| Literature DB >> 22394397 |
Serge Lavoie1, Jean Legault, Charles Gauthier, Vakhtang Mshvildadze, Sylvain Mercier, André Pichette.
Abstract
Abibalsamins A (1) and B (2), two unprecedented tetraterpenoids featuring a 3,4-seco-rearranged lanostane system fused with a β-myrcene lateral chain via a [4 + 2] Diels-Alder cycloaddition, were isolated from the oleoresin of Abies balsamea. Their structures were elucidated by means of extensive 2D NMR, IR, and MS spectroscopy analyses. The absolute configuration of 1 was determined by single-crystal X-ray diffraction. Both compounds exhibited significant cytotoxic activity against cancer cell lines.Entities:
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Year: 2012 PMID: 22394397 DOI: 10.1021/ol300237f
Source DB: PubMed Journal: Org Lett ISSN: 1523-7052 Impact factor: 6.005