Chemistry
Transition State
100%
electronics
73%
Density Functional Theory
62%
Pyrolysis
58%
Free Energy
33%
Electric Field
33%
Catalyst Activity
33%
Reaction Activation Energy
25%
Electron Localization
23%
Statistical Ensemble
22%
Vibronic Coupling
22%
Dipole Moment
22%
Methyl Halides
22%
Enzymatic Hydrolysis
22%
Four Wave Mixing
20%
Nonlinear Optical Property
20%
Density Functional Theory
20%
Carboxamide
19%
DFT-B3LYP Calculation
19%
Ethyl
17%
Hydrogen
17%
Base
16%
Solvent Effect
16%
Decarbonylation
16%
Cob(I)alamin
16%
formation
16%
Molecular Structure
14%
Methane
14%
Electrophilicity
13%
Rate-Determining Step
13%
Cobalamin
13%
Aldehyde
12%
Møller-Plesset Perturbation Theory
12%
Energetics
12%
Antimalarial
11%
Phosphole
11%
Optical Susceptibility
11%
Herbicide
11%
Relaxation
11%
Electronic Property
11%
Ammonia
11%
Heterocyclic Compound
11%
Hole (Electron)
11%
Benzoate
11%
Aromatic Amino Acid
11%
Ethyl Acetate
11%
Mugineic Acid
11%
Hexamethylbenzene
11%
Sulfonylation
11%
Nucleophilic Aromatic Substitution
11%
Atomic Mass
11%
1,2,3-triazole
11%
Quinolone
11%
Chalcone
11%
Lactam Ring
11%
Beta Lactam Antibiotic Agent
11%
Organometallic Complexes
11%
Spin Exchange
11%
Mechanistic Study
11%
Antibiofilm
11%
Fast Pyrolysis
11%
Dapsone
11%
Gaussian Distribution
11%
Flash Vacuum Pyrolysis
11%
Frustrated Lewis Pairs
11%
Nitrogen Dioxide
11%
Dissociation Energy
11%
Biomimetics
11%
Acetyl Group
11%
Ketene
11%
Metal Oxide
11%
Resonance Energy
11%
Isomerization
11%
Imine
11%
Biodiesel
11%
Cannabinoid
11%
Hemolytic
11%
Pectin
11%
Racemization
11%
Halogen
11%
Cellular Imaging
11%
Peroxidase
11%
Sulfide
11%
Glutathione
11%
4-Pyridone
11%
Proline
11%
reductive dehalogenation
11%
Benzene
11%
Hydrogen Sulfide
11%
Compound E
11%
Antioxidant Agent
11%
Glucosidase
11%
stability
11%
Cysteine
11%
Lipid II
11%
Cubic Expansion
11%
Serine
10%
Nucleophilic Substitution
9%
Harmonic Oscillator
9%
Carboxylic Acid
9%
Pharmacology, Toxicology and Pharmaceutical Science
Quantitative Structure-Activity Relationship
62%
Biological Activity
37%
Applicability Domain
31%
Lead Compound
28%
Quantitative Structure Activity Relation
27%
Antimalarial Agent
22%
Cannabinoid
22%
Antioxidant Capacity
20%
Malignant Neoplasm
20%
Cross-Validation
19%
IC50
18%
Antimalarial Activity
18%
Carboxamide
16%
Amino Acid
16%
Non Insulin Dependent Diabetes Mellitus
16%
Antioxidant
14%
Diseases
12%
Dipeptidyl Peptidase IV
11%
4 Pyridone Derivative
11%
Dapsone
11%
Selenium Compound
11%
Estrogen Receptor
11%
Thiosemicarbazone Derivative
11%
G Protein Coupled Receptor 40
11%
Proteinase
11%
SARS Coronavirus
11%
Drug Delivery System
11%
Eupatorium
11%
Controlled Substance
11%
Glucosidase
11%
Toxic Hepatitis
11%
Thiourea
11%
Acrylamide
11%
Glutathione Peroxidase
11%
Ebselen
11%
Carbanion
11%
Quinolone
11%
Aromatic Amino Acid
11%
Cellular Imaging
11%
Chalcone Derivative
11%
Hepatotoxicity
11%
Tellurium Derivative
11%
Base
11%
Methanol
11%
Coronavirinae
11%
Mycobacterium Tuberculosis
11%
Bond Length
11%
4 Hydroxybenzaldehyde
11%
Leucine Rich Repeat Kinase 2
11%
Imine
11%
Parkinson's Disease
11%
Molecular Orbital
11%
Quinazoline Derivative
11%
Pyrimidine Derivative
11%
Benzophenone Derivative
11%
QSAR Study
11%
Tyrosinase
11%
Receptor
9%
Electronegativity
8%
Fourier Transform Infrared Spectroscopy
7%
Hydrogen Peroxide
7%
Breast Cancer
7%
Aldehyde
7%
Virtual Screening
6%
Antiinfective Agent
5%
Hydroxyl Group
5%
Leishmaniasis
5%
Sulfonamide
5%
Oxidoreductase
5%
Drug Development
5%
Antimycobacterial Agent
5%
Thiosemicarbazone
5%
Dicamba
5%
Cinnamic Acid
5%
RNA Directed RNA Polymerase
5%
Papain
5%
Biological Target
5%
Angiotensin I
5%
Carbonate Dehydratase
5%
Proline Derivative
5%
Peptidyl Prolyl Cis Trans Isomerase NIMA Interacting 1
5%
Amastigote
5%
Carbon 13
5%
Aromatic Compound
5%
Binding Site
5%
Enamine
5%
Nucleophile
5%
Carbonyl Derivative
5%
Absorption Distribution Metabolism Excretion
5%