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
Hauptverfasser: Yeap, Joanne Soon-Yee, Tan, Chun-Hoe, Yong, Kien-Thai, Lim, Kuan-Hon, Lim, Siew-Huah, Low, Yun-Yee, Kam, Toh-Seok
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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. [Display omitted] •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.
ISSN:0031-9422
1873-3700
DOI:10.1016/j.phytochem.2020.112391