Chemistry
Synthesis (Chemical)
100%
Occurrence in Nature
39%
Shikimic Acid
36%
Enone
25%
Inhibitor
25%
Acid
24%
(-)-Quinic Acid
20%
Ligand
19%
Application
16%
1,10-phenanthroline
16%
Quinone
15%
Dicoumarol
14%
Arene
14%
Pyrrolidine
14%
Deoxyribonucleic Acid
10%
Toxicity
10%
Bioassay
10%
Quinate
9%
Dehydration
9%
Coumarin
9%
% Inhibition
9%
Crystal Structure
9%
NAD(P)
8%
Procedure
7%
Functionalization
7%
Chemical Reaction
7%
Cytotoxic Agent
7%
Cyclic Structure
7%
Point Group C3
7%
Cyclohex-2-Enone
7%
Metabolite
7%
Structure
7%
Metal Ion
7%
Probe
7%
Terpenoid
7%
Total Synthesis
7%
Hydrophilicity
7%
Biochemical Activity
7%
Antimetabolite
7%
Actinoid Atom
7%
Lanthanoid Atom
7%
Nuclear Energy
7%
Phenanthroline
7%
Transition Element
7%
Chemical Transformation
6%
Shikimate
6%
Martin Dehydration
6%
Enantiopurity
5%
Chemical Kinetics Characteristics
5%
Biochemistry, Genetics and Molecular Biology
Protein
34%
Lysozyme
20%
Sec61
19%
Oxidoreductase
15%
Synthesis
14%
Anabolism
10%
Infectious Agent
9%
Enzyme Activity
8%
Translocon
8%
Endoplasmic-Reticulum-Associated Protein Degradation
7%
Cooperation
7%
Binding Site
7%
Unfolded Protein Response
7%
Caspase 1
7%
Inflammasome
7%
Shiga-Like Toxin
7%
Growth
7%
Interleukin-1
7%
Intracellular Trafficking
7%
Secretion (Process)
7%
Crystal Structure
7%
Protein Catabolism
6%
Dislocation
5%
Small Molecule
5%
Ubiquitin
5%
Homeostasis
5%
Pharmacology, Toxicology and Pharmaceutical Science
Neoplasm
30%
Dicoumarol
19%
Enzyme
18%
Reduced Nicotinamide Adenine Dinucleotide (Phosphate) Dehydrogenase (Quinone)
15%
Oxidoreductase
14%
Quinone Derivative
14%
Biological Product
12%
Coumarin
11%
Natural Product
10%
Malignant Neoplasm
9%
Toxicity
9%
Quantitative Structure-Activity Relationship
9%
Quinic Acid
7%
1,10 Phenanthroline
7%
IC50
7%
Enzyme Inhibition
7%
Ligand
7%
Transition Element
7%
Structure Activity Relationship
7%
Antiinfective Agent
5%
Colon Cancer
5%