NO20082593L - Pyrazolo[4,3-D]pyrimidin-5-yl)derivater anvendt som PDE5 inhibitorer - Google Patents

Pyrazolo[4,3-D]pyrimidin-5-yl)derivater anvendt som PDE5 inhibitorer

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Publication number
NO20082593L
NO20082593L NO20082593A NO20082593A NO20082593L NO 20082593 L NO20082593 L NO 20082593L NO 20082593 A NO20082593 A NO 20082593A NO 20082593 A NO20082593 A NO 20082593A NO 20082593 L NO20082593 L NO 20082593L
Authority
NO
Norway
Prior art keywords
pyrazolo
pyrimidin
derivatives used
pde5 inhibitors
methylpyridin
Prior art date
Application number
NO20082593A
Other languages
English (en)
Inventor
Michael Brent Tollefson
Original Assignee
Pfizer Prod Inc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Pfizer Prod Inc filed Critical Pfizer Prod Inc
Publication of NO20082593L publication Critical patent/NO20082593L/no

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    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/04Ortho-condensed systems
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    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
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Abstract

Foreliggende oppfinnelse omfatter l-(l-(2-etoksyetyI)-3-etyI-7-(4-metyIpyridin-2-ylamino)-1H-pyrazolo[4,3-dlpyrimidin-5-yl)piperidin-4-karboksylsyre og dets salter. Oppfinnelsen innbefatter ytterligere farmasøytiske sammensetninger, behandlingsfremgangsmåter av behandling og syntetiske behandlingsfremgangsmåter relatert til 1-(1-(2-etoksyetyl)-3-etyl-7-(4-metylpyridin-2-ylamino)-1H-pyrazolo[4,3-dlpyrimidin-5-yl)piperidin-4-karboksylsyre og dets salter.
NO20082593A 2005-11-10 2008-06-10 Pyrazolo[4,3-D]pyrimidin-5-yl)derivater anvendt som PDE5 inhibitorer NO20082593L (no)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US73532005P 2005-11-10 2005-11-10
PCT/IB2006/003132 WO2007054778A1 (en) 2005-11-10 2006-10-31 Pyrazolo[4,3-d]pyrimidin-5-yl)derivative used as pde5 inhibitors

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NO20082593L true NO20082593L (no) 2008-07-22

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NO20082593A NO20082593L (no) 2005-11-10 2008-06-10 Pyrazolo[4,3-D]pyrimidin-5-yl)derivater anvendt som PDE5 inhibitorer

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US (2) US20090156618A1 (no)
EP (1) EP1948661B1 (no)
JP (1) JP4208959B1 (no)
KR (1) KR101012592B1 (no)
CN (1) CN101305007B (no)
AP (1) AP2008004437A0 (no)
AR (1) AR057885A1 (no)
AT (1) ATE435865T1 (no)
AU (1) AU2006313486B2 (no)
BR (1) BRPI0618284A2 (no)
CA (1) CA2629339C (no)
CR (1) CR9966A (no)
DE (1) DE602006007728D1 (no)
DK (1) DK1948661T3 (no)
DO (1) DOP2006000248A (no)
EA (1) EA200800920A1 (no)
EC (1) ECSP088441A (no)
ES (1) ES2326919T3 (no)
IL (1) IL190456A (no)
MA (1) MA29943B1 (no)
NL (1) NL2000291C2 (no)
NO (1) NO20082593L (no)
PE (1) PE20070764A1 (no)
RS (1) RS20080197A (no)
TN (1) TNSN08209A1 (no)
TW (1) TW200738723A (no)
UY (1) UY29909A1 (no)
WO (1) WO2007054778A1 (no)
ZA (1) ZA200803173B (no)

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US20110165183A1 (en) * 2008-08-01 2011-07-07 Biocryst Pharmaceuticals, Inc. Piperidine derivatives as jak3 inhibitors
WO2010043633A1 (en) * 2008-10-15 2010-04-22 Palau Pharma, S. A. 2h-pyrazolo [4,3-d]pyrimidin-5-amine derivatives as h4 histamine receptor antagonists for the treatment of allergic, immunological and inflammatory diseases
CN102970965A (zh) * 2010-04-05 2013-03-13 Sk化学公司 含有pde5抑制剂的减少皮肤皱纹的合成物
EP3189835B1 (en) * 2011-02-28 2018-07-25 National Cerebral and Cardiovascular Center Medical agent for suppressing malignant tumor metastasis
MX363696B (es) 2011-04-21 2019-03-28 Origenis Gmbh Pirazolo[4,3-d]pirimidinas utiles como inhibidores de cinasas.
WO2014060112A1 (en) 2012-10-19 2014-04-24 Origenis Gmbh Pyrazolo[4,3-d]pyrimidines as kinase inhibitors
WO2014064566A1 (en) * 2012-10-23 2014-05-01 Pfizer Inc. Use of a tetrasubstituted pyrazolo[4,3-d]pyrimidine compound for treating diabetic nephropathy
CA3128680C (en) 2014-08-12 2025-10-07 The Children's Hospital Of Philadelphia METHODS FOR IMPROVING MYOCARDIAL PERFORMANCE IN PATIENTS WHO HAVE UNDERGONE FONTAN SURGERY, USING UDENAFIL COMPOSITIONS
AU2020356193A1 (en) 2019-09-24 2022-05-19 Children's Hospital Of Philadelphia Methods of improving exercise performance, single ventricular performance, and myocardial performance index (MPI) in single ventricle heart disease, using udenafil compositions

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US8518956B2 (en) 2013-08-27
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PE20070764A1 (es) 2007-08-13
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