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  • Title: Synthesis and biological evaluation of novel spin labeled 18β-glycyrrhetinic acid derivatives.
    Author: Liu Y, Qian K, Wang CY, Chen CH, Yang X, Lee KH.
    Journal: Bioorg Med Chem Lett; 2012 Dec 15; 22(24):7530-3. PubMed ID: 23122524.
    Abstract:
    Eighteen novel spin-labeled 18β-glycyrrhetinic acid (GA) derivatives were designed, synthesized, and evaluated for cytotoxicity against four human tumor cell lines (A-549, DU-145, KB and KBvin). Most of the derivatives showed more significant cytotoxicity than that of the parent compound GA. The best compound, 6j, with a tryptophan amino moiety and piperidine nitroxyl radical showed GI(50) values of 13.7-15.0 μM, and was fivefold more potent than GA. In a mechanism of action study, compound 7a was confirmed as a 20S proteasome inhibitor in both in vitro and cell-based assays. These findings support further optimization efforts based on 18β-GA as a lead compound to develop potential anticancer drug candidates.
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