Abstract
A series of heterocyclic analogues 3-10 of mycophenolic acid were designed as metabolically stable congeners possibly targeted for inosine monophosphate dehydrogenase. The synthesis, cytotoxic and anti-HIV activity of these compounds are described.
| Original language | English |
|---|---|
| Pages (from-to) | 861-866 |
| Number of pages | 6 |
| Journal | Bioorganic and Medicinal Chemistry Letters |
| Volume | 5 |
| Issue number | 8 |
| DOIs | |
| State | Published - Apr 20 1995 |
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