The conversion of 2-β-D-ribofuranosylthiazole-4-carboxamide to an analogue of NAD with potent IMP dehydrogenase-inhibitory properties

David A. Cooney, Hiremagalur N. Jayaram, Gulilat Gebeyehu, Charles R. Betts, James A. Kelley, Victor E. Marquez, David G. Johns

Research output: Contribution to journalArticle

155 Scopus citations
Original languageEnglish (US)
Pages (from-to)2133-2136
Number of pages4
JournalBiochemical Pharmacology
Volume31
Issue number11
DOIs
StatePublished - Jun 1 1982

ASJC Scopus subject areas

  • Biochemistry
  • Pharmacology

Cite this

Cooney, D. A., Jayaram, H. N., Gebeyehu, G., Betts, C. R., Kelley, J. A., Marquez, V. E., & Johns, D. G. (1982). The conversion of 2-β-D-ribofuranosylthiazole-4-carboxamide to an analogue of NAD with potent IMP dehydrogenase-inhibitory properties. Biochemical Pharmacology, 31(11), 2133-2136. https://doi.org/10.1016/0006-2952(82)90436-1