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selenazofurin

Known as: RSC II, 2-ribofuranosylselenazole-4-carboxamide, 4-Selenazolecarboxamide, 2-beta-D-ribofuranosyl- 
 
National Institutes of Health

Papers overview

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Review
2005
Review
2005
  • W. Parker
  • Virus research
  • 2005
  • Corpus ID: 11014735
Thirty years after its synthesis, the mechanism of action of ribavirin is still not completely understood. Although much is known… Expand
Review
1999
Review
1999
Inosine 5 -monophosphate dehydrogenase (IMPDH) is a rate-limiting enzyme for the synthesis of GTP and dGTP. Two isoforms of IMPDH… Expand
Highly Cited
1997
Highly Cited
1997
The synthesis and biological activity of selenophenfurin (5-beta-D-ribofuranosylselenophene-3-carboxamide, 1), the selenophene… Expand
Highly Cited
1996
Highly Cited
1996
We have employed the attenuated vaccine strain 17D of yellow fever virus (YFV) to evaluate the inhibitory effect of a selected… Expand
Highly Cited
1986
Highly Cited
1986
The synthetic "C" nucleoside, tiazofurin (2-beta-D-ribofuranosylthiazole-4-carboxamide), its selenium analogue selenazofurin, and… Expand
Highly Cited
1985
Highly Cited
1985
The mechanism of the cellular toxicity of four inosinate dehydrogenase (IMP-DH) inhibitors with different antitumor and antiviral… Expand
1985
1985
The nucleosides ribavirin, selenazofurin, tiazofurin and bredinin all exhibit the lowering of guanylate pools in vitro and in… Expand
Highly Cited
1985
Highly Cited
1985
A series of dinucleotides, analogous to nicotinamide adenine dinucleotide but containing the five-membered base nucleosides… Expand
Highly Cited
1984
Highly Cited
1984
Binary combinations of the N-nucleoside ribavirin (1-beta-D-ribofuranosyl-1,2,4-triazole-3-carboxamide) and the C-nucleoside… Expand
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1984
1984
The antiviral effects of selenazofurin (2-beta-D-ribofuranosylselenazole-4-carboxamide, selenazole), ribavirin (1-beta-D… Expand
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