Lanostane- and cycloartane-type triterpenoids from Abies balsamea oleoresin

Beilstein J Org Chem. 2013 Jul 4:9:1333-1339. doi: 10.3762/bjoc.9.150. eCollection 2013.

Abstract

Phytochemical analysis of A. balsamea oleoresin led to the isolation of three new 3,4-seco-lanostane triterpenoids 1-3, one new cycloartane triterpenoid 4 along with fourteen known terpenoids. Structure determinations were based on extensive 1D/2D NMR, IR and MS spectroscopic analyses, and comparison with literature data. The isolated compounds were evaluated in vitro for their cytotoxicity against human cell lines (A549, DLD-1, WS1) and their antibacterial activity against E. coli and S. aureus. Abiesonic acid (6) exhibited weak cytotoxic activity against A549 (IC50 = 22 µM) while compounds 1 and 4 were weakly active against S. aureus (MIC = 25 µM).

Keywords: Abies balsamea; cycloartane; lanostane; oleoresin; triterpenoids.