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Chemistry
Catalyst
100%
Natural Product
84%
1,2,3-triazole
67%
Amine
65%
formation
60%
Aldehyde
60%
pre-catalyst
58%
Ambient Reaction Temperature
48%
Suzuki Reaction
46%
Palladium
45%
Thalidomide
44%
Chloride
44%
Ring Formation
44%
Cross-Coupling Reaction
41%
Bioactivity
38%
Rhodium
37%
Diels-Alder Reaction
34%
Cyclic Structure
32%
Boronic Acid
32%
Heck Reaction
32%
Alkyne
31%
Tsuji-Trost Allylation
27%
Electron Density
27%
Intramolecular Heck Reaction
27%
Antineoplastic Agent
27%
Maleic Anhydride
27%
Phosphine
27%
Chemistry
23%
Halide
23%
Azide
21%
Acid Catalyst
20%
Octene
20%
Electrostatic Potential
20%
electronics
20%
Carbene
20%
Maleimide
20%
Benzene
20%
Carboxylic Acid
19%
Aniline
19%
Ruthenium
18%
Catalyst Property
18%
Asymmetric Synthesis
18%
Oxazine
18%
methylation
18%
Chemical Industry
18%
Alkaloid
18%
Cycloaddition
16%
Borylation
16%
Metabolite
15%
Absolute Configuration
13%
Pharmacology, Toxicology and Pharmaceutical Science
Norcantharidin
41%
Thalidomide
27%
Thalidomide Derivative
27%
Phosphoprotein Phosphatase 1
27%
Phosphoprotein Phosphatase 2A
27%
IC50
24%
Sorafenib
20%
Aloxistatin Acid
20%
4 Amino 7 Tert Butyl 5 (4 methylphenyl)pyrazolo[3,4 D]pyrimidine
19%
Liver Cancer
18%
Cantharidin
17%
Carboxamide
17%
Lysergide
13%
Antiinfective Agent
13%
Natural Product
13%
Anti-Inflammatory Drug
13%
Antrodia camphorata
13%
Maleic Anhydride
13%
Alder
13%
Quercetin
13%
Flavonoid
13%
Liver Cell Carcinoma
13%
Adenosine Derivative
13%
Adenosine Receptor Stimulating Agent
13%
Hyperbarism
13%
Antioxidant
13%
Trometamol
13%
Lipoxygenase
13%
Stilbene
13%
Minimum Inhibitory Concentration
13%
Adenosine Receptor Ligands
13%
Lenalidomide
13%
Adenosine
13%
Thioether
13%
Malignant Neoplasm
13%
EC50
13%
Epoxide
13%
Aminoalcohol
13%
Anticarcinogen
13%
Cytotoxicity
13%
Carboxylate
12%
Carcinogen
9%
Biological Activity
6%
Functional Groups
6%
Maleimide
6%
Toluene
6%
Chlorobenzene
6%
Interleukin 6
6%
Pharmaceutical Chemistry
6%
Enzyme Interaction
6%