Keyphrases
Docking Molecular
100%
Antibacterial Activity
71%
Escherichia Coli
62%
Docking Studies
57%
Molecular Dynamics Approach
50%
Chalcone
50%
3-methoxycinnamic Acid
50%
Organic Chemistry
50%
Synthesis Chemistry
50%
Medicinal Chemistry
50%
2-hydroxybenzohydrazide
50%
Chemistry Synthesis
50%
In Vitro Antimalarial Activity
50%
Microwave Irradiation
50%
Benzoyloxy
50%
Cyclooxygenase-1 (COX-1)
50%
Methoxy
50%
Ferulic Acid
35%
Percentage Yield
19%
3D7 Strain
16%
Antimalarial Drugs
16%
Antiplasmodial Activity
16%
Half Maximal Inhibitory Concentration
16%
IC50
16%
Antimalarial Activity
16%
Plasmodium Falciparum 3D7
16%
Candle
16%
Chloroquine Diphosphate
16%
New Antibacterials
12%
Gram-negative
12%
13C NMR
12%
Methyl P-hydroxybenzoate
12%
Diffusion Method
12%
1H-13C
12%
Bacillus Subtilis (B. subtilis)
12%
Gram-positive Bacilli
12%
Halogen Group
12%
CH Group
12%
Molegro Virtual Docker
12%
IR-MS
12%
Fourier Transform Infrared Spectroscopy (FT-IR)
12%
1H nuclear Magnetic Resonance (1H NMR)
12%
Synthetic Derivatives
7%
Molecule Docking
7%
Benzylidene
7%
Condensation Reaction
7%
Compound Synthesis
7%
Methyl Salicylate (MeSA)
7%
Antithrombosis
7%
Biological Activity
7%
Pharmacology, Toxicology and Pharmaceutical Science
Ferulic Acid
50%
Antimalarial Activity
50%
Chalcone
50%
Antiinfective Agent
50%
Antibacterial Activity
50%
IC50
33%
Anti-Inflammatory Drug
20%
Chloroquine
16%
Antiplasmodial Activity
16%
Plasmodium Falciparum 3D7
16%
Antimalarial Agent
16%
Chalcone Derivative
16%
Bond Energy
10%
Antithrombotic Activity
10%
Methyl Paraben
10%
Thrombosis
10%
Biological Activity
10%
Escherichia coli
10%
Carbon 13
10%
Gram Positive Bacterium
10%
Chemistry
Antibacterial
100%
Microwave Irradiation
50%
Chemistry
50%
1H NMR Spectroscopy
29%
Fourier Transform Infrared Spectroscopy
29%
Organic Chemistry
25%
4-Hydroxybenzoate
16%
13C NMR Spectroscopy
16%
Halogen
16%
Condensation Reaction
12%
Green Chemistry
12%
Methyl Salicylate
12%
Ultraviolet Spectrum
12%
