1. Academic Validation
  2. ent-Eudesmane sesquiterpenoids, galloyl esters of the oak lactone precursor, and a 3-O-methylellagic acid glycoside from the wood of Platycarya strobilacea

ent-Eudesmane sesquiterpenoids, galloyl esters of the oak lactone precursor, and a 3-O-methylellagic acid glycoside from the wood of Platycarya strobilacea

  • Phytochemistry. 2011 Jun;72(8):796-803. doi: 10.1016/j.phytochem.2011.02.020.
Hajime Maeda 1 Narumi Kakoki Mami Ayabe Yuki Koga Tomoko Oribe Yosuke Matsuo Takashi Tanaka Isao Kouno
Affiliations

Affiliation

  • 1 Graduate School of Biomedical Sciences, Nagasaki University, Nagasaki, Japan.
Abstract

ent-Eudesmane sesquiterpenoids, 8,11-dihydroxy-2,4-cycloeudesmane, 11-hydroxy-2,4-cycloeudesman-8-one and 2,4-cyclo-7(11)-eudesmen-8-one, were isolated from the wood of Platycarya strobilacea, which has been used as an aromatic tree since at least the 18th century. On charring the wood, 2,4-cyclo-7(11)-eudesmen-8-one was detected in the smoke. In the charred wood, the concentrations of ellagitannins, such as galloyl pedunculagin, dramatically decreased, whereas concentrations of pentagalloyl glucose, and Other gallotannins were relatively stable. In addition, two Other compounds, the 6'-O-m- and p-digalloyl oak lactone precursor and the 3-O-methylellagic acid 4'-O-(4″-O-galloyl)-xylopyranoside, were isolated from the charred wood along with m- and p-digallic acid.

Figures
Products