Abstract
Ten known compounds were isolated from the leaves and barks of Walsura chrysogyne. One of the known compounds which was isolated as crystal was structurally confirmed by X-ray crystallography and named chrysura (5). The stereochemistry of the (20R, 24ξ1)-ocotillone (9) which previously established by chemical methods has been elucidated by interpretation using 1D, 2D NMR and comparison with closely related compounds. Among the isolated compounds, eichlerianic acid (4) and viridiflorol (7) showed the most significant ichthyotoxicity against zebrafish (Danio rerio) with Median Tolerance Limit (TLM) of 6.7 and 15 ppm respectively.
Keywords: Anti-acetylcholinesterase ichthyotoxicity, Walsura chrysogyne and 20R, 24S-epoxy-25-hydroxydammaran-3-one.
Related Books
Advances in Organic Synthesis
The Synthetic Methods, Structures, and Properties of the Ca-C σ Bond Organocalcium Containing Compounds
Advances in Organic Synthesis
Chemistry of Bipyrazoles: Synthesis and Applications
Advances in Organic Synthesis
Advanced Nanocatalysis for Organic Synthesis and Electroanalysis
Advances in Organic Synthesis
Advances in Organic Synthesis
13