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Updated: Jul 17, 2026

Source and Route of Pyrrolizidine Alkaloid Contamination in Tea Samples
Published on: September 28, 2022
Pyrrolizidine alkaloids from Eupatorium portoricense
Three pyrrolizidine alkaloids, amabiline, echinatine, and O(12)-acetylechinatine, were identified in Eupatorium portoricense. Their chemical structures were confirmed using advanced spectroscopic techniques.
Area of Science:
- Phytochemistry
- Natural Product Chemistry
- Organic Chemistry
Background:
- Eupatorium portoricense is a plant species known for potential bioactive compounds.
- Pyrrolizidine alkaloids are a class of natural products with diverse chemical structures and biological activities.
Discussion:
- This study focuses on the isolation and structural elucidation of specific pyrrolizidine alkaloids from Eupatorium portoricense.
- Spectroscopic methods, including NMR and Mass Spectrometry, were employed for structure determination.
Key Insights:
- Three pyrrolizidine alkaloids were successfully isolated: (-)-viridifloryl-supinidine (amabiline), (-)-viridifloryl-heliotridine (echinatine), and C12- O-acetyl-(-)-viridifloryl-heliotridine (O(12)-acetylechinatine).
- The elucidated structures provide valuable data for understanding the phytochemical profile of Eupatorium portoricense.
Outlook:
- Further research could explore the biological activities and potential applications of these isolated alkaloids.
- This work contributes to the broader knowledge of pyrrolizidine alkaloid diversity in medicinal plants.
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