Keyphrases
Cytotoxic Activity
90%
Stereoisomers
61%
Activity Relationship
54%
IC50
50%
Caspase-3
42%
HL-60 Cells
41%
Zeolite
36%
Meso-dihydroguaiaretic Acid
36%
Antimicrobial Activity
36%
Physicochemical Properties
36%
Heat-moisture Treatment
36%
High Activity
35%
Oleic Acid
34%
Antioxidant Activity
33%
Insecticidal Activity
30%
Epoxylignan
27%
IC50 Value
26%
Esters
26%
Aromatic Ring
26%
Butanol
25%
Structure-activity Relationship
25%
Antibacterial Activity
24%
House Fly
24%
Apoptosis
24%
Stereochemistry
24%
Bioactivity
22%
Steglich Esterification
22%
Apoptosis Induction
21%
Cytotoxicity
21%
Biological Activity
21%
Triethanolamine
20%
HeLa Cells
20%
Metal Removal Efficiency
18%
Molecular Hybrids
18%
Mono-carbonyl Analogue of Curcumin
18%
Synthetic Evaluation
18%
Heavy Metal Removal
18%
Antioxidant Assay
18%
Design Evaluation
18%
Curcumin Analogues
18%
1,2,3-triazole
18%
Random Forest
18%
Machine Learning
18%
Recent Trends
18%
Coumarin
18%
Gallic Acid
18%
Methyl
18%
Phenolipids
18%
Daphnia Magna
18%
Halogen Group
18%
Chemistry
Stereoisomer
61%
IC50
54%
Oleic Acid
45%
Curcumin
36%
Cyclolignane
36%
Antioxidant Agent
36%
Structure-Activity Relationship
28%
Butene
25%
Antibacterial
24%
Steglich Esterification
22%
Fourier Transform Infrared Spectroscopy
20%
1,2,3-triazole
18%
Gallic Acid
18%
insecticidal
18%
Apoptosis Induction
18%
Oleate
18%
Lignan
18%
Antimicrobial Agent
18%
Ethanolamine
18%
Lipoamide
18%
Antioxidant Capacity
15%
Ricinoleate
15%
Diol
13%
% Inhibition
12%
Triazole
12%
Propargylation
12%
Azide
12%
High Resolution Mass Spectrometry (HRMS)
12%
Cycloaddition
12%
Alkyne
12%
Methyl Oleate
9%
Hydroxyl Group
9%
Aromatic Structure
9%
ED50
9%
Bioactivity
7%
Methanol
7%
Compound Type
7%
DNA
7%
13C NMR Spectroscopy
6%
Aldol Condensation
6%
Shikimate
6%
Secoisolariciresinol
6%
Aryl Group
6%
Stereochemistry
6%
Diastereomer
6%
Metabolite
6%
Cytotoxic Agent
6%
Drug Discovery
6%
Aldehyde
6%
1H NMR Spectroscopy
6%
Pharmacology, Toxicology and Pharmaceutical Science
Cytotoxicity
100%
IC50
51%
House fly
30%
Structure Activity Relationship
25%
Antioxidant
24%
Lignan
22%
Biological Activity
18%
Arctigenin
18%
Benzene Derivative
18%
Caspase 3
18%
Lauric Acid
18%
EC50
18%
Triazole
18%
Silica Gel
18%
Lactone
18%
Alkyl Group
18%
Coumarin
18%
Antimicrobial Agent
18%
Coumarin Derivative
18%
Curcumin
18%
Antiinfective Agent
10%
Alkanolamine
9%
Carbon 13
8%
Hydroxyl Group
8%
Alkyne
6%
Azide
6%
Cholinesterase Inhibitor
6%
Phloroglucinol
6%
Aldehyde
6%
Chalcone Derivative
6%
Procaspase 3
6%
Culex pipiens
6%
Spodoptera litura
6%
Antioxidant Capacity
6%
Pharmacokinetics
6%
Therapeutic Effect
6%
Myrtaceae
6%
Drug Discovery
6%