Eumitrin L: a new xanthone dimer from the lichen Usnea baileyi
Hoang-Vinh-Truong Phan1,2, Le-Thuy-Thuy-Trang Hoang3,4, Dinh Gia Trung5
1Institute of Fundamental and Applied Sciences, Duy Tan University, Ho Chi Minh City, Vietnam.
Natural Product Research
|July 4, 2025
Summary
A new dimeric xanthone, Eumitrin L, was isolated from lichen U. baileyi. Several compounds showed significant tyrosinase inhibition and antioxidant activity, with protocetraric acid and usnic acid being the most potent.
Area of Science:
- Natural Product Chemistry
- Lichenology
- Pharmacognosy
Background:
- Lichens are a rich source of diverse secondary metabolites.
- Usnea baileyi is a lichen species known for its potential chemical constituents.
Purpose of the Study:
- To isolate and characterize new and known compounds from the lichen U. baileyi.
- To evaluate the isolated compounds for tyrosinase inhibitory and antioxidant activities.
Main Methods:
- Compound isolation using column chromatography.
- Structural elucidation via spectroscopic analyses (1D, 2D NMR, DP4, ECD).
- Bioactivity assays including tyrosinase inhibition and DPPH radical scavenging.
- Molecular docking simulations.
Main Results:
- Isolation of a new dimeric xanthone, Eumitrin L, and 13 known compounds.
- Compounds 6, 7, 8, 11 demonstrated tyrosinase inhibition.
- Compounds 3, 10, 13, 14 exhibited significant antioxidant properties.
- Protocetraric acid (6) and usnic acid (10) were identified as the most active compounds.
Conclusions:
- The lichen U. baileyi produces compounds with notable biological activities.
- Eumitrin L represents a novel dimeric xanthone.
- Protocetraric acid and usnic acid show promise as natural tyrosinase inhibitors and antioxidants.
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