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Three new pterosins from Pteris semipinnata.
Weiren Lu1, Huajun Li1, Lan Cao1
1Jiangxi University of Traditional Chinese Medicine, Nanchang, Jiangxi, PR China.
Natural Product Research
|April 4, 2024
Summary
Three new pterosins were isolated from Pteris semipinnata and showed anti-inflammatory effects by inhibiting NF-κB induction. This study expands the known compounds from this plant species.
Area of Science:
- Natural Product Chemistry
- Pharmacology
- Phytochemistry
Background:
- Pteris semipinnata is a plant species known to contain various bioactive compounds.
- Pterosins are a class of natural products with diverse biological activities.
- Understanding the chemical constituents and pharmacological properties of medicinal plants is crucial for drug discovery.
Purpose of the Study:
- To isolate and characterize new pterosins from Pteris semipinnata.
- To evaluate the anti-inflammatory potential of the isolated novel pterosins.
- To report the first isolation of specific known pterosins from this plant.
Main Methods:
- Isolation of compounds using chromatographic techniques.
- Structure elucidation employing High-Resolution Electrospray Ionization Mass Spectrometry (HRESIMS), Nuclear Magnetic Resonance (NMR) spectroscopy, and Circular Dichroism (CD).
- Assessment of anti-inflammatory activity through inhibition of Nuclear Factor-kappa B (NF-κB) induction.
Main Results:
- Three new pterosins, semipterosin A (1), B (2), and C (3), were identified.
- Eleven known pterosins (4-14) were also isolated, with compounds 6-14 reported for the first time from this plant.
- Compounds 1-3 demonstrated significant inhibition of NF-κB induction, with percentages of 40.7%, 61.9%, and 34.0%, respectively.
Conclusions:
- The chemical investigation of Pteris semipinnata yielded three novel pterosins and eleven known ones.
- The newly isolated pterosins possess notable anti-inflammatory activity, indicated by their ability to inhibit NF-κB.
- This research contributes to the understanding of Pteris semipinnata's chemical diversity and therapeutic potential.
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