Synthesis of the seco-Limonoid BCD Ring System Identifies a Hsp90 Chaperon Machinery (p23) Inhibitor
- David M. Pinkerton,
- Sharon Chow,
- Nada H. Eisa,
- Kashish Kainth,
- Timothy J. Vanden Berg,
- Jed M. Burns
- University of Queensland,
- Mansoura University,
- Augusta University,
- CSIRO,
Sustainable Development Goals
- SDG 3 Good Health and Well
Abstract
D-Ring-seco-limonoids (tetranortriterpenoids), such as gedunin and xylogranin B display anti-cancer activity, acting via inhibition of Hsp90 and/or associated chaperon machinery (e.g., p23). Despite this, these natural products have received relatively little attention, both in terms of an enabling synthetic approach (which would allow access to derivatives), and as a consequence their structure–activity relationship (SAR). Disclosed herein is a generally applicable synthetic route to the BCD ring system of the seco-D-ring double bond containing limonoids. Furthermore, cell based assays revealed the first skeletal fragment that exhibited inhibition of the p23 enzyme at a level which was equipotent to that of gedunin, despite being much less structurally complex.
Publication Information
Output type
Original language
English (US)Pages from-to (Number of pages)
Pages 1451-1455 (5 pages)Journal (Volume, Issue Number)
Chemistry - A European Journal (Volume 25, Issue 6)Publication milestones
- Accepted/In press - 01/01/2018
- Published - 01/28/2019
Publication status
ISSN
0947-6539Publication IDs
- Scopus: 85058946008
- PubMed: 30570197
