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Design and synthesis of heterocyclic analogues of mycophenolic acid as potential chemotherapeutic agents

  • SUNY Buffalo

Research output: Contribution to journalArticlepeer-review

3 Scopus citations

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 languageEnglish
Pages (from-to)861-866
Number of pages6
JournalBioorganic and Medicinal Chemistry Letters
Volume5
Issue number8
DOIs
StatePublished - Apr 20 1995

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