MA27852A1 - Derives de 1-(alkylaminoalkyl-pyrolidin-/piperidinyl)-2,2-diphenylacetamide utilises comme antagonistes du recepteur muscarinique - Google Patents
Derives de 1-(alkylaminoalkyl-pyrolidin-/piperidinyl)-2,2-diphenylacetamide utilises comme antagonistes du recepteur muscariniqueInfo
- Publication number
- MA27852A1 MA27852A1 MA28650A MA28650A MA27852A1 MA 27852 A1 MA27852 A1 MA 27852A1 MA 28650 A MA28650 A MA 28650A MA 28650 A MA28650 A MA 28650A MA 27852 A1 MA27852 A1 MA 27852A1
- Authority
- MA
- Morocco
- Prior art keywords
- compounds
- muscarinic receptor
- pyrolidin
- alkylaminoalkyl
- piperidinyl
- Prior art date
Links
- 229940121948 Muscarinic receptor antagonist Drugs 0.000 title 1
- -1 PIPERIDINYL Chemical class 0.000 title 1
- 150000001875 compounds Chemical class 0.000 abstract 5
- 238000000034 method Methods 0.000 abstract 2
- 102000014415 Muscarinic acetylcholine receptor Human genes 0.000 abstract 1
- 108050003473 Muscarinic acetylcholine receptor Proteins 0.000 abstract 1
- 201000010099 disease Diseases 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
- 239000000543 intermediate Substances 0.000 abstract 1
- 230000001404 mediated effect Effects 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 239000012453 solvate Substances 0.000 abstract 1
Classifications
-
- 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
-
- 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
-
- 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
-
- 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
- A61P11/08—Bronchodilators
-
- 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
- C07D207/04—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
- C07D207/16—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
-
- 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
- C07D211/34—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 carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (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)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pulmonology (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Hydrogenated Pyridines (AREA)
- Pyrrole Compounds (AREA)
- Medicinal Preparation (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Abstract
La présente invention concerne des composés représentés par la formule générale (I) dans laquelle R1-R5 et a-e sont des éléments définis dans la description ; ou des sels ou des solvates ou encore des stéréo-isomères de qualité pharmaceutique de ces composés. L'invention concerne également des compositions pharmaceutiques contenant ces composés ; des procédés et des produits intermédiaires destinés à la préparation de ces composés ; ainsi que des méthodes destinées au traitement d'états pathologiques induits par les récepteurs muscariniques, utilisant ces composés.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US47845603P | 2003-06-13 | 2003-06-13 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MA27852A1 true MA27852A1 (fr) | 2006-04-03 |
Family
ID=33563773
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MA28650A MA27852A1 (fr) | 2003-06-13 | 2005-12-09 | Derives de 1-(alkylaminoalkyl-pyrolidin-/piperidinyl)-2,2-diphenylacetamide utilises comme antagonistes du recepteur muscarinique |
Country Status (22)
| Country | Link |
|---|---|
| US (5) | US7183292B2 (fr) |
| EP (1) | EP1633707A1 (fr) |
| JP (1) | JP2007507496A (fr) |
| KR (1) | KR20060017541A (fr) |
| CN (2) | CN100406435C (fr) |
| AR (1) | AR044676A1 (fr) |
| AU (1) | AU2004253869B2 (fr) |
| BR (1) | BRPI0411358A (fr) |
| CA (1) | CA2525801A1 (fr) |
| CL (1) | CL2004001431A1 (fr) |
| CO (1) | CO5650231A2 (fr) |
| IS (1) | IS8155A (fr) |
| MA (1) | MA27852A1 (fr) |
| MX (1) | MXPA05013256A (fr) |
| MY (1) | MY139290A (fr) |
| NO (1) | NO20060191L (fr) |
| NZ (1) | NZ543805A (fr) |
| PE (1) | PE20050282A1 (fr) |
| RU (1) | RU2337095C2 (fr) |
| TW (1) | TW200510298A (fr) |
| WO (1) | WO2005003090A1 (fr) |
| ZA (1) | ZA200509942B (fr) |
Families Citing this family (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TW200800953A (en) * | 2002-10-30 | 2008-01-01 | Theravance Inc | Intermediates for preparing substituted 4-amino-1-(pyridylmethyl) piperidine |
| PE20040950A1 (es) * | 2003-02-14 | 2005-01-01 | Theravance Inc | DERIVADOS DE BIFENILO COMO AGONISTAS DE LOS RECEPTORES ADRENERGICOS ß2 Y COMO ANTAGONISTAS DE LOS RECEPTORES MUSCARINICOS |
| TW200510298A (en) * | 2003-06-13 | 2005-03-16 | Theravance Inc | Substituted pyrrolidine and related compounds |
| JP2007524641A (ja) * | 2003-07-11 | 2007-08-30 | セラヴァンス, インコーポレーテッド | 置換4−アミノ−1−ベンジルピペリジン化合物 |
| EP1723142A1 (fr) * | 2004-03-11 | 2006-11-22 | Theravance, Inc. | Composes de diphenylmethyle, antagonistes du recepteur muscarinique |
| EP1725525A1 (fr) * | 2004-03-11 | 2006-11-29 | Theravance, Inc. | Composes biphenyle convenant en tant qu'antagonistes du recepteur muscarinique |
| GB0411056D0 (en) | 2004-05-18 | 2004-06-23 | Novartis Ag | Organic compounds |
| TW200540154A (en) * | 2004-06-10 | 2005-12-16 | Theravance Inc | Crystalline form of a substituted pyrrolidine compound |
| GB0516313D0 (en) | 2005-08-08 | 2005-09-14 | Argenta Discovery Ltd | Azole derivatives and their uses |
| KR101495708B1 (ko) * | 2007-02-23 | 2015-02-25 | 세라밴스 바이오파마 알앤디 아이피, 엘엘씨 | 무스카린 수용체 안타고니스트로 유용한 4차 암모늄 디페닐메틸 화합물 |
Family Cites Families (54)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3192206A (en) | 1961-12-04 | 1965-06-29 | Robins Co Inc A H | 4-(omega-aminoalkyl)-3, 3-disubstitutedn-hydrocarbon-2-pyrrolidinones and corresponding-2-thionpyrrolidinones |
| US3192210A (en) | 1961-12-04 | 1965-06-29 | Robins Co Inc A H | 4-(omega-substituted alkyl)-3, 3-disubstituted-1-substituted-2-pyrrolidinones and 4-(omega-substituted alkyl)-3, 3-disubstituted-1-substituted-2-thionpyrrolidinones |
| US3192221A (en) | 1961-12-04 | 1965-06-29 | Robins Co Inc A H | 4-(omega-substituted alkyl)-3, 3-disubstituted-1-substituted-2-pyrrolidinones and 4-(omega-substituted alkyl)-3, 3-disubstituted-1-substituted-2-thionpyrrolidinones and production thereof |
| US3247222A (en) | 1962-12-26 | 1966-04-19 | Robins Co Inc A H | Alpha (nu-hydrocarbonpyrrolidyl-3-) alpha, alpha carbocyclic arylacetamides |
| US3732247A (en) | 1970-08-14 | 1973-05-08 | Robins Co Inc A H | 3-di-substituted methylene pyrrolidines wherein the 1-or n-lower-alkyl substituent contains at least two carbon atoms |
| US3984557A (en) | 1974-12-26 | 1976-10-05 | A. H. Robins Company, Incorporated | Antiarrhythmia compositions and methods |
| US4002766A (en) | 1974-12-26 | 1977-01-11 | A. H. Robins Company, Incorporated | Antiarrhythmia methods |
| BR8007911A (pt) | 1979-12-06 | 1981-06-16 | Glaxo Group Ltd | Inalador aperfeicoado |
| JPS57175165A (en) * | 1981-04-21 | 1982-10-28 | Tokyo Tanabe Co Ltd | Novel 1,4-dihydropyridine-3,5-dicarboxylic diester derivative and its salt |
| EP0069715B1 (fr) | 1981-07-08 | 1986-11-05 | Aktiebolaget Draco | Inhalateur de poudre |
| IL76583A (en) * | 1984-10-19 | 1988-08-31 | Robins Co Inc A H | 1-(aminoalkyl)-alpha'alpha-diaryl pyrrolidinyl,piperidino and homopiperidino acetamides and acetonitriles and pharmaceutical compositions containing them |
| US4594343A (en) | 1984-10-19 | 1986-06-10 | Shanklin Jr James R | 1-[(aminoalkyl and aminoalkylamino)carbonyl and thiocarbonyl]-α,α-diarylpyrrolidine, piperidine and homopiperidineacetamides and acetonitriles |
| AU591152B2 (en) | 1985-07-30 | 1989-11-30 | Glaxo Group Limited | Devices for administering medicaments to patients |
| US4810713A (en) | 1985-12-20 | 1989-03-07 | A. H. Robins Company, Incorporated | Arylalkyl-heterocyclic amines, n-substituted by aryloxyalkyl groups used in a method for allergy treatment |
| EP0228893A3 (fr) | 1985-12-20 | 1990-01-03 | A.H. ROBINS COMPANY, INCORPORATED (a Delaware corporation) | Amines arylalkyl-hétérocycliques N-substitués par un groupe aryloxyalkyl dans le traitement des allergies |
| IN163948B (fr) * | 1986-01-17 | 1988-12-10 | Robins Co Inc A H | |
| US5932594A (en) | 1988-11-01 | 1999-08-03 | Pfizer, Inc. | Muscarinic receptor antagonists |
| US5225183A (en) | 1988-12-06 | 1993-07-06 | Riker Laboratories, Inc. | Medicinal aerosol formulations |
| US5233053A (en) | 1989-03-17 | 1993-08-03 | Pfizer Inc. | Pyrrolidine derivatives |
| GB8906166D0 (en) * | 1989-03-17 | 1989-05-04 | Pfizer Ltd | Therapeutic agents |
| US5070087A (en) | 1989-05-08 | 1991-12-03 | A. H. Robins Company, Incorporated | Aryl(alkyland alkylene)-N-((phenoxy and phenylthio)alkyl) aminoheterocyclics as cardiovascular, anthihistaminic, antisecretory and antiallergy agents |
| GB8928042D0 (en) | 1989-12-12 | 1990-02-14 | Pfizer Ltd | Muscarinic receptor antagonists |
| GB9000301D0 (en) | 1990-01-06 | 1990-03-07 | Pfizer Ltd | Piperidine & pyrrolidine derivatives |
| US5607950A (en) | 1990-01-06 | 1997-03-04 | Pfizer Inc. | Muscarinic receptor antagonists |
| US5486527A (en) | 1990-01-06 | 1996-01-23 | Pfizer Inc. | Anticholinergic agents |
| SK280968B6 (sk) | 1990-03-02 | 2000-10-09 | Glaxo Group Limited | Balenie medikamentu na použite v inhalačnom prístroji |
| JP2997705B2 (ja) * | 1990-08-01 | 2000-01-11 | 株式会社ネオス | 静電荷像現像用トナー |
| JP3005024B2 (ja) * | 1990-08-03 | 2000-01-31 | 株式会社ネオス | 摩擦帯電付与部材 |
| WO1992022286A1 (fr) | 1991-06-12 | 1992-12-23 | Minnesota Mining And Manufacturing Company | Formulations pour aerosol en suspension comprenant du sulfate d'albuterol |
| US5337740A (en) | 1991-08-01 | 1994-08-16 | New England Pharmaceuticals, Inc. | Inhalation devices |
| DK0717987T3 (da) | 1991-12-18 | 2001-11-12 | Minnesota Mining & Mfg | Suspension-aerosol-formuleringer |
| SE9202218D0 (sv) * | 1992-07-22 | 1992-07-22 | Kabi Pharmacia Ab | Pharmacologically active alfa-(tertiary-aminomethyl)-benzenemethanol derivatives, pharmaceutical composition containing them, therapeutical use thereof and processes for their preparation |
| US5239993A (en) | 1992-08-26 | 1993-08-31 | Glaxo Inc. | Dosage inhalator providing optimized compound inhalation trajectory |
| US5415162A (en) | 1994-01-18 | 1995-05-16 | Glaxo Inc. | Multi-dose dry powder inhalation device |
| KR19990008109A (ko) | 1995-04-28 | 1999-01-25 | 나가사까 겐지로 | 1,4-이치환 피페리딘 유도체 |
| JPH0971048A (ja) * | 1995-09-06 | 1997-03-18 | Fuji Photo Film Co Ltd | 感熱記録材料 |
| ATE205490T1 (de) | 1995-10-13 | 2001-09-15 | Banyu Pharma Co Ltd | Substituierte heteroaromatische derivate |
| WO1998054167A1 (fr) | 1997-05-28 | 1998-12-03 | Mitsubishi-Tokyo Pharmaceuticals, Inc. | Composes d'indole |
| AU8357198A (en) | 1997-07-24 | 1999-02-16 | Mitsubishi-Tokyo Pharmaceuticals, Inc. | Aminocycloalkane compounds |
| JPH11100366A (ja) | 1997-09-29 | 1999-04-13 | Kyorin Pharmaceut Co Ltd | 新規n−置換環状アミン誘導体及びその製造法 |
| AU763638B2 (en) | 1998-06-08 | 2003-07-31 | Theravance Biopharma R&D Ip, Llc | Muscarinic receptor antagonists |
| US6409330B1 (en) | 1998-07-14 | 2002-06-25 | Seiko Epson Corporation | Sublimation transfer ink jet recording method and ink composition for use therein |
| US6693202B1 (en) | 1999-02-16 | 2004-02-17 | Theravance, Inc. | Muscarinic receptor antagonists |
| DE19921693A1 (de) | 1999-05-12 | 2000-11-16 | Boehringer Ingelheim Pharma | Neuartige Arzneimittelkompositionen auf der Basis von anticholinergisch wirksamen Verbindungen und ß-Mimetika |
| US6403810B2 (en) * | 2000-07-10 | 2002-06-11 | Hoffmann-La Roche Inc. | Thiophene derivatives |
| US20030018019A1 (en) | 2001-06-23 | 2003-01-23 | Boehringer Ingelheim Pharma Kg | Pharmaceutical compositions based on anticholinergics, corticosteroids and betamimetics |
| TW200800953A (en) * | 2002-10-30 | 2008-01-01 | Theravance Inc | Intermediates for preparing substituted 4-amino-1-(pyridylmethyl) piperidine |
| JP4767842B2 (ja) | 2003-04-01 | 2011-09-07 | セラヴァンス, インコーポレーテッド | β2アドレナリン作用性レセプターアゴニスト活性およびムスカリン性レセプターアンタゴニスト活性を有するジアリールメチル化合物および関連化合物 |
| TW200510298A (en) | 2003-06-13 | 2005-03-16 | Theravance Inc | Substituted pyrrolidine and related compounds |
| JP2007524641A (ja) * | 2003-07-11 | 2007-08-30 | セラヴァンス, インコーポレーテッド | 置換4−アミノ−1−ベンジルピペリジン化合物 |
| PE20050973A1 (es) * | 2003-10-29 | 2005-11-19 | Theravance Inc | Sales de acido naftalen-1,5-disulfonico de un compuesto de 4-amino-1-(piridilmetil)piperidina como antagonistas de receptores muscarinicos |
| EP1723142A1 (fr) | 2004-03-11 | 2006-11-22 | Theravance, Inc. | Composes de diphenylmethyle, antagonistes du recepteur muscarinique |
| EP1725525A1 (fr) | 2004-03-11 | 2006-11-29 | Theravance, Inc. | Composes biphenyle convenant en tant qu'antagonistes du recepteur muscarinique |
| TW200540154A (en) | 2004-06-10 | 2005-12-16 | Theravance Inc | Crystalline form of a substituted pyrrolidine compound |
-
2004
- 2004-06-03 TW TW093115971A patent/TW200510298A/zh unknown
- 2004-06-09 CL CL200401431A patent/CL2004001431A1/es unknown
- 2004-06-10 RU RU2006101151/04A patent/RU2337095C2/ru not_active IP Right Cessation
- 2004-06-10 CA CA002525801A patent/CA2525801A1/fr not_active Abandoned
- 2004-06-10 CN CNB2004800166001A patent/CN100406435C/zh not_active Expired - Fee Related
- 2004-06-10 BR BRPI0411358-6A patent/BRPI0411358A/pt not_active IP Right Cessation
- 2004-06-10 EP EP04776527A patent/EP1633707A1/fr not_active Withdrawn
- 2004-06-10 MX MXPA05013256A patent/MXPA05013256A/es active IP Right Grant
- 2004-06-10 JP JP2006533776A patent/JP2007507496A/ja active Pending
- 2004-06-10 KR KR1020057023698A patent/KR20060017541A/ko not_active Ceased
- 2004-06-10 CN CN2007101399767A patent/CN101108809B/zh not_active Expired - Fee Related
- 2004-06-10 PE PE2004000578A patent/PE20050282A1/es not_active Application Discontinuation
- 2004-06-10 NZ NZ543805A patent/NZ543805A/en unknown
- 2004-06-10 WO PCT/US2004/018813 patent/WO2005003090A1/fr not_active Ceased
- 2004-06-10 US US10/865,527 patent/US7183292B2/en not_active Expired - Lifetime
- 2004-06-10 AU AU2004253869A patent/AU2004253869B2/en not_active Ceased
- 2004-06-11 AR ARP040102027A patent/AR044676A1/es unknown
- 2004-06-11 MY MYPI20042271A patent/MY139290A/en unknown
-
2005
- 2005-11-28 IS IS8155A patent/IS8155A/is unknown
- 2005-12-07 ZA ZA200509942A patent/ZA200509942B/en unknown
- 2005-12-09 MA MA28650A patent/MA27852A1/fr unknown
- 2005-12-14 CO CO05126202A patent/CO5650231A2/es not_active Application Discontinuation
-
2006
- 2006-01-12 NO NO20060191A patent/NO20060191L/no not_active Application Discontinuation
- 2006-11-21 US US11/602,802 patent/US7351718B2/en not_active Expired - Lifetime
- 2006-11-21 US US11/602,703 patent/US7351717B2/en not_active Expired - Lifetime
-
2008
- 2008-01-30 US US12/011,935 patent/US7638639B2/en not_active Expired - Lifetime
- 2008-01-30 US US12/011,939 patent/US7615566B2/en not_active Expired - Lifetime
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| MA28747B1 (fr) | Dérivés de pyridine | |
| MA27774A1 (fr) | Inhibiteurs de phosphatidylinositol 3-kinase | |
| MA31766B1 (fr) | Composés organiques | |
| MA29926B1 (fr) | Derives de pyrazine | |
| MA30696B1 (fr) | Derives de l'acide (3-amino-1,2,3,4-tetrahydro-9h-carbazol-9-yl)-acetique | |
| TNSN04156A1 (fr) | Pyridinones substituees servant de modulateurs de la map-kinase p38 | |
| MA30089B1 (fr) | (arylsulfonyl)-pyrasolopiperidines | |
| TNSN05250A1 (fr) | Pyrimidinones substituees | |
| MA27775A1 (fr) | Composes organiques | |
| MA30411B1 (fr) | Derives de triazolopyrazine utiles comme agent anticancereux | |
| MA31521B1 (fr) | Dérivés de 2,3-dihydrobenzo[1,4] dioxin-2-ylméthyle utilisés en tant qu'antagonistes des alpha2c pour traiter des maladies des systèmes nerveux périphérique et central | |
| MA29772B1 (fr) | Benzimidazoles substitues et procedes de preparation | |
| MA27568A1 (fr) | Derives de pyrrolopyrimidine | |
| TNSN07248A1 (fr) | Derive de pyrrolidyle de composes heteroaromatiques servant d'inhibiteurs de phosphodiesterases | |
| MA29170B1 (fr) | Derives puriniques agissant comme des agonistes du recepteur a2a | |
| MA31373B1 (fr) | Composes amino-heterocycliques | |
| MA27883A1 (fr) | Derives de pyrido [2,1-a] isoquinoline utilises comme inhibiteurs de dpp-iv | |
| TN2009000450A1 (fr) | Derives de pyridine | |
| MA29140B1 (fr) | Dérivés de quinoléine hétéroaromatiques et leur utilisation comme inhibiteurs de PDE10 | |
| MA30911B1 (fr) | Nouveaux derives de sulfonamide en tant qu'antagonistes de bradykinine | |
| MA31952B1 (fr) | Pyrrolopyrimidines et pyrrolopyridines | |
| MA27347A1 (fr) | Inhibiteurs de protease du vih, compositions les contenant, leurs utilisations pharmaceutiques et matieres pour leur synthese | |
| MA30333B1 (fr) | Aminotetrahydropyranes utiles en tant qu'inhibiteurs de la dipeptidyle peptidase-iv pour le traitement ou la prevention du diabete. | |
| TNSN07349A1 (fr) | Derives de n-(n-sulfonylaminomethyl) cyclopropanecarboxamide utiles pour le traitement de la douleur | |
| MA27389A1 (fr) | Derives de benzimidazole nouveaux utiles comme agents antiproliferatifs. |