Antitumor activity of derivatives of mycophenolic acid.

Abstract
One hundred and eight derivatives of mycophenolic acid (MA) from Penicillium were prepared by modifications at the phenolic hydroxyl and/or carboxyl sites. None of these compounds was as effective as MA in suppressing cell growth of L-5178Y leukemia cells in vitro, whereas several compounds with changes at the hydroxyl and carboxyl groups were more effective than MA against Ehrlich solid carcinoma and L-1210 leukemia in mice.

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