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      Antiproliferative triterpene saponins from Entada africana.

      Journal of Natural Products
      Animals, Antineoplastic Agents, Phytogenic, chemistry, isolation & purification, pharmacology, Drug Screening Assays, Antitumor, Fabaceae, Humans, Macrophages, drug effects, Mali, Mice, Molecular Structure, Nuclear Magnetic Resonance, Biomolecular, Plant Roots, Plants, Medicinal, Saponins, Triterpenes

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          Abstract

          Nine new ester saponins (1-9) were isolated from the roots of Entada africana. Their structures were elucidated by 1D and 2D NMR experiments including 1D and 2D TOCSY, DQF-COSY, HSQC, and HMBC spectroscopy, as well as ESIMS analysis, and chemical methods. The aglycon moieties were found to be echinocystic acid for compounds 1, 2, 4-6, 8, and 9 and acacic acid for 3 and 7. All isolated compounds were tested for their antiproliferative activity against the J774.A1, HEK-293, and WEHI-164 cell lines. Moderate to high cytotoxic potency was found for almost all compounds tested.

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