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 inhibitorerInfo
- 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
Links
- 229940123333 Phosphodiesterase 5 inhibitor Drugs 0.000 title 1
- -1 Pyrazolo [4,3-D] pyrimidin-5-yl Chemical group 0.000 title 1
- 239000002590 phosphodiesterase V inhibitor Substances 0.000 title 1
- IQZQWPRZFLHJFI-UHFFFAOYSA-N 1-[1-(2-ethoxyethyl)-3-ethyl-7-[(4-methylpyridin-2-yl)amino]pyrazolo[4,3-d]pyrimidin-5-yl]piperidine-4-carboxylic acid Chemical compound C=12N(CCOCC)N=C(CC)C2=NC(N2CCC(CC2)C(O)=O)=NC=1NC1=CC(C)=CC=N1 IQZQWPRZFLHJFI-UHFFFAOYSA-N 0.000 abstract 2
- 238000000034 method Methods 0.000 abstract 2
- 150000003839 salts Chemical class 0.000 abstract 2
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic 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
- C07D487/04—Ortho-condensed systems
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- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic 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
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
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- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
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- Neurology (AREA)
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- Diabetes (AREA)
- Cardiology (AREA)
- Endocrinology (AREA)
- Heart & Thoracic Surgery (AREA)
- Physical Education & Sports Medicine (AREA)
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- Hematology (AREA)
- Urology & Nephrology (AREA)
- Reproductive Health (AREA)
- Ophthalmology & Optometry (AREA)
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- Psychology (AREA)
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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 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NO20082593L true NO20082593L (no) | 2008-07-22 |
Family
ID=37685872
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO20082593A NO20082593L (no) | 2005-11-10 | 2008-06-10 | Pyrazolo[4,3-D]pyrimidin-5-yl)derivater anvendt som PDE5 inhibitorer |
Country Status (29)
| Country | Link |
|---|---|
| US (2) | US20090156618A1 (sr) |
| EP (1) | EP1948661B1 (sr) |
| JP (1) | JP4208959B1 (sr) |
| KR (1) | KR101012592B1 (sr) |
| CN (1) | CN101305007B (sr) |
| AP (1) | AP2008004437A0 (sr) |
| AR (1) | AR057885A1 (sr) |
| AT (1) | ATE435865T1 (sr) |
| AU (1) | AU2006313486B2 (sr) |
| BR (1) | BRPI0618284A2 (sr) |
| CA (1) | CA2629339C (sr) |
| CR (1) | CR9966A (sr) |
| DE (1) | DE602006007728D1 (sr) |
| DK (1) | DK1948661T3 (sr) |
| DO (1) | DOP2006000248A (sr) |
| EA (1) | EA200800920A1 (sr) |
| EC (1) | ECSP088441A (sr) |
| ES (1) | ES2326919T3 (sr) |
| IL (1) | IL190456A (sr) |
| MA (1) | MA29943B1 (sr) |
| NL (1) | NL2000291C2 (sr) |
| NO (1) | NO20082593L (sr) |
| PE (1) | PE20070764A1 (sr) |
| RS (1) | RS20080197A (sr) |
| TN (1) | TNSN08209A1 (sr) |
| TW (1) | TW200738723A (sr) |
| UY (1) | UY29909A1 (sr) |
| WO (1) | WO2007054778A1 (sr) |
| ZA (1) | ZA200803173B (sr) |
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| RU2011105768A (ru) * | 2008-08-01 | 2012-09-10 | Биокрист Фармасьютикалз, Инк. (Us) | Производные пиперидина в качестве ингибиторов jakз |
| 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 |
| EP2556820A4 (en) * | 2010-04-05 | 2015-01-21 | Sk Chemicals Co Ltd | COMPOSITION CONTAINING PDE5 INHIBITOR FOR MITIGATION OF SKIN WRINKLES |
| EP3189835B1 (en) * | 2011-02-28 | 2018-07-25 | National Cerebral and Cardiovascular Center | Medical agent for suppressing malignant tumor metastasis |
| AU2012244550C1 (en) | 2011-04-21 | 2017-06-22 | Origenis Gmbh | Pyrazolo [4, 3-d] pyrimidines useful as kinase inhibitors |
| WO2014060112A1 (en) | 2012-10-19 | 2014-04-24 | Origenis Gmbh | Pyrazolo[4,3-d]pyrimidines as kinase inhibitors |
| CA2888160A1 (en) * | 2012-10-23 | 2014-05-01 | Pfizer Inc. | Use of a tetrasubstituted pyrazolo[4,3-d]pyrimidine compound for treating diabetic nephropathy |
| MX390977B (es) | 2014-08-12 | 2025-03-21 | Mezzion Pharma Co Ltd | Metodos para mejorar el rendimiento miocardico en pacientes con cirugia de fontan que utilizan composiciones de udenafilo |
| MX2022003593A (es) | 2019-09-24 | 2022-09-19 | Mezzion Pharma Co Ltd | Métodos para mejorar el rendimiento del ejercicio, el rendimiento ventricular único y el índice de rendimiento del miocardio (mpi) en la enfermedad cardiaca del ventrículo único, utilizando composiciones de udenafil. |
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| EP0960102A1 (en) | 1996-07-08 | 1999-12-01 | Du Pont Pharmaceuticals Company | AMIDINOINDOLES, AMIDINOAZOLES, AND ANALOGS THEREOF AS INHIBITORS OF FACTOR Xa AND OF THROMBIN |
| ES2203078T3 (es) | 1998-04-20 | 2004-04-01 | Pfizer Inc. | Parazolopirimidinonas inhibidoras de gmpc pde5 para el tratamiento de la disfuncion sexual. |
| GB9822238D0 (en) * | 1998-10-12 | 1998-12-09 | Pfizer Ltd | Process for preparation of pyrazolo[4,3-D]pyrimidin-7-ones and intermediates thereof |
| ES2205945T3 (es) | 1998-10-23 | 2004-05-01 | Pfizer Inc. | Pirazolopirimidinonas inhibidoras de gmpc pde5 para el tratamiento de disfunciones sexuales. |
| DE19942474A1 (de) | 1999-09-06 | 2001-03-15 | Merck Patent Gmbh | Pyrazolo[4,3-d]pyrimidine |
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| KR100824193B1 (ko) * | 2003-04-29 | 2008-04-21 | 화이자 인코포레이티드 | 고혈압 치료에 유용한5,7-디아미노피라졸로[4,3-d]피리미딘 |
| WO2004103407A2 (en) | 2003-05-22 | 2004-12-02 | Altana Pharma Ag | Composition comprising a pde4 inhibitor and a pde5 inhibitor |
| CA2545340A1 (en) | 2003-11-10 | 2005-05-26 | Synta Pharmaceuticals, Corp. | Fused heterocyclic compounds |
| GB0327319D0 (en) * | 2003-11-24 | 2003-12-24 | Pfizer Ltd | Novel pharmaceuticals |
| GB0327323D0 (en) * | 2003-11-24 | 2003-12-31 | Pfizer Ltd | Novel pharmaceuticals |
| JP2007532526A (ja) * | 2004-04-07 | 2007-11-15 | ファイザー・インク | ピラゾロ[4,3−d]ピリミジン類 |
| CA2572331A1 (en) | 2004-07-02 | 2006-02-09 | Exelixis, Inc. | C-met modulators and method of use |
| EP1809632A2 (en) * | 2004-10-28 | 2007-07-25 | Pharmacia & Upjohn Company LLC | Pyrazolo[4,3-d]pyrimidine derivatives useful as pde-5 inhibitors |
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