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      Neolignanamides, lignanamides, and other phenolic compounds from the root bark of Lycium chinense.

      Journal of Natural Products
      Acrylamides, chemistry, isolation & purification, pharmacology, Bicyclo Compounds, Heterocyclic, Biphenyl Compounds, Drugs, Chinese Herbal, Free Radical Scavengers, Lycium, Molecular Structure, Naphthalenes, Nuclear Magnetic Resonance, Biomolecular, Phenols, Picrates, Plant Bark, Stereoisomerism

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          Abstract

          Seven new neolignanamides (1-7), including two pairs of cis- and trans-isomers, and a new lignanamide (8) were isolated from the EtOAc-soluble fraction of an EtOH extract of the root bark of Lycium chinense, together with 22 known phenolic compounds (9-30), four of which were obtained from the genus Lycium for the first time. Compounds 5, 6, and 7 are unusual dimers having a rare connection mode between the two cinnamic acid amide units, while compounds 6, 7, and 8 are the first naturally occurring dimers derived from two dissimilar cinnamic acid amides. The cinnamic acid amides, neolignanamides, and lignanamides possess moderate radical-scavenging activity against the DPPH (2,2-diphenyl-1-picrylhydrazyl) and superoxide radicals.

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