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Title: Total Synthesis and Anticancer Activity of Novel Pulsatilla Saponin D Analogues. Author: Kim M, Park Y, Chung WY, Park KK, Jung M. Journal: Chem Pharm Bull (Tokyo); 2015; 63(9):669-77. PubMed ID: 26329860. Abstract: Novel saponins that retain a free carboxyl group at the C-17 position and various sugars linked at the C-3 position of hederagenin aglycone were synthesized via stereospecific glycosylation. Since these natural products represented by Pulsatilla saponin D (PSD) were obtained in very small amounts, the total synthesis developed in this paper will resolve this problem of scarcity. The two types of synthesized arabinose- and rhamnose-cored saponins showed potent anticancer activity against a human lung cancer cell line (A549), and most disaccharide moiety saponins possessed more potent anti-lung cancer activity. Among the novel PSD analogues containing disaccharide saponins, compound 10i showed anti-lung cancer activity (6.6 µM) that was four-fold more potent than the clinical agent Iressa (26.08 µM).[Abstract] [Full Text] [Related] [New Search]