Tricolorin A, major phytogrowth inhibitor from Ipomoea tricolor
| Přístupová URL adresa: | https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a26a9d06e37b52e8fe8875025c45883b http://www.scopus.com/inward/record.url?eid=2-s2.0-0027155930&partnerID=MN8TOARS |
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| Přírůstkové číslo: | edsair.doi.dedup.....a26a9d06e37b52e8fe8875025c45883b |
| Autor: | A. D. Kinghorn, Rogelio Pereda-Miranda, D. B. M. Wickramaratne, Rachel Mata, Ana Luisa Anaya, John M. Pezzuto |
| Předmět: |
Magnetic Resonance Spectroscopy
Molecular Conformation Pharmaceutical Science Biology Ipomoea Analytical Chemistry chemistry.chemical_compound Ipomoea tricolor Drug Discovery Botany Radicle Tumor Cells Cultured Glycosides Phorbol 12 13-Dibutyrate Protein Kinase C Antibacterial agent Pharmacology chemistry.chemical_classification Chromatography Plants Medicinal Herbicides Plant Extracts Organic Chemistry Glycoside Brain biology.organism_classification Antineoplastic Agents Phytogenic Complementary and alternative medicine chemistry Phorbol Molecular Medicine Drug Screening Assays Antitumor Weed Convolvulaceae |
| Zdroj: | Scopus-Elsevier |
| Popis: | The allelopathic potential of Ipomoea tricolor (Convolvulaceae), used in Mexican traditional agriculture as a weed controller, has been demonstrated by measuring the inhibitory activity of organic extracts on seedling growth of Amaranthus leucocarpus and Echinochloa crus-galli. Bioactivity-directed fractionation of the active CHCl3 extract led to the isolation of the allelopathic principle, which turned out to be a mixture of the so-called "resin glycosides" of convolvulaceous plants. The structure of tricolorin A, the major phytogrowth inhibitor present in the active fraction, was elucidated as (11S)-hydroxyhexadecanoic acid 11-O-alpha-L-rhamnopyranosyl-(1-->3)-O-alpha-L-[2-O-(2S-methylbutyryl)-4 -O- (2S-methylbutyryl)] rhamnopyranosyl-(1-->2)-O-beta-D-glucopyranosyl-(1-->2)-beta-D-fucopyran oside- (1,3"-lactone)[1], based on chemical methods and spectral analysis including 1H-1H COSY, 1H-13CHETCOR, long range 1H-13C COLOC, and selective INEPT experiments. Bioassays showed that radicle elongation of the two weed seedlings tested was inhibited by tricolorin A [1] with IC50 values ranging from 12 to 37 microM. Staphylococcus aureus was sensitive to compound 1 with an MIC value of 1.8 micrograms/ml. Significant cytotoxic activity against cultured P-388 and human breast cancer cells (ED50 2.2 micrograms/ml) was demonstrated for compound 1, and it also inhibited phorbol 12,13-dibutyrate binding using calf brain homogenate as a source of protein kinase C (IC50 43 microM). |
| Databáze: | OpenAIRE |
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