Planta Med 2008; 74 - PB144
DOI: 10.1055/s-0028-1084489

New 2-acetoxy fatty acid methyl esters from Nepeta parnassica

G Gkinis 1, E Ioannou 1, C Vagias 1, O Tzakou 1, V Roussis 1
  • 1Department of Pharmacognosy and Chemistry of Natural Products, School of Pharmacy, University of Athens, Panepistimiopolis Zografou, Athens 15771, Greece

The genus Nepeta (Lamiaceae) comprises approximately 250 species of annual or perennial herbs distributed in temperate Europe, Asia and Africa [1]. Nepetalactones, iridoids and their glucosides, diterpenes and triterpenes are reported in the literature as major constituents of Nepeta species. Their extracts and essential oils have exhibited analgesic, anti-inflammatory, antiviral, antioxidant and antimicrobial activities. Nepeta parnassica Heldr. & Sart. is an aromatic perennial herb, endemic to Greece and South Albania [2].

The dichloromethane extract of the aerial parts of wild N. parnassica populations collected from Mt. Parnassos (Greece) was subjected to a series of chromatographic separations to yield three new fatty acid methyl esters bearing an acetoxy group at C-2 (1-3), in addition to the new nepetalactone dimer, nepetaparnone, and the new pimarane derivative, parnapimarol [3]. The structure elucidation of 1-3 was based on analyses of their spectroscopic data (1D and 2D NMR, IR, MS).

References: 1. Mabberley, D.J. (1997) The Plant Book: A Portable Dictionary of the Vascular Plants. Cambridge University Press. Cambridge.

2. Turner, C. (1972) Flora Europaea, Vol. 3 (Tutin, T.G.; Heywood, V.H.; Burges, N.A.; Moore, D.M.; Valentine, D.H.; Walters, S.M.; Webb, D.A., Eds.). Cambridge University Press. Cambridge.

3. Gkinis, G. et al. (2008)J. Nat Prod. In press.