| Literature DB >> 32388425 |
Anna Korda1, Lucie Rárová2, Zbigniew Pakulski3, Miroslav Strnad4, Jana Oklešťková2, Kinga Kuczynska1, Piotr Cmoch1, Katarzyna Gwardiak1, Romuald Karczewski1.
Abstract
Triterpene bidesmosides are considered as highly cytotoxic saponins, usually less toxic against normal cells than monodesmosides, and less haemolytic. Biological activity of the betulin-type bidesmosides, rarely found in Nature, and seldom prepared due to serious synthetic problems, is poorly recognized. We report herein a protocol for the preparation of disubstituted lupane saponins (betulin bidesmosides) by treatment of their benzoates with potassium carbonate in dichloromethane / methanol solution. Cytotoxicity of all compounds was tested in vitro for a series of cancer cell lines, as well as normal human skin BJ fibroblasts. Presence of l-rhamnose moiety is crucial for cytotoxicity of betulin bidesmosides. On the other hand, l-arabinose fragment connected to lupane C-3 carbon atom significantly decreases activity. Presented results clearly show that betulin bidesmosides have significant clinical potential as anticancer agents.Entities:
Keywords: Betulin bidesmosides; Birch bark; Cytotoxic activity; Structure–activity relationship; Synthesis
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Year: 2020 PMID: 32388425 DOI: 10.1016/j.bioorg.2020.103868
Source DB: PubMed Journal: Bioorg Chem ISSN: 0045-2068 Impact factor: 5.275