MA29943B1 - Derives de pyrazolo[4,3-d] pyrimidine-5-yle utilises comme inhibiteurs de pde5 - Google Patents
Derives de pyrazolo[4,3-d] pyrimidine-5-yle utilises comme inhibiteurs de pde5Info
- Publication number
- MA29943B1 MA29943B1 MA30918A MA30918A MA29943B1 MA 29943 B1 MA29943 B1 MA 29943B1 MA 30918 A MA30918 A MA 30918A MA 30918 A MA30918 A MA 30918A MA 29943 B1 MA29943 B1 MA 29943B1
- Authority
- MA
- Morocco
- Prior art keywords
- pyrazolo
- yle
- pyrimidine
- derivatives
- formula
- Prior art date
Links
- 229940123333 Phosphodiesterase 5 inhibitor Drugs 0.000 title 1
- 239000002590 phosphodiesterase V inhibitor Substances 0.000 title 1
- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 abstract 2
- 239000002253 acid Substances 0.000 abstract 2
- 101100189582 Dictyostelium discoideum pdeD gene Proteins 0.000 abstract 1
- 102000004190 Enzymes Human genes 0.000 abstract 1
- 108090000790 Enzymes Proteins 0.000 abstract 1
- 101150098694 PDE5A gene Proteins 0.000 abstract 1
- -1 PYRIMIDIN-5-YL Chemical class 0.000 abstract 1
- 102100029175 cGMP-specific 3',5'-cyclic phosphodiesterase Human genes 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 238000001308 synthesis method Methods 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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- A61K31/33—Heterocyclic compounds
- 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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Abstract
LA PRÉSENTE INVENTION CONCERNE UN ACIDE 1-(1-(2-ÉTHOXYÉTHYL-3-ÉTHYL-7-(4-MÉTHYLPYRIDIN-2- YLAMINO)-LH-PYRAZOLO[4,3-D]PYRIMIDIN-5-YL)PIPÉRIDINE 4-CARBOXYLIQUE REPRÉSENTÉ PAR LA FORMULE (I) ET SES SELS. L'INVENTION CONCERNE ÉGALEMENT DES COMPOSITIONS PHARMACEUTIQUES, DES MÉTHODES DE TRAITEMENT ET DES PROCÉDÉS DE SYNTHÈSE CONCERNANT LA FORMULE (I). L'ACIDE REPRÉSENTÉ PAR LA FORMULE (I) ET SES SELS S'UTILISENT POUR INHIBER L'ENZYME PDE5.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US73532005P | 2005-11-10 | 2005-11-10 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MA29943B1 true MA29943B1 (fr) | 2008-11-03 |
Family
ID=37685872
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MA30918A MA29943B1 (fr) | 2005-11-10 | 2008-05-09 | Derives de pyrazolo[4,3-d] pyrimidine-5-yle utilises comme inhibiteurs de pde5 |
Country Status (29)
| Country | Link |
|---|---|
| US (2) | US20090156618A1 (fr) |
| EP (1) | EP1948661B1 (fr) |
| JP (1) | JP4208959B1 (fr) |
| KR (1) | KR101012592B1 (fr) |
| CN (1) | CN101305007B (fr) |
| AP (1) | AP2008004437A0 (fr) |
| AR (1) | AR057885A1 (fr) |
| AT (1) | ATE435865T1 (fr) |
| AU (1) | AU2006313486B2 (fr) |
| BR (1) | BRPI0618284A2 (fr) |
| CA (1) | CA2629339C (fr) |
| CR (1) | CR9966A (fr) |
| DE (1) | DE602006007728D1 (fr) |
| DK (1) | DK1948661T3 (fr) |
| DO (1) | DOP2006000248A (fr) |
| EA (1) | EA200800920A1 (fr) |
| EC (1) | ECSP088441A (fr) |
| ES (1) | ES2326919T3 (fr) |
| IL (1) | IL190456A (fr) |
| MA (1) | MA29943B1 (fr) |
| NL (1) | NL2000291C2 (fr) |
| NO (1) | NO20082593L (fr) |
| PE (1) | PE20070764A1 (fr) |
| RS (1) | RS20080197A (fr) |
| TN (1) | TNSN08209A1 (fr) |
| TW (1) | TW200738723A (fr) |
| UY (1) | UY29909A1 (fr) |
| WO (1) | WO2007054778A1 (fr) |
| ZA (1) | ZA200803173B (fr) |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BRPI0916931A2 (pt) * | 2008-08-01 | 2015-11-24 | Biocryst Pharm Inc | agentes terapêuticos |
| WO2010043633A1 (fr) * | 2008-10-15 | 2010-04-22 | Palau Pharma, S. A. | Dérivés de 2h-pyrazolo[4,3-d]pyrimidin-5-amine utilisés comme antagonistes des récepteurs h4 de l'histamine pour le traitement de maladies allergiques, immunologiques et inflammatoires |
| EP2556820A4 (fr) * | 2010-04-05 | 2015-01-21 | Sk Chemicals Co Ltd | Composition contenant un inhibiteur de pde5 pour l'atténuation des rides de la peau |
| EP2682128B1 (fr) * | 2011-02-28 | 2017-11-08 | National Cerebral and Cardiovascular Center | Peptide natriurétique auriculaire ou peptide cérébral natriurétique pour le prévention de la métastase |
| CN103492389B (zh) | 2011-04-21 | 2016-09-14 | 原真股份有限公司 | 用作激酶抑制剂的吡唑并[4,3-d]嘧啶 |
| US9637491B2 (en) | 2012-10-19 | 2017-05-02 | Origenis Gmbh | Pyrazolo[4,3-D]pyrimidines as kinase inhibitors |
| CA2888160A1 (fr) * | 2012-10-23 | 2014-05-01 | Pfizer Inc. | Utilisation d'une pyrazolo[4,3-d]pyrimidine tetrasubstituee pour le traitement de la nephropathie diabetique |
| MY200278A (en) | 2014-08-12 | 2023-12-18 | Mezzion Pharma Co Ltd | Methods of improving exercise capacity in fontan patients using udenafil compositions |
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| AU3645697A (en) | 1996-07-08 | 1998-02-02 | Du Pont Pharmaceuticals Company | Amidinoindoles, amidinoazoles, and analogs thereof as inhibitors of factor xa and of thrombin |
| SK15532000A3 (sk) | 1998-04-20 | 2001-12-03 | Pfizer Inc. | Pyrazolopyrimidínové inhibítory cgmp pde5 na použitie na liečbu sexuálnych dysfunkcií, spôsob ich prípravy, medziprodukty a farmaceutický prostriedok s ich obsahom |
| GB9822238D0 (en) * | 1998-10-12 | 1998-12-09 | Pfizer Ltd | Process for preparation of pyrazolo[4,3-D]pyrimidin-7-ones and intermediates thereof |
| AU5995699A (en) | 1998-10-23 | 2000-05-15 | Bunnage, Mark Edward | Pyrazolopyrimidinone cgmp pde5 inhibitors for the treatment of sexual dysfunction |
| DE19942474A1 (de) | 1999-09-06 | 2001-03-15 | Merck Patent Gmbh | Pyrazolo[4,3-d]pyrimidine |
| CN1249051C (zh) | 2000-04-28 | 2006-04-05 | 阿卡蒂亚药品公司 | 毒蕈碱性激动剂 |
| DE10031584A1 (de) | 2000-06-29 | 2002-01-10 | Merck Patent Gmbh | 5-Aminoalkyl-pyrazolo[4,3-d]pyrimidine |
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| EP1348707B1 (fr) | 2002-03-28 | 2010-08-25 | Ustav Experimentalni Botaniky AV CR, v.v.i. (Institute of Experimental Botany Academy of Sciences of the Czech Republic, PRO) | Pyrazolo[4,3-d]pyrimidines, procédé pour leur préparation et application thérapeutique |
| EA008596B1 (ru) * | 2003-04-29 | 2007-06-29 | Пфайзер Инк. | 5,7-ДИАМИНОПИРАЗОЛО[4,3-d]ПИРИМИДИНЫ, ПОЛЕЗНЫЕ ПРИ ЛЕЧЕНИИ ГИПЕРТЕНЗИИ |
| CA2525946C (fr) | 2003-05-22 | 2013-01-29 | Altana Pharma Ag | Composition contenant un inhibiteur de pde4 et un inhibiteur de pde5 |
| TWI344364B (en) | 2003-11-10 | 2011-07-01 | Synta Pharmaceuticals Corp | Fused heterocyclic compounds |
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| CA2562251C (fr) * | 2004-04-07 | 2009-04-28 | Pfizer Inc. | Pyrazolo'4,3-d pyrimidines |
| AU2005270068B2 (en) | 2004-07-02 | 2012-04-19 | Exelixis, Inc. | C-Met modulators and method of use |
| EP1809632A2 (fr) * | 2004-10-28 | 2007-07-25 | Pharmacia & Upjohn Company LLC | Derives de pyrazolo [4,3-d] pyrimidine utiles comme inhibiteurs de pde-5 |
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