Two guaianolide sesquiterpenoid tetramers named ainsliatetramers A and B were separated from . Through spectroscopic analyses, especially the band-selective CT-HSQC and CT-HMBC techniques, the complex skeleton was constructed from four sesquiterpene units via three different linkages. A biosynthetic pathway was proposed featuring a Michael addition and a regular and a hetero-Diels-Alder cycloaddition. Both exhibited potent cytotoxicity against human cancer cell lines with IC values ranging from 2 to 15 μM.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1021/acs.orglett.9b02909 | DOI Listing |
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!