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Chemistry
Heterocyclic Compound
83%
Antimicrobial Agent
69%
Pyridine
55%
1,2,4-Triazole
44%
Antibacterial
42%
Hydrazide
40%
Nucleoside
38%
1,3,4-oxadiazole
37%
Hydrazone
36%
Pyrimidine
35%
Furan
33%
Cyclocondensation Reaction
32%
Nucleoside Analog
31%
Amine
30%
Acetylation
30%
Condensation
28%
1,3,4-thiadiazole
27%
Thiadiazole
27%
Ethyl
27%
1H NMR Spectroscopy
25%
formation
24%
NMR Spectroscopy
19%
Aldehyde
19%
Hydrazine Hydrate
18%
Monosaccharide
18%
Pyridone
16%
Tetrazole
16%
Oxadiazole
16%
Dye-Sensitized Solar Cell
16%
Carbazole
16%
Carbon Disulfide
15%
Aldose
15%
Alkaline Condition
14%
Alkylation
13%
Antiviral Agent
13%
Antiviral Drug
13%
Elemental Analysis
13%
Cyclization Reaction
12%
Antibacterial Agent
12%
Acidic Condition
12%
Donor
12%
Sodium Salt
11%
Glucosidase
11%
Cobalt
11%
Palladium
11%
Methylquinoline
11%
Anti HIV
11%
2-Deoxy-D-Glucose
11%
Light Harvesting
11%
Cycloaddition
11%
Pharmacology, Toxicology and Pharmaceutical Science
Antiinfective Agent
100%
Hydrazide
57%
Oxadiazole Derivative
55%
Antimicrobial Agent
50%
Acyclic Nucleoside
50%
Thiadiazoles
46%
Antiviral Activity
37%
Nucleoside Analog
37%
Pyrimidine
35%
Antibacterial Activity
33%
Antivirus Agent
33%
Pyridine Derivative
27%
Triazole
24%
HIV
22%
Quinazoline
22%
Technetium 99m
22%
1,3,4 Oxadiazole Derivative
22%
Furan
19%
Heterocyclic Compound
16%
Anti-Human Immunodeficiency Virus
16%
Biological Activity
16%
Pyridone Derivative
16%
Acetic Anhydride
16%
Hepatitis B Virus
15%
1,3,4 Thiadiazole Derivative
14%
Malonic Acid Derivative
12%
Triazole Derivative
11%
Cuprous Ion
11%
Solid Malignant Neoplasm
11%
Neoplasm
11%
Formate
11%
Antitumor Activity
11%
Tetrazole Derivative
11%
Amitrole
11%
Pyrazolone
11%
Microwave Irradiation
11%
Hypoxia
11%
Quinazoline Derivative
11%
Biodistribution
11%
Pyrazole Derivative
11%
Anticonvulsant Activity
11%
Tosyl
11%
Intercalating Agent
11%
Nucleoside
11%
Glucose
11%
Nucleic Acid
11%
Elemental Analysis
10%
Aldehyde
9%
Acetohydrazide
9%
Glycoside
9%