Macroline, talpinine, and sarpagine alkaloids from Alstonia penangiana. An NMR-based method for differentiating between A. penangiana and A. macrophylla
Fourteen previously undescribed alkaloids comprising two N-1-hydroxymethylmacroline alkaloids, one talpinine-type oxindole acetal, a pair of equilibrating talpinine-type oxindole hemiacetals, eight oxidized derivatives of sarpagine- and akuammiline-type indole alkaloids, in addition to alstochalotin...
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Veröffentlicht in: | Phytochemistry (Oxford) 2020-08, Vol.176, p.112391-112391, Article 112391 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Fourteen previously undescribed alkaloids comprising two N-1-hydroxymethylmacroline alkaloids, one talpinine-type oxindole acetal, a pair of equilibrating talpinine-type oxindole hemiacetals, eight oxidized derivatives of sarpagine- and akuammiline-type indole alkaloids, in addition to alstochalotine a diastereomer of gelsochalotine recently isolated from Gelsemium elegans, were isolated from the leaf and stem-bark extracts of Alstonia penangiana. The structures and relative configurations of these alkaloids were established using NMR, MS, and in one instance, confirmed by X-ray diffraction analysis. An NMR-based method is described as a useful chemotaxonomic tool for differentiating between A. penangiana and A. macrophylla. Several of the alkaloids isolated showed appreciable growth inhibitory effects when tested against a number of human cancer cell lines.
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•Fourteen undescribed alkaloids were isolated from Alstonia penangiana.•Several of the alkaloids showed cytotoxicity against HT-29 or HCT 116 cells.•A 1H-NMR-based method differentiates between A. penangiana and A. macrophylla. |
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ISSN: | 0031-9422 1873-3700 |
DOI: | 10.1016/j.phytochem.2020.112391 |