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FIELD OF THE INVENTION
The present invention is directed to inhibition of purine receptors as a therapeutic strategy in spinal cord and brain injury.
BACKGROUND OF THE INVENTION
Acute spinal injury is a major public health problem. Spinal cord injuries resulting in paralysis or other severe
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FIELD OF THE INVENTION
The invention relates to methods and compositions for modulating the axonal outgrowth of central nervous system neurons. In particular, the invention provides means of internalized purine administration.
BACKGROUND OF THE INVENTION
After early childhood, injury to the central
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FIELD OF INVENTION
The present invention relates to new 2,6,9-substituted purine derivatives and their biological applications. In particular, the invention relates to purine derivatives having antiproliferative properties which are useful in the treatment of proliferative disorders such as cancer,
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FIELD OF INVENTION
The present invention relates to new 2,6,9-substituted purine derivatives and their biological applications. In particular, the invention relates to purine derivatives having antiproliferative properties which are useful in the treatment of proliferative disorders such as cancer,
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RELATED APPLICATIONS
This application is a continuation of PCT/GB2003/003554, filed on Aug. 13, 2003, which claims priority to GB 0219054.4 filed on Aug. 15, 2002. The entire contents of both of these applications are hereby incorporated herein by reference.
FIELD OF INVENTION
The present invention
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Log In / Enskri
FIELD OF INVENTION
The present invention relates to new 2,6,9-substituted purine derivatives and their biological applications. In particular, the invention relates to purine derivatives having antiproliferative properties which are useful in the treatment of proliferative disorders such as cancer,
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FIELD OF THE INVENTION
This invention pertains to A.sub.3 and A.sub.1 adenosine receptor agonists, pharmaceutical compositions comprising such agonists, and a method of use thereof, for example, in treating various medical disorders.
BACKGROUND OF THE INVENTION
Extracellular adenosine acts as a
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BACKGROUND OF THE INVENTION
Extracellular adenosine acts as a local modulator at four subtypes of adenosine receptors, namely, A.sub.1, A.sub.2A, A.sub.2B, and A.sub.3, which are involved in numerous physiological and pathophysiological processes. Fredholm et al., Pharmacol. Rev. 2001; 53:527-52.
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FIELD
This relates to the field of small molecule PNPase substrates and inhibitors as well as potassium-sparing diuretics and natriuretics and methods of their use.
BACKGROUND
With the notable exceptions of mineralocorticoid antagonists and epithelial sodium channel (ENaC) inhibitors, most
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