Related Experiment Video
Updated: Jun 20, 2026

Floral-Dip Transformation of Flax (Linum usitatissimum) to Generate Transgenic Progenies with a High Transformation Rate
Published on: December 19, 2014
The phenylpropanoids of Aster flaccidus
Zhen-ling Liu1, Ying-qian Liu, Lei Zhao
1College of Chemistry and Chemical Engineering, State Key Laboratory of Applied Organic Chemistry, Lanzhou University, Lanzhou 730000, PR China. liuzhl@lzu.edu.cn
Two new compounds from Aster flaccidus bge were identified. Compound 2 shows significant antitumor activity against human liver carcinoma cells, while neither compound demonstrated notable anti-HIV-1 activity.
Area of Science:
- Natural Product Chemistry
- Pharmacology
- Medicinal Chemistry
Background:
- Aster flaccidus bge is a traditional medicine in northwestern China.
- Phenylpropanoids are a class of organic compounds with diverse biological activities.
Purpose of the Study:
- To isolate and identify new phenylpropanoids from Aster flaccidus bge.
- To evaluate the anti-HIV-1 and antitumor activities of the isolated compounds.
Main Methods:
- Isolation of compounds using chloroform extraction.
- Structure elucidation using 1D and 2D NMR spectroscopy and HRMS analysis.
- In vitro anti-HIV-1 and antitumor assays against BEL 7402 cell line.
Main Results:
- Two new phenylpropanoids, including a lignan, were identified: (7'R, 8S)-9'-lariciresinol-(alpha-methyl)-butanoate (1) and 5,9-dimethoxyl-7-(alpha-methyl)-butanoxyl-phenyl-2E-propenol-(alpha-methyl)-butanoate (2).
- Compounds 1 and 2 exhibited weak anti-HIV-1 activity (Therapeutic Index [TI] = 1.0-1.1).
- Compound 2 displayed significant antitumor activity against BEL 7402 cells, with IC50 values decreasing from 106.67+/-8.47 microM at 24 h to 50.51+/-6.11 microM at 72 h.
Conclusions:
- Aster flaccidus bge contains novel phenylpropanoids with potential therapeutic applications.
- Compound 2 shows promising antitumor properties warranting further investigation.
- The isolated compounds are not effective against HIV-1 at the tested concentrations.
Related Concept Videos
Adrenergic Agonists: Chemistry and Structure-Activity Relationship
Aromatic ring substitutions: Substituting the aromatic ring with –OH groups at positions 3 and 4 yields catecholamines (e.g., epinephrine), which have a high affinity for adrenoceptors. Hydrogen bonding between –OH groups and receptors enhances adrenergic activity.
Separation of the aromatic...
Introduction to Seed Plants
Fungal Phylum Ascomycota
Drugs Affecting GI Tract Motility: Other Laxatives
Osmotic or saline laxatives, like magnesium hydroxide or milk of...
Antiasthma Drugs: Methylxanthines
Theophylline is thought to inhibit phosphodiesterase enzymes, increasing intracellular levels of cyclic adenosine monophosphate (cAMP) and cyclic guanosine monophosphate (cGMP). This rise in cAMP and cGMP concentrations stimulates cardiac function,...
Antiasthma Drugs: Leukotriene Modifiers
Leukotriene modifiers work through two distinct mechanisms:
