Literature DB >> 22394397

Abibalsamins A and B, two new tetraterpenoids from Abies balsamea oleoresin.

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.

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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


  2 in total

1.  Abieslactone induces cell cycle arrest and apoptosis in human hepatocellular carcinomas through the mitochondrial pathway and the generation of reactive oxygen species.

Authors:  Guo-Wei Wang; Chao Lv; Zhi-Ran Shi; Ren-Tao Zeng; Xue-Yun Dong; Wei-Dong Zhang; Run-Hui Liu; Lei Shan; Yun-Heng Shen
Journal:  PLoS One       Date:  2014-12-11       Impact factor: 3.240

2.  Lanostane- and cycloartane-type triterpenoids from Abies balsamea oleoresin.

Authors:  Serge Lavoie; Charles Gauthier; Jean Legault; Sylvain Mercier; Vakhtang Mshvildadze; André Pichette
Journal:  Beilstein J Org Chem       Date:  2013-07-04       Impact factor: 2.883

  2 in total

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