PE20070764A1 - Acido 1-(1-(2-etoxietil)-3-etil-7-(4-metilpiridin-2-ilamino)-1h-pirazolo[4,3-d]pirimidin-5-il)piperidina-4-carboxilico y las sales del mismo - Google Patents
Acido 1-(1-(2-etoxietil)-3-etil-7-(4-metilpiridin-2-ilamino)-1h-pirazolo[4,3-d]pirimidin-5-il)piperidina-4-carboxilico y las sales del mismoInfo
- Publication number
- PE20070764A1 PE20070764A1 PE2006001379A PE2006001379A PE20070764A1 PE 20070764 A1 PE20070764 A1 PE 20070764A1 PE 2006001379 A PE2006001379 A PE 2006001379A PE 2006001379 A PE2006001379 A PE 2006001379A PE 20070764 A1 PE20070764 A1 PE 20070764A1
- Authority
- PE
- Peru
- Prior art keywords
- salts
- ilamino
- methylpyridin
- pyrazolo
- pyrimidin
- Prior art date
Links
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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
REFERIDA AL COMPUESTO ACIDO 1-(1-(2-ETOXIETIL)-3-ETIL-7-(4-METILPIRIDIN-2-ILAMINO)-1H-PIRAZOLO[4,3-D]PIRIMIDIN-5-IL)PIPERIDINA-4-CARBOXILICO Y SALES FARMACEUTICAMENTE ACEPTABLES DEL MISMO. DENTRO DE LAS SALES SE ENCUENTRAN LA SAL CLORHIDRATO, BORATO, FOSFATO, CARBONATO, ETANOSULFONATO, ENTRE OTRAS. TAMBIEN ESTA REFERIDA A UNA COMPOSICION FARMACEUTICA Y A UN PROCEDIMIENTO DE PREPARACION. DICHO COMPUESTO ES INHIBIDOR DE LA ENZIMA FOSFODIESTERAA DE TIPO 5 (PDE5) ESPECIFICA DE MONOFOSFATO DE GUANILATO CICLICO Y ES UTIL EN EL TRATAMIENTO DE ENFERMEDADES CARDIOVASCULARES, METABOLICAS, DEL SISTEMA NERVIOSO CENTRAL, DISFUNCION SEXUAL, ENTRE OTRAS
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US73532005P | 2005-11-10 | 2005-11-10 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PE20070764A1 true PE20070764A1 (es) | 2007-08-13 |
Family
ID=37685872
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PE2006001379A PE20070764A1 (es) | 2005-11-10 | 2006-11-07 | Acido 1-(1-(2-etoxietil)-3-etil-7-(4-metilpiridin-2-ilamino)-1h-pirazolo[4,3-d]pirimidin-5-il)piperidina-4-carboxilico y las sales del mismo |
Country Status (30)
| Country | Link |
|---|---|
| US (2) | US20090156618A1 (es) |
| EP (1) | EP1948661B1 (es) |
| JP (1) | JP4208959B1 (es) |
| KR (1) | KR101012592B1 (es) |
| CN (1) | CN101305007B (es) |
| AP (1) | AP2008004437A0 (es) |
| AR (1) | AR057885A1 (es) |
| AT (1) | ATE435865T1 (es) |
| AU (1) | AU2006313486B2 (es) |
| BR (1) | BRPI0618284A2 (es) |
| CA (1) | CA2629339C (es) |
| CR (1) | CR9966A (es) |
| DE (1) | DE602006007728D1 (es) |
| DK (1) | DK1948661T3 (es) |
| DO (1) | DOP2006000248A (es) |
| EA (1) | EA200800920A1 (es) |
| EC (1) | ECSP088441A (es) |
| ES (1) | ES2326919T3 (es) |
| HK (1) | HK1120803A1 (es) |
| IL (1) | IL190456A (es) |
| MA (1) | MA29943B1 (es) |
| NL (1) | NL2000291C2 (es) |
| NO (1) | NO20082593L (es) |
| PE (1) | PE20070764A1 (es) |
| RS (1) | RS20080197A (es) |
| TN (1) | TNSN08209A1 (es) |
| TW (1) | TW200738723A (es) |
| UY (1) | UY29909A1 (es) |
| WO (1) | WO2007054778A1 (es) |
| ZA (1) | ZA200803173B (es) |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2010014930A2 (en) * | 2008-08-01 | 2010-02-04 | Biocryst Pharmaceuticals, Inc. | Therapeutic agents |
| 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 |
| WO2012118042A1 (ja) * | 2011-02-28 | 2012-09-07 | 独立行政法人国立循環器病研究センター | 悪性腫瘍転移抑制用医薬 |
| TWI606049B (zh) | 2011-04-21 | 2017-11-21 | 原真股份有限公司 | 新穎激酶抑制劑 |
| US9637491B2 (en) | 2012-10-19 | 2017-05-02 | Origenis Gmbh | Pyrazolo[4,3-D]pyrimidines as kinase inhibitors |
| CN104755086A (zh) * | 2012-10-23 | 2015-07-01 | 辉瑞公司 | 四取代的吡唑并[4,3-d]嘧啶化合物用于治疗糖尿病肾病的用途 |
| KR20170066334A (ko) | 2014-08-12 | 2017-06-14 | 주식회사 메지온 | 유데나필 조성물을 이용하여 폰탄 환자에서 심근 성능을 개선시키는 방법 |
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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 |
| HUP0102543A3 (en) | 1998-04-20 | 2002-01-28 | Pfizer | Pyrazolopyrimidinone cgmp pde5 inhibitors for the treatment of sexual dysfunction and medicaments containing them |
| GB9822238D0 (en) * | 1998-10-12 | 1998-12-09 | Pfizer Ltd | Process for preparation of pyrazolo[4,3-D]pyrimidin-7-ones and intermediates thereof |
| BR9915532A (pt) | 1998-10-23 | 2001-08-14 | Pfizer | Inibidores de cgmp pde5 de pirazolopirimidinona para tratamento da disfunção sexual |
| DE19942474A1 (de) | 1999-09-06 | 2001-03-15 | Merck Patent Gmbh | Pyrazolo[4,3-d]pyrimidine |
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| WO2004096810A1 (en) * | 2003-04-29 | 2004-11-11 | Pfizer Limited | 5,7-diaminopyrazolo`4,3-d!pyrimidines useful in the treatment of hypertension |
| WO2004103407A2 (en) | 2003-05-22 | 2004-12-02 | Altana Pharma Ag | Composition comprising a pde4 inhibitor and a pde5 inhibitor |
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-
2006
- 2006-10-27 NL NL2000291A patent/NL2000291C2/nl not_active IP Right Cessation
- 2006-10-31 CN CN2006800416985A patent/CN101305007B/zh not_active Expired - Fee Related
- 2006-10-31 DK DK06809195T patent/DK1948661T3/da active
- 2006-10-31 DE DE602006007728T patent/DE602006007728D1/de active Active
- 2006-10-31 BR BRPI0618284-4A patent/BRPI0618284A2/pt not_active Application Discontinuation
- 2006-10-31 JP JP2008539522A patent/JP4208959B1/ja not_active Expired - Fee Related
- 2006-10-31 KR KR1020087011230A patent/KR101012592B1/ko not_active IP Right Cessation
- 2006-10-31 RS RSP-2008/0197A patent/RS20080197A/sr unknown
- 2006-10-31 ES ES06809195T patent/ES2326919T3/es active Active
- 2006-10-31 EA EA200800920A patent/EA200800920A1/ru unknown
- 2006-10-31 AT AT06809195T patent/ATE435865T1/de not_active IP Right Cessation
- 2006-10-31 EP EP06809195A patent/EP1948661B1/en active Active
- 2006-10-31 AP AP2008004437A patent/AP2008004437A0/xx unknown
- 2006-10-31 AU AU2006313486A patent/AU2006313486B2/en not_active Ceased
- 2006-10-31 CA CA2629339A patent/CA2629339C/en not_active Expired - Fee Related
- 2006-10-31 WO PCT/IB2006/003132 patent/WO2007054778A1/en active Application Filing
- 2006-11-07 PE PE2006001379A patent/PE20070764A1/es not_active Application Discontinuation
- 2006-11-08 AR ARP060104894A patent/AR057885A1/es unknown
- 2006-11-09 US US11/558,306 patent/US20090156618A1/en not_active Abandoned
- 2006-11-09 DO DO2006P000248A patent/DOP2006000248A/es unknown
- 2006-11-09 UY UY29909A patent/UY29909A1/es not_active Application Discontinuation
- 2006-11-09 TW TW095141515A patent/TW200738723A/zh unknown
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2008
- 2008-03-26 IL IL190456A patent/IL190456A/en not_active IP Right Cessation
- 2008-04-10 ZA ZA200803173A patent/ZA200803173B/xx unknown
- 2008-05-08 EC EC2008008441A patent/ECSP088441A/es unknown
- 2008-05-09 CR CR9966A patent/CR9966A/es not_active Application Discontinuation
- 2008-05-09 TN TNP2008000209A patent/TNSN08209A1/fr unknown
- 2008-05-09 MA MA30918A patent/MA29943B1/fr unknown
- 2008-06-10 NO NO20082593A patent/NO20082593L/no not_active Application Discontinuation
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2009
- 2009-01-02 HK HK09100008.1A patent/HK1120803A1/xx not_active IP Right Cessation
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2010
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