| Literature DB >> 25039009 |
Simeon Fogue Kouam1, Alain Wembe Ngouonpe2, Marc Lamshöft3, Ferdinand Mouafo Talontsi3, Jonathan O Bauer4, Carsten Strohmann4, Bonaventure Tchaleu Ngadjui5, Hartmut Laatsch6, Michael Spiteller7.
Abstract
The stem bark of Polyalthia oliveri was screened for its chemical constituents using liquid chromatography high resolution mass spectrometry resulting in the isolation of three indolosesquiterpene alkaloids named 8α-polyveolinone (1), N-acetyl-8α-polyveolinone (2) and N-acetyl-polyveoline (3), together with three known compounds, dehydro-O-methylisopiline (4), N-methylurabaine (5) and polycarpol (6). The structures of the compounds were elucidated by means of high resolution mass spectrometry and different NMR techniques and chemical transformations. Their absolute configurations were assigned by ab-initio calculation of CD and ORD data (for 2 and 3) and X-ray diffraction analysis (for 2). Compounds 2 and 3 exhibited moderate antiplasmodial activity against erythrocytic stages of chloroquine-sensitive Plasmodium falciparum NF54 strain and low cytotoxicity on rat skeletal myoblast (L6) cell line.Entities:
Keywords: Absolute configuration; Annonaceae; Antiplasmodial; Cytotoxicity; High resolution mass spectrometry; Indolosesquiterpenes; Polyalthia oliveri
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Year: 2014 PMID: 25039009 DOI: 10.1016/j.phytochem.2014.06.015
Source DB: PubMed Journal: Phytochemistry ISSN: 0031-9422 Impact factor: 4.072