SV2004001373A - Inhibidores de pde9 para tratamiento de transtornos cardiovasculares. ref. pcs22051 - Google Patents
Inhibidores de pde9 para tratamiento de transtornos cardiovasculares. ref. pcs22051Info
- Publication number
- SV2004001373A SV2004001373A SV2002001373A SV2002001373A SV2004001373A SV 2004001373 A SV2004001373 A SV 2004001373A SV 2002001373 A SV2002001373 A SV 2002001373A SV 2002001373 A SV2002001373 A SV 2002001373A SV 2004001373 A SV2004001373 A SV 2004001373A
- Authority
- SV
- El Salvador
- Prior art keywords
- rent
- optionally replaced
- treatment
- pde9 inhibitors
- cardiovascular disorders
- Prior art date
Links
- 229940076380 PDE9 inhibitor Drugs 0.000 title abstract 3
- 208000024172 Cardiovascular disease Diseases 0.000 title abstract 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical group [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 abstract 3
- 102100027217 CD82 antigen Human genes 0.000 abstract 1
- 101100166631 Homo sapiens CD82 gene Proteins 0.000 abstract 1
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 abstract 1
- 101100364863 Solanum lycopersicum SAR2 gene Proteins 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 229920006395 saturated elastomer Polymers 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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- A61P9/14—Vasoprotectives; Antihaemorrhoidals; Drugs for varicose therapy; Capillary stabilisers
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
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- Endocrinology (AREA)
- Reproductive Health (AREA)
- Cardiology (AREA)
- Urology & Nephrology (AREA)
- Heart & Thoracic Surgery (AREA)
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- Ophthalmology & Optometry (AREA)
- Neurosurgery (AREA)
- Biomedical Technology (AREA)
- Dermatology (AREA)
- Pregnancy & Childbirth (AREA)
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- Hospice & Palliative Care (AREA)
- Psychiatry (AREA)
- Immunology (AREA)
- Toxicology (AREA)
- Obesity (AREA)
- Oncology (AREA)
- Emergency Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
LA INVENCION SE REFIERE A LOS INHIBIDORES PDE9 PARA EL TRATAMIENTO DE TRASTORNOS CARDIOVASCULARES. LOS INHIBIDORES PDE9 PREERIDOS SON COMPUESTOS DE LA FORMULA I EN LOS QUE R1 ES H O ALQUILO C1-6, EN EL QUE R1 ESTA UNIDO BIEN A N1 O N2; R2 CES ALQUILO C1-6 OPCIONALMENTE SUSTITUIDO CON HIDROXI O ALCOXI; CICLOALQUILO C3-7 OPCIONALMENTE SUSTITUIDO CON ALQUILO, HIDROXI, O ALCOXI; UN HETEROCICLO SATURADO DE 5-6 MIEMBROS OPCIONALMENTE SUSTITUIDO CON ALQUILO, HIDROXI O ALCOXI; HET1 O AR1; R3 ES ALQUILO C1-6 OPCIONALMENTE SUSTITUIDO CON 1 O 2 GRUPOS INDEPENDIENTEMENTE SELECCIONADOS ENTRE: AR2; CICLOALQUILO C3-7 OPCIONALMENTE SUTITUIDO CON ALQUILO C1-6; O AR2; SAR2; NHC(O) ALQUILO C1-6; HET2; XANTENO Y NAFTALENO.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB0126395A GB0126395D0 (en) | 2001-11-02 | 2001-11-02 | Pyrazolo[4,3]pyrimidine derivatives and their use in treating disease |
| GB0130695A GB0130695D0 (en) | 2001-12-21 | 2001-12-21 | Pyrazola[4,3]pyrimidine |
| GB0216761A GB0216761D0 (en) | 2002-07-18 | 2002-07-18 | PDE9 Inhibitors for treating cardiovascular disorders |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SV2004001373A true SV2004001373A (es) | 2004-01-07 |
Family
ID=27256310
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SV2002001373A SV2004001373A (es) | 2001-11-02 | 2002-11-01 | Inhibidores de pde9 para tratamiento de transtornos cardiovasculares. ref. pcs22051 |
Country Status (14)
| Country | Link |
|---|---|
| EP (1) | EP1440073A1 (es) |
| JP (1) | JP2005511575A (es) |
| AR (1) | AR037329A1 (es) |
| BR (1) | BR0214096A (es) |
| CA (1) | CA2466824A1 (es) |
| DO (1) | DOP2002000482A (es) |
| HN (1) | HN2002000317A (es) |
| MX (1) | MXPA04004171A (es) |
| PA (1) | PA8557401A1 (es) |
| PE (1) | PE20030702A1 (es) |
| SV (1) | SV2004001373A (es) |
| TW (1) | TW200300081A (es) |
| UY (1) | UY27522A1 (es) |
| WO (1) | WO2003037899A1 (es) |
Families Citing this family (68)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR20040066788A (ko) | 2001-08-31 | 2004-07-27 | 더 락커펠러 유니버시티 | 프스포다이에스터레이즈 활성 및 뇌에서프스포다이에스터레이즈 1b 매개되는 신호의 조절 |
| WO2003049679A2 (en) | 2001-12-06 | 2003-06-19 | Merck & Co., Inc. | Mitotic kinesin inhibitors |
| DE10238722A1 (de) * | 2002-08-23 | 2004-03-11 | Bayer Ag | Selektive Phosphodiesterase 9A-Inhibitoren als Arzneimittel zur Verbesserung kognitiver Prozesse |
| DE10238724A1 (de) | 2002-08-23 | 2004-03-04 | Bayer Ag | Alkyl-substituierte Pyrazolpyrimidine |
| DE10238723A1 (de) | 2002-08-23 | 2004-03-11 | Bayer Ag | Phenyl-substituierte Pyrazolyprimidine |
| US7141669B2 (en) | 2003-04-23 | 2006-11-28 | Pfizer Inc. | Cannabiniod receptor ligands and uses thereof |
| DE102004004142A1 (de) * | 2003-05-09 | 2004-11-25 | Bayer Healthcare Ag | 6-Cyclylmethyl- und 6-Alkylmethyl-substituierte Pyrazolopyrimidine |
| DE10320785A1 (de) | 2003-05-09 | 2004-11-25 | Bayer Healthcare Ag | 6-Arylmethyl-substituierte Pyrazolopyrimidine |
| US8044060B2 (en) | 2003-05-09 | 2011-10-25 | Boehringer Ingelheim International Gmbh | 6-cyclylmethyl- and 6-alkylmethyl pyrazolo[3,4-D]pyrimidines, methods for their preparation and methods for their use to treat impairments of perception, concentration learning and/or memory |
| JP2006525966A (ja) * | 2003-05-09 | 2006-11-16 | バイエル・ヘルスケア・アクチェンゲゼルシャフト | 6−シクリルメチル−および6−アルキルメチル置換ピラゾロピリミジン類 |
| DE10328479A1 (de) * | 2003-06-25 | 2005-01-13 | Bayer Ag | 6-Arylamino-5-cyano-4-pyrimidinone |
| WO2005012256A1 (en) | 2003-07-22 | 2005-02-10 | Astex Therapeutics Limited | 3, 4-disubstituted 1h-pyrazole compounds and their use as cyclin dependent kinases (cdk) and glycogen synthase kinase-3 (gsk-3) modulators |
| DE102004001873A1 (de) | 2004-01-14 | 2005-09-29 | Bayer Healthcare Ag | Cyanopyrimidinone |
| US20080125403A1 (en) | 2004-04-02 | 2008-05-29 | Merck & Co., Inc. | Method of Treating Men with Metabolic and Anthropometric Disorders |
| US7067659B2 (en) * | 2004-04-23 | 2006-06-27 | Duke University | Reactive oxygen generating enzyme inhibitor with nitric oxide bioactivity and uses thereof |
| US8404718B2 (en) | 2005-01-21 | 2013-03-26 | Astex Therapeutics Limited | Combinations of pyrazole kinase inhibitors |
| AR054425A1 (es) | 2005-01-21 | 2007-06-27 | Astex Therapeutics Ltd | Sales de adicion de piperidin 4-il- amida de acido 4-(2,6-dicloro-benzoilamino) 1h-pirazol-3-carboxilico. |
| DE102005024494A1 (de) * | 2005-05-27 | 2006-11-30 | Bayer Healthcare Ag | Verwendung von Cyanopyrimidinen |
| US8293754B2 (en) | 2005-06-14 | 2012-10-23 | Aska Pharmaceutical Co., Ltd. | Thienopyrimidine derivatives |
| EP1919287A4 (en) * | 2005-08-23 | 2010-04-28 | Intra Cellular Therapies Inc | ORGANIC COMPOUNDS FOR TREATING A REDUCED DOPAMINE RECEPTOR SIGNALING ACTIVITY |
| WO2007143705A2 (en) | 2006-06-06 | 2007-12-13 | Intra-Cellular Therapies, Inc. | Organic compounds |
| AU2007282678B2 (en) * | 2006-08-08 | 2012-09-27 | Aska Pharmaceutical Co., Ltd. | Quinazoline derivative |
| EP2123301A4 (en) * | 2006-12-13 | 2010-11-03 | Aska Pharm Co Ltd | Therapeutic agent for urinary tract disease |
| JP5578786B2 (ja) * | 2006-12-13 | 2014-08-27 | あすか製薬株式会社 | キノキサリン誘導体 |
| CA2678575C (en) * | 2007-02-16 | 2013-10-08 | Emisphere Technologies, Inc. | Compounds having a cyclic moiety and compositions for delivering active agents |
| SI2152712T1 (sl) * | 2007-05-11 | 2012-03-30 | Pfizer | Amino heterociklične spojine |
| WO2009068617A1 (en) * | 2007-11-30 | 2009-06-04 | Boehringer Ingelheim International Gmbh | 1, 5-dihydro-pyrazolo (3, 4-d) pyrimidin-4-one derivatives and their use as pde9a modulators for the teatment of cns disorders |
| CA2707218A1 (en) | 2007-12-06 | 2009-06-11 | Intra-Cellular Therapies, Inc. | Organic compounds |
| UA105362C2 (en) | 2008-04-02 | 2014-05-12 | Бьорингер Ингельхайм Интернациональ Гмбх | 1-heterocyclyl-1, 5-dihydro-pyrazolo [3, 4-d] pyrimidin-4-one derivatives and their use as pde9a modulators |
| MX2011002340A (es) | 2008-09-08 | 2011-04-04 | Boehringer Ingelheim Int | Pirazolopirimidinas y su uso para el tratamiento de trastornos del snc. |
| AU2009307884B2 (en) | 2008-10-22 | 2014-07-31 | Merck Sharp & Dohme Corp. | Novel cyclic benzimidazole derivatives useful anti-diabetic agents |
| CN102271509A (zh) | 2008-10-31 | 2011-12-07 | 默沙东公司 | 用于抗糖尿病药的新型环苯并咪唑衍生物 |
| JP5813511B2 (ja) | 2008-12-06 | 2015-11-17 | イントラ−セルラー・セラピーズ・インコーポレイテッドIntra−Cellular Therapies, Inc. | 有機化合物 |
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| US3939161A (en) * | 1973-10-29 | 1976-02-17 | Abbott Laboratories | 1,3-Dimethyl- 1H-pyrazolo(4,3-D) pyrimidine-7 (6H)-ones |
| US4666908A (en) * | 1985-04-05 | 1987-05-19 | Warner-Lambert Company | 5-Substituted pyrazolo[4,3-d]pyrimidine-7-ones and methods of use |
| GB9722520D0 (en) * | 1997-10-24 | 1997-12-24 | Pfizer Ltd | Compounds |
| DE19838705A1 (de) * | 1998-08-26 | 2000-03-02 | Bayer Ag | Neue Dihydro-(1,2,3)-triazolo-[4,5-d]pyrimidin-7-one |
| IL139457A0 (en) * | 1999-11-08 | 2001-11-25 | Pfizer | Compounds for the treatment of female sexual dysfunction |
| EP1363914A1 (en) * | 2001-02-05 | 2003-11-26 | Dr. Reddy's Laboratories Ltd. | Aryl substituted alkylcarboxylic acids as hypocholesterolemic agents |
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2002
- 2002-10-01 HN HN2002000317A patent/HN2002000317A/es unknown
- 2002-10-09 DO DO2002000482A patent/DOP2002000482A/es unknown
- 2002-10-22 WO PCT/IB2002/004385 patent/WO2003037899A1/en not_active Ceased
- 2002-10-22 EP EP02777623A patent/EP1440073A1/en not_active Withdrawn
- 2002-10-22 JP JP2003540180A patent/JP2005511575A/ja active Pending
- 2002-10-22 MX MXPA04004171A patent/MXPA04004171A/es unknown
- 2002-10-22 CA CA002466824A patent/CA2466824A1/en not_active Abandoned
- 2002-10-22 BR BR0214096-9A patent/BR0214096A/pt not_active IP Right Cessation
- 2002-10-29 PA PA20028557401A patent/PA8557401A1/es unknown
- 2002-10-30 UY UY27522A patent/UY27522A1/es not_active Application Discontinuation
- 2002-10-30 PE PE2002001070A patent/PE20030702A1/es not_active Application Discontinuation
- 2002-10-31 AR ARP020104152A patent/AR037329A1/es unknown
- 2002-11-01 SV SV2002001373A patent/SV2004001373A/es not_active Application Discontinuation
- 2002-11-01 TW TW091132424A patent/TW200300081A/zh unknown
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| AR037329A1 (es) | 2004-11-03 |
| PA8557401A1 (es) | 2003-11-12 |
| TW200300081A (en) | 2003-05-16 |
| PE20030702A1 (es) | 2003-08-21 |
| EP1440073A1 (en) | 2004-07-28 |
| MXPA04004171A (es) | 2004-09-06 |
| HN2002000317A (es) | 2003-05-21 |
| UY27522A1 (es) | 2003-06-30 |
| DOP2002000482A (es) | 2003-05-31 |
| CA2466824A1 (en) | 2003-05-08 |
| WO2003037899A1 (en) | 2003-05-08 |
| BR0214096A (pt) | 2004-09-28 |
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