMR Spectroscopy 33%
• Antibacterial 33%
• Antifungal 33%
• Elemental Analysis 33%
• Inhibition of Growth 33%
• Hydrazine Hydrate 33%
• Heterocyclic Compound 33%
• Transfer RNA 33%
• Glucosamine 33%
• Methionine 33%

Pharmacology, Toxicology and Pharmaceutical Science

• Thiophene 100%
• Benzamide Derivative 100%
• Antimicrobial Agent 100%
• Imine 100%
• Benzamide 66%
• Escherichia coli 66%
• Antibacterial Activity 33%
• Candida Albicans 33%
• Antifungal Activity 33%
• Methionine Transfer RNA 33%
• Synthetase 33%
• Receptor 33%
• Carbon 13 33%
• Elemental Analysis 33%
• Hydrazine 33%
• Glucosamine 33%
• Pseudomonas 33%