Methanocarba cycloalkyl nucleoside analogues

C - Chemistry – Metallurgy – 07 – D

Patent

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Details

C07D 471/04 (2006.01) A61K 31/505 (2006.01) A61K 31/52 (2006.01) A61P 29/00 (2006.01) A61P 35/00 (2006.01) C07D 235/00 (2006.01) C07D 239/00 (2006.01) C07D 239/54 (2006.01) C07D 239/56 (2006.01) C07D 239/58 (2006.01) C07D 473/34 (2006.01) C07D 487/04 (2006.01)

Patent

CA 2397366

The present invention provides novel nucleoside and nucleotide derivatives that are useful agonists or antagonists of P1 or P2 receptors. For example, the present invention provides a compound of formula A-M, wherein A is modified adenine or uracil and M is a constrained cycloalkyl group. The adenine or uracil is bonded to the constrained cycloakyl group. The compounds of the present invention are useful in the treatment or prevention of various diseases including airway diseases (through A2B, A3, P2Y2 receptors), cancer (through A3, P2 receptors), cardiac arrhythmias (through A1 receptors), cardiac ischemia (through A1, A3 receptors), epilepsy (through A1, P2X receptors), and Huntington's Disease (through A2A receptors).

L'invention concerne de nouveaux dérivés nucléosidiques et nucléotidiques qui constituent des agonistes ou des antagonistes utiles de récepteurs P1 ou P2. Par exemple, l'invention concerne un composé représenté par la formule A-M, dans laquelle A représente adénine ou uracile modifié(e), et M représente un groupe cycloalkyle contraint. L'adénine ou l'uracile est lié(e) au groupe cycloakyle contraint. Les composés de l'invention sont utiles dans le traitement ou la prévention de diverses affections, par exemple des maladies des voies respiratoires (par les récepteurs A¿2B?, A¿3?, P2Y¿2?), le cancer (par les récepteurs A¿3?, P2), des arythmies cardiaques (par les récepteurs A¿1?), l'ischémie cardiaque (par les récepteurs A¿1?, A¿3?), l'épilepsie (par les récepteurs A¿1?, P2X) et la maladie de Huntington (par les récepteurs A¿2A?).

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