Inside Back Cover: Total Synthesis and Biological Assessment of MandelalideA
The picture shows the marine macrolide mandelalideA together with the starting materials and advanced intermediates that have enabled a highly convergent total synthesis of the macrolactone core of this complex natural product. Like other bioactive macrocycles, mandelalideA is of polyketide origin a...
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Veröffentlicht in: | Chemistry : a European journal 2016-01, Vol.22 (4), p.1531 |
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Hauptverfasser: | , , |
Format: | Artikel |
Sprache: | eng |
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Online-Zugang: | Volltext |
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Zusammenfassung: | The picture shows the marine macrolide mandelalideA together with the starting materials and advanced intermediates that have enabled a highly convergent total synthesis of the macrolactone core of this complex natural product. Like other bioactive macrocycles, mandelalideA is of polyketide origin and it has been described to exhibit antiproliferative activity against some human cancer cell lines, but not others. Here, mandelalideA was found to reduce the proliferation of two lung cancer cell lines with nM potency, but it did not kill all cells even at much higher concentrations. More information can be found in the Full Paper by K.-H. Altmann etal. on page1292ff. |
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ISSN: | 0947-6539 1521-3765 |
DOI: | 10.1002/chem.201504918 |