Chemistry
1,4-naphthoquinone
20%
Agarose
10%
Antibacterial Agent
40%
Antifungal Agent
40%
Antimicrobial Agent
20%
Application
24%
Aqueous Solution
10%
Base
10%
Biomass
20%
Boiling Point
20%
Boric Acid
10%
Buchwald-Hartwig Cross Coupling Reaction
20%
Buffer Solution
16%
Carbohydrate
40%
Carbon
20%
Carbon Aerogel
20%
Carboxylic Acid
20%
Catalyst
16%
Chemical Reaction
19%
Cyclic Acetal
20%
Cycloaddition
13%
Electrolyte
16%
Ester
40%
Ethylenediaminetetraacetic Acid
10%
Green
23%
Heteroatom
20%
Hydrogel
20%
Ion
13%
Lewis Acid
20%
Linezolid
20%
Methanol
10%
Nitrogen
10%
Organic Chemistry
20%
Organic Synthesis
19%
Oxazolidinone
13%
Oxygen Reduction Reaction
40%
Porosity
20%
Probe
20%
Procedure
20%
Purification
13%
Pyrolysis
10%
Rate
20%
Resistance
13%
Solvent
60%
Supercapacitors
40%
Surface Area
16%
Synthesis (Chemical)
100%
Tris
10%
Vacuum
20%
Water Type
26%
Pharmacology, Toxicology and Pharmaceutical Science
1,4 Naphthoquinone
20%
Alkaloid
10%
Anaerobic Bacterium
20%
Anthracycline
5%
Antibacterial Activity
28%
Antifungal
20%
Antifungal Activity
6%
Antifungal Agent
53%
Antiinfective Agent
60%
Bacterium
10%
Bioassay
10%
Biological Activity
10%
Carbohydrate
40%
Carbon
5%
Compounds of Lead
5%
Coniine
20%
Conium
10%
Conium maculatum
20%
Cyclin Dependent Kinase
20%
Enzyme
20%
Ester
40%
Fungus
10%
Glycosyltransferase
5%
Kanamycin
20%
Kanamycin A
13%
Kanamycin A Derivative
6%
Kanamycin B
20%
Kanamycin Derivative
20%
Lead Compounds
11%
Lethality
10%
Linezolid
20%
Linezolid
6%
Methyltransferase
10%
Meticillin
5%
Mouse
10%
Naphthalene
5%
Natural Product
5%
Nicotinic Receptor
10%
Oxazolidinone Derivative
13%
Oxazolidinone Derivative
10%
Piperidine Derivative
10%
Polyketide Synthase
20%
Pretomanid
6%
Quinone Derivative
10%
Solvent
20%
Staphylococcus Aureus
5%
Streptomyces
10%
Toxicity
26%
Triazole
20%
Water
20%
