ES2176471T3 - Inhibidores ciclicos gmp-especificos de la fosfodiesterasa. - Google Patents
Inhibidores ciclicos gmp-especificos de la fosfodiesterasa.Info
- Publication number
- ES2176471T3 ES2176471T3 ES96923986T ES96923986T ES2176471T3 ES 2176471 T3 ES2176471 T3 ES 2176471T3 ES 96923986 T ES96923986 T ES 96923986T ES 96923986 T ES96923986 T ES 96923986T ES 2176471 T3 ES2176471 T3 ES 2176471T3
- Authority
- ES
- Spain
- Prior art keywords
- rent
- sub
- gmp
- phosphodiesterase
- sup
- Prior art date
- Legal status (The legal status 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 status listed.)
- Expired - Lifetime
Links
- 102000004861 Phosphoric Diester Hydrolases Human genes 0.000 title 1
- 108090001050 Phosphoric Diester Hydrolases Proteins 0.000 title 1
- 239000003112 inhibitor Substances 0.000 title 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical class [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 3
- 229910052739 hydrogen Inorganic materials 0.000 abstract 3
- 239000001257 hydrogen Substances 0.000 abstract 3
- 229910052736 halogen Inorganic materials 0.000 abstract 2
- 150000002367 halogens Chemical class 0.000 abstract 2
- 229940124639 Selective inhibitor Drugs 0.000 abstract 1
- 230000009286 beneficial effect Effects 0.000 abstract 1
- 239000002131 composite material Substances 0.000 abstract 1
- 230000005764 inhibitory process Effects 0.000 abstract 1
- 239000012453 solvate Substances 0.000 abstract 1
- 230000001225 therapeutic effect Effects 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/12—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains three hetero rings
- C07D471/14—Ortho-condensed systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P15/00—Drugs for genital or sexual disorders; Contraceptives
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P15/00—Drugs for genital or sexual disorders; Contraceptives
- A61P15/10—Drugs for genital or sexual disorders; Contraceptives for impotence
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Veterinary Medicine (AREA)
- Public Health (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)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Reproductive Health (AREA)
- Endocrinology (AREA)
- Gynecology & Obstetrics (AREA)
- Diabetes (AREA)
- Hematology (AREA)
- Obesity (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Abstract
UN COMPUESTO DE FORMULA (I) Y SUS SOLVATOS, EN LOS QUE R SUP,0} REPRESENTA HIDROGENO, HALOGENO O ALQUILO C SUB,1} UB,6}; R SUP,1} REPRESENTA HIDROGENO O ALQUILO C SUB,1} B,6}; R SUP,2} REPRESENTA EL ANILLO BICICLICO (1) QUE PUEDE ESTAR OPCIONALMENTE SUSTITUIDO POR UNO O MAS GRUPOS SELECCIONADOS DE HALOGENO Y ALQUILO C SUB,1} NTA HIDROGENO O ALQUILO C SUB,1} PRESENTE INVENCION ES UN INHIBIDOR POTENTE Y SELECTIVO DE LA PDE ESPECIFICA DE CGMP Y POSEE UTILIDAD EN DIVERSAS AREAS TERAPEUTICAS EN LAS QUE DICHA INHIBICION ES BENEFICIOSA.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GBGB9514465.5A GB9514465D0 (en) | 1995-07-14 | 1995-07-14 | Chemical compounds |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES2176471T3 true ES2176471T3 (es) | 2002-12-01 |
Family
ID=10777696
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES96923986T Expired - Lifetime ES2176471T3 (es) | 1995-07-14 | 1996-07-11 | Inhibidores ciclicos gmp-especificos de la fosfodiesterasa. |
Country Status (24)
| Country | Link |
|---|---|
| US (1) | US5981527A (es) |
| EP (1) | EP0846118B1 (es) |
| JP (1) | JP4150818B2 (es) |
| CN (1) | CN1069318C (es) |
| AR (1) | AR003455A1 (es) |
| AT (1) | ATE216997T1 (es) |
| AU (1) | AU702324B2 (es) |
| BR (1) | BR9609780A (es) |
| CA (1) | CA2226761A1 (es) |
| CO (1) | CO4700455A1 (es) |
| CZ (1) | CZ3298A3 (es) |
| DE (1) | DE69621026T2 (es) |
| ES (1) | ES2176471T3 (es) |
| GB (1) | GB9514465D0 (es) |
| HR (1) | HRP960321B1 (es) |
| HU (1) | HUP9900006A3 (es) |
| IL (1) | IL122923A0 (es) |
| MX (1) | MX9800411A (es) |
| NO (1) | NO980154L (es) |
| PL (1) | PL324527A1 (es) |
| SK (1) | SK3898A3 (es) |
| WO (1) | WO1997003985A1 (es) |
| YU (1) | YU42296A (es) |
| ZA (1) | ZA965934B (es) |
Families Citing this family (89)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB9401090D0 (en) * | 1994-01-21 | 1994-03-16 | Glaxo Lab Sa | Chemical compounds |
| US6143746A (en) * | 1994-01-21 | 2000-11-07 | Icos Corporation | Tetracyclic cyclic GMP-specific phosphodiesterase inhibitors, process of preparation and use |
| US6046206A (en) * | 1995-06-07 | 2000-04-04 | Cell Pathways, Inc. | Method of treating a patient having a precancerous lesions with amide quinazoline derivatives |
| US6232312B1 (en) | 1995-06-07 | 2001-05-15 | Cell Pathways, Inc. | Method for treating patient having precancerous lesions with a combination of pyrimidopyrimidine derivatives and esters and amides of substituted indenyl acetic acides |
| US5874440A (en) * | 1995-06-07 | 1999-02-23 | Cell Pathways, Inc. | Method of treating a patient having precancerous lesions with phenyl pyrimidinone derivatives |
| US6200980B1 (en) | 1995-06-07 | 2001-03-13 | Cell Pathways, Inc. | Method of treating a patient having precancerous lesions with phenyl purinone derivatives |
| US6262059B1 (en) | 1995-06-07 | 2001-07-17 | Cell Pathways, Inc. | Method of treating a patient having precancerous lesions with quinazoline derivatives |
| US6060477A (en) * | 1995-06-07 | 2000-05-09 | Cell Pathways, Inc. | Method of treating a patient having precancerous lesions with phenyl cycloamino pyrimidinone derivatives |
| GB9514473D0 (en) * | 1995-07-14 | 1995-09-13 | Glaxo Lab Sa | Chemical compounds |
| US6331543B1 (en) | 1996-11-01 | 2001-12-18 | Nitromed, Inc. | Nitrosated and nitrosylated phosphodiesterase inhibitors, compositions and methods of use |
| DE69833254T2 (de) | 1997-06-23 | 2006-11-02 | Cellegy Pharmaceuticals, Inc., Brisbane | Microdosistherapie von gefässbedingten erscheinungen durch no-donoren |
| ES2137113B1 (es) | 1997-07-29 | 2000-09-16 | Almirall Prodesfarma Sa | Nuevos derivados de triazolo-piridazinas heterociclicos. |
| US5852035A (en) * | 1997-12-12 | 1998-12-22 | Cell Pathways, Inc. | Method for inhibiting neoplastic cells and related conditions by exposure to substituted N- arylmethyl and heterocyclmethyl-1H-pyrazolo (3,4-B) quinolin-4-amines |
| US6046199A (en) * | 1998-01-14 | 2000-04-04 | Cell Pathways, Inc. | Method of inhibiting neoplastic cells with tetracyclic pyrido[3,4-B]indole derivatives |
| US6410584B1 (en) | 1998-01-14 | 2002-06-25 | Cell Pathways, Inc. | Method for inhibiting neoplastic cells with indole derivatives |
| US5942520A (en) * | 1998-01-27 | 1999-08-24 | Cell Pathways, Inc. | Method for inhibiting neoplastic cells by exposure to substituted N-cycloalkylmethyl-1-H-pyrazolo (3,4-B) quinolone-4 amines |
| US5990117A (en) * | 1998-04-15 | 1999-11-23 | Cell Pathways, Inc. | Method for inhibiting neoplastic cells and related conditions by exposure to quinazoline derivatives |
| US6124303A (en) * | 1998-09-11 | 2000-09-26 | Cell Pathways, Inc. | Method for inhibiting neoplastic cells and related conditions by exposure to 9-substituted 2-(2-N-aloxyphenyl) purin-6-ones |
| US6268372B1 (en) | 1998-09-11 | 2001-07-31 | Cell Pathways, Inc. | Method for inhibiting neoplastic cells and related conditions by exposure to 2,9-disubstituted purin-6-ones |
| US6326379B1 (en) | 1998-09-16 | 2001-12-04 | Bristol-Myers Squibb Co. | Fused pyridine inhibitors of cGMP phosphodiesterase |
| US6200771B1 (en) | 1998-10-15 | 2001-03-13 | Cell Pathways, Inc. | Method of using a novel phosphodiesterase in pharmaceutical screeing to identify compounds for treatment of neoplasia |
| US6133271A (en) * | 1998-11-19 | 2000-10-17 | Cell Pathways, Inc. | Method for inhibiting neoplastic cells and related conditions by exposure thienopyrimidine derivatives |
| US6187779B1 (en) | 1998-11-20 | 2001-02-13 | Cell Pathways, Inc. | Method for inhibiting neoplastic cells and related conditions by exposure to 2,8-disubstituted quinazoline derivatives |
| US6369092B1 (en) | 1998-11-23 | 2002-04-09 | Cell Pathways, Inc. | Method for treating neoplasia by exposure to substituted benzimidazole derivatives |
| US6486155B1 (en) | 1998-11-24 | 2002-11-26 | Cell Pathways Inc | Method of inhibiting neoplastic cells with isoquinoline derivatives |
| US6034099A (en) * | 1998-11-24 | 2000-03-07 | Cell Pathways, Inc. | Method for inhibiting neoplastic lesions by administering 4-(arylmethylene)- 2, 3- dihydro-pyrazol-3-ones |
| US6077842A (en) * | 1998-11-24 | 2000-06-20 | Cell Pathways, Inc. | Method of inhibiting neoplastic cells with pyrazolopyridylpyridazinone derivatives |
| US6020379A (en) * | 1999-02-19 | 2000-02-01 | Cell Pathways, Inc. | Position 7 substituted indenyl-3-acetic acid derivatives and amides thereof for the treatment of neoplasia |
| US6451807B1 (en) | 1999-04-30 | 2002-09-17 | Lilly Icos, Llc. | Methods of treating sexual dysfunction in an individual suffering from a retinal disease, class 1 congestive heart failure, or myocardial infarction using a PDE5 inhibitor |
| HUP0001632A3 (en) | 1999-04-30 | 2001-12-28 | Lilly Icos Llc Wilmington | Pharmaceutical compositions comprising selective phosphodiestherase inhibitors |
| AU4663100A (en) | 1999-04-30 | 2000-11-17 | Lilly Icos Llc | Treatment of female arousal disorder |
| UA72922C2 (uk) * | 1999-08-03 | 2005-05-16 | Ліллі Айкос Ллк | ФАРМАЦЕВТИЧНА КОМПОЗИЦІЯ З <font face="Symbol">b</font>-КАРБОЛІНОМ (ВАРІАНТИ) ТА СПОСІБ ЛІКУВАННЯ СЕКСУАЛЬНОЇ ДИСФУНКЦІЇ |
| US20040152106A1 (en) * | 1999-10-07 | 2004-08-05 | Robertson Harold A. | Gene necessary for striatal function, uses thereof, and compounds for modulating same |
| WO2001024781A2 (en) * | 1999-10-07 | 2001-04-12 | Novaneuron Inc. | Gene necessary for striatal function, uses thereof, and compounds for modulating same |
| KR20020038941A (ko) | 1999-10-11 | 2002-05-24 | 디. 제이. 우드, 스피겔 알렌 제이 | 포스포디에스테라아제 억제제로서의5-(2-치환된-5-헤테로사이클릴설포닐피리드-3-일)-디하이드로피라졸로[4,3-d]피리미딘-7-온 |
| US20040254153A1 (en) * | 1999-11-08 | 2004-12-16 | Pfizer Inc | Compounds for the treatment of female sexual dysfunction |
| IL139454A0 (en) | 1999-11-08 | 2001-11-25 | Pfizer | Compounds for the treatment of female sexual dysfunction |
| US6569638B1 (en) | 2000-03-03 | 2003-05-27 | Cell Pathways, Inc | Method for screening compounds for the treatment of neoplasia |
| AU2001255849B8 (en) | 2000-04-19 | 2006-04-27 | Lilly Icos, Llc. | PDE-V inhibitors for treatment of Parkinson's Disease |
| WO2001078781A2 (en) * | 2000-04-19 | 2001-10-25 | Johns Hopkins University | Methods for prevention and treatment of gastrointestinal disorders |
| JP2004501920A (ja) * | 2000-06-23 | 2004-01-22 | リリー アイコス リミテッド ライアビリティ カンパニー | 環状gmp特異的ホスホジエステラーゼ阻害剤 |
| CA2423357C (en) * | 2000-08-02 | 2008-05-27 | Lilly Icos Llc | Fused heterocyclic derivatives as phosphodiesterase inhibitors |
| US6503894B1 (en) | 2000-08-30 | 2003-01-07 | Unimed Pharmaceuticals, Inc. | Pharmaceutical composition and method for treating hypogonadism |
| MXPA03001958A (es) * | 2000-09-06 | 2003-06-24 | Tanabe Seiyaku Co | Preparaciones para administrar oral. |
| US6821978B2 (en) * | 2000-09-19 | 2004-11-23 | Schering Corporation | Xanthine phosphodiesterase V inhibitors |
| ATE297926T1 (de) * | 2000-10-02 | 2005-07-15 | Lilly Icos Llc | Hexahydropyrazino(1'2':1,6)-pyrido(3,4-b)indole 1,4-dion-derivate zur behandlung von cardiovaskulären erkrankungen und erektionsstörungen |
| AU2002213419A1 (en) | 2000-10-02 | 2002-04-15 | Lilly Icos Llc | Condensed pyridoindole derivatives |
| DE60122559T2 (de) * | 2000-11-06 | 2006-12-07 | Lilly Icos Llc, Wilmington | Indolderivate als pde5-inhibitoren |
| WO2002038563A2 (en) * | 2000-11-08 | 2002-05-16 | Lilly Icos Llc | Condensed pyrazindione derivatives as pde inhibitors |
| JP4179784B2 (ja) * | 2001-02-15 | 2008-11-12 | 田辺三菱製薬株式会社 | 口腔内速崩壊性錠 |
| DE10118305A1 (de) * | 2001-04-12 | 2002-10-17 | Bayer Ag | Zusammensetzungen zur nasalen Applikation |
| DE10118306A1 (de) | 2001-04-12 | 2002-10-17 | Bayer Ag | Imidazotriazinonhaltige Zusammensetzungen zur nasalen Applikation |
| ES2286291T3 (es) * | 2001-06-05 | 2007-12-01 | Lilly Icos Llc | Compustos tetraciclicos como inhibidores de pde5. |
| US6984641B2 (en) | 2001-06-21 | 2006-01-10 | Lilly Icos Llc. | Carboline derivatives as PDE5 inhibitors |
| CA2465893A1 (en) * | 2001-11-09 | 2003-05-22 | Schering Corporation | Polycyclic guanine derivative phosphodiesterase v inhibitors |
| CA2469075C (en) * | 2001-12-20 | 2011-09-13 | Applied Research Systems Ars Holding N.V. | Pyrrolidine derivatives as prostaglandin modulators |
| US7893101B2 (en) | 2002-03-20 | 2011-02-22 | Celgene Corporation | Solid forms comprising (+)-2-[1-(3-ethoxy-4-methoxyphenyl)-2-methylsulfonylethyl]-4-acetylaminoisoindoline-1,3-dione, compositions thereof, and uses thereof |
| US7276529B2 (en) | 2002-03-20 | 2007-10-02 | Celgene Corporation | Methods of the treatment or prevention of exercise-induced asthma using (+)-2-[1-(3-ethoxy-4-methoxyphenyl)-2-methylsulfonylethyl]-4-acetylaminoisoindoline-1,3-dione |
| US6962940B2 (en) | 2002-03-20 | 2005-11-08 | Celgene Corporation | (+)-2-[1-(3-Ethoxy-4-methoxyphenyl)-2-methylsulfonylethyl]-4-acetylaminoisoindoline-1,3-dione: methods of using and compositions thereof |
| US7208516B2 (en) | 2002-03-20 | 2007-04-24 | Celgene Corporation | Methods of the treatment of psoriatic arthritis using (+)-2-[1-(3-ethoxy-4-methoxyphenyl)-2-methylsulfonylethyl]-4-acetylaminoisoindoline-1,3-dione |
| CN100430395C (zh) * | 2002-07-31 | 2008-11-05 | 利利艾科斯有限公司 | 改进的皮克特-施彭格勒反应和由该反应制备得到的产物 |
| JP2007501866A (ja) | 2003-06-13 | 2007-02-01 | マイクロバイア インコーポレイテッド | 胃腸疾患の治療のための方法および組成物 |
| US8063214B2 (en) * | 2004-10-28 | 2011-11-22 | Dr. Reddy's Laboratories Limited | Polymorphic forms of tadalafil |
| US8506934B2 (en) | 2005-04-29 | 2013-08-13 | Robert I. Henkin | Methods for detection of biological substances |
| JP2009506069A (ja) | 2005-08-26 | 2009-02-12 | ブレインセルス,インコーポレイティド | ムスカリン性受容体調節による神経発生 |
| EP2258359A3 (en) | 2005-08-26 | 2011-04-06 | Braincells, Inc. | Neurogenesis by muscarinic receptor modulation with sabcomelin |
| JP2009512711A (ja) | 2005-10-21 | 2009-03-26 | ブレインセルス,インコーポレイティド | Pde阻害による神経新生の調節 |
| EP2314289A1 (en) | 2005-10-31 | 2011-04-27 | Braincells, Inc. | Gaba receptor mediated modulation of neurogenesis |
| AU2006311577B2 (en) | 2005-11-09 | 2013-02-07 | Zalicus Inc. | Methods, compositions, and kits for the treatment of medical conditions |
| US20100216734A1 (en) | 2006-03-08 | 2010-08-26 | Braincells, Inc. | Modulation of neurogenesis by nootropic agents |
| CA2651862A1 (en) | 2006-05-09 | 2007-11-22 | Braincells, Inc. | 5 ht receptor mediated neurogenesis |
| AU2007249399A1 (en) | 2006-05-09 | 2007-11-22 | Braincells, Inc. | Neurogenesis by modulating angiotensin |
| WO2008030651A1 (en) * | 2006-09-08 | 2008-03-13 | Braincells, Inc. | Combinations containing a 4-acylaminopyridine derivative |
| US20100184806A1 (en) | 2006-09-19 | 2010-07-22 | Braincells, Inc. | Modulation of neurogenesis by ppar agents |
| US8293489B2 (en) | 2007-01-31 | 2012-10-23 | Henkin Robert I | Methods for detection of biological substances |
| US8580801B2 (en) | 2008-07-23 | 2013-11-12 | Robert I. Henkin | Phosphodiesterase inhibitor treatment |
| US20100216805A1 (en) | 2009-02-25 | 2010-08-26 | Braincells, Inc. | Modulation of neurogenesis using d-cycloserine combinations |
| WO2013106547A1 (en) | 2012-01-10 | 2013-07-18 | President And Fellows Of Harvard College | Beta-cell replication promoting compounds and methods of their use |
| WO2014055801A1 (en) | 2012-10-05 | 2014-04-10 | Henkin Robert I | Phosphodiesterase inhibitors for treating taste and smell disorders |
| CN104230960B (zh) * | 2013-06-06 | 2017-02-15 | 山东轩竹医药科技有限公司 | 四并环类间变性淋巴瘤激酶抑制剂 |
| WO2015089105A1 (en) | 2013-12-09 | 2015-06-18 | Respira Therapeutics, Inc. | Pde5 inhibitor powder formulations and methods relating thereto |
| CN104804016B (zh) * | 2014-01-23 | 2017-06-20 | 山东轩竹医药科技有限公司 | 四并环类间变性淋巴瘤激酶抑制剂 |
| CN106233141B (zh) | 2014-02-18 | 2018-08-21 | 罗伯特·I·汉金 | 用于诊断和治疗味觉或嗅觉的损失和/或失真的方法和组合物 |
| JP6687550B2 (ja) | 2014-06-23 | 2020-04-22 | セルジーン コーポレイション | 肝疾患又は肝機能異常を治療するためのアプレミラスト |
| WO2019123285A1 (en) | 2017-12-20 | 2019-06-27 | Novartis Ag | Fused tricyclic pyrazolo-dihydropyrazinyl-pyridone compounds as antivirals |
| KR20200135961A (ko) * | 2018-02-28 | 2020-12-04 | 페로 테라퓨틱스 인코포레이티드 | 페롭토시스 유도 활성을 갖는 화합물 및 이의 사용 방법 |
| US11040964B2 (en) | 2019-02-27 | 2021-06-22 | Ferro Therapeutics, Inc. | Compounds and methods of use |
| US12569493B2 (en) | 2020-03-24 | 2026-03-10 | Cyrano Therapeutics Inc. | Treatment of chemosensory dysfunction from a coronavirus infection |
| EP4684777A1 (en) | 2024-07-24 | 2026-01-28 | Adalvo Limited | A fixed-dose pharmaceutical composition comprising (2s)-2-[(4,6-dimethylpyrimidin-2-yl)oxy]-3-methoxy-3,3-diphenylpropanoic acid and (6r,12ar)-6-(1,3-benzodioxol-5-yl)-2-methyl-2,3,6,7,12,12a-hexahydropyrazino{1',2:1,6]pyrido[3,4-b]indole-1,4-dione |
Family Cites Families (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3644384A (en) * | 1969-06-09 | 1972-02-22 | Sterling Drug Inc | Certain 2-(alpha-haloacetyl) - 1 2 3 4-tetrahydro - 9h - pyrido(3 4-b)indole-3-carboxylates and derivatives |
| US3717638A (en) * | 1971-03-11 | 1973-02-20 | Sterling Drug Inc | 1,2,3,4,6,7,12,12A-OCTAHYDRO-2-PHENYLPYRAZINO[2',1':6,1]PYRIDO[3,4-b]INDOLES AND INTERMEDIATES THEREFOR |
| US3917599A (en) * | 1973-03-30 | 1975-11-04 | Council Scient Ind Res | 2-Substituted-1,2,3,4,6,7,12,12A-octahydropyrazino(2{40 ,1{40 :6,1)pyrido(3,4-B)indoles |
| GB1454171A (en) * | 1973-10-19 | 1976-10-27 | Council Scient Ind Res | Tetracyclic compounds |
| US4188390A (en) * | 1977-11-05 | 1980-02-12 | Pfizer Inc. | Antihypertensive 4-amino-2-[4-(1,4-benzodioxan-2-carbonyl) piperazin-1-yl or homopiperazin-1-yl]quinazolines |
| US4656174A (en) * | 1982-07-24 | 1987-04-07 | Pfizer Inc. | Quinoline therapeutic agents |
| IT1217190B (it) * | 1988-04-22 | 1990-03-14 | Recordati Chem Pharm | Composti utili per il trattamento e diagnosi di disfunzioni frettili |
| EP0357122A3 (en) * | 1988-08-29 | 1991-10-23 | Duphar International Research B.V | Use of beta-carbolines, their bio-isosteric benzofuran and benzothiophene analogues for the manufacture of a medicament having cytostatic properties |
| DE3830096A1 (de) * | 1988-09-03 | 1990-03-15 | Hoechst Ag | Piperazindione mit psychotroper wirkung |
| FR2649613B1 (fr) * | 1989-07-11 | 1991-09-27 | Virag Ronald | Medicament vaso-actif |
| JPH0344324A (ja) * | 1989-07-13 | 1991-02-26 | Kazuoki Tsuchiya | 性機能賦活剤 |
| ATE113839T1 (de) * | 1990-05-31 | 1994-11-15 | Pfizer | Arzneimittel gegen impotenz. |
| US5270323A (en) * | 1990-05-31 | 1993-12-14 | Pfizer Inc. | Method of treating impotence |
| GB9013750D0 (en) * | 1990-06-20 | 1990-08-08 | Pfizer Ltd | Therapeutic agents |
| GB9114760D0 (en) * | 1991-07-09 | 1991-08-28 | Pfizer Ltd | Therapeutic agents |
| GB9218322D0 (en) * | 1992-08-28 | 1992-10-14 | Pfizer Ltd | Therapeutic agents |
| GB9311920D0 (en) * | 1993-06-09 | 1993-07-28 | Pfizer Ltd | Therapeutic agents |
| GB9401090D0 (en) * | 1994-01-21 | 1994-03-16 | Glaxo Lab Sa | Chemical compounds |
-
1995
- 1995-07-14 GB GBGB9514465.5A patent/GB9514465D0/en active Pending
-
1996
- 1996-07-05 HR HR960321A patent/HRP960321B1/xx not_active IP Right Cessation
- 1996-07-11 HU HU9900006A patent/HUP9900006A3/hu unknown
- 1996-07-11 SK SK38-98A patent/SK3898A3/sk unknown
- 1996-07-11 CZ CZ9832A patent/CZ3298A3/cs unknown
- 1996-07-11 ES ES96923986T patent/ES2176471T3/es not_active Expired - Lifetime
- 1996-07-11 PL PL96324527A patent/PL324527A1/xx unknown
- 1996-07-11 CA CA002226761A patent/CA2226761A1/en not_active Abandoned
- 1996-07-11 MX MX9800411A patent/MX9800411A/es not_active Application Discontinuation
- 1996-07-11 AT AT96923986T patent/ATE216997T1/de active
- 1996-07-11 DE DE69621026T patent/DE69621026T2/de not_active Expired - Fee Related
- 1996-07-11 CN CN96196751A patent/CN1069318C/zh not_active Expired - Fee Related
- 1996-07-11 AU AU64192/96A patent/AU702324B2/en not_active Ceased
- 1996-07-11 WO PCT/EP1996/003025 patent/WO1997003985A1/en not_active Ceased
- 1996-07-11 JP JP50624997A patent/JP4150818B2/ja not_active Expired - Fee Related
- 1996-07-11 BR BR9609780A patent/BR9609780A/pt not_active Application Discontinuation
- 1996-07-11 US US09/000,192 patent/US5981527A/en not_active Expired - Lifetime
- 1996-07-11 IL IL12292396A patent/IL122923A0/xx unknown
- 1996-07-11 EP EP96923986A patent/EP0846118B1/en not_active Expired - Lifetime
- 1996-07-12 ZA ZA9605934A patent/ZA965934B/xx unknown
- 1996-07-12 CO CO96036775A patent/CO4700455A1/es unknown
- 1996-07-12 YU YU42296A patent/YU42296A/sh unknown
- 1996-07-12 AR ARP960103558A patent/AR003455A1/es unknown
-
1998
- 1998-01-13 NO NO980154A patent/NO980154L/no not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| JP4150818B2 (ja) | 2008-09-17 |
| EP0846118A1 (en) | 1998-06-10 |
| GB9514465D0 (en) | 1995-09-13 |
| HUP9900006A3 (en) | 1999-11-29 |
| JPH11509535A (ja) | 1999-08-24 |
| SK3898A3 (en) | 1998-11-04 |
| HRP960321B1 (en) | 2003-06-30 |
| ATE216997T1 (de) | 2002-05-15 |
| CO4700455A1 (es) | 1998-12-29 |
| US5981527A (en) | 1999-11-09 |
| HUP9900006A2 (hu) | 1999-04-28 |
| HRP960321A2 (en) | 1998-08-31 |
| ZA965934B (en) | 1997-02-03 |
| NO980154L (no) | 1998-03-10 |
| BR9609780A (pt) | 1999-03-09 |
| MX9800411A (es) | 1998-04-30 |
| DE69621026D1 (de) | 2002-06-06 |
| PL324527A1 (en) | 1998-06-08 |
| DE69621026T2 (de) | 2002-08-22 |
| EP0846118B1 (en) | 2002-05-02 |
| NO980154D0 (no) | 1998-01-13 |
| AU702324B2 (en) | 1999-02-18 |
| AU6419296A (en) | 1997-02-18 |
| YU42296A (sh) | 1998-12-23 |
| CN1195349A (zh) | 1998-10-07 |
| CN1069318C (zh) | 2001-08-08 |
| AR003455A1 (es) | 1998-08-05 |
| IL122923A0 (en) | 1998-08-16 |
| CZ3298A3 (cs) | 1998-06-17 |
| CA2226761A1 (en) | 1997-02-06 |
| WO1997003985A1 (en) | 1997-02-06 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| ES2176471T3 (es) | Inhibidores ciclicos gmp-especificos de la fosfodiesterasa. | |
| ES2170252T3 (es) | Tetrahidroimidazopiridoindoldionas como inhibidores de cgmp especifico pde. | |
| DK0563345T3 (da) | Nye 4-arylpiperaziner og 4-arylpiperidiner | |
| ES2122543T3 (es) | Derivados tetraciclicos, proceso de preparacion y utilizacion. | |
| ES2188957T3 (es) | N-(4-(heteroarilmetil)fenil)-heteroarilaminas. | |
| ES2062009T4 (es) | Agentes antifungicos derivados de triazol | |
| NO944430D0 (no) | 4-mercaptoacetylamino-[2Åbenzazepinon(3)-derivater, og anvendelse som enkefalinaseinhibitorer | |
| ES2062395T3 (es) | Nuevos compuestos de bencimidazol y su uso. | |
| UY26727A1 (es) | Derivados de tropano útiles en terapia | |
| FI964004A0 (fi) | Serotoniiniantagonistien (5HT3) käyttö fibromyalgian hoitoon | |
| ES2160237T3 (es) | O-carbamoil-fenilalaninol que tiene sustituyente en anillo de benceno, sus sales farmaceuticamente utiles, y metodo para la preparacion de los mismos. | |
| ES2196554T3 (es) | Derivados del 1,4-diazacicloheptano y su empleo en tintes para el cabello por oxidacion. | |
| ES2087477T3 (es) | Derivados de pirimidina-4-carboxamida, su preparacion y su aplicacion en terapeutica. | |
| ES2074060T3 (es) | Nuevos ciano y alenil derivados de aristeromicina/adenosina acetilenicos. | |
| DK0734461T3 (da) | Anvendelse af et apparat til dannelse af exciteret gas | |
| ES2171911T3 (es) | Poliaminas conformacionalmente restringidas y su uso como agentes antineoplasicos. | |
| ES2110260T3 (es) | Androstenonas. | |
| DK0638068T3 (da) | Fremgangsmåde til fremstilling af (S)-3-amino-1-substitueret-pyrrolidiner | |
| DE69416518D1 (de) | Neue 9-n-bicyclische nucleosidverbindungen nützlich als selektive inhibitoren von proinflammatorische cytokinen | |
| DK0417473T3 (da) | Fremgangsmåde til behandling af cardial samt vaskulær hypertrofi og hyperplasi | |
| ES470296A1 (es) | Mejoras introducidas en un procedimiento para la preparacionde fluormetal-aminoacidos | |
| CO5011097A1 (es) | Derivados de 8-azabiciclo [3.2.1]octan-3-metanamina . | |
| ATE196508T1 (de) | Enantiomere von cyclopenten-derivaten | |
| ES2046189T3 (es) | Derivados de dihidropiridina y composiciones de los mismos. | |
| ES2059550T3 (es) | Derivados de la bencimidazola, su preparacion y su aplicacion en terapeutica. |