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Biochemically active sesquiterpene lactones from Ratibida mexicana
M R Calera1, F Soto, P Sanchez
1Facultad de Química, Universidad Nacional Autónoma de México, México, D.F.
Phytochemistry
|September 1, 1995
Summary
Two sesquiterpene lactones from Ratibida mexicana roots inhibit plant growth, fungal pathogens, and tumor cells. Isoalloalantolactone also inhibits Photosystem II in photosynthesis.
Area of Science:
- Natural Product Chemistry
- Phytochemistry
- Plant Biochemistry
Background:
- Ratibida mexicana is a plant species with potential medicinal properties.
- Sesquiterpene lactones are a class of natural compounds known for diverse biological activities.
Purpose of the Study:
- To isolate and characterize bioactive compounds from Ratibida mexicana roots.
- To evaluate the herbicidal, cytotoxic, and antifungal activities of isolated compounds.
- To investigate the mechanism of action of isoalloalantolactone on photosynthesis.
Main Methods:
- Bioactivity-directed fractionation of methanol extract.
- Isolation and structural elucidation of sesquiterpene lactones.
- Bioassays for radicle growth inhibition, cytotoxicity, and antifungal activity.
- Photosynthetic electron transport studies.
Main Results:
- Two sesquiterpene lactones, isoalloalantolactone and elema-1,3,11-trien-8,12-olide, were isolated.
- Both compounds inhibited radicle growth of Amaranthus hypochondriacus and Echinochloa crus-galli.
- Moderate cytotoxic activity against solid tumor cell lines and significant inhibition of phytopathogenic fungi were observed.
- Isoalloalantolactone inhibited ATP synthesis and electron transport, specifically Photosystem II, acting as a Hill's reaction inhibitor.
Conclusions:
- Sesquiterpene lactones from Ratibida mexicana exhibit significant herbicidal, cytotoxic, and antifungal properties.
- Isoalloalantolactone's inhibition of Photosystem II offers insights into its mode of action.
- These findings highlight the potential of Ratibida mexicana as a source of novel bioactive compounds.