MA30162B1 - Nouveaux derives de pyrrole a cycles fusionnes - Google Patents
Nouveaux derives de pyrrole a cycles fusionnesInfo
- Publication number
- MA30162B1 MA30162B1 MA31116A MA31116A MA30162B1 MA 30162 B1 MA30162 B1 MA 30162B1 MA 31116 A MA31116 A MA 31116A MA 31116 A MA31116 A MA 31116A MA 30162 B1 MA30162 B1 MA 30162B1
- Authority
- MA
- Morocco
- Prior art keywords
- pyrrole derivatives
- new fused
- fused cycle
- cycle
- new
- Prior art date
Links
- KAESVJOAVNADME-UHFFFAOYSA-N Pyrrole Chemical class C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 title 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 239000003814 drug Substances 0.000 abstract 1
- 229940079593 drug Drugs 0.000 abstract 1
- 150000003233 pyrroles Chemical class 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/04—Indoles; Hydrogenated indoles
- C07D209/30—Indoles; Hydrogenated indoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to carbon atoms of the hetero ring
- C07D209/42—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
- A61K31/4025—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil not condensed and containing further heterocyclic rings, e.g. cromakalim
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/06—Antiasthmatics
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/12—Drugs for disorders of the urinary system of the kidneys
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/02—Drugs for dermatological disorders for treating wounds, ulcers, burns, scars, keloids, or the like
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- 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
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/08—Antiallergic agents
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
- A61P7/02—Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/04—Inotropic agents, i.e. stimulants of cardiac contraction; Drugs for heart failure
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
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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
- C07D401/06—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 linked by a carbon chain containing only aliphatic carbon atoms
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/06—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/06—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D407/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00
- C07D407/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing two hetero rings
- C07D407/06—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/06—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
-
- 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
- C07D471/02—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 two hetero rings
- C07D471/04—Ortho-condensed systems
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- 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
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
- C07D495/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D495/04—Ortho-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- Medicinal Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Engineering & Computer Science (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Cardiology (AREA)
- Diabetes (AREA)
- Pulmonology (AREA)
- Heart & Thoracic Surgery (AREA)
- Hematology (AREA)
- Immunology (AREA)
- Urology & Nephrology (AREA)
- Rheumatology (AREA)
- Hospice & Palliative Care (AREA)
- Physical Education & Sports Medicine (AREA)
- Endocrinology (AREA)
- Obesity (AREA)
- Pain & Pain Management (AREA)
- Vascular Medicine (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Emergency Medicine (AREA)
- Dermatology (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Indole Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
Abstract
Nouveaux dérivés de pyrrole à cycles fusionnés La présente invention concerne des dérivés de pyrrole condensés nouveaux de formule (I) dans laquelle A, Ar, R1, R2, R2', R2'' et n répondent aux définitions figurant dans la description et dans les revendications, ainsi que leurs sels physiologiquement acceptables. Ces composés inhibent la kymase et peuvent être utilisés comme médicaments.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP05112210 | 2005-12-15 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MA30162B1 true MA30162B1 (fr) | 2009-01-02 |
Family
ID=37782002
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MA31116A MA30162B1 (fr) | 2005-12-15 | 2008-07-11 | Nouveaux derives de pyrrole a cycles fusionnes |
Country Status (20)
| Country | Link |
|---|---|
| US (1) | US7696240B2 (fr) |
| EP (1) | EP1966134B1 (fr) |
| JP (1) | JP4955012B2 (fr) |
| KR (1) | KR101355754B1 (fr) |
| CN (1) | CN101351446B (fr) |
| AR (1) | AR058338A1 (fr) |
| AU (1) | AU2006326136B2 (fr) |
| BR (1) | BRPI0619963A2 (fr) |
| CA (1) | CA2637740A1 (fr) |
| CR (1) | CR10027A (fr) |
| EC (1) | ECSP088549A (fr) |
| IL (1) | IL191768A0 (fr) |
| MA (1) | MA30162B1 (fr) |
| MY (1) | MY146491A (fr) |
| NO (1) | NO20082561L (fr) |
| NZ (1) | NZ568594A (fr) |
| RU (1) | RU2434853C2 (fr) |
| TW (1) | TWI363755B (fr) |
| UA (1) | UA95788C2 (fr) |
| WO (1) | WO2007068621A1 (fr) |
Families Citing this family (28)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU2004312530A1 (en) * | 2003-12-29 | 2005-07-21 | Sepracor Inc. | Pyrrole and pyrazole DAAO inhibitors |
| JP2009500425A (ja) | 2005-07-06 | 2009-01-08 | セプラコア インコーポレーテッド | エスゾピクロン及びトランス4−(3,4−ジクロロフェニル)−1,2,3,4−テトラヒドロ−n−メチル−1−ナフタレンアミン又はトランス4−(3,4−ジクロロフェニル)−1,2,3,4−テトラヒドロ−1−ナフタレンアミンの組み合わせ、並びに閉経期並びに気分、不安、及び認知障害の治療方法 |
| WO2007047146A2 (fr) * | 2005-10-11 | 2007-04-26 | Intermune, Inc. | Inhibiteurs de réplication virale |
| NZ569608A (en) * | 2006-01-06 | 2011-09-30 | Sepracor Inc | Tetralone-based monoamine reuptake inhibitors |
| BRPI0706365A2 (pt) | 2006-01-06 | 2011-03-22 | Sepracor Inc | Cicloalquilaminas como inibidores da recaptação de monoamina |
| DK2816024T3 (en) | 2006-03-31 | 2017-10-30 | Sunovion Pharmaceuticals Inc | CHIRALE AMINER |
| US7884124B2 (en) * | 2006-06-30 | 2011-02-08 | Sepracor Inc. | Fluoro-substituted inhibitors of D-amino acid oxidase |
| US20080058395A1 (en) * | 2006-06-30 | 2008-03-06 | Sepracor Inc. | Fused heterocyclic inhibitors of D-amino acid oxidase |
| US7579370B2 (en) * | 2006-06-30 | 2009-08-25 | Sepracor Inc. | Fused heterocycles |
| EP2057162A2 (fr) * | 2006-06-30 | 2009-05-13 | Sepracor Inc. | Inhibiteurs hétérocycliques fusionnés de la d-aminoacide-oxydase |
| TW200819447A (en) * | 2006-08-31 | 2008-05-01 | Smithkline Beecham Corp | Chemical compounds |
| US7902252B2 (en) * | 2007-01-18 | 2011-03-08 | Sepracor, Inc. | Inhibitors of D-amino acid oxidase |
| US20090099248A1 (en) * | 2007-01-18 | 2009-04-16 | Sepracor Inc. | Inhibitors of d-amino acid oxidase |
| MX2009008439A (es) * | 2007-02-12 | 2009-08-13 | Intermune Inc | Nuevos inhibidores de la replicacion del virus de hepatitis c. |
| MY162157A (en) * | 2007-04-16 | 2017-05-31 | Abbott Lab | Substituted indole mcl-1 inhibitors |
| AU2008259841B2 (en) | 2007-05-31 | 2015-02-05 | Sunovion Pharmaceuticals Inc. | Phenyl substituted cycloalkylamines as monoamine reuptake inhibitors |
| WO2008153129A1 (fr) * | 2007-06-14 | 2008-12-18 | Teijin Pharma Limited | Agent pour abaisser le taux d'acide urique |
| WO2010017418A1 (fr) * | 2008-08-07 | 2010-02-11 | Sepracor Inc. | Promédicaments d'inhibiteurs hétérocycliques fusionnés de la d-amino acide oxydase |
| US9062056B2 (en) | 2008-09-09 | 2015-06-23 | Boehringer Ingelheim International Gmbh | Aza-benzimidazolone Chymase inhibitors |
| WO2011017634A2 (fr) * | 2009-08-07 | 2011-02-10 | Sepracore Inc. | Promédicaments d'inhibiteurs hétérocycliques fusionnés de la d-aminoacide oxydase |
| SG181883A1 (en) | 2009-12-25 | 2012-08-30 | Daiichi Sankyo Co Ltd | Seven-membered ring compound and pharmaceutical use therefor |
| EP2731439A4 (fr) * | 2011-07-12 | 2014-12-03 | Merck Sharp & Dohme | INHIBITEURS DE LA KINASE TrkA, COMPOSITIONS EN CONTENANT ET MÉTHODES ASSOCIÉES |
| KR101739259B1 (ko) | 2015-04-22 | 2017-05-25 | 광운대학교 산학협력단 | 신규 피롤 단량체 및 그 제조방법, 피롤 단량체로부터 합성된 고분자 또는 화합물 및 그 제조방법 |
| CA3001065A1 (fr) | 2015-10-14 | 2017-04-20 | Xiaoxi WEI | Compositions et procedes permettant de reduire la formation de cristaux de glace |
| EP3386949A4 (fr) * | 2015-12-07 | 2019-11-20 | Wake Forest University Health Sciences | Inhibiteurs de glycolate oxydase et méthodes d'utilisation pour le traitement des calculs rénaux |
| WO2018200608A1 (fr) * | 2017-04-26 | 2018-11-01 | The Board Of Trustees Of The University Of Illinois | Activateurs de nrf et de hif/inhibiteurs de hdac et méthodes thérapeutiques utilisant ceux-ci |
| WO2019199979A1 (fr) | 2018-04-10 | 2019-10-17 | The General Hospital Corporation | Composés antibactériens |
| CN112028815A (zh) * | 2019-06-03 | 2020-12-04 | 中国药科大学 | 吲哚类衍生物及其医药用途 |
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| WO2000010568A1 (fr) | 1998-08-24 | 2000-03-02 | Draheim Susan E | Procedes et compositions pour traiter la parodontopathie a l'aide d'un inhibiteur de phospholipase secretoire a¿2? |
| CZ27399A3 (cs) | 1999-01-26 | 2000-08-16 | Ústav Experimentální Botaniky Av Čr | Substituované dusíkaté heterocyklické deriváty, způsob jejich přípravy, tyto deriváty pro použití jako léčiva, farmaceutická kompozice a kombinovaný farmaceutický přípravek tyto deriváty obsahující a použití těchto derivátů pro výrobu léčiv |
| GB9902047D0 (en) | 1999-01-29 | 1999-03-17 | Cerebrus Ltd | Chemical compounds XI |
| GB9902455D0 (en) | 1999-02-05 | 1999-03-24 | Zeneca Ltd | Chemical compounds |
| GB9902453D0 (en) | 1999-02-05 | 1999-03-24 | Zeneca Ltd | Chemical compounds |
| GB9902459D0 (en) | 1999-02-05 | 1999-03-24 | Zeneca Ltd | Chemical compounds |
| FR2796274B1 (fr) * | 1999-07-16 | 2001-09-21 | Oreal | Utilisation de l'acide 4,6-dimethoxy-indole 2-carboxylique ou de ses derives pour stimuler ou induire la pousse des cheveux et/ou stopper leur chute |
| DE19951360A1 (de) * | 1999-10-26 | 2001-05-03 | Aventis Pharma Gmbh | Substituierte Indole |
| WO2001032621A1 (fr) * | 1999-10-29 | 2001-05-10 | Wakunaga Pharmaceutical Co., Ltd. | Nouveaux derives d'indole, et medicaments contenant lesdits derives comme principe actif |
| IL150594A0 (en) | 2000-01-07 | 2003-02-12 | Ustav Ex Botan Adademie Ved Ce | Purine derivatives, process for their preparation and use |
| ES2295128T3 (es) * | 2000-01-17 | 2008-04-16 | Teijin Pharma Limited | Derivados de bencimidazol como inhibidores de quimasa humana. |
| US20030083315A1 (en) * | 2000-01-17 | 2003-05-01 | Naoki Tsuchiya | Human chymase inhibitors |
| JP4180365B2 (ja) | 2000-07-31 | 2008-11-12 | エフ.ホフマン−ラ ロシュ アーゲー | ピペラジン誘導体 |
| AU2002211901A1 (en) | 2000-10-10 | 2002-04-22 | Smithkline Beecham Corporation | Substituted indoles, pharmaceutical compositions containing such indoles and their use as PPAR-gamma binding agents |
| EP1362854B1 (fr) | 2001-02-22 | 2007-10-31 | Teijin Pharma Limited | Dérivé benzo[b]thiophène et procédé de production correspondant |
| US6710068B2 (en) | 2001-04-11 | 2004-03-23 | Idenix Pharmaceuticals, Inc. | Phenylindoles for the treatment of HIV |
| TWI317634B (en) * | 2001-12-13 | 2009-12-01 | Nat Health Research Institutes | Aroyl indoles compounds |
| WO2004080965A1 (fr) | 2003-03-14 | 2004-09-23 | Kyowa Hakko Kogyo Co., Ltd. | Antagoniste du recepteur du neuropeptide ff |
| JP2007516203A (ja) * | 2003-07-09 | 2007-06-21 | バイオリポックス エービー | 炎症の治療に有用なインドール類 |
| US7265148B2 (en) | 2003-09-25 | 2007-09-04 | Wyeth | Substituted pyrrole-indoles |
| US20050089936A1 (en) * | 2003-10-23 | 2005-04-28 | Jianping Cai | Combinatorial library of 3-aryl-1H-indole-2-carboxylic acid amides |
| US7396940B2 (en) * | 2003-10-23 | 2008-07-08 | Hoffmann-La Roche Inc. | Combinatorial library of 3-aryl-1H-indole-2-carboxylic acid |
| ES2315877T3 (es) | 2004-06-18 | 2009-04-01 | Biolipox Ab | Indoles utiles en el tratamiento de inflamaciones. |
| CA2609980C (fr) | 2005-05-27 | 2015-10-13 | Queen's University At Kingston | Traitement de troubles du repliement des proteines |
-
2006
- 2006-05-12 UA UAA200808861A patent/UA95788C2/ru unknown
- 2006-12-05 MY MYPI20081926A patent/MY146491A/en unknown
- 2006-12-05 RU RU2008128347/04A patent/RU2434853C2/ru not_active IP Right Cessation
- 2006-12-05 CA CA002637740A patent/CA2637740A1/fr not_active Abandoned
- 2006-12-05 JP JP2008544957A patent/JP4955012B2/ja not_active Expired - Fee Related
- 2006-12-05 BR BRPI0619963-1A patent/BRPI0619963A2/pt not_active IP Right Cessation
- 2006-12-05 US US11/634,584 patent/US7696240B2/en not_active Expired - Fee Related
- 2006-12-05 WO PCT/EP2006/069292 patent/WO2007068621A1/fr not_active Ceased
- 2006-12-05 EP EP06841282.4A patent/EP1966134B1/fr active Active
- 2006-12-05 CN CN2006800471484A patent/CN101351446B/zh not_active Expired - Fee Related
- 2006-12-05 NZ NZ568594A patent/NZ568594A/en not_active IP Right Cessation
- 2006-12-05 AU AU2006326136A patent/AU2006326136B2/en not_active Ceased
- 2006-12-05 KR KR1020087014264A patent/KR101355754B1/ko not_active Expired - Fee Related
- 2006-12-13 TW TW095146710A patent/TWI363755B/zh not_active IP Right Cessation
- 2006-12-13 AR ARP060105492A patent/AR058338A1/es not_active Application Discontinuation
-
2008
- 2008-05-27 IL IL191768A patent/IL191768A0/en unknown
- 2008-05-28 CR CR10027A patent/CR10027A/es not_active Application Discontinuation
- 2008-06-02 NO NO20082561A patent/NO20082561L/no not_active Application Discontinuation
- 2008-06-13 EC EC2008008549A patent/ECSP088549A/es unknown
- 2008-07-11 MA MA31116A patent/MA30162B1/fr unknown
Also Published As
| Publication number | Publication date |
|---|---|
| RU2434853C2 (ru) | 2011-11-27 |
| BRPI0619963A2 (pt) | 2011-10-25 |
| MY146491A (en) | 2012-08-15 |
| IL191768A0 (en) | 2008-12-29 |
| EP1966134B1 (fr) | 2014-03-12 |
| US20070142452A1 (en) | 2007-06-21 |
| AR058338A1 (es) | 2008-01-30 |
| CA2637740A1 (fr) | 2007-06-21 |
| EP1966134A1 (fr) | 2008-09-10 |
| JP4955012B2 (ja) | 2012-06-20 |
| JP2009519291A (ja) | 2009-05-14 |
| ECSP088549A (es) | 2008-07-30 |
| TWI363755B (en) | 2012-05-11 |
| AU2006326136B2 (en) | 2012-08-16 |
| KR101355754B1 (ko) | 2014-01-27 |
| KR20080070062A (ko) | 2008-07-29 |
| HK1127058A1 (en) | 2009-09-18 |
| UA95788C2 (en) | 2011-09-12 |
| CN101351446B (zh) | 2011-10-05 |
| RU2008128347A (ru) | 2010-01-20 |
| NO20082561L (no) | 2008-08-27 |
| NZ568594A (en) | 2011-08-26 |
| CR10027A (es) | 2008-07-29 |
| WO2007068621A1 (fr) | 2007-06-21 |
| TW200732303A (en) | 2007-09-01 |
| AU2006326136A1 (en) | 2007-06-21 |
| US7696240B2 (en) | 2010-04-13 |
| CN101351446A (zh) | 2009-01-21 |
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