
doi: 10.1055/s-2002-32068
pmid: 12058326
Seven alkaloids were isolated from Sprekelia formosissima, and five from Hymenocallis x festalis. Tazettine, lycorine, haemanthidine and haemanthamine were evaluated for antiproliferative and multidrug resistance (mdr) reversing activity on mouse lymphoma cells. Lycorine, haemanthidine and haemanthamine displayed pronounced cell growth inhibitory activities against both drug-sensitive and drug-resistant cell lines, but did not significantly inhibit mdr-1 p-glycoprotein. Thus, the tested alkaloids are apparently not substrates for the mdr efflux pump. Assays for interactions with DNA and RNA revealed that the antiproliferative effects of lycorine and haemanthamine result from their complex formation with RNA.
Aniline Compounds, Molecular Structure, Plant Stems, DNA, Dioxoles, Nucleic Acid Denaturation, Antineoplastic Agents, Phytogenic, Drug Resistance, Multiple, Phenanthridines, Magnoliopsida, Mice, Alkaloids, RNA, Transfer, Verapamil, Amaryllidaceae Alkaloids, Tumor Cells, Cultured, Animals, Leukemia L5178
Aniline Compounds, Molecular Structure, Plant Stems, DNA, Dioxoles, Nucleic Acid Denaturation, Antineoplastic Agents, Phytogenic, Drug Resistance, Multiple, Phenanthridines, Magnoliopsida, Mice, Alkaloids, RNA, Transfer, Verapamil, Amaryllidaceae Alkaloids, Tumor Cells, Cultured, Animals, Leukemia L5178
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