PE20070460A1 - Derivados de carboxamida como antagonista del receptor muscarinico - Google Patents
Derivados de carboxamida como antagonista del receptor muscarinicoInfo
- Publication number
- PE20070460A1 PE20070460A1 PE2006001136A PE2006001136A PE20070460A1 PE 20070460 A1 PE20070460 A1 PE 20070460A1 PE 2006001136 A PE2006001136 A PE 2006001136A PE 2006001136 A PE2006001136 A PE 2006001136A PE 20070460 A1 PE20070460 A1 PE 20070460A1
- Authority
- PE
- Peru
- Prior art keywords
- methyl
- diphenylhexanamide
- halo
- alkyl
- optionally substituted
- Prior art date
Links
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
- C07D207/04—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
- C07D207/12—Oxygen or sulfur atoms
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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
- A61K31/397—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having four-membered rings, e.g. azetidine
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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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- 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
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4409—Non condensed pyridines; Hydrogenated derivatives thereof only substituted in position 4, e.g. isoniazid, iproniazid
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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
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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
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/08—Bronchodilators
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- 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
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/10—Antimycotics
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
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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
-
- 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
- A61P37/02—Immunomodulators
- A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
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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
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D205/00—Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom
- C07D205/02—Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom not condensed with other rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D205/00—Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom
- C07D205/02—Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom not condensed with other rings
- C07D205/04—Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
-
- 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
-
- 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
- C07D211/40—Oxygen atoms
- C07D211/44—Oxygen atoms attached in position 4
- C07D211/46—Oxygen atoms attached in position 4 having a hydrogen atom as the second substituent in position 4
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Immunology (AREA)
- Pulmonology (AREA)
- Epidemiology (AREA)
- Transplantation (AREA)
- Communicable Diseases (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Oncology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Hydrogenated Pyridines (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Pyrrole Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
SE REFIERE A COMPUESTOS DE FORMULA (I) DONDE R1 ES CN O CONH2; A ES UN COMPUESTO DE FORMULA (i), (ii) O (iii); R2 Y R3 SON METILO O FORMAN UN CICLOPENTANO JUNTO CON EL ATOMO DE CARBONO AL QUE ESTAN UNIDOS; p ES 0 O 1; A1 ES FENILO OPCIONALMENTE SUSTITUIDO CON HALO, CN, CF3, ENTRE OTROS SUSTITUYENTES, NAFTILO OPCIONALMENTE SUSTITUIDO CON HALO, OCF3, ALQUILO(C1-C4), ENTRE OTROS SUSTITUYENTES, O UN HETEROCICLICO DE 9 A 10 MIEMBROS QUE CONTIENE DE 1 A 3 HETEROATOMOS SELECCIONADOS DE O, S O N OPCIONALMENTE SUSTITUIDO CON OR4, HALO, ALQUILO(C1-C4), DONDE R4 ES H O ALQUILO(C1-C4). SON COMPUESTOS PREFERIDOS: 5-METIL-5-[(3S)-3-FENOXIPIRROLIDIN-1-IL]-2,2-DIFENILHEXANAMIDA, 5-METIL-5-[(3R)-3-FENOXIPIRROLIDIN-1-IL]-2,2-DIFENILHEXANAMIDA, 5-[(3S)-3-(3-HIDROXIFENOXI)PIRROLIDIN-1-IL]-5-METIL-2,2-DIFENILHEXANAMIDA, ENTRE OTROS. SE REFIERE TAMBIEN A UNA COMPOSICION FARMACEUTICA. DICHOS COMPUESTOS SON ANTAGONISTAS DEL RECEPTOR MUSCARINICO M3 SIENDO UTILES EN EL TRATAMIENTO DE ENFERMEDAD PULMONAR OBSTRUCTIVA CRONICA, BRONQUITIS, ASMA, BRONQUIECTASIA
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US71946705P | 2005-09-21 | 2005-09-21 | |
| US71947705P | 2005-09-21 | 2005-09-21 | |
| US71946805P | 2005-09-21 | 2005-09-21 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PE20070460A1 true PE20070460A1 (es) | 2007-05-14 |
Family
ID=37698323
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PE2006001136A PE20070460A1 (es) | 2005-09-21 | 2006-09-19 | Derivados de carboxamida como antagonista del receptor muscarinico |
Country Status (43)
Families Citing this family (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2008002246A1 (en) * | 2006-06-28 | 2008-01-03 | Astrazeneca Ab | A pharmaceutical composition comprising an ikk2 inhibitor and a second active ingrdient. |
| JP2010504316A (ja) * | 2006-09-22 | 2010-02-12 | ファイザー・リミテッド | ムスカリン様受容体アンタゴニストとしてのアゼチジン誘導体 |
| BRPI0808413A2 (pt) * | 2007-03-16 | 2014-07-15 | Pfizer Ltd | Sal de hidrocloreto de 5-[3-(3-hidroxifenóxi)azetidin-1-il]-5-metil-2,2-difenilhe xanamida, composição farmacêutica contendo o mesmo, bem como uso |
| JP5801997B2 (ja) | 2009-07-07 | 2015-10-28 | ファイザー・リミテッドＰｆｉｚｅｒ Ｌｉｍｉｔｅｄ | 薬品の組合せを吸入するための投薬ユニット、投薬ユニットのパック、および吸入器 |
| CN103201244B (zh) * | 2010-08-26 | 2015-06-17 | 阿尔比马尔公司 | 用于制备1-溴代-2-(环丙基甲氧基)-5-氟代-4-甲氧基苯的方法 |
| CN103242214B (zh) * | 2013-05-02 | 2016-04-06 | 陕西步长高新制药有限公司 | 一种吲哚衍生物及其制备方法 |
| KR101538846B1 (ko) * | 2013-07-30 | 2015-07-22 | 동아에스티 주식회사 | 신규한 바이페닐 유도체 및 그의 제조방법 |
| WO2018167804A1 (en) * | 2017-03-15 | 2018-09-20 | Mylan Laboratories Limited | Novel polymorphs of (5-[3-(3-hydroxyphenoxy)azetidin-1-yl]-5-methyl-2,2-diphenylhexanamide hydrochloride |
| US10342786B2 (en) | 2017-10-05 | 2019-07-09 | Fulcrum Therapeutics, Inc. | P38 kinase inhibitors reduce DUX4 and downstream gene expression for the treatment of FSHD |
| AU2018346712B2 (en) | 2017-10-05 | 2021-04-01 | Fulcrum Therapeutics, Inc. | P38 kinase inhibitors reduce DUX4 and downstream gene expression for the treatment of FSHD |
| CN111423434A (zh) * | 2019-01-09 | 2020-07-17 | 四川海思科制药有限公司 | 一种碳酰胺衍生物及其制备方法 |
| US20220380307A1 (en) * | 2019-06-25 | 2022-12-01 | Mylan Laboratories Limited | Methods and intermediates for preparing hydrochloride salt of 5-[3-(3-hydroxyphenoxy)azetidin-1-yl]-5-methyl-2,2-diphenylhexanamide |
| EP4171525A1 (en) | 2020-06-26 | 2023-05-03 | Mylan Pharma UK Limited | Formulations including 5-[3-(3-hydroxyphenoxy)azetidin-1-yl]-5-methyl-2,2-diphenylhexanamide |
| WO2023049696A1 (en) * | 2021-09-21 | 2023-03-30 | Corteva Agriscience Llc | Methylation of 2-chloro-6-fluorophenol |
Family Cites Families (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2886574A (en) * | 1956-11-19 | 1959-05-12 | Upjohn Co | Quaternary ammonium salts of 2, 2-diphenyl-4, 4-dimethyl-4-pyrrolidino-butyramide |
| US4219559A (en) * | 1979-01-10 | 1980-08-26 | Janssen Pharmaceutica N.V. | N-Heterocyclyl-4-piperidinamines |
| GB8824262D0 (en) * | 1988-10-17 | 1988-11-23 | 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 |
| US5849761A (en) | 1995-09-12 | 1998-12-15 | Regents Of The University Of California | Peripherally active anti-hyperalgesic opiates |
| AU733209B2 (en) * | 1996-12-02 | 2001-05-10 | Kyorin Pharmaceutical Co. Ltd. | Novel n-substituted pyrrolidine derivatives and process for preparing the same |
| DE59611439D1 (de) * | 1996-12-17 | 2007-09-06 | Filtertek Bv | Rückschlagventil, insbesondere für die Medizintechnik |
| 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 |
| US6673908B1 (en) * | 1999-02-22 | 2004-01-06 | Nuvelo, Inc. | Tumor necrosis factor receptor 2 |
| GB0011838D0 (en) | 2000-05-17 | 2000-07-05 | Astrazeneca Ab | Chemical compounds |
| US6667344B2 (en) * | 2001-04-17 | 2003-12-23 | Dey, L.P. | Bronchodilating compositions and methods |
| EA006505B1 (ru) | 2001-12-20 | 2005-12-29 | Лабораториос С.А.Л.В.А.Т.,С.А. | Производные карбамата 1-алкил-1-азониабицикло[2.2.2]октана и их применение в качестве антагонистов мускаринового рецептора |
| MXPA03000145A (es) | 2002-01-07 | 2003-07-15 | Pfizer | Compuestos de oxo u oxi-piridina como moduladores de receptores 5-ht4. |
| EP1375508A1 (en) | 2002-06-27 | 2004-01-02 | Aventis Pharma Deutschland GmbH | N6-substituted adenosine analogues and their use as pharmaceutical agents |
| US20060094716A1 (en) | 2002-09-17 | 2006-05-04 | Actelion Pharmaceuticals Ltd | 1-Pyridin-4-yl-urea derivatives |
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2006
- 2006-09-01 ES ES06795581T patent/ES2318794T3/es active Active
- 2006-09-01 CA CA2623332A patent/CA2623332C/en active Active
- 2006-09-01 JP JP2008531819A patent/JP4221447B1/ja not_active Expired - Fee Related
- 2006-09-01 EA EA200800540A patent/EA013083B1/ru unknown
- 2006-09-01 AT AT06795581T patent/ATE420069T1/de active
- 2006-09-01 ME MEP-2009-96A patent/ME01106B/me unknown
- 2006-09-01 RS RSP-2009/0103A patent/RS50855B/sr unknown
- 2006-09-01 DK DK06795581T patent/DK1928821T3/da active
- 2006-09-01 PL PL06795581T patent/PL1928821T3/pl unknown
- 2006-09-01 AU AU2006293618A patent/AU2006293618B9/en active Active
- 2006-09-01 PT PT06795581T patent/PT1928821E/pt unknown
- 2006-09-01 BR BRPI0616111A patent/BRPI0616111B8/pt active IP Right Grant
- 2006-09-01 DE DE602006004768T patent/DE602006004768D1/de active Active
- 2006-09-01 NZ NZ566023A patent/NZ566023A/en unknown
- 2006-09-01 RS RS20080119A patent/RS51680B/en unknown
- 2006-09-01 WO PCT/IB2006/002727 patent/WO2007034325A1/en active Application Filing
- 2006-09-01 AP AP2008004368A patent/AP1983A/xx active
- 2006-09-01 GE GEAP200610573A patent/GEP20104880B/en unknown
- 2006-09-01 CN CN2006800348189A patent/CN101268046B/zh active Active
- 2006-09-01 SI SI200630186T patent/SI1928821T1/sl unknown
- 2006-09-01 EP EP06795581A patent/EP1928821B1/en active Active
- 2006-09-01 KR KR1020087006784A patent/KR100976909B1/ko active IP Right Grant
- 2006-09-01 MX MX2008002805A patent/MX2008002805A/es active IP Right Grant
- 2006-09-18 US US11/522,840 patent/US7772223B2/en active Active
- 2006-09-18 AR ARP060104081A patent/AR055171A1/es active IP Right Grant
- 2006-09-18 UY UY29798A patent/UY29798A1/es active IP Right Grant
- 2006-09-19 PE PE2006001136A patent/PE20070460A1/es active IP Right Grant
- 2006-09-19 NL NL2000241A patent/NL2000241C2/nl not_active IP Right Cessation
- 2006-09-20 TW TW095134738A patent/TWI322143B/zh active
- 2006-09-20 DO DO2006000202A patent/DOP2006000202A/es unknown
- 2006-09-20 GT GT200600422A patent/GT200600422A/es unknown
- 2006-09-21 HN HN2006032615A patent/HN2006032615A/es unknown
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2008
- 2008-02-11 IL IL189453A patent/IL189453A/en active IP Right Grant
- 2008-02-12 ZA ZA200801432A patent/ZA200801432B/xx unknown
- 2008-02-25 NO NO20081001A patent/NO340975B1/no unknown
- 2008-03-12 EC EC2008008265A patent/ECSP088265A/es unknown
- 2008-03-13 CR CR9814A patent/CR9814A/es unknown
- 2008-03-19 MA MA30766A patent/MA29839B1/fr unknown
- 2008-03-19 TN TNP2008000137A patent/TNSN08137A1/fr unknown
- 2008-03-21 MY MYPI20080778A patent/MY143581A/en unknown
- 2008-11-06 HK HK08112121.9A patent/HK1117163A1/xx unknown
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2009
- 2009-03-02 HR HR20090127T patent/HRP20090127T3/xx unknown
- 2009-03-12 CY CY20091100283T patent/CY1108880T1/el unknown
- 2009-09-09 US US12/556,285 patent/US8268881B2/en active Active
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2010
- 2010-06-03 CU CU2010000115A patent/CU20100115A7/es active IP Right Grant
- 2010-07-01 US US12/828,732 patent/US8486992B2/en active Active
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2013
- 2013-05-09 CR CR20130209A patent/CR20130209A/es unknown
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