MA30607B1 - N-phenylmethyl -5-oxo-proline-2-amides substitues tenant lieu d'antagonistes du recepteur p2x7 et procedes d'utilisation - Google Patents
N-phenylmethyl -5-oxo-proline-2-amides substitues tenant lieu d'antagonistes du recepteur p2x7 et procedes d'utilisationInfo
- Publication number
- MA30607B1 MA30607B1 MA31599A MA31599A MA30607B1 MA 30607 B1 MA30607 B1 MA 30607B1 MA 31599 A MA31599 A MA 31599A MA 31599 A MA31599 A MA 31599A MA 30607 B1 MA30607 B1 MA 30607B1
- Authority
- MA
- Morocco
- Prior art keywords
- phenylmethyl
- proline
- oxo
- substituted
- methods
- Prior art date
Links
- 102100037602 P2X purinoceptor 7 Human genes 0.000 title abstract 4
- 101710189965 P2X purinoceptor 7 Proteins 0.000 title abstract 4
- 239000002464 receptor antagonist Substances 0.000 title 1
- 229940044551 receptor antagonist Drugs 0.000 title 1
- 206010061218 Inflammation Diseases 0.000 abstract 1
- 230000003042 antagnostic effect Effects 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 230000000694 effects Effects 0.000 abstract 1
- 230000004054 inflammatory process Effects 0.000 abstract 1
- 230000001404 mediated effect Effects 0.000 abstract 1
- 230000004770 neurodegeneration Effects 0.000 abstract 1
- 230000036407 pain Effects 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D207/18—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member
- C07D207/22—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D207/24—Oxygen or sulfur atoms
- C07D207/26—2-Pyrrolidones
- C07D207/273—2-Pyrrolidones with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to other ring carbon atoms
- C07D207/277—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D207/28—2-Pyrrolidone-5- carboxylic acids; Functional derivatives thereof, e.g. esters, nitriles
-
- 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
-
- 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
- A61K31/4015—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 having oxo groups directly attached to the heterocyclic ring, e.g. piracetam, ethosuximide
-
- 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
- A61P19/08—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
- A61P19/10—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease for osteoporosis
-
- 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
- A61P25/02—Drugs for disorders of the nervous system for peripheral neuropathies
-
- 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
- A61P25/04—Centrally acting analgesics, e.g. opioids
-
- 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
- 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
- A61P37/00—Drugs for immunological or allergic disorders
-
- 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
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D207/18—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member
- C07D207/22—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D207/24—Oxygen or sulfur atoms
- C07D207/26—2-Pyrrolidones
- C07D207/273—2-Pyrrolidones with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to other ring carbon atoms
- C07D207/277—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Engineering & Computer Science (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Rheumatology (AREA)
- Pain & Pain Management (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Psychiatry (AREA)
- Hospice & Palliative Care (AREA)
- Immunology (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Plural Heterocyclic Compounds (AREA)
- Pyrrole Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Abstract
La présente invention concerne de nouveaux dérivés d'oxoprolinamide de formule (I) qui modulent la fonction du récepteur P2X7 et sont capables d'antagoniser les effets de l'ATP au niveau du récepteur P2X7, et l'utilisation de ces composés ou de leurs compositions pharmaceutiques dans le traitement d'affections médiées par le récepteur P2X7, par exemple la douleur, l'inflammation et la neurodégénérescence.
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB0613473A GB0613473D0 (en) | 2006-07-06 | 2006-07-06 | Novel compounds |
| GB0622825A GB0622825D0 (en) | 2006-11-15 | 2006-11-15 | Novel compounds |
| GB0705263A GB0705263D0 (en) | 2007-03-19 | 2007-03-19 | Novel compounds |
| GB0711439A GB0711439D0 (en) | 2007-06-13 | 2007-06-13 | Novel receptor antagonists and their methods of use |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MA30607B1 true MA30607B1 (fr) | 2009-07-01 |
Family
ID=38508907
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MA31599A MA30607B1 (fr) | 2006-07-06 | 2009-01-30 | N-phenylmethyl -5-oxo-proline-2-amides substitues tenant lieu d'antagonistes du recepteur p2x7 et procedes d'utilisation |
Country Status (25)
| Country | Link |
|---|---|
| US (2) | US7718693B2 (fr) |
| EP (1) | EP2049478B1 (fr) |
| JP (1) | JP5283620B2 (fr) |
| KR (2) | KR101398264B1 (fr) |
| AR (1) | AR061815A1 (fr) |
| AU (1) | AU2007271182B2 (fr) |
| BR (1) | BRPI0714062A2 (fr) |
| CA (1) | CA2655675A1 (fr) |
| CR (2) | CR10545A (fr) |
| CY (1) | CY1113415T1 (fr) |
| DK (1) | DK2049478T3 (fr) |
| EA (1) | EA016076B1 (fr) |
| ES (1) | ES2385505T3 (fr) |
| HR (1) | HRP20120505T1 (fr) |
| IL (1) | IL196181A0 (fr) |
| MA (1) | MA30607B1 (fr) |
| MX (1) | MX2009000117A (fr) |
| NO (1) | NO20090267L (fr) |
| PE (1) | PE20080997A1 (fr) |
| PL (1) | PL2049478T3 (fr) |
| PT (1) | PT2049478E (fr) |
| SI (1) | SI2049478T1 (fr) |
| TW (1) | TW200819127A (fr) |
| UA (1) | UA100227C2 (fr) |
| WO (1) | WO2008003697A1 (fr) |
Families Citing this family (67)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8063050B2 (en) | 2006-07-06 | 2011-11-22 | Array Biopharma Inc. | Hydroxylated and methoxylated pyrimidyl cyclopentanes as AKT protein kinase inhibitors |
| DE602007011628D1 (de) | 2006-07-06 | 2011-02-10 | Array Biopharma Inc | Dihydrofuropyrimidine als akt-proteinkinaseinhibitoren |
| KR101398264B1 (ko) * | 2006-07-06 | 2014-05-26 | 글락소 그룹 리미티드 | P2x7수용체 길항제로서의 치환된 n페닐메틸5옥소프롤린2아미드 및 그의 사용 방법 |
| MX2008016203A (es) | 2006-07-06 | 2009-01-27 | Array Biopharma Inc | Ciclopenta [d] pirimidinas como inhibidores de la proteina cinasa akt. |
| JP5231411B2 (ja) | 2006-07-06 | 2013-07-10 | アレイ バイオファーマ、インコーポレイテッド | Aktプロテインキナーゼ阻害剤としてのジヒドロチエノピリミジン |
| DE102006047617B4 (de) * | 2006-10-09 | 2008-11-27 | Clariant International Limited | Verfahren zur Herstellung basischer (Meth)acrylamide |
| DE102006047619B4 (de) * | 2006-10-09 | 2008-11-13 | Clariant International Limited | Verfahren zur Herstellung basischer Fettsäureamide |
| RU2454974C2 (ru) * | 2006-10-22 | 2012-07-10 | Айдев Текнолоджиз, Инк. | Устройства и способы для продвижения стентов |
| GB0705882D0 (en) | 2007-03-27 | 2007-05-02 | Glaxo Group Ltd | Novel compounds |
| US20100168171A1 (en) * | 2007-03-28 | 2010-07-01 | Paul John Beswick | Piperidinone Carboxamide Derivatives as P2X7 Modulators |
| EP2139875A2 (fr) * | 2007-03-29 | 2010-01-06 | Glaxo Group Limited | Dérivés d'oxazolidine et de morpholine carboxamide comme modulateurs de p2x7 |
| CA2682649A1 (fr) | 2007-04-03 | 2008-10-09 | Glaxo Group Limited | Derives imidazolidine carboxamide comme modulateurs de p2x7 |
| US8846683B2 (en) | 2007-07-05 | 2014-09-30 | Array Biopharma, Inc. | Pyrimidyl cyclopentanes as Akt protein kinase inhibitors |
| US9409886B2 (en) | 2007-07-05 | 2016-08-09 | Array Biopharma Inc. | Pyrimidyl cyclopentanes as AKT protein kinase inhibitors |
| CA2692502C (fr) | 2007-07-05 | 2016-03-01 | Array Biopharma Inc. | Cyclopentanes de pyrimidyle comme inhibiteurs de proteines kinases akt |
| KR101624361B1 (ko) | 2007-07-05 | 2016-05-25 | 어레이 바이오파마 인크. | Akt 단백질 키나제 억제제로서의 피리미딜 시클로펜탄 |
| WO2009074518A1 (fr) * | 2007-12-12 | 2009-06-18 | Glaxo Group Limited | Combinaisons formées de modulateurs au prolinamide du récepteur p2x7 et d'autres agents thérapeutiques |
| GB0724625D0 (en) * | 2007-12-18 | 2008-01-30 | Glaxo Group Ltd | Novel compounds |
| AU2008337506A1 (en) * | 2007-12-18 | 2009-06-25 | Glaxo Group Limited | 5-oxo-3-pyrrolidinecarboxamide derivatives as P2X7 modulators |
| NZ586720A (en) | 2008-01-09 | 2012-11-30 | Array Biopharma Inc | Hydroxylated pyrimidyl cyclopentane as akt protein kinase inhibitor |
| EP2247578B1 (fr) | 2008-01-09 | 2013-05-22 | Array Biopharma, Inc. | Pyrimidylcyclopentanes hydroxylés utilisés comme inhibiteurs de protéine kinase akt |
| GB0803729D0 (en) * | 2008-02-29 | 2008-04-09 | Ge Healthcare Ltd | Imaging the central nervous system |
| NZ587799A (en) | 2008-03-25 | 2012-06-29 | Affectis Pharmaceuticals Ag | Novel p2x7r antagonists and their use |
| DE102008017213B4 (de) * | 2008-04-04 | 2012-08-09 | Clariant International Limited | Kontinuierliches Verfahren zur Herstellung von Amiden aliphatischer Hydroxycarbonsäuren |
| DE102008017216B4 (de) * | 2008-04-04 | 2013-08-14 | Clariant International Ltd. | Kontinuierliches Verfahren zur Herstellung von Fettsäureamiden |
| DE102008017219A1 (de) * | 2008-04-04 | 2009-10-08 | Clariant International Ltd. | Verfahren zur Herstellung von Amiden in Gegenwart von überhitztem Wasser |
| DE102008017214B4 (de) * | 2008-04-04 | 2012-02-16 | Clariant International Limited | Kontinuierliches Verfahren zur Herstellung von Fettsäurealkanolamiden |
| DE102008017217A1 (de) * | 2008-04-04 | 2009-10-08 | Clariant International Ltd. | Kontinuierliches Verfahren zur Herstellung von Amiden aromatischer Carbonsäuren |
| DE102008017215B4 (de) * | 2008-04-04 | 2012-08-09 | Clariant International Ltd. | Kontinuierliches Verfahren zur Herstellung von Amiden ethylenisch ungesättigter Carbonsäuren |
| DE102008017218B4 (de) * | 2008-04-04 | 2011-09-22 | Clariant International Ltd. | Kontinuierliches Verfahren zur Herstellung von Amiden niederer aliphatischer Carbonsäuren |
| WO2010077836A2 (fr) * | 2009-01-05 | 2010-07-08 | Boehringer Ingelheim International Gmbh | Composés pyrrolidines qui modulent le récepteur cb2 |
| EP2243772B1 (fr) | 2009-04-14 | 2012-01-18 | Affectis Pharmaceuticals AG | Nouveaux antagonistes P2X7R et leur utilisation |
| DE102009031059A1 (de) | 2009-06-30 | 2011-01-05 | Clariant International Ltd. | Vorrichtung zur kontinuierlichen Durchführung chemischer Reaktionen bei hohen Temperaturen |
| DE102009042523B4 (de) | 2009-09-22 | 2012-02-16 | Clariant International Ltd. | Vorrichtung und Verfahren zur kontinuierlichen Durchführung heterogen katalysierter chemischer Reaktionen bei hohen Temperaturen |
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| CN104623665B (zh) * | 2009-12-08 | 2018-01-12 | 范德比尔特大学 | 用于静脉采集和自体移植的改进的方法和组合物 |
| EA201290876A1 (ru) | 2010-03-05 | 2013-03-29 | Президент Энд Феллоуз Оф Гарвард Колледж | Композиции индуцированных дендритных клеток и их использование |
| CN102858741A (zh) | 2010-05-14 | 2013-01-02 | 阿费克蒂斯制药股份公司 | 制备p2x7r拮抗剂的新方法 |
| DE102010056565A1 (de) | 2010-12-30 | 2012-07-05 | Clariant International Ltd. | Verfahren zur Modifizierung Hydroxylgruppen tragender Polymere |
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| BR112013017316A2 (pt) * | 2011-01-04 | 2019-09-24 | Novartis Ag | compostos de indol ou análogos dos mesmos para o tratamento de degeneração macular relacionada à idade (amd) |
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| ES2786298T3 (es) * | 2011-03-03 | 2020-10-09 | Zalicus Pharmaceuticals Ltd | Inhibidores de benzimidazol del canal de sodio |
| MY179607A (en) | 2011-04-01 | 2020-11-11 | Genentech Inc | Combinations of akt inhibitor compounds and abiraterone, and methods of use |
| BR112013025397A2 (pt) | 2011-04-01 | 2019-09-24 | Deepak Sampath | combinação de um composto, composto de fórmula i ou um sal farmaceuticamente aceitável do mesmo, uso, kit, produto, método para tratamento de um distúrbio hiperproliferativo e método para tratamento de uma doença ou afecção modulada por quinase akt em um mamífero |
| WO2012163456A1 (fr) | 2011-05-27 | 2012-12-06 | Affectis Pharmaceuticals Ag | Nouveaux antagonistes de p2x7r et leur utilisation |
| WO2012163792A1 (fr) | 2011-05-27 | 2012-12-06 | Affectis Pharmaceuticals Ag | Nouveaux antagonistes de p2x7r et leur utilisation |
| CN103687860B (zh) | 2011-07-22 | 2016-06-08 | 埃科特莱茵药品有限公司 | 作为p2x7受体拮抗剂的杂环酰胺衍生物 |
| BR112014017735B1 (pt) | 2012-01-20 | 2022-06-28 | Idorsia Pharmaceuticals Ltd | Compostos derivados de amida heterocíclicos como antagonistas do receptor de p2x7, composição farmacêutica, e, uso de um composto |
| US9075975B2 (en) * | 2012-02-21 | 2015-07-07 | Andrew Bud | Online pseudonym verification and identity validation |
| JP6295269B2 (ja) | 2012-12-12 | 2018-03-14 | イドーシア ファーマシューティカルズ リミテッドIdorsia Pharmaceuticals Ltd | P2x7受容体アンタゴニストとしてのインドールカルボキサミド誘導体 |
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Family Cites Families (23)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2651639A (en) * | 1951-08-22 | 1953-09-08 | American Cyanamid Co | 2-pyrrolidone-5-carboxamide derivatives and methods of preparing the same |
| FR2273533A1 (fr) | 1974-06-04 | 1976-01-02 | Ferlux Sa | Nouveaux derives n-substitues d'acides pyrrolidones-2 carboxyliques-5 |
| JPH0699307B2 (ja) * | 1987-08-20 | 1994-12-07 | キッセイ薬品工業株式会社 | 抗痴呆剤 |
| US4772601A (en) * | 1988-01-25 | 1988-09-20 | Hoechst-Roussel Pharmaceuticals, Inc. | 5-Substituted 1-(4-(1-pyrrolidinyl)-2-butynyl)-2-pyrrolidinones, pharmaceutical compositions and use |
| WO1997017958A1 (fr) | 1995-11-13 | 1997-05-22 | Smithkline Beecham Corporation | Composes hemoregulateurs |
| US6054579A (en) * | 1997-06-26 | 2000-04-25 | Leukosite, Inc. | Synthesis of substituted lactams |
| SE9704544D0 (sv) * | 1997-12-05 | 1997-12-05 | Astra Pharma Prod | Novel compounds |
| SE9704546D0 (sv) * | 1997-12-05 | 1997-12-05 | Astra Pharma Prod | Novel compounds |
| WO2000033788A2 (fr) * | 1998-12-11 | 2000-06-15 | American Biogenetic Sciences Inc. | Composes heterocycliques azotes substitues et leur utilisation therapeutique |
| CN1215028C (zh) | 2002-05-24 | 2005-08-17 | 中国科学院上海有机化学研究所 | 外消旋的联二酚的光学拆分方法 |
| US7288538B2 (en) * | 2003-02-20 | 2007-10-30 | Encysive Pharmaceuticals, Inc. | Phenylenediamine urotensin-II receptor antagonists and CCR-9 antagonists |
| EP1663185B1 (fr) * | 2003-09-22 | 2008-12-10 | onepharm Research & Development GmbH | Prevention et traitement de la perte osseuse induite par inflammation et/ou immuno-mediee |
| US20080021034A1 (en) * | 2006-04-10 | 2008-01-24 | Painceptor Pharma Corporation | Compositions and methods for modulating gated ion channels |
| WO2008005368A2 (fr) * | 2006-06-30 | 2008-01-10 | Abbott Laboratories | Pipérazines en tant qu'antagonistes de p2x7 |
| KR101398264B1 (ko) | 2006-07-06 | 2014-05-26 | 글락소 그룹 리미티드 | P2x7수용체 길항제로서의 치환된 n페닐메틸5옥소프롤린2아미드 및 그의 사용 방법 |
| DK2046740T3 (da) * | 2006-07-22 | 2012-08-20 | Oxagen Ltd | Forbindelser med CRTH2-antagonistisk virkning |
| MX2009005478A (es) * | 2006-11-27 | 2009-08-12 | Lundbeck & Co As H | Derivados de heteroarilamida. |
| JP2010520875A (ja) * | 2007-03-09 | 2010-06-17 | レノビス, インコーポレイテッド | P2x7調節因子としてのビシクロヘテロアリール化合物およびその使用 |
| GB0705882D0 (en) * | 2007-03-27 | 2007-05-02 | Glaxo Group Ltd | Novel compounds |
| US20100168171A1 (en) * | 2007-03-28 | 2010-07-01 | Paul John Beswick | Piperidinone Carboxamide Derivatives as P2X7 Modulators |
| EP2139875A2 (fr) * | 2007-03-29 | 2010-01-06 | Glaxo Group Limited | Dérivés d'oxazolidine et de morpholine carboxamide comme modulateurs de p2x7 |
| CA2682649A1 (fr) * | 2007-04-03 | 2008-10-09 | Glaxo Group Limited | Derives imidazolidine carboxamide comme modulateurs de p2x7 |
| EP2592082A1 (fr) * | 2007-04-10 | 2013-05-15 | H. Lundbeck A/S | Analogues d'hétéroaryl-amide utilisés en tant qu'antagonistes de P2X7 |
-
2007
- 2007-07-03 KR KR1020097002352A patent/KR101398264B1/ko not_active Expired - Fee Related
- 2007-07-03 DK DK07787001.2T patent/DK2049478T3/da active
- 2007-07-03 BR BRPI0714062-2A patent/BRPI0714062A2/pt not_active IP Right Cessation
- 2007-07-03 PL PL07787001T patent/PL2049478T3/pl unknown
- 2007-07-03 KR KR1020147001116A patent/KR20140016431A/ko not_active Ceased
- 2007-07-03 JP JP2009517252A patent/JP5283620B2/ja not_active Expired - Fee Related
- 2007-07-03 PT PT07787001T patent/PT2049478E/pt unknown
- 2007-07-03 US US11/772,977 patent/US7718693B2/en not_active Expired - Fee Related
- 2007-07-03 UA UAA200900103A patent/UA100227C2/uk unknown
- 2007-07-03 SI SI200730962T patent/SI2049478T1/sl unknown
- 2007-07-03 WO PCT/EP2007/056675 patent/WO2008003697A1/fr not_active Ceased
- 2007-07-03 MX MX2009000117A patent/MX2009000117A/es active IP Right Grant
- 2007-07-03 EP EP07787001A patent/EP2049478B1/fr not_active Not-in-force
- 2007-07-03 EA EA200970085A patent/EA016076B1/ru not_active IP Right Cessation
- 2007-07-03 CA CA002655675A patent/CA2655675A1/fr not_active Abandoned
- 2007-07-03 AU AU2007271182A patent/AU2007271182B2/en not_active Ceased
- 2007-07-03 HR HRP20120505TT patent/HRP20120505T1/hr unknown
- 2007-07-03 ES ES07787001T patent/ES2385505T3/es active Active
- 2007-07-04 TW TW096124227A patent/TW200819127A/zh unknown
- 2007-07-04 PE PE2007000855A patent/PE20080997A1/es not_active Application Discontinuation
- 2007-07-04 AR ARP070102985A patent/AR061815A1/es unknown
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2008
- 2008-12-19 CR CR10545A patent/CR10545A/es unknown
- 2008-12-25 IL IL196181A patent/IL196181A0/en unknown
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2009
- 2009-01-16 NO NO20090267A patent/NO20090267L/no not_active Application Discontinuation
- 2009-01-30 MA MA31599A patent/MA30607B1/fr unknown
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2010
- 2010-02-18 US US12/708,077 patent/US8048907B2/en not_active Expired - Fee Related
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- 2012-07-26 CY CY20121100671T patent/CY1113415T1/el unknown
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2014
- 2014-11-10 CR CR20140515A patent/CR20140515A/es unknown
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