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Published on: January 26, 2016
Five undescribed cyclopeptides from Cordyceps militaris
Wei Yang1, Cong Fu2, Bin-Yuan Hu2
1School of Pharmacy, Chengdu University of Traditional Chinese Medicine, Chengdu, 611137, PR China; Institute for Inheritance-Based Innovation of Chinese Medicine, Marshall Laboratory of Biomedical Engineering, School of Pharmacy, Shenzhen University Medical School, Shenzhen University, Shenzhen, 518055, PR China.
Five new cyclopeptides, Ustiloxins I-M, were isolated from Cordyceps militaris. Compounds 4 and 5 demonstrated significant toxicity against human triple-negative breast cancer cells.
Area of Science:
- Natural Products Chemistry
- Medicinal Chemistry
- Pharmacology
Background:
- Cordyceps militaris is a fungus known for producing bioactive compounds.
- Cyclopeptides represent a class of natural products with diverse biological activities.
- Triple-negative breast cancer remains a challenging disease with limited targeted therapies.
Purpose of the Study:
- To isolate and characterize novel cyclopeptides from Cordyceps militaris.
- To evaluate the cytotoxic effects of these compounds on human triple-negative breast cancer cells.
Main Methods:
- Isolation of cyclopeptides using chromatographic techniques.
- Structure elucidation employing spectroscopic methods (NMR, MS) and X-ray crystallography.
- Computational methods for structure assignment.
- In vitro cytotoxicity assays using human triple-negative breast cancer cell lines.
Main Results:
- Five new cyclopeptides, Ustiloxins I-M (1-5), were isolated and characterized.
- The structures of Ustiloxins I and M (1 and 5) were confirmed by crystallography.
- Spectroscopic and computational analyses determined the structures of Ustiloxins J-L (2-4).
- Ustiloxins L (4) and M (5) exhibited cytotoxicity against triple-negative breast cancer cells with IC50 values of 64.29 μM and 28.89 μM, respectively.
Conclusions:
- Cordyceps militaris produces novel cyclopeptides with potential anticancer properties.
- Ustiloxins L and M show promising activity against human triple-negative breast cancer cells, warranting further investigation.
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