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Paeoveitols A-E from Paeonia veitchii.
Wen-Juan Liang1, Yun-Bao Ma1, Chang-An Geng1
1State Key Laboratory of Phytochemistry and Plant Resources in West China, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming 650201, PR China.
Fitoterapia
|August 5, 2015
Summary
Five new compounds, Paeoveitols A-E, were isolated from Paeonia veitchii. Compound 4 demonstrated weak agitation of the human melatonin receptor 1 (MT1) in vitro.
Area of Science:
- Phytochemistry
- Natural Product Chemistry
- Pharmacology
Background:
- Paeonia veitchii is a plant with a history of traditional medicinal use.
- Investigating its chemical constituents may reveal novel bioactive compounds.
- The human melatonin receptor 1 (MT1) is a target for various physiological processes.
Purpose of the Study:
- To isolate and characterize new chemical constituents from Paeonia veitchii.
- To evaluate the biological activity of isolated compounds, specifically their effect on the human melatonin receptor 1 (MT1).
Main Methods:
- Isolation of compounds using chromatographic techniques.
- Structure elucidation through comprehensive spectroscopic analyses (IR, UV, MS, 1D and 2D NMR).
- Determination of absolute configuration via single-crystal X-ray diffraction.
- In vitro assay for human MT1 receptor agitation using HEK293 cells.
Main Results:
- Five new compounds, Paeoveitols A-E (1-5), were isolated, including three monoterpenes and two benzofuran derivatives.
- The structures of all compounds were elucidated.
- Compound 4 exhibited weak agitation activity at the human MT1 receptor (22.52% at 1.79 mM).
Conclusions:
- Paeonia veitchii yielded five novel compounds, Paeoveitols A-E.
- Compound 4 shows preliminary weak activity at the human MT1 receptor, warranting further investigation.
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