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Conversion of 2-beta-D-ribofuranosylselenazole-4-carboxamide to an analogue of NAD with potent IMP dehydrogenase-inhibitory properties.
- Source :
-
Biochemical pharmacology [Biochem Pharmacol] 1983 Sep 01; Vol. 32 (17), pp. 2633-6. - Publication Year :
- 1983
- Subjects :
- Animals
Gas Chromatography-Mass Spectrometry
Mice
Selenium chemical synthesis
IMP Dehydrogenase antagonists & inhibitors
Ketone Oxidoreductases antagonists & inhibitors
Leukemia P388 drug therapy
Leukemia, Experimental drug therapy
NAD analogs & derivatives
Organoselenium Compounds
Ribavirin analogs & derivatives
Ribavirin toxicity
Ribonucleosides chemical synthesis
Ribonucleosides toxicity
Selenium toxicity
Subjects
Details
- Language :
- English
- ISSN :
- 0006-2952
- Volume :
- 32
- Issue :
- 17
- Database :
- MEDLINE
- Journal :
- Biochemical pharmacology
- Publication Type :
- Academic Journal
- Accession number :
- 6137224
- Full Text :
- https://doi.org/10.1016/0006-2952(83)90038-2