WO2010059838A3 - Pde4 inhibitors selective for the long form of pde4 for treating inflammation and avoiding side effects - Google Patents

Pde4 inhibitors selective for the long form of pde4 for treating inflammation and avoiding side effects Download PDF

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WO2010059838A3
WO2010059838A3 PCT/US2009/065164 US2009065164W WO2010059838A3 WO 2010059838 A3 WO2010059838 A3 WO 2010059838A3 US 2009065164 W US2009065164 W US 2009065164W WO 2010059838 A3 WO2010059838 A3 WO 2010059838A3
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pde4
side effects
treating inflammation
long form
avoiding side
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PCT/US2009/065164
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French (fr)
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WO2010059838A2 (en
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Jasbir Singh
Mark Gurney
Alexander Kiselyov
Olefur Magnusson
Alex Burgin
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Decode Genetics Ehf
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    • C07C217/80Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having amino groups and etherified hydroxy groups bound to carbon atoms of six-membered aromatic rings of the same carbon skeleton having amino groups and etherified hydroxy groups bound to carbon atoms of non-condensed six-membered aromatic rings
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    • C07C217/82Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having amino groups and etherified hydroxy groups bound to carbon atoms of six-membered aromatic rings of the same carbon skeleton having amino groups and etherified hydroxy groups bound to carbon atoms of non-condensed six-membered aromatic rings of the same non-condensed six-membered aromatic ring
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    • C07C217/86Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having amino groups and etherified hydroxy groups bound to carbon atoms of six-membered aromatic rings of the same carbon skeleton having amino groups and etherified hydroxy groups bound to carbon atoms of non-condensed six-membered aromatic rings of the same non-condensed six-membered aromatic ring the oxygen atom of at least one of the etherified hydroxy groups being further bound to an acyclic carbon atom to an acyclic carbon atom of a hydrocarbon radical containing six-membered aromatic rings
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Abstract

The present invention relates to compounds which are inhibitors of phosphodiesterase-4 (PDE4) useful for the treatment and prevention of stroke, myocardial infarct, cardiovascular inflammatory diseases and disorders and central nervous system disorders, to compounds with a selectivity for a non-catalytic portion of PDE4, to methods of determining this selectivity.
PCT/US2009/065164 2008-11-20 2009-11-19 Pde4 inhibitors selective for the long form of pde4 for treating inflammation and avoiding side effects WO2010059838A2 (en)

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KR101774035B1 (en) 2009-10-30 2017-09-01 얀센 파마슈티카 엔.브이. IMIDAZO[l,2-b]PYRIDAZINE DERIVATIVES AND THEIR USE AS PDE1O INHIBITORS
AR080754A1 (en) 2010-03-09 2012-05-09 Janssen Pharmaceutica Nv IMIDAZO DERIVATIVES (1,2-A) PIRAZINA AND ITS USE AS PDE10 INHIBITORS
EA027418B1 (en) 2011-06-27 2017-07-31 Янссен Фармацевтика Нв 1-ARYL-4-METHYL-[1,2,4]TRIAZOLO[4,3-a]QUINOXALINE DERIVATIVES, PHARMACEUTICAL COMPOSITION BASED THEREON, PROCESSES FOR PREPARING AND USING THE SAME, INTERMEDIATES
CA2872216C (en) 2012-06-26 2021-07-20 Janssen Pharmaceutica Nv Combinations comprising pde 2 inhibitors such as 1-aryl-4-methyl-[1,2,4] triazolo [4,3-a] quinoxaline compounds and pde 10 inhibitors for use in the treatment of neurological or metabolic disorders
CA2875057C (en) 2012-07-09 2021-07-13 Janssen Pharmaceutica Nv Imidazo[1,2-b]pyridazine and imidazo[1,2-a]pyrazine compounds and their use as inhibitors of the phosphodiesterase 10 enzyme
WO2014066659A1 (en) 2012-10-25 2014-05-01 Tetra Discovery Partners, Llc. Heteroaryl inhibitors of pde4
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