MA29379B1 - Derives de pyrrolidine 3,4-substitues pour le traitement de l'hypertension - Google Patents
Derives de pyrrolidine 3,4-substitues pour le traitement de l'hypertensionInfo
- Publication number
- MA29379B1 MA29379B1 MA30268A MA30268A MA29379B1 MA 29379 B1 MA29379 B1 MA 29379B1 MA 30268 A MA30268 A MA 30268A MA 30268 A MA30268 A MA 30268A MA 29379 B1 MA29379 B1 MA 29379B1
- Authority
- MA
- Morocco
- Prior art keywords
- treatment
- compounds
- pyrrolidine compounds
- substituted pyrrolidine
- substituted
- Prior art date
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Classifications
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- A—HUMAN NECESSITIES
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- 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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- 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
- C07D207/263—2-Pyrrolidones with only hydrogen atoms or radicals containing only hydrogen and carbon atoms directly attached to other ring carbon atoms
- C07D207/27—2-Pyrrolidones with only hydrogen atoms or radicals containing only hydrogen and carbon atoms directly attached to other ring carbon atoms with substituted hydrocarbon radicals directly attached to the ring nitrogen atom
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- A61K31/34—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having five-membered rings with one oxygen as the only ring hetero atom, e.g. isosorbide
- A61K31/341—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having five-membered rings with one oxygen as the only ring hetero atom, e.g. isosorbide not condensed with another ring, e.g. ranitidine, furosemide, bufetolol, muscarine
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- A61K31/35—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having six-membered rings with one oxygen as the only ring hetero atom
- A61K31/351—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having six-membered rings with one oxygen as the only ring hetero atom not condensed with another ring
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- A61K31/352—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having six-membered rings with one oxygen as the only ring hetero atom condensed with carbocyclic rings, e.g. methantheline
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- 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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- A61K31/403—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
- A61K31/4035—Isoindoles, e.g. phthalimide
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- 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
- A61K31/416—1,2-Diazoles condensed with carbocyclic ring systems, e.g. indazole
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- A61K31/42—Oxazoles
- A61K31/422—Oxazoles not condensed and containing further heterocyclic rings
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- 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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- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/445—Non condensed piperidines, e.g. piperocaine
- A61K31/4523—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
- A61K31/454—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. pimozide, domperidone
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- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
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- A—HUMAN NECESSITIES
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- 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
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- C—CHEMISTRY; METALLURGY
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- C07D—HETEROCYCLIC COMPOUNDS
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- 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
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Abstract
L'INVENTION CONCERNE L'UTILISATION DE COMPOSÉS PYRROLIDINE (3,4-DI-, 3,3,4-TRI, 3,4,4-TRI- OR 3,3,4,4-TÉTRA-)SUBSTITUÉS DANS LA PRÉPARATION D'UNE FORMULATION PHARMACEUTIQUE DESTINÉE AU TRAITEMENT D'UNE MALADIE DÉPENDANT DE L'ACTIVITÉ DE LA RÉNINE; L'UTILISATION D'UN COMPOSÉ DE CETTE CLASSE DANS LE TRAITEMENT D'UNE MALADIE DÉPENDANT DE L'ACTIVITÉ DE LA RÉNINE; DES COMPOSÉS QUI FONT PARTIE D'UNE SOUS-CLASSE DESDITS COMPOSÉS PYRROLIDINE SUBSTITUÉS ET QUI SONT DESTINÉS AU DIAGNOSTIC ET AU TRAITEMENT THÉRAPEUTIQUE D'UN ANIMAL À SANG CHAUD, EN PARTICULIER AU TRAITEMENT D'UNE MALADIE (D'UN TROUBLE) DÉPENDANT DE L'ACTIVITÉ DE LA RÉNINE; DE NOUVEAUX COMPOSÉS QUI FONT PARTIE D'UNE SOUS-CLASSE DESDITS COMPOSÉS PYRROLIDINE SUBSTITUÉS; DES FORMULATIONS PHARMACEUTIQUES COMPRENANT LESDITS COMPOSÉS PYRROLIDINE, ET/OU UN PROCÉDÉ DE TRAITEMENT QUI CONSISTE À ADMINISTRER LESDITS COMPOSÉS PYRROLIDINE SUBSTITUÉS, UN PROCÉDÉ DE FABRICATION EN PARTICULIER DESDITS NOUVEAUX COMPOSÉS PYRROLIDINE SUBSTITUÉS, AINSI QUE DE NOUVEAUX INTERMÉDIAIRES, DES MATIÈRES PREMIÈRES ET/OU DES ÉTAPES PARTIELLES DE LEUR SYNTHÈSE. LES COMPOSÉS PYRROLIDINE SUBSTITUÉS DE L'INVENTION RÉPONDENT À LA FORMULE (I) SUIVANTE, DANS LAQUELLE R1, R2, R3, R4, R5 ET T SONT TELS QUE DÉFINIS DANS LA DESCRIPTION.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
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GBGB0505969.6A GB0505969D0 (en) | 2005-03-23 | 2005-03-23 | Organic compounds |
Publications (1)
Publication Number | Publication Date |
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MA29379B1 true MA29379B1 (fr) | 2008-04-01 |
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MA30268A MA29379B1 (fr) | 2005-03-23 | 2007-10-02 | Derives de pyrrolidine 3,4-substitues pour le traitement de l'hypertension |
Country Status (26)
Country | Link |
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US (1) | US7807709B2 (fr) |
EP (1) | EP1863477B1 (fr) |
JP (1) | JP5171612B2 (fr) |
KR (1) | KR20070113254A (fr) |
CN (1) | CN101146530B (fr) |
AR (1) | AR053832A1 (fr) |
AT (1) | ATE486597T1 (fr) |
AU (1) | AU2006226554B2 (fr) |
BR (1) | BRPI0609671A2 (fr) |
CA (1) | CA2600063A1 (fr) |
DE (1) | DE602006017980D1 (fr) |
ES (1) | ES2355742T3 (fr) |
GB (1) | GB0505969D0 (fr) |
GT (1) | GT200600089A (fr) |
IL (1) | IL185242A0 (fr) |
MA (1) | MA29379B1 (fr) |
MX (1) | MX2007011694A (fr) |
NO (1) | NO20075365L (fr) |
PE (1) | PE20061325A1 (fr) |
PL (1) | PL1863477T3 (fr) |
PT (1) | PT1863477E (fr) |
RU (1) | RU2419606C2 (fr) |
TN (1) | TNSN07361A1 (fr) |
TW (1) | TW200700061A (fr) |
WO (1) | WO2006100036A1 (fr) |
ZA (1) | ZA200706697B (fr) |
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GB0514203D0 (en) | 2005-07-11 | 2005-08-17 | Novartis Ag | Organic compounds |
PT2420491E (pt) | 2005-12-30 | 2013-10-14 | Novartis Ag | Compostos de piperidina 3,5-substituída como inibidores de renina |
GB0611696D0 (en) * | 2006-06-13 | 2006-07-26 | Novartis Ag | Organic compounds |
EP2119702A4 (fr) | 2007-01-31 | 2010-12-08 | Dainippon Sumitomo Pharma Co | Dérivé d'amide |
NZ582098A (en) | 2007-06-25 | 2012-03-30 | Novartis Ag | N5-(2-ethoxyethyl)-n3-(2-pyridinyl)-3,5-piperidinedicarboxamide derivatives for use as renin inhibitors |
US9408914B2 (en) | 2010-04-28 | 2016-08-09 | Kyowa Hakko Kirin Co., Ltd. | Cationic lipid |
MX349484B (es) | 2011-03-16 | 2017-07-31 | Mitsubishi Tanabe Pharma Corp | Compuesto heterocíclico saturado que contiene nitrógeno. |
JP2013095755A (ja) | 2011-11-02 | 2013-05-20 | Kyowa Hakko Kirin Co Ltd | カチオン性脂質 |
US20140045913A1 (en) | 2011-12-12 | 2014-02-13 | Kyowa Hakko Kirin Co., Ltd. | Lipid nano particles comprising combination of cationic lipid |
CN103420890B (zh) * | 2012-05-15 | 2015-06-24 | 天津药物研究院 | 3-吡咯甲酸衍生物及其制备方法和用途 |
AU2013291125A1 (en) | 2012-07-16 | 2015-01-22 | Dicerna Pharmaceuticals, Inc. | RNAi pharmaceutical composition capable of suppressing expression of KRAS gene |
BR112016014830A2 (pt) | 2013-12-23 | 2017-09-19 | Bayer Pharma AG | Conjugados de fármaco de anticorpo (adcs) com inibidores de ksp |
JP6743015B2 (ja) | 2014-12-15 | 2020-08-19 | バイエル ファーマ アクチエンゲゼルシャフト | Ksp阻害剤の脱グリコシル化抗tweakr抗体との抗体薬物複合体(adc類) |
CA2990076A1 (fr) | 2015-06-22 | 2016-12-29 | Bayer Pharma Aktiengesellschaft | Conjugues anticorps-medicament (adc) et conjugues lieur-promedicament (apdc) a groupes enzymatiquement clivables |
US20180318438A1 (en) | 2015-06-23 | 2018-11-08 | Bayer Pharma Aktiengesellschaft | Antibody drug conjugates of kinesin spindel protein (ksp) inhibitors with anti-tweakr-antibodies |
US11001636B2 (en) | 2016-06-15 | 2021-05-11 | Bayer Pharma Aktiengesellschaft | Specific antibody-drug-conjugates (ADCs) with KSP inhibitors and anti-CD123-antibodies |
WO2018114804A1 (fr) | 2016-12-21 | 2018-06-28 | Bayer Pharma Aktiengesellschaft | Conjugués anticorps-principe actif (adc) spécifiques renfermant des inhibiteurs de ksp |
IL310558A (en) | 2016-12-21 | 2024-03-01 | Bayer Pharma AG | Drug-antibody conjugates with enzymatically cleavable groups |
US20230113948A1 (en) * | 2019-12-20 | 2023-04-13 | Arbutus Biopharma Corporation | Synthetic processes and intermediates |
CN111423411B (zh) * | 2020-04-02 | 2021-04-16 | 南京生命源医药科技有限公司 | 一种新型肾素抑制剂 |
WO2024033374A1 (fr) | 2022-08-11 | 2024-02-15 | Syngenta Crop Protection Ag | Nouveaux composés arylcarboxamide ou arylthioamide |
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EP0242789A3 (fr) * | 1986-04-25 | 1990-09-05 | Dainippon Pharmaceutical Co., Ltd. | Dérivés de quinoléine et procédés pour leur préparation |
AU671092B2 (en) | 1991-12-18 | 1996-08-15 | Schering Corporation | Imidazolyl or imidazoylalkyl substituted with a four or five membered nitrogen containing heterocyclic ring |
IL111176A0 (en) | 1993-10-07 | 1994-12-29 | Du Pont Merck Pharma | Dipeptide boronic acid inhibitors of trypsin-like enzymes and pharmaceutical compositions containing them |
JP2001526178A (ja) | 1997-08-28 | 2001-12-18 | メルク エンド カムパニー インコーポレーテッド | ピロリジン系およびピペリジン系ケモカイン受容体活性調節剤 |
CA2333554A1 (fr) | 1998-06-17 | 1999-12-23 | Chu-Baio Xue | Acides hydroxamiques cycliques utilises en tant qu'inhibiteurs de metalloproteases |
US6610692B1 (en) | 1998-10-30 | 2003-08-26 | Merck & Co., Inc. | Thrombin inhibitors |
AU3386500A (en) | 1999-03-02 | 2000-09-21 | Merck & Co., Inc. | 3-cyclopropyl and 3-cyclobutyl pyrrolidine modulators of chemokine receptor activity |
US6489354B1 (en) * | 1999-03-02 | 2002-12-03 | Merck & Co., Inc. | 3-alkyl substituted pyrrolidine modulators of chemokine receptor activity |
US6303593B1 (en) | 1999-03-02 | 2001-10-16 | Merck & Co., Inc. | 3-thienyl and 3-furanyl pyrrolidine modulators of chemokine receptor activity |
WO2000051610A1 (fr) | 1999-03-02 | 2000-09-08 | Merck & Co., Inc. | Modulateurs de l'activite de recepteurs de chemokine a base de pyrrolidine |
PL360678A1 (en) | 2000-03-17 | 2004-09-20 | Bristol-Myers Squibb Pharma Company | Cyclic beta-amino acid derivatives as inhibitors of matrix metalloproteases and tnf-alpha |
FR2811673B1 (fr) | 2000-07-17 | 2002-09-13 | Rhodia Chimie Sa | Utilisation de composes insatures comprenant un heterocycle comme stabilisants de polymeres halogenes |
US7125887B2 (en) | 2000-10-11 | 2006-10-24 | Merck & Co., Inc. | Pyrrolidine modulators of CCR5 chemokine receptor activity |
US6740649B2 (en) | 2001-09-17 | 2004-05-25 | Bristol-Myers Squibb Company | Cyclic hydroxamic acids as inhibitors of matrix metalloproteinases and/or TNF- α converting enzyme (TACE) |
WO2003031443A1 (fr) | 2001-10-04 | 2003-04-17 | Morphochem Aktiengesellschaft für kombinatorische Chemie | Antibiotiques a action duale renfermant une oxazolidinone et une quinolone ou une fraction de naphthyridinone |
AU2003301959A1 (en) | 2002-05-20 | 2004-06-03 | Bristol-Myers Squibb Company | Substituted cycloalkyl p1' hepatitis c virus inhibitors |
GB0212410D0 (en) | 2002-05-29 | 2002-07-10 | Novartis Ag | Organic compounds |
PL374860A1 (en) | 2002-07-09 | 2005-11-14 | Bristol-Myers Squibb Company | Substituted heterocyclic derivatives useful as antidiabetic and antiobesity agents and method |
AU2004293178B8 (en) | 2003-11-26 | 2009-01-08 | Novartis Ag | Organic compounds |
JP2007518777A (ja) | 2004-01-23 | 2007-07-12 | シュペーデル・エクスペリメンタ・アーゲー | アミノアルコール誘導体およびレニン阻害剤としてのその使用 |
CN1910135A (zh) | 2004-01-23 | 2007-02-07 | 斯皮德尔实验股份公司 | 氨基醇衍生物及其作为血管紧张肽原酶抑制剂的活性 |
PL1735270T3 (pl) | 2004-01-23 | 2010-12-31 | Novartis Ag | Dwuaminoalkohole i ich zastosowanie jako inhibitorów reniny |
BRPI0508969A (pt) | 2004-03-19 | 2007-08-21 | Speedel Experimenta Ag | compostos orgánicos |
US7851634B2 (en) | 2004-03-19 | 2010-12-14 | Novartis Ag | 5-amino 4-hydroxy-7-(1H-indolmethyl)-8-methylnonamide derivatives as renin inhibitors for the treatment of hypertension |
CN1273452C (zh) * | 2004-06-01 | 2006-09-06 | 中国医学科学院医药生物技术研究所 | 7-(4,4-二甲基-3-氨甲基吡咯烷-1-基)取代的新喹啉羧酸衍生物及其制法 |
TW200631929A (en) | 2004-12-10 | 2006-09-16 | Speedel Experimenta Ag | ω -phenyloctanamides |
GB0428526D0 (en) | 2004-12-30 | 2005-02-09 | Novartis Ag | Organic compounds |
GB0500784D0 (en) | 2005-01-14 | 2005-02-23 | Novartis Ag | Organic compounds |
US20080176947A1 (en) | 2005-03-11 | 2008-07-24 | Peter Herold | Heterocyclic-Substituted Alkanamides Useful as Renin Inhibitors |
-
2005
- 2005-03-23 GB GBGB0505969.6A patent/GB0505969D0/en not_active Ceased
-
2006
- 2006-02-22 GT GT200600089A patent/GT200600089A/es unknown
- 2006-03-21 CA CA002600063A patent/CA2600063A1/fr not_active Abandoned
- 2006-03-21 AT AT06707621T patent/ATE486597T1/de active
- 2006-03-21 MX MX2007011694A patent/MX2007011694A/es active IP Right Grant
- 2006-03-21 DE DE602006017980T patent/DE602006017980D1/de active Active
- 2006-03-21 KR KR1020077021868A patent/KR20070113254A/ko not_active Application Discontinuation
- 2006-03-21 PT PT06707621T patent/PT1863477E/pt unknown
- 2006-03-21 PL PL06707621T patent/PL1863477T3/pl unknown
- 2006-03-21 CN CN2006800094939A patent/CN101146530B/zh not_active Expired - Fee Related
- 2006-03-21 US US11/909,402 patent/US7807709B2/en not_active Expired - Fee Related
- 2006-03-21 ES ES06707621T patent/ES2355742T3/es active Active
- 2006-03-21 BR BRPI0609671-9A patent/BRPI0609671A2/pt not_active IP Right Cessation
- 2006-03-21 RU RU2007138892/04A patent/RU2419606C2/ru not_active IP Right Cessation
- 2006-03-21 WO PCT/EP2006/002578 patent/WO2006100036A1/fr active Application Filing
- 2006-03-21 JP JP2008502310A patent/JP5171612B2/ja not_active Expired - Fee Related
- 2006-03-21 AR ARP060101103A patent/AR053832A1/es unknown
- 2006-03-21 EP EP06707621A patent/EP1863477B1/fr active Active
- 2006-03-21 AU AU2006226554A patent/AU2006226554B2/en not_active Ceased
- 2006-03-22 TW TW095109927A patent/TW200700061A/zh unknown
- 2006-03-23 PE PE2006000322A patent/PE20061325A1/es not_active Application Discontinuation
-
2007
- 2007-08-13 IL IL185242A patent/IL185242A0/en unknown
- 2007-08-13 ZA ZA200706697A patent/ZA200706697B/xx unknown
- 2007-09-21 TN TNP2007000361A patent/TNSN07361A1/en unknown
- 2007-10-02 MA MA30268A patent/MA29379B1/fr unknown
- 2007-10-19 NO NO20075365A patent/NO20075365L/no not_active Application Discontinuation
Also Published As
Publication number | Publication date |
---|---|
ATE486597T1 (de) | 2010-11-15 |
EP1863477B1 (fr) | 2010-11-03 |
US7807709B2 (en) | 2010-10-05 |
AU2006226554B2 (en) | 2010-03-11 |
TNSN07361A1 (en) | 2008-12-31 |
CA2600063A1 (fr) | 2006-09-28 |
AU2006226554A1 (en) | 2006-09-28 |
JP2008534457A (ja) | 2008-08-28 |
EP1863477A1 (fr) | 2007-12-12 |
DE602006017980D1 (de) | 2010-12-16 |
TW200700061A (en) | 2007-01-01 |
CN101146530B (zh) | 2011-05-18 |
AR053832A1 (es) | 2007-05-23 |
RU2419606C2 (ru) | 2011-05-27 |
ES2355742T3 (es) | 2011-03-30 |
GB0505969D0 (en) | 2005-04-27 |
GT200600089A (es) | 2006-11-08 |
KR20070113254A (ko) | 2007-11-28 |
WO2006100036A1 (fr) | 2006-09-28 |
MX2007011694A (es) | 2007-11-15 |
RU2007138892A (ru) | 2009-04-27 |
CN101146530A (zh) | 2008-03-19 |
IL185242A0 (en) | 2008-06-05 |
BRPI0609671A2 (pt) | 2010-04-20 |
NO20075365L (no) | 2007-12-27 |
PE20061325A1 (es) | 2007-01-05 |
JP5171612B2 (ja) | 2013-03-27 |
PL1863477T3 (pl) | 2011-04-29 |
ZA200706697B (en) | 2008-10-29 |
US20080194549A1 (en) | 2008-08-14 |
PT1863477E (pt) | 2011-02-10 |
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