Pharmacology, Toxicology and Pharmaceutical Science
1,3,4 Oxadiazole Derivative
22%
1,3,4 Thiadiazole Derivative
18%
Acetic Acid Derivative
11%
Acetohydrazide
12%
Acyclic Nucleoside
55%
Aldehyde
18%
Amitrole
11%
Anti-Human Immunodeficiency Virus
22%
Antibacterial Activity
33%
Anticonvulsant Activity
11%
Antiinfective Agent
100%
Antimicrobial Agent
62%
Antitumor Activity
11%
Antiviral Activity
37%
Antiviral Drug
16%
Antivirus Agent
16%
Biodistribution
11%
Biological Activity
16%
Cuprous Ion
11%
Cytotoxicity
11%
Elemental Analysis
10%
Formate
11%
Furan
27%
Hepatitis B Virus
11%
Heterocyclic Compound
33%
HIV
38%
Hydrazide
72%
Hydrazine Derivative
11%
Hypoxia
11%
Malignant Neoplasm
11%
Malonic Acid Derivative
14%
Metal Complex
8%
Microwave Irradiation
11%
Neoplasm
11%
Nucleoside Analog
42%
Oxadiazole Derivative
68%
Pyrazole Derivative
11%
Pyrazolone
11%
Pyridine Derivative
44%
Pyrimidine
37%
Quinazoline
22%
Quinazoline Derivative
11%
Solid Malignant Neoplasm
11%
Technetium 99m
22%
Tetrazole Derivative
11%
Thiadiazoles
64%
Thiosemicarbazide
16%
Triazole
37%
Triazole Derivative
22%
Uracil
11%
Chemistry
1,2,4-Triazole
38%
1,3,4-oxadiazole
33%
1,3,4-thiadiazole
25%
1H NMR Spectroscopy
25%
2-Deoxy-D-Glucose
11%
Acetylation
34%
Acidic Condition
12%
Aldehyde
13%
Aldose
15%
Alkaline Condition
12%
Alkylation
13%
Anti HIV
11%
Antibacterial
33%
Antibacterial Agent
13%
Antifungal
11%
Antimicrobial Agent
58%
Bioactivity
14%
Carbazole
11%
Carbon Disulfide
25%
Cobalt
11%
Condensation
24%
Crystal Structure
11%
Cyclocondensation Reaction
36%
Donor
11%
Dye-Sensitized Solar Cell
11%
Elemental Analysis
12%
Essential Oil
11%
Ethyl
19%
Ethylenediamine
11%
formation
26%
Furan
27%
Glucosidase
11%
Heterocyclic Compound
77%
Hydrazide
35%
Hydrazine Hydrate
22%
Hydrazone
35%
Methylquinoline
11%
Monosaccharide
21%
NMR Spectroscopy
19%
Nucleoside
22%
Nucleoside Analog
31%
Oxadiazole
13%
Oxidative Cyclization
11%
Palladium
11%
Pyridone
22%
Sodium Salt
11%
Tetrazole
22%
Thiadiazole
22%
Thiazole
11%
Triazole
11%