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Two new bioactive iridoids from Rothmannia wittii
Nattapong Chaipukdee1, Kwanjai Kanokmedhakul1, Somdej Kanokmedhakul1
1Natural Products Research Unit, Department of Chemistry, Center of Excellence for Innovation in Chemistry, Faculty of Science, Khon Kaen University, Khon Kaen 40002, Thailand.
Researchers isolated two new iridoids from Rothmannia wittii, with one showing antimycobacterial activity against Mycobacterium tuberculosis and the other exhibiting cytotoxicity against cancer cell lines.
Area of Science:
- Natural Product Chemistry
- Pharmacology
Background:
- Rothmannia wittii is a plant species with potential medicinal properties.
- Phytochemical investigation of medicinal plants is crucial for discovering novel therapeutic compounds.
Purpose of the Study:
- To isolate and identify chemical constituents from the bark and fruit of Rothmannia wittii.
- To evaluate the biological activities of the isolated compounds.
Main Methods:
- Compounds were isolated using chromatographic techniques.
- Structural elucidation was performed using various spectroscopic methods (e.g., NMR, MS).
- Biological activities, including antimycobacterial and cytotoxic effects, were assessed using standard assays.
Main Results:
- Two new iridoids, 6β-hydroxy-10-O-acetylgenipin (1) and 10-O-acetylmacrophyllide (2), were identified.
- Six known iridoids, benzoic acid, vanillic acid, and stigmasterol were also isolated.
- Iridoid 1 demonstrated antimycobacterial activity against Mycobacterium tuberculosis (MIC = 12.50 μg/mL).
- Iridoid 2 showed cytotoxicity against the NCI-H187 cancer cell line (IC50 = 6.82 μg/mL).
- Compounds 2 and 5 exhibited weak cytotoxicity against KB and MCF-7 cell lines, while compound 4 was active against NCI-H187.
Conclusions:
- Rothmannia wittii is a source of novel iridoids with significant biological activities.
- The isolated compounds, particularly iridoids 1 and 2, show potential for development as therapeutic agents against tuberculosis and cancer.
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