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5-iodotubercidin

Known as: 5'-iodotubericidin 
National Institutes of Health

Related topics

Related topics

3 relations

Broader (2)

Enzyme InhibitorsTubercidin
analogs & derivatives

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2012
Highly Cited
2012
A small-molecule inhibitor of Haspin alters the kinetochore functions of Aurora B
A chemical biology study characterizes the role of Haspin kinase in centromere recruitment of the chromosome passenger complex… 
Highly Cited
2008
Highly Cited
2008
HIF-1-dependent repression of adenosine kinase attenuates hypoxia-induced vascular leak.
Extracellular adenosine has been implicated in vascular adaptation to hypoxia. Based on the observation that increases in… 
Highly Cited
2005
Highly Cited
2005
Clozapine and the mitogen-activated protein kinase signal transduction pathway: Implications for antipsychotic actions
Highly Cited
2000
Highly Cited
2000
Adenosine kinase inhibitors. 1. Synthesis, enzyme inhibition, and antiseizure activity of 5-iodotubercidin analogues.
Adenosine receptor agonists produce a wide variety of therapeutically useful pharmacologies. However, to date they have failed to… 
Highly Cited
1998
Highly Cited
1998
Antinociception by adenosine analogs and inhibitors of adenosine metabolism in an inflammatory thermal hyperalgesia model in the rat
Highly Cited
1998
Highly Cited
1998
Inhibition of adenosine kinase during oxygen-glucose deprivation in rat cortical neuronal cultures
Highly Cited
1996
Highly Cited
1996
Adenosine kinase inhibitors augment release of adenosine from spinal cord slices.
Highly Cited
1995
Highly Cited
1995
Involvement of adenosine deaminase and adenosine kinase in regulating extracellular adenosine concentration in rat hippocampal slices
1986
1986
Regional distribution of adenosine uptake in guinea-pig brain slices and the effect of some inhibitors: Evidence for nitrobenzylthioinosine-sensitive and insensitive sites?
1986
1986
Studies on several pyrrolo[2,3-d]pyrimidine analogues of adenosine which lack significant agonist activity at A1 and A2 receptors but have potent pharmacological activity in vivo.
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