Gardenifolins A-H, Scalemic Neolignans from Gardenia ternifolia: Chiral Resolution, Configurational Assignment, and Cytotoxic Activities against the HeLa Cancer Cell Line

Keyphrases

• Cytotoxic Activity 100%
• Circular Dichroism Spectroscopy 100%
• Chiral Resolution 100%
• HeLa Cancer Cells 100%
• Configurational Assignment 100%
• Neolignan 100%
• Gardenia Ternifolia 100%
• Induced Apoptosis 50%
• High Activity 50%
• Furan 50%
• Ring Systems 50%
• IC50 Value 50%
• HeLa Cells 50%
• Cytotoxic Effect 50%
• 2D NMR 50%
• 1D NMR 50%
• Absolute Configuration 50%
• Human Cancer 50%
• HeLa Cell Line 50%
• Stereoisomers 50%
• NMR Techniques 50%
• Two-peak 50%
• Dihydrofuran 50%
• Diastereomers 50%
• Stereogenic Centers 50%
• Rubiaceae 50%
• Helicity Rules 50%
• Tropical Plants 50%
• Single Electronics 50%
• Reversed-phase Chromatography 50%
• Stem Bark Extract 50%
• Chiral Phase 50%
• Double Bond Geometry 50%
• Electronic Circular Dichroism Spectrum 50%
• Relative Configuration 50%
• Stereoisomeric 50%
• Phase-coupled 50%

Chemistry

• Circular Dichroism 100%
• Electronic Circular Dichroism 100%
• Chirality in Separations 100%
• Neolignan 100%
• Enantiomer 66%
• Purity 33%
• Cyclic Structure 33%
• IC50 33%
• Two-Dimensional NMR 33%
• 1D NMR Spectroscopy 33%
• Absolute Configuration 33%
• Nuclear Overhauser Effect 33%
• High Performance Liquid Chromatography 33%
• Double Bond 33%
• Diastereomer 33%
• Dihydrofuran 33%
• Furan 33%
• Stereoisomer 33%
• Reverse Phase Liquid Chromatography 33%