MA28461B1 - Derives d'heteroaryl- et phenylsulfamoyle substitues - Google Patents

Derives d'heteroaryl- et phenylsulfamoyle substitues

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Publication number
MA28461B1
MA28461B1 MA29311A MA29311A MA28461B1 MA 28461 B1 MA28461 B1 MA 28461B1 MA 29311 A MA29311 A MA 29311A MA 29311 A MA29311 A MA 29311A MA 28461 B1 MA28461 B1 MA 28461B1
Authority
MA
Morocco
Prior art keywords
phenylsulfamoyl
derivatives
substituted heteroaryl
heteroaryl
substituted
Prior art date
Application number
MA29311A
Other languages
English (en)
Inventor
Ernest Seiichi Hamanaka
Marcus Eugene Kehrli Jr
Original Assignee
Pfizer Prod Inc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=34960729&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=MA28461(B1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Pfizer Prod Inc filed Critical Pfizer Prod Inc
Publication of MA28461B1 publication Critical patent/MA28461B1/fr

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    • C07C311/15—Sulfonamides having sulfur atoms of sulfonamide groups bound to carbon atoms of six-membered aromatic rings
    • C07C311/21—Sulfonamides having sulfur atoms of sulfonamide groups bound to carbon atoms of six-membered aromatic rings having the nitrogen atom of at least one of the sulfonamide groups bound to a carbon atom of a six-membered aromatic ring
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    • C07C323/49—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and nitrogen atoms, not being part of nitro or nitroso groups, bound to the same carbon skeleton having at least one of the nitrogen atoms, not being part of nitro or nitroso groups, further bound to other hetero atoms to sulfur atoms
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    • C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
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    • C07D213/72—Nitrogen atoms
    • C07D213/75—Amino or imino radicals, acylated by carboxylic or carbonic acids, or by sulfur or nitrogen analogues thereof, e.g. carbamates
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Families Citing this family (23)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7262318B2 (en) * 2004-03-10 2007-08-28 Pfizer, Inc. Substituted heteroaryl- and phenylsulfamoyl compounds
RU2342130C2 (ru) * 2004-05-25 2008-12-27 Пфайзер Продактс Инк. Применение агониста рецептора, активируемого пероксисомным пролифератором, для увеличения концентрации сывороточной глюкозы у жвачного животного
US20050288340A1 (en) * 2004-06-29 2005-12-29 Pfizer Inc Substituted heteroaryl- and phenylsulfamoyl compounds
CA2621406A1 (fr) * 2005-09-07 2007-03-15 Plexxikon, Inc. Composes actifs sur les ppar
US7888376B2 (en) 2005-11-23 2011-02-15 Bristol-Myers Squibb Company Heterocyclic CETP inhibitors
US7790770B2 (en) 2005-11-23 2010-09-07 Bristol-Myers Squibb Company Heterocyclic CETP inhibitors
US7652023B2 (en) 2005-11-23 2010-01-26 Bristol-Myers Squibb Company Heterocyclic CETP inhibitors
GB0526252D0 (en) * 2005-12-22 2006-02-01 Novartis Ag Organic compounds
WO2007091140A1 (fr) * 2006-02-06 2007-08-16 Pfizer Products Inc. Composés substitués de phénylsulfamoyle agonistes du ppar
US20100069443A1 (en) * 2006-09-07 2010-03-18 National University Corporation Okayama University Compound with benzamide skeleton having cyclooxygenase-1 (cox-1)-selective inhibitory activity
EP2129382A4 (fr) * 2007-02-21 2011-01-19 Univ Michigan Compositions et procédés de tranquillisation du muscle cardiaque
US8119693B2 (en) 2007-05-08 2012-02-21 Sanford-Burnham Medical Research Institute Tissue non-specific alkaline phosphatase inhibitors and uses thereof for treating vascular calcification
EP2464350B1 (fr) * 2009-09-11 2016-08-24 Nestec S.A. Compositions et procédés destinés à améliorer les fonctions cognitives et associées chez les animaux
KR101194995B1 (ko) * 2009-10-14 2012-10-29 주식회사 이큐스앤자루 신규한 2-페닐-벤즈이미다졸 또는 2-페닐-벤즈옥사졸 유도체 또는 이의 약학적으로 허용가능한 염, 이의 제조방법 및 이를 유효성분으로 함유하는 항바이러스용 약학적 조성물
US8546412B2 (en) * 2011-12-21 2013-10-01 Abbott Cardiovascular Systems, Inc. Methods of treating heart failure
US20170298081A1 (en) * 2014-08-08 2017-10-19 Kasuma Partners Inc. Condensed heterocyclic compound
CA2957785C (fr) 2014-08-11 2023-01-03 Angion Biomedica Corporation Inhibiteurs de cytochrome p450 et leurs utilisations
CA2970819A1 (fr) 2014-12-31 2016-07-07 Angion Biomedica Corp. Methodes et agents pour traiter une maladie
US12098119B2 (en) * 2017-08-10 2024-09-24 Nutshell Biotech (Shanghai) Co., Ltd. Compound used as SIRT6 small-molecule allosteric activator and pharmaceutical composition thereof
AU2019207491A1 (en) 2018-01-10 2020-07-30 Cura Therapeutics, Llc Pharmaceutical compositions comprising phenylsulfonamides, and their therapeutic applications
WO2021007478A1 (fr) 2019-07-11 2021-01-14 Cura Therapeutics, Llc Composés de sulfone et leurs compositions pharmaceutiques, et leurs applications thérapeutiques pour le traitement de maladies neurodégénératives
US12377084B2 (en) * 2019-11-14 2025-08-05 Grey Wolf Therapeutics Limited ERAP1 modulators
WO2023146844A1 (fr) * 2022-01-25 2023-08-03 University Of Houston System Composés anti-inflammatoires non stéroïdiens

Family Cites Families (104)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB378179A (en) 1930-08-04 1932-08-11 American Safety Navigation Com Improvement in boat-launching devices
CH507249A (de) * 1968-05-31 1971-05-15 Sandoz Ag Verfahren zur Herstellung von 2-Brom-a-ergokryptin
US3806542A (en) * 1969-06-10 1974-04-23 Ciba Geigy Corp 5-arylsulfamyl-anthranilic acids
US3658990A (en) * 1969-06-10 1972-04-25 Ciba Geigy Corp Diuretic compositions
US3843662A (en) * 1971-12-09 1974-10-22 Pfizer 2-halo-5-(substituted piperidino sulfonyl)benzoic acids
US3812104A (en) * 1971-06-25 1974-05-21 Ciba Geigy Corp 5-arylsulfamyl-anthranilic acids
CH558789A (de) 1971-08-19 1975-02-14 Ciba Geigy Ag Verfahren zur herstellung der neuen 5-(2-aminophenylsulfamoyl)-4-chlor-n-furfryl-anthranilsaeure und ihrer salze.
US3992441A (en) * 1972-12-26 1976-11-16 Pfizer Inc. Sulfamylbenzoic acids
US4377521A (en) * 1972-12-26 1983-03-22 Pfizer Inc. Sulfamylbenzoic acids
US4062950A (en) * 1973-09-22 1977-12-13 Bayer Aktiengesellschaft Amino sugar derivatives
US3879402A (en) * 1973-09-26 1975-04-22 Pfizer Process for preparing 2-chloro-5-sulfamoylbenzoic acids
US3894033A (en) * 1974-05-16 1975-07-08 Pfizer 5-Aryltetrazoles
US3929803A (en) * 1974-05-28 1975-12-30 Pfizer Aryl carboxylic acids
JPS5612114B2 (fr) * 1974-06-07 1981-03-18
NO154918C (no) * 1977-08-27 1987-01-14 Bayer Ag Analogifremgangsmaate til fremstilling av terapeutisk aktive derivater av 3,4,5-trihydroksypiperidin.
JPS5953920B2 (ja) * 1977-12-28 1984-12-27 東洋醸造株式会社 新規なアミノ糖化合物およびその製法
CA1121290A (fr) * 1978-02-14 1982-04-06 Yasuji Suhara Derives amines d'un sucre
US4231938A (en) * 1979-06-15 1980-11-04 Merck & Co., Inc. Hypocholesteremic fermentation products and process of preparation
US4444784A (en) * 1980-08-05 1984-04-24 Merck & Co., Inc. Antihypercholesterolemic compounds
US4450171A (en) * 1980-08-05 1984-05-22 Merck & Co., Inc. Antihypercholesterolemic compounds
ES505959A0 (es) * 1980-10-09 1982-09-01 Hoechst Ag Procedimiento para la preparacion de un inactivador de alfa-amilasa
JPS5817167B2 (ja) 1980-11-10 1983-04-05 持田製薬株式会社 抗ウイルス作用を有する医薬組成物
EP0068408A1 (fr) 1980-11-10 1983-01-05 Mochida Pharmaceutical Co., Ltd. Compositions antivirales et méthode pour le traitement des maladies virales
DE3166093D1 (en) * 1981-01-05 1984-10-18 Takeda Chemical Industries Ltd N-substituted pseudo-aminosugars, their production and use
SE8203877L (sv) 1981-06-22 1982-12-23 Hodogaya Chemical Co Ltd Aminosulfonylbensoesyraderivat
US4495439A (en) * 1981-09-02 1985-01-22 Tokyo Shibaura Denki Kabushiki Kaisha Magnetic focusing type cathode ray tube
DK161312C (da) * 1982-03-11 1991-12-09 Pfizer Analogifremgangsmaade til fremstilling af 2-aminoalkoxymethyl-4-phenyl-6-methyl-1,4-dihydropyridin-3,5-dicarboxylsyreestere eller syreadditionssalte deraf samt phthalimidoderivater til anvendelse som udgangsmateriale ved fremgangsmaaden
US4448784A (en) * 1982-04-12 1984-05-15 Hoechst-Roussel Pharmaceuticals, Inc. 1-(Aminoalkylphenyl and aminoalkylbenzyl)-indoles and indolines and analgesic method of use thereof
US4739073A (en) * 1983-11-04 1988-04-19 Sandoz Pharmaceuticals Corp. Intermediates in the synthesis of indole analogs of mevalonolactone and derivatives thereof
DK520784A (da) * 1984-01-21 1985-07-22 Hoechst Ag Cycliske polypeptider, deres fremstilling og anvendelse
US4634765A (en) * 1984-12-18 1987-01-06 Merrell Dow Pharmaceuticals Inc. Homodisaccharide hypoglycemic agents
GB8501372D0 (en) * 1985-01-18 1985-02-20 Smith Kline French Lab Chemical compounds
US5061798A (en) * 1985-01-18 1991-10-29 Smith Kline & French Laboratories, Ltd. Benzyl pyridyl and pyridazinyl compounds
GB8531071D0 (en) * 1985-12-17 1986-01-29 Boots Co Plc Therapeutic compound
GB8608335D0 (en) * 1986-04-04 1986-05-08 Pfizer Ltd Pharmaceutically acceptable salts
US5041432A (en) * 1987-01-30 1991-08-20 E. I. Du Pont De Nemours And Company Steroid derivatives useful as hypocholesterolemics
JP2569746B2 (ja) * 1987-08-20 1997-01-08 日産化学工業株式会社 キノリン系メバロノラクトン類
US5192772A (en) * 1987-12-09 1993-03-09 Nippon Shinyaku Co. Ltd. Therapeutic agents
US4804770A (en) * 1988-04-29 1989-02-14 E. R. Squibb & Sons, Inc. Process for preparing a keto-phosphonate intermediate useful in preparing HMG-CoA reductase inhibitors
EP0344383A1 (fr) * 1988-06-02 1989-12-06 Merrell Dow Pharmaceuticals Inc. Inhibiteurs d'alpha-glucosidase
JP2681162B2 (ja) 1988-07-04 1997-11-26 コニカ株式会社 ハロゲン化銀カラー写真感光材料
DE3836675A1 (de) * 1988-10-28 1990-05-03 Hoechst Ag Glykosidase-inhibitor salbostatin, verfahren zu seiner herstellung und seine verwendung
FI94339C (fi) * 1989-07-21 1995-08-25 Warner Lambert Co Menetelmä farmaseuttisesti käyttökelpoisen /R-(R*,R*)/-2-(4-fluorifenyyli)- , -dihydroksi-5-(1-metyylietyyli)-3-fenyyli-4-/(fenyyliamino)karbonyyli/-1H-pyrroli-1-heptaanihapon ja sen farmaseuttisesti hyväksyttävien suolojen valmistamiseksi
US5504078A (en) * 1990-06-08 1996-04-02 Merrell Dow Pharmaceuticals Inc. α-glucosidase inhibitors
EP0618803A4 (fr) * 1991-12-19 1995-03-22 Southwest Found Biomed Res Polypeptide inhibant la proteine de transfert aux esters de cholesteryl, anticorps contre le polypeptide synthetique et traitements prophylactiques et therapeutiques anti-atherosclerose.
RU94046149A (ru) * 1992-05-28 1996-11-27 Пфайзер Инк. (US) Новые n-арил и n-гетероарил производные мочевины как ингибиторы ацил кофермента а:холестерин ацил трансферазы (асат) фармацевтическая композиция, способ ингибирования (асат)
FR2692575B1 (fr) * 1992-06-23 1995-06-30 Sanofi Elf Nouveaux derives du pyrazole, procede pour leur preparation et compositions pharmaceutiques les contenant.
US5284971A (en) * 1992-07-16 1994-02-08 Syntex (U.S.A.) Inc. 4-(3-cyclohexyl-4-hydroxy or-methoxy phenylsulfonyl) 3,5 dibromo phenyl acetic thyromimetic cholesterol-lowering agents
EP0580550B1 (fr) * 1992-07-21 1997-10-22 Novartis AG Dérivés de l'acide oxamique utilisés comme agents hypocholestérémiques
WO1994007867A1 (fr) * 1992-09-28 1994-04-14 Pfizer Inc. Pyrimidines substituees pour le controle des complications diabetiques
JPH06332264A (ja) * 1993-05-24 1994-12-02 Hodogaya Chem Co Ltd 静電荷像現像用トナー
US5596106A (en) * 1994-07-15 1997-01-21 Eli Lilly And Company Cannabinoid receptor antagonists
DE4435477A1 (de) * 1994-10-04 1996-04-11 Bayer Ag Cycloalkano-indol- und -azaindol-derivate
AU697744C (en) * 1994-10-27 2002-08-22 Elanco Animal Health Ireland Limited Apolipoprotein-B synthesis inhibitors
US5521186A (en) * 1994-10-27 1996-05-28 Janssen Pharmaceutica N.V. Apolipoprotein-β synthesis inhibitors
MX9709875A (es) * 1995-06-06 1998-03-31 Pfizer N-(indol-2-carbonil)-glicinamidas substituidas y derivados como inhibidores de glicogeno fosforilasa, composiciones que las contienen y uso de las mismas.
US5919795A (en) * 1995-06-07 1999-07-06 Pfizer Inc. Biphenyl-2-carboxylic acid-tetrahydro-isoquinolin-6-yl amide derivatives, their preparation and their use as inhibitors of microsomal triglyceride transfer protein and/or apolipoprotein B (Apo B) secretion
JP3656680B2 (ja) * 1995-09-21 2005-06-08 株式会社リコー 可逆性感熱発色組成物、およびそれを用いた可逆性記録媒体
TR199901180T2 (xx) * 1996-11-27 1999-08-23 Pfizer Inc. Apo B-Salg�lama/MTP inhibit�r amidler.
IL131493A (en) * 1997-03-04 2004-05-12 Monsanto Co Aromatic compounds of the hydroxamic sulfonyl alpha-deroxamic acid and their use in the preparation of drugs for the treatment of a condition associated with pathological activity of the metalloprotease matrix
US6794511B2 (en) * 1997-03-04 2004-09-21 G. D. Searle Sulfonyl aryl or heteroaryl hydroxamic acid compounds
US6696449B2 (en) * 1997-03-04 2004-02-24 Pharmacia Corporation Sulfonyl aryl hydroxamates and their use as matrix metalloprotease inhibitors
US7863444B2 (en) 1997-03-19 2011-01-04 Abbott Laboratories 4-aminopyrrolopyrimidines as kinase inhibitors
IL133870A0 (en) * 1997-07-11 2001-04-30 Smithkline Beecham Plc Sulphonamide derivatives being 5-ht6 receptor antagonists and process for their preparation
US6268387B1 (en) * 1997-12-23 2001-07-31 Warner-Lambert Company Thiourea and benzamide compounds, compositions and methods of treating or preventing inflammatory diseases and atherosclerosis
AU759255B2 (en) * 1998-01-29 2003-04-10 Amgen, Inc. PPAR-gamma modulators
US6583157B2 (en) * 1998-01-29 2003-06-24 Tularik Inc. Quinolinyl and benzothiazolyl modulators
AU765603C (en) * 1998-04-14 2004-08-05 General Hospital Corporation, The Methods for treating neuropsychiatric disorders
CZ302691B6 (cs) * 1998-07-08 2011-09-07 Sanofi - Aventis Deutschland GmbH N-Arylamidová sloucenina, zpusob její prípravy, farmaceutický prostredek tuto slouceninu obsahující, tato sloucenina pro použití jako aktivátor a pro použití k terapii nebo profylaxi
IL141769A0 (en) * 1998-09-11 2002-03-10 Aventis Pharma Sa Azetidine derivatives, preparation and medicines containing them
US6197786B1 (en) * 1998-09-17 2001-03-06 Pfizer Inc 4-Carboxyamino-2-substituted-1,2,3,4-tetrahydroquinolines
GT199900147A (es) * 1998-09-17 1999-09-06 1, 2, 3, 4- tetrahidroquinolinas 2-sustituidas 4-amino sustituidas.
FR2789079B3 (fr) * 1999-02-01 2001-03-02 Sanofi Synthelabo Derive d'acide pyrazolecarboxylique, sa preparation, les compositions pharmaceutiques en contenant
JP2001089412A (ja) 1999-09-22 2001-04-03 Otsuka Pharmaceut Co Ltd ベンゼン誘導体またはその医薬的に許容される塩
GB0007934D0 (en) 2000-03-31 2000-05-17 Darwin Discovery Ltd Chemical compounds
US6653332B2 (en) * 2000-05-03 2003-11-25 Tularik Inc. Combination therapeutic compositions and method of use
UA82048C2 (uk) * 2000-11-10 2008-03-11 Эли Лилли Энд Компани Агоністи альфа-рецепторів, активованих проліфератором пероксисом
GEP20053675B (en) * 2001-03-30 2005-11-25 Pfizer Prod Inc Pyridazinone Aldose Reductase Inhibitors
CN1543451A (zh) 2001-06-07 2004-11-03 过氧化物酶体增生剂激活的受体的调节剂
US6540436B2 (en) * 2001-07-23 2003-04-01 Rain Bird Corporation Deep root watering unit
TW550839B (en) * 2001-07-25 2003-09-01 Shinetsu Handotai Kk Light emitting element and method for manufacturing thereof
GB2378179A (en) * 2001-08-03 2003-02-05 Pantherix Ltd Aromatic sulfonamides and their use in treating bacterial diseases
US7371777B2 (en) * 2001-08-17 2008-05-13 Eisai Co., Ltd. Cyclic compound and PPAR agonist
GB0121337D0 (en) * 2001-09-04 2001-10-24 Astrazeneca Ab Chemical compounds
AU2002347985A1 (en) 2001-11-15 2003-06-10 Eli Lilly And Company Peroxisome proliferator activated receptor alpha agonists
JP2003292439A (ja) * 2002-02-04 2003-10-15 Sumitomo Pharmaceut Co Ltd 新規ピロール誘導体からなるｐｐａｒ活性化剤
ES2292937T3 (es) * 2002-02-21 2008-03-16 Eli Lilly And Company Moduladores para el receptor activado por el proliferador de peroxisomas.
AU2003219934A1 (en) * 2002-03-06 2003-09-22 Merck And Co., Inc. Method of treatment or prevention of obesity
WO2003087044A2 (fr) 2002-04-09 2003-10-23 7Tm Pharma A/S Nouveaux composes carboxamide utiles pour soigner les troubles associes au recepteur mch
AU2003250117B2 (en) * 2002-07-29 2007-05-10 F. Hoffmann-La Roche Ag Novel benzodioxoles
AU2003262947A1 (en) * 2002-08-30 2004-03-19 Pharmacia And Upjohn Company Method of preventing or treating atherosclerosis or restenosis
US7329658B2 (en) * 2003-02-06 2008-02-12 Pfizer Inc Cannabinoid receptor ligands and uses thereof
US20040204450A1 (en) * 2003-03-28 2004-10-14 Pfizer Inc Quinoline and quinoxaline compounds
US7141669B2 (en) * 2003-04-23 2006-11-28 Pfizer Inc. Cannabiniod receptor ligands and uses thereof
US7145012B2 (en) * 2003-04-23 2006-12-05 Pfizer Inc. Cannabinoid receptor ligands and uses thereof
US20050022815A1 (en) * 2003-06-25 2005-02-03 Sunrise Medical Hhg Inc. Apparatus and method for monitoring supplemental oxygen usage
WO2005014532A1 (fr) * 2003-08-08 2005-02-17 Transtech Pharma, Inc. Composes aryle et heteroaryle, compositions et procedes associes
KR100799802B1 (ko) * 2004-02-04 2008-01-31 화이자 프로덕츠 인크. 치환된 퀴놀린 화합물
EP1737809B1 (fr) * 2004-02-27 2013-09-18 Amgen, Inc Composes, compositions pharmaceutiques et procedes d'utilisation dans le traitement de troubles metaboliques
CA2555914A1 (fr) * 2004-03-08 2005-09-22 Amgen Inc. Modulation therapeutique de l'activite de recepteur de ppar-gamma
US7262318B2 (en) * 2004-03-10 2007-08-28 Pfizer, Inc. Substituted heteroaryl- and phenylsulfamoyl compounds
NZ550114A (en) * 2004-04-20 2011-02-25 Transtech Pharma Inc Substituted thiazole and pyrimidine derivatives as melanocortin receptor modulators
US6967808B1 (en) * 2004-05-13 2005-11-22 Hitachi Global Storage Technologies Netherlands B.V. Data recording system with servo pattern having pseudo-random binary sequences
US20050288340A1 (en) * 2004-06-29 2005-12-29 Pfizer Inc Substituted heteroaryl- and phenylsulfamoyl compounds

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CA2559035A1 (fr) 2005-10-06
JP2007528387A (ja) 2007-10-11
KR20070001173A (ko) 2007-01-03
EA200601442A1 (ru) 2007-02-27
SV2005002047A (es) 2005-12-13
WO2005092845A1 (fr) 2005-10-06
AP2006003714A0 (en) 2006-08-31
TW200610525A (en) 2006-04-01
BRPI0508555A (pt) 2007-08-07
US20060258723A1 (en) 2006-11-16
ECSP066834A (es) 2006-12-29
DOP2005000034A (es) 2005-12-15
NL1028519A1 (nl) 2005-09-13
PA8625701A1 (es) 2006-01-25
NO20064615L (no) 2006-12-07
EP1725524A1 (fr) 2006-11-29
US7262318B2 (en) 2007-08-28
US20050228015A1 (en) 2005-10-13
AR048260A1 (es) 2006-04-12
DOP2005000025A (es) 2006-11-15
AU2005225628A1 (en) 2005-10-06
AU2005225628B2 (en) 2008-09-11
IL177631A0 (en) 2006-12-31
NL1028519C2 (nl) 2006-06-22
UY28794A1 (es) 2005-10-31
PE20051147A1 (es) 2006-01-28

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