NO20015599L - Hjelpemidler eller preventive midler for sykdom assosiert med kjemokiner - Google Patents
Hjelpemidler eller preventive midler for sykdom assosiert med kjemokinerInfo
- Publication number
- NO20015599L NO20015599L NO20015599A NO20015599A NO20015599L NO 20015599 L NO20015599 L NO 20015599L NO 20015599 A NO20015599 A NO 20015599A NO 20015599 A NO20015599 A NO 20015599A NO 20015599 L NO20015599 L NO 20015599L
- Authority
- NO
- Norway
- Prior art keywords
- chemokines
- remedies
- preventive agents
- illness associated
- prophylactics
- Prior art date
Links
- 102000019034 Chemokines Human genes 0.000 title abstract 3
- 108010012236 Chemokines Proteins 0.000 title abstract 3
- 230000003449 preventive effect Effects 0.000 title 1
- 201000010099 disease Diseases 0.000 abstract 2
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 2
- 230000000069 prophylactic effect Effects 0.000 abstract 2
- 150000003839 salts Chemical class 0.000 abstract 2
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 1
- 102100021943 C-C motif chemokine 2 Human genes 0.000 abstract 1
- 101710155857 C-C motif chemokine 2 Proteins 0.000 abstract 1
- 101710151805 Mitochondrial intermediate peptidase 1 Proteins 0.000 abstract 1
- 239000002253 acid Substances 0.000 abstract 1
- 239000004480 active ingredient Substances 0.000 abstract 1
- -1 cyclic amine Chemical class 0.000 abstract 1
- 201000008383 nephritis Diseases 0.000 abstract 1
- 206010039073 rheumatoid arthritis Diseases 0.000 abstract 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D223/00—Heterocyclic compounds containing seven-membered rings having one nitrogen atom as the only ring hetero atom
- C07D223/02—Heterocyclic compounds containing seven-membered rings having one nitrogen atom as the only ring hetero atom not condensed with other rings
- C07D223/06—Heterocyclic compounds containing seven-membered rings having one nitrogen atom as the only ring hetero atom not condensed with other rings 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
- C07D223/12—Nitrogen atoms not forming part of a nitro radical
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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
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- 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
- A61K31/401—Proline; Derivatives thereof, e.g. captopril
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- A—HUMAN NECESSITIES
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- 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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- 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
- A61K31/403—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 condensed with carbocyclic rings, e.g. carbazole
- A61K31/404—Indoles, e.g. pindolol
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- A61K31/415—1,2-Diazoles
- A61K31/4155—1,2-Diazoles non condensed and containing further heterocyclic rings
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- A61K31/4164—1,3-Diazoles
- A61K31/4178—1,3-Diazoles not condensed 1,3-diazoles and containing further heterocyclic rings, e.g. pilocarpine, nitrofurantoin
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- A61K31/4164—1,3-Diazoles
- A61K31/4184—1,3-Diazoles condensed with carbocyclic rings, e.g. benzimidazoles
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- A61K31/422—Oxazoles not condensed and containing further heterocyclic rings
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- A61K31/423—Oxazoles condensed with carbocyclic rings
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- A61K31/427—Thiazoles not condensed and containing further heterocyclic rings
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- 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
-
- 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
- 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
-
- 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
-
- 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
- C07D207/04—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 no double bonds between ring members or between ring members and non-ring members
- C07D207/08—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 no double bonds between ring members or between ring members and non-ring members with hydrocarbon radicals, substituted by hetero atoms, attached to ring carbon atoms
- C07D207/09—Radicals substituted by nitrogen atoms, not forming part of a nitro radical
-
- 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
- C07D207/04—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 no double bonds between ring members or between ring members and non-ring members
- C07D207/10—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 no double bonds between ring members or between ring members and non-ring members 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
- C07D207/14—Nitrogen atoms not forming part of a nitro radical
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
- C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D211/06—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
- C07D211/08—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms
- C07D211/18—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D211/26—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms with hydrocarbon radicals, substituted by nitrogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
- C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D211/06—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
- C07D211/36—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members 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
- C07D211/56—Nitrogen atoms
- C07D211/58—Nitrogen atoms attached in position 4
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Organic Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Neurology (AREA)
- Pulmonology (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Biomedical Technology (AREA)
- Cardiology (AREA)
- Neurosurgery (AREA)
- Heart & Thoracic Surgery (AREA)
- Immunology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Hydrogenated Pyridines (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP17585699 | 1999-05-18 | ||
| JP25146499 | 1999-09-06 | ||
| PCT/JP2000/003203 WO2000069432A1 (fr) | 1999-05-18 | 2000-05-18 | Moyens de traitement et de prevention contre les maladies associees a des chimiokines |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| NO20015599D0 NO20015599D0 (no) | 2001-11-16 |
| NO20015599L true NO20015599L (no) | 2001-11-16 |
Family
ID=26496987
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO20015599A NO20015599L (no) | 1999-05-18 | 2001-11-16 | Hjelpemidler eller preventive midler for sykdom assosiert med kjemokiner |
Country Status (13)
| Country | Link |
|---|---|
| US (1) | US7390830B1 (fr) |
| EP (1) | EP1179341B1 (fr) |
| KR (1) | KR100673340B1 (fr) |
| CN (1) | CN1240699C (fr) |
| AT (1) | ATE308985T1 (fr) |
| AU (1) | AU779954B2 (fr) |
| CA (1) | CA2373942A1 (fr) |
| DE (1) | DE60023878T2 (fr) |
| DK (1) | DK1179341T3 (fr) |
| ES (1) | ES2250132T3 (fr) |
| NO (1) | NO20015599L (fr) |
| NZ (1) | NZ515374A (fr) |
| WO (1) | WO2000069432A1 (fr) |
Families Citing this family (42)
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| US6316623B1 (en) * | 1998-08-21 | 2001-11-13 | Isis Pharmaceuticals, Inc. | Ethylenediamine compound libraries |
| WO2001043746A1 (fr) * | 1999-12-14 | 2001-06-21 | Nippon Shinyaku Co., Ltd. | Composition medicinale |
| US6492521B2 (en) * | 2000-11-03 | 2002-12-10 | Cytec Technology Corp. | Hindered amine light stabilizers based on multi-functional carbonyl compounds and methods of making same |
| EP1470119A4 (fr) | 2001-06-13 | 2005-10-19 | Genesoft Pharmaceuticals Inc | Composes benzothiophene presentant une activite anti-infectieuse |
| US6867221B2 (en) * | 2001-08-30 | 2005-03-15 | Kowa Co., Ltd. | Cyclic amine compounds and pharmaceutical composition containing the same |
| JP2005170790A (ja) * | 2002-01-09 | 2005-06-30 | Ajinomoto Co Inc | N−アルキルスルフォニル置換アミド誘導体 |
| PA8575901A1 (es) * | 2002-07-18 | 2004-07-20 | Pfizer Prod Inc | Derivados de piperidina novedosos |
| EP1539151B1 (fr) | 2002-08-02 | 2009-03-18 | Genesoft Pharmaceuticals, Inc. | Composes biaryle a action anti-infectieuse |
| WO2004039318A2 (fr) | 2002-10-25 | 2004-05-13 | Genesoft Pharmaceuticals, Inc. | Composes biaryle anti-infectieux |
| GEP20115290B (en) | 2002-11-27 | 2011-09-26 | Incyte Corp | 3-aminopyrrolidine derivatives as modulators of chemokine receptors |
| CA2508769A1 (fr) | 2002-12-10 | 2004-06-24 | Oscient Pharmaceuticals Corporation | Composes antibacteriens possedant un motif (pyrrole carboxamide)-(benzamide)-(imidazole carboxamide) |
| EP2385040A1 (fr) | 2003-03-14 | 2011-11-09 | ONO Pharmaceutical Co., Ltd. | Dérivés hétérocycliques renfermant de l'azote et médicaments contenant ces dérivés comme principe actif |
| US7498323B2 (en) | 2003-04-18 | 2009-03-03 | Ono Pharmaceuticals Co., Ltd. | Spiro-piperidine compounds and medicinal use thereof |
| JP4768620B2 (ja) * | 2003-05-15 | 2011-09-07 | ジェネンテック, インコーポレイテッド | 敗血症の予防及び治療のための方法及び組成物 |
| US7405210B2 (en) | 2003-05-21 | 2008-07-29 | Osi Pharmaceuticals, Inc. | Pyrrolopyridine-2-carboxylic acid amide inhibitors of glycogen phosphorylase |
| US7378409B2 (en) | 2003-08-21 | 2008-05-27 | Bristol-Myers Squibb Company | Substituted cycloalkylamine derivatives as modulators of chemokine receptor activity |
| EP1524265A1 (fr) * | 2003-10-15 | 2005-04-20 | Newron Pharmaceuticals S.p.A. | Dérivés de prolinamide en tant que bloqueurs du canal sodium et/ou calcium ou inhibiteurs sélectifs de MAO-B |
| JP4740151B2 (ja) | 2003-12-18 | 2011-08-03 | インサイト コーポレイション | ケモカイン受容体のモジュレーターとしての3‐シクロアルキルアミノピロリジン誘導体 |
| GB0401334D0 (en) * | 2004-01-21 | 2004-02-25 | Novartis Ag | Organic compounds |
| ATE483708T1 (de) | 2004-03-08 | 2010-10-15 | Prosidion Ltd | Pyrrolopyridin-2-carbonsäurehydrazide als inhibitoren von glykogenphosphorylase |
| CN1950085A (zh) | 2004-05-11 | 2007-04-18 | 因赛特公司 | 作为趋化因子受体调节剂的3-(4-杂芳基环己基氨基)环戊烷羧酰胺 |
| TW200602314A (en) | 2004-05-28 | 2006-01-16 | Tanabe Seiyaku Co | A novel pyrrolidine compound and a process for preparing the same |
| KR20070043770A (ko) * | 2004-06-14 | 2007-04-25 | 데이진 화-마 가부시키가이샤 | 아세트아미드피롤리딘 유도체의 제조 방법 및 그 중간체화합물 |
| WO2006019497A2 (fr) | 2004-06-17 | 2006-02-23 | Neurocrine Biosciences, Inc. | Composes somniferes et procedes associes |
| WO2006030925A1 (fr) | 2004-09-13 | 2006-03-23 | Ono Pharmaceutical Co., Ltd. | Derive heterocyclique azote et medicament le contenant en tant que principe actif |
| DE602005013275D1 (de) | 2004-12-02 | 2009-04-23 | Prosidion Ltd | Pyrrolopyridin-2-karbonsäureamide |
| TW200633998A (en) * | 2004-12-08 | 2006-10-01 | Nissan Chemical Ind Ltd | Substituted heterocyclic compounds and thrombopoietin receptor activators |
| CN101155802A (zh) * | 2005-04-07 | 2008-04-02 | 帝人制药株式会社 | 氨基吡咯烷衍生物的晶体及其制备方法 |
| EP1889622A4 (fr) | 2005-05-31 | 2009-12-23 | Ono Pharmaceutical Co | Compose de spiropiperidine et son utilisation medicinale |
| JP5251127B2 (ja) | 2005-10-28 | 2013-07-31 | 小野薬品工業株式会社 | 塩基性基を含有する化合物およびその用途 |
| PL1961744T3 (pl) | 2005-11-18 | 2013-09-30 | Ono Pharmaceutical Co | Związek zawierający grupę zasadową oraz jego zastosowanie |
| US8003642B2 (en) | 2006-03-10 | 2011-08-23 | Ono Pharmaceutical Co., Ltd. | Nitrogenated heterocyclic derivative, and pharmaceutical agent comprising the derivative as active ingredient |
| EP2042503B1 (fr) | 2006-05-16 | 2013-01-30 | Ono Pharmaceutical Co., Ltd. | Composé ayant un groupe acide qui peut être protégé et utilisation dudit composé |
| EP2055705A4 (fr) | 2006-07-31 | 2014-08-20 | Ono Pharmaceutical Co | Composé auquel un groupe cyclique est lié par une liaison spiro et son utilisation |
| AU2007319660A1 (en) * | 2006-10-05 | 2008-05-22 | Centocor Ortho Biotech Inc. | CCR2 antagonists for treatment of fibrosis |
| WO2009104557A1 (fr) * | 2008-02-21 | 2009-08-27 | 株式会社カネカ | Procédé de production de dérivé de n-(3-pyrrolidinyl)glycine |
| WO2010129351A1 (fr) | 2009-04-28 | 2010-11-11 | Schepens Eye Research Institute | Procédé pour identifier et pour traiter une dégénérescence maculaire liée à l'âge |
| KR101151415B1 (ko) | 2009-07-10 | 2012-06-01 | 양지화학 주식회사 | Ccr2 길항제로서의 피페라지닐에틸 3-아미노피롤리딘 유도체 |
| EP3371164B1 (fr) * | 2015-11-06 | 2022-03-16 | Neurocrine Biosciences, Inc. | Dérivés carboxamides de n-[2-(1-benzylpipéridin-4-yl)éthyl]-4-(pyrazin-2-yl)-pipérazine-1- et composés similaires en tant qu'antagonists du récepteur muscarinique 4 (m4) pour traiter des maladies neurologiques |
| RU2018146946A (ru) * | 2016-06-08 | 2020-07-10 | Глэксосмитклайн Интеллекчуал Проперти Дивелопмент Лимитед | Химические соединения |
| CN106916168B (zh) * | 2017-03-13 | 2019-08-27 | 牡丹江医学院 | 一种治疗重症胰腺炎的化合物及其制备方法 |
| EP4069367B1 (fr) | 2019-12-06 | 2024-05-15 | Neurocrine Biosciences, Inc. | Antagonistes du récepteur muscarinique 4 et procédés d'utilisation |
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| US4443461A (en) | 1981-09-10 | 1984-04-17 | John Wyeth & Brother Limited | N-[2-[[1-[1H-Indolylalkyl- or oxoalkyl]-4-piperidinyl]-amino]-2-oxoethyl]-arylcarboxamide derivatives |
| GB2106108B (en) | 1981-09-10 | 1985-05-01 | Wyeth John & Brother Ltd | Piperidine derivatives |
| GR81827B (fr) | 1983-03-21 | 1984-12-12 | Boehringer Ingelheim Ltd | |
| AU598750B2 (en) * | 1985-09-27 | 1990-07-05 | Mitsubishi Chemical Corporation | Phenylalanine derivative and proteinase inhibitor |
| WO1997024325A1 (fr) | 1995-12-28 | 1997-07-10 | Takeda Chemical Industries, Ltd. | DERIVES DE DIPHENYLMETHANE UTILISES COMME ANTAGONISTES DU RECEPTEUR MIP-1α/RANTES |
| EP0915888A1 (fr) | 1996-04-24 | 1999-05-19 | Takeda Chemical Industries, Ltd. | Derives d'imidazopyridine reunis par fusion antihyperlipidemiants utilises comme agents |
| WO1997044329A1 (fr) | 1996-05-20 | 1997-11-27 | Teijin Limited | Derives de diamine cyclique de diarylaklyle utilises en tant qu'antagonistes des recepteurs de chimiokines |
| EP0920306A2 (fr) | 1996-07-12 | 1999-06-09 | Leukosite, Inc. | Antagonistes des recepteurs de la chemokine et procedes d'utilisation de ces derniers |
| EP0916668A4 (fr) | 1996-07-29 | 2000-08-16 | Banyu Pharma Co Ltd | Antagonistes de recepteurs de chemokines |
| EP0927167A1 (fr) | 1996-08-14 | 1999-07-07 | Warner-Lambert Company | Derives 2-phenyle benzimidazole en tant qu'antagonistes de mcp-1 |
| AU5604998A (en) | 1996-12-13 | 1998-07-03 | Merck & Co., Inc. | Spiro-substituted azacycles as modulators of chemokine receptor activity |
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| WO1998025617A1 (fr) | 1996-12-13 | 1998-06-18 | Merck & Co., Inc. | Arylpiperazines substituees utilisees comme modulateurs de l'activite du recepteur de la chemokine |
| WO1998027815A1 (fr) | 1996-12-20 | 1998-07-02 | Merck & Co., Inc. | Aminoquinoleines substituees utilisees comme modulateurs de l'activite des recepteurs de la chemokine |
| AR011057A1 (es) | 1997-01-08 | 2000-08-02 | Smithkline Beecham Corp | Uso de bis-acridinas sustituidas y compuestos afines para la preparacion de medicamentos y dichos compuestos |
| AU6133098A (en) | 1997-01-21 | 1998-08-07 | Merck & Co., Inc. | 3,3-disubstituted piperidines as modulators of chemokine receptor activity |
| ATE421954T1 (de) | 1997-02-26 | 2009-02-15 | Pfizer | Heteroaryl-hexansäureamid-derivate, ihre herstellung und ihre verwendung als selektive inhibitoren der bindung von mip-1-alpha an seinen ccr1 rezeptor |
| HUP0001285A3 (en) * | 1997-05-08 | 2000-10-30 | Smithkline Beecham Corp Philap | Pyrrolidine derivatives as protease inhibitors, process for producing them and pharmaceutical compositions containing them |
| ZA985542B (en) | 1997-07-03 | 1999-04-07 | Smithkline Beecham Corp | Substituted benzanilides as CCR5 receptor ligands antiinflammatory agents and antiviral agents |
| IL125658A0 (en) | 1997-08-18 | 1999-04-11 | Hoffmann La Roche | Ccr-3 receptor antagonists |
| ID24475A (id) * | 1997-11-18 | 2000-07-20 | Teijin Limeted Cs | Turunan-turunan amina siklik dan penggunaannya sebagai obat |
| DE19837485A1 (de) | 1998-08-12 | 2000-02-17 | Siemens Ag | Verfahren zum Erkennen von Schäden an Schienenfahrzeugen und/oder Gleisen |
| EP1131290B1 (fr) | 1998-11-20 | 2008-02-20 | F. Hoffmann-La Roche Ag | Piperidines comme antagonistes du recepteur ccr-3 |
| JP3593037B2 (ja) | 1998-11-20 | 2004-11-24 | エフ.ホフマン−ラ ロシュ アーゲー | ピロリジン誘導体ccr−3受容体アンタゴニスト |
| EP1140086A4 (fr) | 1998-12-18 | 2002-04-03 | Du Pont Pharm Co | N-ureidoalkyl-piperidines utilisees en tant que modulateurs de l'activite des recepteurs des chimiokines |
| CA2346933A1 (fr) | 1998-12-18 | 2000-06-22 | Dupont Pharmaceuticals Company | N-ureidoalkyl-piperidines utilisees en tant que modulateurs de l'activite des recepteurs des chimiokines |
| WO2000069815A1 (fr) * | 1999-05-13 | 2000-11-23 | Teijin Limited | Derives d'amines cycliques ureido-substituees et leur utilisation en tant que medicament |
| KR100667645B1 (ko) | 1999-08-04 | 2007-02-28 | 데이진 가부시키가이샤 | 환상 아민 ccr3 길항제 |
| US6410566B1 (en) * | 2000-05-16 | 2002-06-25 | Teijin Limited | Cyclic amine derivatives and their use as drugs |
-
2000
- 2000-05-18 WO PCT/JP2000/003203 patent/WO2000069432A1/fr not_active Ceased
- 2000-05-18 KR KR1020017014579A patent/KR100673340B1/ko not_active Expired - Fee Related
- 2000-05-18 NZ NZ515374A patent/NZ515374A/en unknown
- 2000-05-18 CA CA002373942A patent/CA2373942A1/fr not_active Abandoned
- 2000-05-18 EP EP00927808A patent/EP1179341B1/fr not_active Expired - Lifetime
- 2000-05-18 DK DK00927808T patent/DK1179341T3/da active
- 2000-05-18 US US09/959,635 patent/US7390830B1/en not_active Expired - Fee Related
- 2000-05-18 CN CNB008104905A patent/CN1240699C/zh not_active Expired - Fee Related
- 2000-05-18 AU AU46147/00A patent/AU779954B2/en not_active Ceased
- 2000-05-18 ES ES00927808T patent/ES2250132T3/es not_active Expired - Lifetime
- 2000-05-18 DE DE60023878T patent/DE60023878T2/de not_active Expired - Fee Related
- 2000-05-18 AT AT00927808T patent/ATE308985T1/de not_active IP Right Cessation
-
2001
- 2001-11-16 NO NO20015599A patent/NO20015599L/no not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| ES2250132T3 (es) | 2006-04-16 |
| DK1179341T3 (da) | 2006-03-27 |
| ATE308985T1 (de) | 2005-11-15 |
| US7390830B1 (en) | 2008-06-24 |
| KR100673340B1 (ko) | 2007-02-28 |
| EP1179341B1 (fr) | 2005-11-09 |
| WO2000069432A1 (fr) | 2000-11-23 |
| NO20015599D0 (no) | 2001-11-16 |
| EP1179341A4 (fr) | 2003-10-29 |
| AU779954B2 (en) | 2005-02-24 |
| EP1179341A1 (fr) | 2002-02-13 |
| CN1384743A (zh) | 2002-12-11 |
| DE60023878D1 (de) | 2005-12-15 |
| CA2373942A1 (fr) | 2000-11-23 |
| CN1240699C (zh) | 2006-02-08 |
| NZ515374A (en) | 2004-09-24 |
| AU4614700A (en) | 2000-12-05 |
| DE60023878T2 (de) | 2006-07-20 |
| KR20020015322A (ko) | 2002-02-27 |
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