Chemistry
Natural Product
100%
1,2,3-triazole
93%
Thalidomide
77%
Palladium
67%
formation
67%
Ring Formation
61%
Cyclic Structure
58%
Cross-Coupling Reaction
58%
Rhodium
51%
Diels-Alder Reaction
48%
Bioactivity
46%
Heck Reaction
45%
Suzuki Reaction
45%
Tsuji-Trost Allylation
38%
Electron Density
38%
Intramolecular Heck Reaction
38%
Antineoplastic Agent
38%
Alkyne
35%
Halide
32%
Catalysis
29%
Acid Catalyst
29%
Ruthenium
29%
Octene
29%
Electrostatic Potential
29%
Boronic Acid
29%
electronics
29%
Carbene
29%
Benzene
29%
Metabolite
29%
Asymmetric Synthesis
25%
Azide
25%
Oxazine
25%
methylation
25%
Chemical Industry
25%
Carboxylic Acid
23%
amination
22%
Absolute Configuration
19%
1,3,4-oxadiazole
19%
Crystal Structure
19%
Antibacterial Agent
19%
Coupling Reaction
19%
Ferrocene
19%
Ketones
19%
Arylation
19%
Benzazepine
19%
Diels-Alder Cycloaddition
19%
Sesquiterpenoid
19%
Psychodysleptic
19%
Catalyst Property
19%
Maleimide
19%
Pharmacology, Toxicology and Pharmaceutical Science
Norcantharidin
77%
Natural Product
67%
Triazole Derivative
58%
Thalidomide
58%
4 Amino 7 Tert Butyl 5 (4 methylphenyl)pyrazolo[3,4 D]pyrimidine
47%
IC50
41%
Thalidomide Derivative
38%
Alder
38%
Sulfonyl
38%
Phosphoprotein Phosphatase 1
38%
Phosphoprotein Phosphatase 2A
38%
Antrodia camphorata
38%
Maleic Anhydride
38%
Antiinfective Agent
35%
Sorafenib
29%
Alkyne
29%
Anti-Inflammatory Drug
29%
Maleimide
29%
Liver Cancer
25%
Cantharidin
24%
Anticarcinogen
19%
Quercetin
19%
Flavonoid
19%
Sucrose Ester Derivative
19%
Liver Cell Carcinoma
19%
Lysergic Acid
19%
Adenosine Derivative
19%
Adenosine Receptor Stimulating Agent
19%
Tosyl
19%
Hyperbarism
19%
Azide
19%
Antioxidant
19%
Trometamol
19%
Lipoxygenase
19%
Stilbene
19%
Minimum Inhibitory Concentration
19%
Biological Activity
19%
Adenosine Receptor Ligands
19%
Lenalidomide
19%
Psychotomimetic
19%
Morpholine Derivative
19%
Adenosine
19%
Lysergide
19%
Thioether
19%
Tumor Necrosis
19%
Benzaldehyde
19%
Lithium Derivative
19%
Malignant Neoplasm
19%
EC50
19%
Aldehyde
19%