% IMPORTANT: The following is UTF-8 encoded.  This means that in the presence
% of non-ASCII characters, it will not work with BibTeX 0.99 or older.
% Instead, you should use an up-to-date BibTeX implementation like “bibtex8” or
% “biber”.

@ARTICLE{Muharini:836428,
      author       = {Muharini, Rini and Díaz, Adriana and Ebrahim, Weaam and
                      Mándi, Attila and Kurtán, Tibor and Rehberg, Nidja and
                      Kalscheuer, Rainer and Hartmann, Rudolf and Orfali, Raha S.
                      and Lin, Wenhan and Liu, Zhen and Proksch, Peter},
      title        = {{A}ntibacterial and {C}ytotoxic {P}henolic {M}etabolites
                      from the {F}ruits of {A}morpha fruticosa},
      journal      = {Journal of natural products},
      volume       = {80},
      number       = {1},
      issn         = {0163-3864},
      address      = {Washington, DC},
      publisher    = {Soc.},
      reportid     = {FZJ-2017-05549},
      pages        = {169–180},
      year         = {2017},
      abstract     = {Fourteen new natural products, namely,
                      2-[(Z)-styryl]-5-geranylresorcin-1-carboxylic acid (1),
                      amorfrutin D (2), 4-O-demethylamorfrutin D (3),
                      8-geranyl-3,5,7-trihydroxyflavanone (4),
                      8-geranyl-5,7,3′-trihydroxy-4′-methoxyisoflavone (5),
                      6-geranyl-5,7,3′-trihydroxy-4′-methoxyisoflavone (6),
                      8-geranyl-7,3′-dihydroxy-4′-methoxyisoflavone (7),
                      3-O-demethyldalbinol (8),
                      6a,12a-dehydro-3-O-demethylamorphigenin (9),
                      (6aR,12aR,5′R)-amorphigenin (10), amorphispironones B and
                      C (11 and 12), resokaempferol
                      3-O-β-d-glucopyranosyl-(1→2)-β-d-glucopyranoside-7-O-α-l-rhamnopyranoside
                      (13), and daidzein
                      7-O-β-d-glucopyranosyl-(1→2)-β-d-glucopyranoside (14),
                      together with 40 known compounds, were isolated from the
                      fruits of Amorpha fruticosa. The structures of the new
                      compounds were elucidated by 1D and 2D NMR spectroscopic
                      analysis as well as from the mass spectrometry data. ECD
                      calculations were performed to determine the absolute
                      configurations of 11 and 15. Compounds 1, 4–6, and 16–23
                      showed potent to moderate antibacterial activities against
                      several Gram-positive bacteria with MIC values ranging from
                      3.1 to 100 μM. In addition, compounds 11 and 24–33 were
                      significantly cytotoxic against the L5178Y mouse lymphoma
                      cell line and exhibited IC50 values from 0.2 to 10.2 μM.},
      cin          = {ICS-6},
      ddc          = {500},
      cid          = {I:(DE-Juel1)ICS-6-20110106},
      pnm          = {551 - Functional Macromolecules and Complexes (POF3-551)},
      pid          = {G:(DE-HGF)POF3-551},
      typ          = {PUB:(DE-HGF)16},
      UT           = {WOS:000393089600023},
      pubmed       = {pmid:28075580},
      doi          = {10.1021/acs.jnatprod.6b00809},
      url          = {https://juser.fz-juelich.de/record/836428},
}