Related Experiment Video
Updated: Jan 1, 2026

A Customizable Approach for the Enzymatic Production and Purification of Diterpenoid Natural Products
Published on: October 4, 2019
Thorectandrols C, D, and E, new sesterterpenes from the marine sponge Thorectandra sp
Romila D Charan1, Tawnya C McKee, Michael R Boyd
1Molecular Targets Drug Discovery Program, Center for Cancer Research, National Cancer Institute, Frederick, Maryland 21702-1201, USA.
Abstract:
Extracts of the marine sponge Thorectandra sp. have been found to contain three new sesterterpenes, thorectandrols C (4), D (5), and E (6), together with the known compounds luffarin R (7), luffarin V (8), and palauolide (9). The structures were determined by extensive NMR spectral data analysis. Their relative stereochemistry was defined using NOE correlations and coupling constants, while CD data were used to suggest their absolute stereochemistry. Cytotoxicity data for compounds 4-9 as well as the previously reported compounds thorectandrols A and B and palauolol (1-3) against six or more human tumor cell lines are also reported.
More Related Videos
16:03A Fish-feeding Laboratory Bioassay to Assess the Antipredatory Activity of Secondary Metabolites from the Tissues of Marine Organisms
Published on: January 11, 2015
09:26Cellular Lipid Extraction for Targeted Stable Isotope Dilution Liquid Chromatography-Mass Spectrometry Analysis
Published on: November 17, 2011
Related Concept Videos
Biosynthesis of Lipids
Thermal and Photochemical Electrocyclic Reactions: Overview