Publications by authors named "Nicole Darbour"

Article Synopsis
  • The study analyzed the phytochemical properties of Marrubium deserti, resulting in the discovery of new labdane diterpenes named marrulibacetal A and desertine, along with various known compounds.
  • A total of 13 phenolic compounds and terpenoids were isolated, including several derivatives of apigenin and phenylethanoid glucosides.
  • The antioxidant activities of some compounds were tested with promising results, showing superior capacity compared to trolox, and exhibited potential genotoxic and antigenotoxic effects on Escherichia coli.
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Bio-guided fractionation of the roots of Paris polyphylla (Trilliaceae), based on inhibition of P-glycoprotein-mediated daunorubicin efflux in K562/R7 cell line, led to isolation and identification of the three saponins 3-O-Rha(1-->2)[Ara(1-->4)]Glc-pennogenine, gracillin and polyphyllin D, and the two ecdysteroids 20-hydroxyecdysone and pinnatasterone. These compounds were tested for multidrug reversion on P-glycoprotein (ABCB1) with both drug-selected and transfected cell lines, and also on Breast Cancer Resistance Protein (BCRP/ABCG2). By contrast to a weak efficiency on BCRP, the three saponins displayed significant effects as inhibitors of P-glycoprotein-mediated drug efflux.

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From the dichloromethane extract of aerial parts of Ferula vesceritensis (Apiaceae), 11 sesquiterpene derivatives were isolated. Among them five were compounds designated as 10-hydroxylancerodiol-6-anisate, 2,10-diacetyl-8-hydroxyferutriol-6-anisate, 10-hydroxylancerodiol-6-benzoate, vesceritenone and epoxy-vesceritenol. The six known compounds were identified as feselol, farnesiferol A, lapidol, 2-acetyl-jaeschkeanadiol-6-anisate, lasidiol-10-anisate and 10-oxo-jaesckeanadiol-6-anisate.

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Article Synopsis
  • A new isoflavone called 5,7-dihydroxy-4'-methoxy-3'-(2,3-dihydroxy-3-methylbutyl)isoflavone was discovered in the stem bark of Ficus nymphaefolia Mill.
  • Eight known isoflavones were also identified, including genistein and erycibenin A.
  • The structures of these compounds were determined through advanced spectral analysis techniques, specifically 1D and 2D NMR experiments.
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