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Keyphrases
Methanol
100%
Computational Approach
100%
Seed Extract
100%
Chemical Fingerprinting
100%
Spectroscopic Approach
100%
Hydrazinecarbothioamide
100%
Spiranthes Spiralis
100%
Antioxidant Activity
66%
Bioactive Compounds
33%
Functional Groups
33%
Well-defined
33%
Phytochemicals
33%
Mutagenicity
33%
Molecular Docking
33%
Morphological Properties
33%
Major Constituents
33%
Biotechnological Applications
33%
Fourier Transform Infrared Spectroscopy (FT-IR)
33%
Methanol Extract
33%
Phenolic Compounds
33%
Microscopic Analysis
33%
Tannin Content
33%
Total Phenolic Content
33%
Absorption Bands
33%
Gas Chromatography-mass Spectrometry
33%
1,3-dioxane
33%
Electrophilicity
33%
Phenolic Content
33%
Computational Analysis
33%
Flavonoid Content
33%
Antioxidant Potential
33%
DPPH Radical Scavenging Activity
33%
Spectrometry Analysis
33%
Binding Affinity
33%
Reduced Density Gradient
33%
Weak Interactions
33%
IC50 Value
33%
Toxicity Profile
33%
In Silico
33%
Antioxidant Phytochemicals
33%
Phytochemical Content
33%
Lowest Unoccupied Molecular Orbital
33%
Chemically Stable
33%
Highest Occupied Molecular Orbital
33%
Fusiform
33%
Noncovalent Interactions
33%
Molecular Electrostatic Potential
33%
Low Binding Energy
33%
Global Reactivity Descriptors
33%
Bioactive Potential
33%
Absorption Distribution Metabolism Excretion
33%
Basal Cell
33%
Toxicity Prediction
33%
Metabolic Prediction
33%
Absorption Prediction
33%
Testa
33%
Interaction Zone
33%
Pharmacological Applications
33%
Hydroxyacetic Acid
33%
GPR52
33%
Acid Hydrazide
33%
Compound Proteins
33%
Seed Shape
33%
Gradient Mapping
33%
Strong Antioxidant
33%
Compound Polysaccharide
33%
Mixed Toxicity
33%
Distribution Prediction
33%
Chemistry
Methanol
100%
Antioxidant Capacity
100%
IC50
50%
Fourier Transform Infrared Spectroscopy
50%
Antioxidant Agent
50%
Electrostatic Force
50%
1,3-dioxane
50%
Electrophilicity
50%
Phenolic Compound
50%
Lowest Unoccupied Molecular Orbital
50%
Kd
50%
Highest Occupied Molecular Orbital
50%
Non-Covalent Interactions
50%
Electrostatic Potential
50%
Hydrazide
50%
Binding Energy
50%
Tannin
50%
Absorption Spectra
50%
Flavonoid
50%
Polysaccharide
50%
Molecular Docking
50%
Mutagenicity
50%
Pharmacology, Toxicology and Pharmaceutical Science
Antioxidant Capacity
100%
Methanol
100%
Phytochemical
100%
Molecular Orbital
100%
Functional Groups
50%
Flavonoid
50%
Mutagenicity
50%
1,4-Dioxane
50%
Non-Covalent Interactions
50%
1,1 Diphenyl 2 Picrylhydrazyl
50%
Polysaccharide
50%
Receptor
50%
IC50
50%
Antioxidant
50%
Fourier Transform Infrared Spectroscopy
50%
Tannin
50%
Hydrazide
50%
Absorption Distribution Metabolism Excretion
50%
Glycolic Acid
50%