Abstract
The non-natural enantiomeric forms of narciclasine and lycoricidine ((-)-1 and (-)-2, respectively), as well as congeners 3-6 are available through chemoenzymatic synthesis. Accordingly, they have now been tested for their cytotoxic effects in a 13-member human cancer cell-line panel and found to be only weakly active. In contrast, an authentic sample of the natural enantiomeric form of narciclasine ((+)-1) was found to be highly active in the same screens.
| Original language | English |
|---|---|
| Pages (from-to) | 685-691 |
| Number of pages | 7 |
| Journal | Chemistry and Biodiversity |
| Volume | 6 |
| Issue number | 5 |
| DOIs | |
| Publication status | Published - May 2009 |
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