Abstract
Phytochemical study of the leaves of the medicinal plant Isodon rubescens led to the isolation of three novel abietane diterpenoids, rubesanolides C-E (1-3). These diterpenes contain a unique γ-lactone subgroup formed between C-8 and C-20. Their structures were determined from analysis of spectroscopic data, and were further confirmed by X-ray crystallographic data. The compounds were evaluated for their antibacterial activity, and rubesanolide D (2) demonstrated inhibition activity against biofilm formation of the dental bacterium Streptococcus mutans.
| Original language | English |
|---|---|
| Pages (from-to) | 5039-5044 |
| Number of pages | 6 |
| Journal | Organic and Biomolecular Chemistry |
| Volume | 10 |
| Issue number | 26 |
| DOIs | |
| Publication status | Published - 14 Jul 2012 |
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