Antimalarial, Cytotoxic, and Antifungal Alkaloids from Duguetia hadrantha

Bioassay-guided isolation of Duguetia hadrantha yielded two new 4,5-dioxo-1-azaaporphinoids, hadranthine A (1) and hadranthine B (2), together with the known alkaloids imbiline-1 (3), sampangine (4), and 3-methoxysampangine (5), whose structures were determined primarily from 2D-NMR 1H−13C HMBC, and...

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Veröffentlicht in:Journal of natural products (Washington, D.C.) D.C.), 2001-05, Vol.64 (5), p.559-562
Hauptverfasser: Muhammad, Ilias, Dunbar, D. Chuck, Takamatsu, Satoshi, Walker, Larry A, Clark, Alice M
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Sprache:eng
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Zusammenfassung:Bioassay-guided isolation of Duguetia hadrantha yielded two new 4,5-dioxo-1-azaaporphinoids, hadranthine A (1) and hadranthine B (2), together with the known alkaloids imbiline-1 (3), sampangine (4), and 3-methoxysampangine (5), whose structures were determined primarily from 2D-NMR 1H−13C HMBC, and 1H−15N HMBC experiments. This is the first report of the co-occurrence of the copyrine alkaloids 4 and 5, as well as the first report of either copyrine or imbiline type alkaloids from a Duguetia species. Compounds 1, 4, and 5 demonstrated in vitro antimalarial activity against Plasmodium falciparum (W-2 clone), while 2 was inactive. Instead, 2 showed in vitro cytotoxicity to selected human cancer cell lines (IC50 = 3−6 μg/mL against SK-MEL, KB, BT-549, and SK-OV-3), and 4 was also cytotoxic to human malignant melanoma (IC50 = 0.37 μg/mL). Sampangine (4) also inhibited cell aggregation with a MIC value of
ISSN:0163-3864
1520-6025
DOI:10.1021/np000436s