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The Synthesis and Biological Evaluation of Two Analogues of the C-Riboside Showdomycin

Renner, Jens (author)
Kruszelnicki, Irma (author)
Adamiak, Beata (author)
Gothenburg University,Göteborgs universitet,Institutionen för laboratoriemedicin, Avdelningen för klinisk virologi,Institute of Laboratory Medicine, Dept of Clinical Virology
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Willis, Anthony C (author)
Hammond, Edward (author)
Su, Stephen (author)
Burns, Christopher (author)
Trybala, Edward, 1955 (author)
Gothenburg University,Göteborgs universitet,Institutionen för laboratoriemedicin, Avdelningen för klinisk virologi,Institute of Laboratory Medicine, Dept of Clinical Virology
Ferro, Vito (author)
Banwell, Martin G (author)
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 (creator_code:org_t)
2005
2005
English.
In: Australian Journal of Chemistry. ; 58:2, s. 86-93
  • Journal article (peer-reviewed)
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  • Two novel analogues, 2 and 3, of the C-riboside showdomycin (1) have been prepared by exploiting the N-TIPS-substituted pyrrole 7 as a synthetic equivalent for the maleimide C3 anion. The tetraacetate precursor, 12, of target 2 as well as target 3 itself were subjected to single-crystal X-ray analyses. Analogues 2 and 3 as well as showdomycin and its anomer (4) have each been evaluated in various assays for their cytotoxic, anti-bacterial, and anti-viral effects.

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