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Bioorg. Med. Chem. Lett. · Apr 2004
Modified norcantharidins; synthesis, protein phosphatases 1 and 2A inhibition, and anticancer activity.
- Matthew E Hart, A Richard Chamberlin, Cecilia Walkom, Jennette A Sakoff, and Adam McCluskey.
- Department of Chemistry, University of California at Irvine, Irvine, CA 92697, USA.
- Bioorg. Med. Chem. Lett. 2004 Apr 19; 14 (8): 1969-73.
AbstractFourteen modified norcantharidin analogues have been synthesised and screened for their ability to inhibit the serine/threonine protein phosphatases 1 and 2A. The most potent compounds found were 10 (PP1 IC(50)=13+/-5 microM; PP2A IC(50)=7+/-3 microM) and 16 (PP1 IC(50)=18+/-8 microM; PP2A IC(50)=3.2+/-0.4 microM). Overall, only analogues possessing at least one acidic residue at the former anhydride warhead displayed any PP1 or PP2A inhibitory action. The ability of these analogues to inhibit PP1 and PP2A correlates well with their observed anti-cancer activity against a panel of five cancer cell lines: A2780 (human ovarian carcinoma), G401 (human kidney carcinoma), HT29 (human colorectal carcinoma), H460 (human lung carcinoma) and L1210 (murine leukemia).
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