MA28746B1 - Dérivés de quinazoline-4-yl-pipéridine et cinnoline-4-yl-pipéridine servant d'inhibiteurs de PDE10 pour le traitement de troubles du SNC - Google Patents
Dérivés de quinazoline-4-yl-pipéridine et cinnoline-4-yl-pipéridine servant d'inhibiteurs de PDE10 pour le traitement de troubles du SNCInfo
- Publication number
- MA28746B1 MA28746B1 MA29625A MA29625A MA28746B1 MA 28746 B1 MA28746 B1 MA 28746B1 MA 29625 A MA29625 A MA 29625A MA 29625 A MA29625 A MA 29625A MA 28746 B1 MA28746 B1 MA 28746B1
- Authority
- MA
- Morocco
- Prior art keywords
- piperidine
- treatment
- compounds
- cinnolin
- quinazolin
- Prior art date
Links
- 239000003112 inhibitor Substances 0.000 title abstract 3
- 208000015114 central nervous system disease Diseases 0.000 title abstract 2
- AZIPZWKZCFUTLU-UHFFFAOYSA-N 4-piperidin-1-ylcinnoline Chemical class C1CCCCN1C1=CN=NC2=CC=CC=C12 AZIPZWKZCFUTLU-UHFFFAOYSA-N 0.000 title 1
- VIMMTIWARBDYNN-UHFFFAOYSA-N 4-piperidin-1-ylquinazoline Chemical compound C1CCCCN1C1=NC=NC2=CC=CC=C12 VIMMTIWARBDYNN-UHFFFAOYSA-N 0.000 title 1
- 150000001875 compounds Chemical class 0.000 abstract 4
- 102000004861 Phosphoric Diester Hydrolases Human genes 0.000 abstract 2
- 108090001050 Phosphoric Diester Hydrolases Proteins 0.000 abstract 2
- 210000003169 central nervous system Anatomy 0.000 abstract 2
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 2
- 229940124639 Selective inhibitor Drugs 0.000 abstract 1
- 239000000543 intermediate Substances 0.000 abstract 1
- 125000002183 isoquinolinyl group Chemical class C1(=NC=CC2=CC=CC=C12)* 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- -1 piperidyl-substituted quinazoline Chemical class 0.000 abstract 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/08—Antiepileptics; Anticonvulsants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/14—Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/14—Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
- A61P25/16—Anti-Parkinson drugs
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/18—Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/22—Anxiolytics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/24—Antidepressants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/30—Drugs for disorders of the nervous system for treating abuse or dependence
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/30—Drugs for disorders of the nervous system for treating abuse or dependence
- A61P25/32—Alcohol-abuse
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/30—Drugs for disorders of the nervous system for treating abuse or dependence
- A61P25/34—Tobacco-abuse
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/30—Drugs for disorders of the nervous system for treating abuse or dependence
- A61P25/36—Opioid-abuse
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
- A61P31/14—Antivirals for RNA viruses
- A61P31/18—Antivirals for RNA viruses for HIV
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- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
- C07D491/04—Ortho-condensed systems
Landscapes
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Biomedical Technology (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Veterinary Medicine (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Addiction (AREA)
- Psychiatry (AREA)
- Psychology (AREA)
- Virology (AREA)
- Pain & Pain Management (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Molecular Biology (AREA)
- Tropical Medicine & Parasitology (AREA)
- AIDS & HIV (AREA)
- Hospice & Palliative Care (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Abstract
Dérivés de quinazoline-4-yl-pipéridine et cinnoline-4-yl-pipéridine servant d'inhibiteurs de PDE10 pour le traitement de troubles du SNC La présente invention concerne des dérivés de quinazoline et isoquinoléine à substituant pipéridyle nouveaux de formule (I) qui servent d'inhibiteurs efficaces de phosphodiestérases (PDE). La présente invention concerne également des composés qui sont des inhibiteurs sélectifs de la PDE10. La présente invention concerne en outre les intermédiaires pour la préparation de ces composés ; des compositions pharmaceutiques comprenant ces composés ; et l'utilisation de ces composés dans des méthodes pour le traitement de certains troubles du système nerveux central (SNC) ou d'autres troubles.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US59094304P | 2004-07-23 | 2004-07-23 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MA28746B1 true MA28746B1 (fr) | 2007-07-02 |
Family
ID=34972555
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MA29625A MA28746B1 (fr) | 2004-07-23 | 2007-01-23 | Dérivés de quinazoline-4-yl-pipéridine et cinnoline-4-yl-pipéridine servant d'inhibiteurs de PDE10 pour le traitement de troubles du SNC |
Country Status (25)
| Country | Link |
|---|---|
| US (1) | US20060019975A1 (fr) |
| EP (1) | EP1773805A1 (fr) |
| JP (1) | JP2008507500A (fr) |
| CN (1) | CN1989124A (fr) |
| AP (1) | AP2007003891A0 (fr) |
| AR (1) | AR050433A1 (fr) |
| AU (1) | AU2005266080A1 (fr) |
| BR (1) | BRPI0513475A (fr) |
| CA (1) | CA2574685A1 (fr) |
| CR (1) | CR8861A (fr) |
| EA (1) | EA200700097A1 (fr) |
| EC (1) | ECSP077193A (fr) |
| GT (1) | GT200500198A (fr) |
| IL (1) | IL180205A0 (fr) |
| MA (1) | MA28746B1 (fr) |
| MX (1) | MX2007000878A (fr) |
| NL (1) | NL1029596C2 (fr) |
| NO (1) | NO20065948L (fr) |
| PE (1) | PE20060570A1 (fr) |
| SV (1) | SV2006002175A (fr) |
| TN (1) | TNSN07021A1 (fr) |
| TW (1) | TW200616641A (fr) |
| UY (1) | UY29028A1 (fr) |
| WO (1) | WO2006011040A1 (fr) |
| ZA (1) | ZA200700223B (fr) |
Families Citing this family (45)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP4797021B2 (ja) * | 2004-10-01 | 2011-10-19 | メルク・シャープ・エンド・ドーム・コーポレイション | 糖尿病の治療または予防用のジペプチジルペプチダ−ゼ−iv阻害剤としてのアミノピペリジン |
| RU2007131400A (ru) * | 2005-03-01 | 2009-04-10 | Вайет (Us) | Соединения циннолина и их применение в качестве модуляторов х-рецепторов печени |
| JP2009524637A (ja) * | 2006-01-27 | 2009-07-02 | ファイザー・プロダクツ・インク | アミノフタラジン誘導体化合物 |
| CA2643963A1 (fr) * | 2006-02-21 | 2007-08-30 | Amgen Inc. | Derives de cinnoline en tant qu'inhibiteurs de phosphodiesterase 10 |
| WO2007098214A1 (fr) * | 2006-02-21 | 2007-08-30 | Amgen Inc. | Dérivés cinnoline comme inhibiteurs de phosphodiestérase 10 |
| US20070287707A1 (en) * | 2006-02-28 | 2007-12-13 | Arrington Mark P | Phosphodiesterase 10 inhibitors |
| US20090099175A1 (en) * | 2006-03-01 | 2009-04-16 | Arrington Mark P | Phosphodiesterase 10 inhibitors |
| US20070265258A1 (en) * | 2006-03-06 | 2007-11-15 | Ruiping Liu | Quinazoline derivatives as phosphodiesterase 10 inhibitors |
| WO2007103554A1 (fr) * | 2006-03-08 | 2007-09-13 | Amgen Inc. | Dérivés de quinoline et d'isoquinoline en tant qu'inhibiteurs de phosphodiestérase 10 |
| US8173806B2 (en) * | 2006-03-17 | 2012-05-08 | Mitsubishi Gas Chemical Company, Inc. | Method for production of quinazolin-4-one derivative |
| ES2392553T3 (es) * | 2006-07-10 | 2012-12-11 | H. Lundbeck A/S | Derivados (3-aril-piperazina-1-ilo) de 6,7-dialcoxiquinazolina, 6,7-dialcoxiftalazina y 6,7-dialcoxiisoquinolina |
| EP1903038A1 (fr) * | 2006-09-07 | 2008-03-26 | Bayer Schering Pharma Aktiengesellschaft | Dérivés N-(1-hetaryl-piperidine-4-yl)-(het)arylamide utilisées comme modulateurs du recepteur EP2 |
| EP1903037A1 (fr) * | 2006-09-07 | 2008-03-26 | Bayer Schering Pharma Aktiengesellschaft | Dérivés de 1-[(hétéro)aryl]-3-[hétéroaryl-pipéridine-4-yl]thiourée en tant que modulateurs de récepteurs EP2 |
| WO2009025839A2 (fr) * | 2007-08-22 | 2009-02-26 | Amgen Inc. | Inhibiteurs de phosphodiestérase 10 |
| US7858620B2 (en) * | 2007-09-19 | 2010-12-28 | H. Lundbeck A/S | Cyanoisoquinoline |
| TW200918519A (en) * | 2007-09-19 | 2009-05-01 | Lundbeck & Co As H | Cyanoisoquinoline |
| ES2397934T3 (es) | 2008-12-17 | 2013-03-12 | Amgen Inc. | Compuestos de aminopiridina y carboxipiridina como inhibidores de fosfodiesterasa 10 |
| CA2765750A1 (fr) | 2009-06-19 | 2010-12-23 | H. Lundbeck A/S | Nouveau derive de phenylimidazole en tant qu'inhibiteur de l'enzyme pde10a |
| TWI481607B (zh) | 2009-12-17 | 2015-04-21 | Lundbeck & Co As H | 作為pde10a酵素抑制劑的2-芳基咪唑衍生物 |
| TWI485151B (zh) | 2009-12-17 | 2015-05-21 | Lundbeck & Co As H | 作為pde10a酵素抑制劑之雜芳香族苯基咪唑衍生物 |
| TW201200516A (en) | 2009-12-17 | 2012-01-01 | Lundbeck & Co As H | Phenylimidazole derivatives comprising an ethynylene linker as PDE10A enzyme inhibitors |
| TWI487705B (zh) | 2009-12-17 | 2015-06-11 | Lundbeck & Co As H | 作為pde10a酵素抑制劑之雜芳香族芳基三唑衍生物 |
| MX2012013128A (es) | 2010-05-13 | 2013-03-20 | Amgen Inc | Compuestos heterociclicos de nitrogeno como inhibidores de la fosfodiesterasa 10. |
| JP2013526546A (ja) | 2010-05-13 | 2013-06-24 | アムジエン・インコーポレーテツド | Pde10阻害剤としてのヘテロアリ−ルオキシヘテロシクリル化合物 |
| AU2011253058A1 (en) | 2010-05-13 | 2012-12-06 | Amgen Inc. | Heteroaryloxycarbocyclyl compounds as PDE10 inhibitors |
| WO2011143365A1 (fr) | 2010-05-13 | 2011-11-17 | Amgen Inc. | Composés azotés hétérocycliques convenant comme inhibiteurs de la pde10 |
| TW201215607A (en) | 2010-07-02 | 2012-04-16 | Lundbeck & Co As H | Aryl-and heteroarylamid derivatives as PDE10A enzyme inhibitor |
| TW201206935A (en) | 2010-07-16 | 2012-02-16 | Lundbeck & Co As H | Triazolo-and pyrazoloquinazoline derivatives as PDE10A enzyme inhibitor |
| DE102010042833B4 (de) | 2010-10-22 | 2018-11-08 | Helmholtz-Zentrum Dresden - Rossendorf E.V. | Neue Halogenalkoxychinazoline, deren Herstellung und Verwendung |
| JO3089B1 (ar) | 2010-11-19 | 2017-03-15 | H Lundbeck As | مشتقات ايميدازول كمثبطات لانزيمات pde10a |
| CA2827724A1 (fr) | 2011-02-18 | 2012-08-23 | Allergan, Inc. | Derives de 6,7-dialkoxy-3-isoquinolinol substitues en tant qu'inhibiteurs de la phosphodiesterase 10 (pde10a) |
| WO2013045607A1 (fr) | 2011-09-30 | 2013-04-04 | H. Lundbeck A/S | Dérivés tricycliques hétéroaromatiques liés à de la quinazoline pouvant être utilisés en tant qu'inhibiteurs de l'enzyme pde10a |
| WO2013050527A1 (fr) | 2011-10-05 | 2013-04-11 | H. Lundbeck A/S | Dérivés de quinazoline en tant qu'inhibiteurs de l'enzyme pde10a |
| TWI570124B (zh) | 2011-12-21 | 2017-02-11 | H 朗德貝克公司 | 作為pde10a酵素抑制劑的喹啉衍生物 |
| WO2013127817A1 (fr) | 2012-02-27 | 2013-09-06 | H. Lundbeck A/S | Dérivés d'imidazole comme inhibiteurs de l'enzyme pde10a |
| TW201348231A (zh) | 2012-02-29 | 2013-12-01 | Amgen Inc | 雜雙環化合物 |
| ES2617863T3 (es) | 2012-06-04 | 2017-06-20 | Actelion Pharmaceuticals Ltd. | Derivados de bencimidazol-prolina |
| EA201500399A1 (ru) | 2012-10-10 | 2015-09-30 | Актелион Фармасьютиклз Лтд. | Антагонисты рецептора орексина, которые представляют собой производные [орто-би-(гетеро)арил]-[2-(мета-би-(гетеро)арил)пирролидин-1-ил]метанона |
| WO2014071044A1 (fr) | 2012-11-01 | 2014-05-08 | Allergan, Inc. | Dérivés de 6,7-dialcoxy-3-isoquinoline substitués à titre d'inhibiteurs de phosphodiestérase 10 (pde10a) |
| CA2902135A1 (fr) | 2013-03-12 | 2014-09-18 | Actelion Pharmaceuticals Ltd | Derives d'amide d'azetidine en tant qu'antagonistes des recepteurs d'orexine |
| SI3077391T1 (sl) | 2013-12-04 | 2018-11-30 | Idorsia Pharmaceuticals Ltd | Uporaba benzimidazol-prolinskih derivatov |
| US9200016B2 (en) | 2013-12-05 | 2015-12-01 | Allergan, Inc. | Substituted 6, 7-dialkoxy-3-isoquinoline derivatives as inhibitors of phosphodiesterase 10 (PDE 10A) |
| KR20160138084A (ko) * | 2014-04-04 | 2016-12-02 | 하. 룬드벡 아크티에셀스카브 | Pde1 저해제인 할로겐화된 퀴나졸린-thf-아민 |
| CN106632089B (zh) * | 2016-11-04 | 2019-06-18 | 中山大学 | 一类喹唑啉类化合物及其制备方法与应用 |
| CR20220236A (es) | 2019-11-28 | 2022-10-03 | Bayer Pharma AG | Aminoquinolonas sustituidas como inhibidores de dgk alfa para la activación inmune |
Family Cites Families (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3517005A (en) * | 1967-10-26 | 1970-06-23 | Pfizer & Co C | Certain 2- and 4-substituted quinazolines |
| GB1460389A (en) * | 1974-07-25 | 1977-01-06 | Pfizer Ltd | 4-substituted quinazoline cardiac stimulants |
| IN148482B (fr) * | 1977-06-03 | 1981-03-07 | Pfizer | |
| JPS60120872A (ja) * | 1983-12-01 | 1985-06-28 | Kyowa Hakko Kogyo Co Ltd | 新規なヘテロ環状化合物及び強心剤 |
| US5721237A (en) * | 1991-05-10 | 1998-02-24 | Rhone-Poulenc Rorer Pharmaceuticals Inc. | Protein tyrosine kinase aryl and heteroaryl quinazoline compounds having selective inhibition of HER-2 autophosphorylation properties |
| US5624926A (en) * | 1993-02-18 | 1997-04-29 | Kyowa Hakko Kogyo Co., Ltd. | Piperidinyl-dioxoquinazolines as adenosine reuptake inhibitors |
| US5614627A (en) * | 1993-09-10 | 1997-03-25 | Eisai Co., Ltd. | Quinazoline compounds |
| JP3919272B2 (ja) * | 1996-12-18 | 2007-05-23 | エーザイ・アール・アンド・ディー・マネジメント株式会社 | キナゾリン系化合物 |
| US20030032579A1 (en) * | 2001-04-20 | 2003-02-13 | Pfizer Inc. | Therapeutic use of selective PDE10 inhibitors |
| US7074801B1 (en) * | 2001-04-26 | 2006-07-11 | Eisai Co., Ltd. | Nitrogen-containing condensed cyclic compound having a pyrazolyl group as a substituent group and pharmaceutical composition thereof |
| JP4782564B2 (ja) * | 2002-07-10 | 2011-09-28 | メルク セローノ ソシエテ アノニム | アゾリジノン−ビニル縮合−ベンゼン誘導体 |
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2005
- 2005-07-08 US US11/178,104 patent/US20060019975A1/en not_active Abandoned
- 2005-07-11 BR BRPI0513475-7A patent/BRPI0513475A/pt not_active Application Discontinuation
- 2005-07-11 WO PCT/IB2005/002177 patent/WO2006011040A1/fr not_active Ceased
- 2005-07-11 AU AU2005266080A patent/AU2005266080A1/en not_active Abandoned
- 2005-07-11 CN CNA2005800248487A patent/CN1989124A/zh active Pending
- 2005-07-11 JP JP2007522057A patent/JP2008507500A/ja not_active Withdrawn
- 2005-07-11 AP AP2007003891A patent/AP2007003891A0/xx unknown
- 2005-07-11 MX MX2007000878A patent/MX2007000878A/es unknown
- 2005-07-11 CA CA002574685A patent/CA2574685A1/fr not_active Abandoned
- 2005-07-11 EA EA200700097A patent/EA200700097A1/ru unknown
- 2005-07-11 EP EP05759014A patent/EP1773805A1/fr not_active Withdrawn
- 2005-07-20 PE PE2005000840A patent/PE20060570A1/es not_active Application Discontinuation
- 2005-07-21 GT GT200500198A patent/GT200500198A/es unknown
- 2005-07-21 AR ARP050103018A patent/AR050433A1/es unknown
- 2005-07-21 UY UY29028A patent/UY29028A1/es not_active Application Discontinuation
- 2005-07-22 NL NL1029596A patent/NL1029596C2/nl not_active IP Right Cessation
- 2005-07-22 TW TW094124808A patent/TW200616641A/zh unknown
- 2005-07-22 SV SV2005002175A patent/SV2006002175A/es not_active Application Discontinuation
-
2006
- 2006-12-20 IL IL180205A patent/IL180205A0/en unknown
- 2006-12-21 NO NO20065948A patent/NO20065948L/no not_active Application Discontinuation
-
2007
- 2007-01-08 ZA ZA200700223A patent/ZA200700223B/xx unknown
- 2007-01-18 CR CR8861A patent/CR8861A/es not_active Application Discontinuation
- 2007-01-22 TN TNP2007000021A patent/TNSN07021A1/fr unknown
- 2007-01-23 MA MA29625A patent/MA28746B1/fr unknown
- 2007-01-23 EC EC2007007193A patent/ECSP077193A/es unknown
Also Published As
| Publication number | Publication date |
|---|---|
| ECSP077193A (es) | 2007-02-28 |
| SV2006002175A (es) | 2006-02-15 |
| CR8861A (es) | 2007-03-02 |
| ZA200700223B (en) | 2008-08-27 |
| NL1029596A1 (nl) | 2006-01-24 |
| WO2006011040A1 (fr) | 2006-02-02 |
| TNSN07021A1 (fr) | 2008-06-02 |
| JP2008507500A (ja) | 2008-03-13 |
| EA200700097A1 (ru) | 2007-06-29 |
| GT200500198A (es) | 2006-03-02 |
| BRPI0513475A (pt) | 2008-05-06 |
| CA2574685A1 (fr) | 2006-02-02 |
| EP1773805A1 (fr) | 2007-04-18 |
| AU2005266080A1 (en) | 2006-02-02 |
| AP2007003891A0 (en) | 2007-02-28 |
| MX2007000878A (es) | 2007-03-12 |
| AR050433A1 (es) | 2006-10-25 |
| TW200616641A (en) | 2006-06-01 |
| IL180205A0 (en) | 2007-07-04 |
| UY29028A1 (es) | 2006-02-24 |
| CN1989124A (zh) | 2007-06-27 |
| PE20060570A1 (es) | 2006-07-14 |
| US20060019975A1 (en) | 2006-01-26 |
| NL1029596C2 (nl) | 2006-09-06 |
| NO20065948L (no) | 2007-01-23 |
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