Keyphrases
1D NMR
31%
2D NMR
31%
A549
16%
Absolute Configuration
17%
Active Sites
14%
Aerial Parts
13%
Alkaloids
20%
Ancistrocladus
10%
Anti-austerity Strategy
10%
Antiausterity Activity
36%
Antiausterity Agents
31%
Antibacterial Activity
24%
Antiproliferative Activity
15%
Arctigenin
9%
Bacillus Subtilis (B. subtilis)
10%
Benzalacetone Synthase
11%
Biological Activity
11%
Boesenbergia Pandurata
10%
Caesalpinia Crista
10%
Caesalpinia Sappan
11%
Cancer Cell Lines
31%
Cancer Cells
26%
Cell Death
12%
Chalcone Synthase
11%
Chemical Constituents
27%
Chemical Structure
12%
Chloroform
17%
Colony Formation
12%
Condensation
13%
Crystallization
18%
Cytotoxic Activity
48%
Cytotoxicity
48%
Dichloromethane
10%
Diterpenes
33%
Diterpenoids
15%
Enzymatic Formation
10%
Escherichia Coli
15%
HeLa
30%
HeLa Cells
11%
Highly Oxygenated Molecules
19%
HR-ESI-MS
15%
Human Pancreatic Cancer
13%
Human Pancreatic Cancer Cell Line
41%
Human Pancreatic Cancer Cells
44%
IC50
36%
IC50 Value
50%
Indonesia
12%
Inhibitory Activity
27%
Isolated Compounds
41%
Isopimarane
14%
Kaempferia Pulchra
14%
Lianas
12%
Lignans
12%
Malonyl-CoA
18%
Marine Sponge
18%
MCF-7
11%
Medicinal Plants
13%
MeOH Extract
14%
Methanolic Extract
10%
MIC Values
11%
Myanmar
62%
Naphthylisoquinoline Alkaloids
16%
Natural Products
16%
Nitric Oxide Inhibition
15%
Nutrient Starvation
32%
Nutrient-limited Conditions
31%
Nutrient-rich Conditions
14%
Orthosiphon Stamineus
19%
PANC-1
92%
PANC-1 Cells
43%
Pancreatic Cancer
10%
Pancreatic Cancer Cells
14%
Phytochemical Study
32%
Plant Polyketides
11%
Plant Type
20%
Plant-specific
11%
Polyketide Synthase
17%
Polyketides
18%
Positive Control
14%
Preferential Cytotoxicity
52%
Prenylation
10%
Propolis
12%
Quassinoids
13%
Securidaca Longepedunculata
10%
Specific Types
10%
Spectroscopic Analysis
31%
Spectroscopic Data
13%
Spectroscopic Techniques
16%
Staphylococcus Aureus
13%
Structure-activity Relationship
11%
Total Synthesis
12%
Traditional Medicine
10%
Tumor Microenvironment
10%
Type III Polyketide Synthase
48%
Unnatural
15%
Vietnam
15%
Vietnamese
18%
Viral Protein R
17%
Wood
14%
Xanthones
12%
Pharmacology, Toxicology and Pharmaceutical Science
2 Oxoglutaric Acid
8%
Acetic Acid Derivative
6%
Acridone Derivative
5%
Alkadiene
5%
Aloe
5%
Amino Acid
9%
Antibacterial Activity
23%
Anticarcinogen
19%
Antiinfective Agent
9%
Antimalarial Activity
5%
Antioxidant Capacity
8%
Antiproliferative Activity
15%
Antivirus Agent
7%
Arctigenin
7%
Bacillus Subtilis
10%
Benzylideneacetone
10%
Biological Activity
9%
Breast Cancer
11%
Caesalpinia
11%
Calotropis gigantea
5%
Cell Viability
5%
Chalcone Synthase
7%
Chloroform
7%
Chromone Derivative
7%
Chrysin
6%
Coumarin Derivative
7%
Coumaroyl-CoA
5%
Crystallization
8%
Cytotoxicity
100%
Dimethylallyltransferase
5%
Disease
7%
Diterpene
16%
Diterpenoid
26%
Drug Development
5%
Drug Discovery
6%
Escherichia coli
10%
Fibrosarcoma
5%
Flavonoid
12%
Glucopyranoside
5%
Glucosidase
5%
Glycoside
14%
Huperzia
5%
IC50
65%
Iridoid
6%
Kaempferia
18%
Klebsiella pneumoniae
6%
Liana
8%
Lignan
9%
Lung Cancer
7%
Malignant Neoplasm
52%
Malonyl-CoA
13%
Medicinal Plant
27%
Melanoma
6%
Natural Product
13%
Nitric Oxide
9%
Orthosiphon stamineus
8%
Oxygenase
8%
Pancreas Cancer
60%
Phytochemical
23%
Picrasma
8%
Polyketide
13%
Polyketide Synthase
39%
Propolis
21%
Pyrone Derivative
5%
Quassinoid
11%
Rhubarb
5%
Sesquiterpene
6%
Sesquiterpenoid
6%
Staphylococcus Aureus
13%
Structure Activity Relationship
12%
Synthetase
29%
Triterpene
10%
Triterpenoid
5%
Tumor Microenvironment
6%
Uterine Cervix Cancer
11%
Uvaria
5%
Vpr Protein
16%
Xanthine Oxidase
6%