Chemical composition of the bark of Tetrapterys mucronata and identification of acetylcholinesterase inhibitory constituents.
Marcos Marçal Ferreira Queiroz, Emerson Ferreira Queiroz, Maria Luiza Zeraik, Samad Nejad Ebrahimi, Laurence Marcourt, Muriel Cuendet, Ian Castro-Gamboa, Matthias Hamburger, Vanderlan Da Silva Bolzani, Jean‐Luc Wolfender
Journal of Natural Products March 28, 2014 DOI: 10.1021/np401003p (opens in new tab)
Study at a glance
AI-extracted from the abstract| Characteristics | Phytochemical and pharmacological analysis Peer reviewed |
|---|---|
| Population | Bark of Tetrapterys mucronata |
| Measures | TLC bioautography assay, HPLC-microfractionation in 96-well plates, AChE inhibition bioautography, IC50 |
| Key points | The ethanolic bark extract of Tetrapterys mucronata inhibited acetylcholinesterase in vitro. Twenty-two compounds were isolated, including six new natural products, and compounds 1, 5, 6, 9, and 10 inhibited AChE with IC50 values below 15 μM. |
Abstract
The secondary metabolite content of Tetrapterys mucronata, a poorly studied plant that is used occasionally in Brazil for the preparation of a psychotropic plant decoction called "Ayahuasca", was determined to establish its chemical composition and to search for acetylcholinesterase (AChE) inhibitors. The ethanolic extract of the bark of T. mucronata exhibited in vitro AChE inhibition in a TLC bioautography assay. To localize the active compounds, biological profiling for AChE inhibition was performed using at-line HPLC-microfractionation in 96-well plates and subsequent AChE inhibition bioautography. The analytical HPLC-PDA conditions were transferred geometrically to a preparative medium-pressure liquid chromatography column using chromatographic calculations for the efficient isolation of the active compounds at the milligram scale. Twenty-two compounds were isolated, of which six are new natural products. The structures of the new compounds (9, 10, 16-18, and 20) were elucidated by spectroscopic data interpretation. Compounds 1, 5, 6, 9, and 10 inhibited AChE with IC50 values below 15 μM.
Citations in the library
Cited by 2
Cites 2
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