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      Synthesis and cytotoxicity of bidesmosidic betulin and betulinic acid saponins.

      Journal of Natural Products
      Antineoplastic Agents, Phytogenic, chemical synthesis, chemistry, pharmacology, Drug Screening Assays, Antitumor, Humans, Molecular Structure, Saponins, Structure-Activity Relationship, Triterpenes

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          Abstract

          The naturally occurring cytotoxic saponin 28-O-beta-d-glucopyranosylbetulinic acid 3beta-O-alpha-l-arabinopyranoside (3) was easily synthesized along with seven bidesmosidic saponins starting from the lupane-type triterpenoids betulin (1) and betulinic acid (2). As highlighted by the preliminary cytotoxicity evaluation against A549, DLD-1, MCF7, and PC-3 human cancer cell lines, the bidesmosidic betulin saponin 22a, bearing alpha-l-rhamnopyranoside moieties at both C-3 and C-28 positions, was determined to be a potent cytotoxic agent (IC(50) 1.8-1.9 microM).

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