GT200100036A - Derivados de eteres de pirazol como agentes antiinflamatorios / analgesicos. - Google Patents
Derivados de eteres de pirazol como agentes antiinflamatorios / analgesicos.Info
- Publication number
- GT200100036A GT200100036A GT200100036A GT200100036A GT200100036A GT 200100036 A GT200100036 A GT 200100036A GT 200100036 A GT200100036 A GT 200100036A GT 200100036 A GT200100036 A GT 200100036A GT 200100036 A GT200100036 A GT 200100036A
- Authority
- GT
- Guatemala
- Prior art keywords
- eteres
- pirazol
- derivatives
- treatment
- inflammatory
- Prior art date
Links
- 239000000730 antalgic agent Substances 0.000 title 1
- 239000002260 anti-inflammatory agent Substances 0.000 title 1
- 230000003110 anti-inflammatory effect Effects 0.000 title 1
- YZXBAPSDXZZRGB-DOFZRALJSA-N arachidonic acid Chemical compound CCCCC\C=C/C\C=C/C\C=C/C\C=C/CCCC(O)=O YZXBAPSDXZZRGB-DOFZRALJSA-N 0.000 abstract 2
- 201000010099 disease Diseases 0.000 abstract 2
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 2
- 241000282472 Canis lupus familiaris Species 0.000 abstract 1
- 206010061218 Inflammation Diseases 0.000 abstract 1
- 229940114079 arachidonic acid Drugs 0.000 abstract 1
- 235000021342 arachidonic acid Nutrition 0.000 abstract 1
- 210000001072 colon Anatomy 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 230000004054 inflammatory process Effects 0.000 abstract 1
- 244000144972 livestock Species 0.000 abstract 1
- 230000001404 mediated effect Effects 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/02—Stomatological preparations, e.g. drugs for caries, aphtae, periodontitis
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
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- A—HUMAN NECESSITIES
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- A61P11/06—Antiasthmatics
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- A61P13/12—Drugs for disorders of the urinary system of the kidneys
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- A—HUMAN NECESSITIES
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- A61P19/08—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
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- A—HUMAN NECESSITIES
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- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
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- A61P9/12—Antihypertensives
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/14—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three 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
- C07D231/18—One oxygen or sulfur atom
- C07D231/20—One oxygen atom attached in position 3 or 5
- C07D231/22—One oxygen atom attached in position 3 or 5 with aryl radicals attached to ring nitrogen atoms
- C07D231/24—One oxygen atom attached in position 3 or 5 with aryl radicals attached to ring nitrogen atoms having sulfone or sulfonic acid radicals in the molecule
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Veterinary Medicine (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- Neurosurgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Cardiology (AREA)
- Pulmonology (AREA)
- Diabetes (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Rheumatology (AREA)
- Pain & Pain Management (AREA)
- Heart & Thoracic Surgery (AREA)
- Endocrinology (AREA)
- Hematology (AREA)
- Psychiatry (AREA)
- Hospice & Palliative Care (AREA)
- Dermatology (AREA)
- Urology & Nephrology (AREA)
- Emergency Medicine (AREA)
- Psychology (AREA)
- Obesity (AREA)
- Ophthalmology & Optometry (AREA)
- Tropical Medicine & Parasitology (AREA)
- Reproductive Health (AREA)
- Vascular Medicine (AREA)
- Oncology (AREA)
Abstract
LA PRESENTE INVECION TRATA DE DERIVADOS DE ETERES, TIOETERES Y AMINA DE PIRAZOL SUS METODOS DE TRATAMIENTO DE ENFERMEDADES Y SU COMPOSICIONES FARMACEUTICAS PARA EL TRATAMIENTO DE ENFERMEDADES MEDIADAS POR LA CILOOXIGENASA. LOS COMPUESTOS DE ESTA INVENCION INHIBEN LA BIOSINTESIS DE LAS PROTAGLANDINAS MEDIANTE LA INTERVENCION DE LA ACCION DE LA ENCIMA CICLOOXIGENASA SOBRE EL ACIDO ARAQUIDONICO, Y POR TANTO RESULTAN UTILES PARA EL TRATAMIENTO O EL ALIVIO DE LA INFLAMANCION, COMO LA ARTRITIS, LA NEURODEGENERACION Y EL CANCER DEL COLON EN MAMIFEROS, PREFERIBLEMENTE SERES HUMANOS, PERROS, GATOS O GANADO.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US18686900P | 2000-03-03 | 2000-03-03 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GT200100036A true GT200100036A (es) | 2001-12-18 |
Family
ID=22686598
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GT200100036A GT200100036A (es) | 2000-03-03 | 2001-03-02 | Derivados de eteres de pirazol como agentes antiinflamatorios / analgesicos. |
Country Status (16)
| Country | Link |
|---|---|
| US (3) | US6878726B2 (es) |
| EP (1) | EP1259504A1 (es) |
| JP (1) | JP2003525288A (es) |
| AR (1) | AR027967A1 (es) |
| AU (2) | AU2001232175B2 (es) |
| BR (1) | BR0108908A (es) |
| CA (1) | CA2401697A1 (es) |
| CO (1) | CO5271651A1 (es) |
| GT (1) | GT200100036A (es) |
| HN (1) | HN2001000037A (es) |
| MX (1) | MXPA02008627A (es) |
| PA (1) | PA8513101A1 (es) |
| PE (1) | PE20011164A1 (es) |
| TN (1) | TNSN01035A1 (es) |
| WO (1) | WO2001064669A1 (es) |
| ZA (1) | ZA200207015B (es) |
Families Citing this family (33)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU2001232175B2 (en) * | 2000-03-03 | 2005-07-07 | Pfizer Products Inc. | Pyrazole ether derivatives as anti-inflammatory/analgesic agents |
| US20040092552A1 (en) * | 2000-04-25 | 2004-05-13 | Brown David L | 2-Fluorobenzenesulfonyl compounds for the treatment of inflammation |
| SI1441714T1 (sl) * | 2001-10-25 | 2008-06-30 | Novartis Ag | Kombinacije, ki obsegajo selektivni inhibitor ciklooksigenaze-2 |
| WO2003037336A1 (en) * | 2001-11-02 | 2003-05-08 | Pfizer Products Inc. | 1-(5-sulfonyl-pyridin-2-yl)-5-(methylidene-cycloalkylmethoxy)-1h-pyrazole-4-carbonitrile derivatives and other compounds as cyclooxygenase inhibitors for the treatment of arthritis, neurodegeneration and colon cancer |
| WO2003037335A1 (en) | 2001-11-02 | 2003-05-08 | Pfizer Products Inc. | 5-heteroatom-substituted pyrazoles |
| WO2003037351A1 (en) * | 2001-11-02 | 2003-05-08 | Pfizer Products Inc. | Heterocyclo-alkylsulfonyl pyrazoles and their use as cox-2 inhibitors |
| JP2005515171A (ja) | 2001-11-02 | 2005-05-26 | ファイザー・プロダクツ・インク | 5−ヘテロ原子含有ピラゾールの効率的な合成法 |
| WO2003037352A1 (en) * | 2001-11-02 | 2003-05-08 | Pfizer Products Inc. | 1-phenyl-5-n-heterocyclyl-pyrazoles as cyclooxygenase inhibitors for the treatment of inflammation associated disorders |
| WO2003037330A1 (en) | 2001-11-02 | 2003-05-08 | Pfizer Products Inc. | Sulfonyl-and sulfonylheteroaryl-pyrazoles with a hydrazinyl or nitrogen oxide substituent at the 5-position for use as cyclooxygenase inhibitors |
| ES2263058T3 (es) * | 2002-08-19 | 2006-12-01 | Glaxo Group Limited | Derivados de pirimidina como inhibidores selectivos de cox-2. |
| EA015104B1 (ru) | 2003-08-01 | 2011-06-30 | Мицубиси Танабе Фарма Корпорейшн | Новые соединения, обладающие ингибирующей активностью в отношении натрийзависимого транспортера |
| US8785403B2 (en) | 2003-08-01 | 2014-07-22 | Mitsubishi Tanabe Pharma Corporation | Glucopyranoside compound |
| AR048377A1 (es) | 2003-08-01 | 2006-04-26 | Janssen Pharmaceutica Nv | Benzoimidazol-, benzotriazol- y benzoimidazolona - o- glucosidos sustituidos |
| CA2549015A1 (en) | 2003-08-01 | 2005-02-10 | Janssen Pharmaceutica N.V. | Substituted fused heterocyclic c-glycosides |
| EA010655B1 (ru) | 2003-08-01 | 2008-10-30 | Янссен Фармацевтика Н.В. | Замещенные индазол-о-глюкозиды |
| UY30730A1 (es) | 2006-12-04 | 2008-07-03 | Mitsubishi Tanabe Pharma Corp | Forma cristalina del hemihidrato de 1-(b (beta)-d-glucopiranosil) -4-metil-3-[5-(4-fluorofenil) -2-tienilmetil]benceno |
| CN101801371B (zh) | 2007-09-10 | 2012-11-28 | 詹森药业有限公司 | 可用作sglt抑制剂的化合物的制备方法 |
| CL2008003653A1 (es) | 2008-01-17 | 2010-03-05 | Mitsubishi Tanabe Pharma Corp | Uso de un inhibidor de sglt derivado de glucopiranosilo y un inhibidor de dppiv seleccionado para tratar la diabetes; y composicion farmaceutica. |
| US9056850B2 (en) | 2008-10-17 | 2015-06-16 | Janssen Pharmaceutica N.V. | Process for the preparation of compounds useful as inhibitors of SGLT |
| WO2010126580A1 (en) | 2009-04-27 | 2010-11-04 | Dow Agrosciences, Llc | Insecticidal pyridine compounds |
| US20110009347A1 (en) | 2009-07-08 | 2011-01-13 | Yin Liang | Combination therapy for the treatment of diabetes |
| RS55909B1 (sr) | 2009-10-14 | 2017-09-29 | Janssen Pharmaceutica Nv | Proces za pripremu jedinjenja koja su korisna kao inhibitori sglt2 |
| NZ703128A (en) | 2010-05-11 | 2016-04-29 | Janssen Pharmaceutica Nv | Pharmaceutical formulations comprising 1 - (beta-d-glucopyranosyl) - 2 -thienylmethylbenzene derivatives as inhibitors of sglt |
| EP2697218B1 (en) | 2011-04-13 | 2016-05-25 | Janssen Pharmaceutica NV | Process for the preparation of compounds useful as inhibitors of sglt2 |
| US9035044B2 (en) | 2011-05-09 | 2015-05-19 | Janssen Pharmaceutica Nv | L-proline and citric acid co-crystals of (2S, 3R, 4R, 5S,6R)-2-(3-((5-(4-fluorophenyl)thiopen-2-yl)methyl)4-methylphenyl)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol |
| CN104302640A (zh) | 2012-03-16 | 2015-01-21 | 埃克希金医药品有限公司 | 3,5-二氨基吡唑激酶抑制剂 |
| JO3215B1 (ar) | 2012-08-09 | 2018-03-08 | Phenex Pharmaceuticals Ag | حلقات غير متجانسة بها 5 ذرات تحتوي على النيتروجين بها استبدال بكربوكساميد أو سلفوناميد كمعدلات لمستقبل نووي غير محمي RORy |
| NZ631142A (en) | 2013-09-18 | 2016-03-31 | Axikin Pharmaceuticals Inc | Pharmaceutically acceptable salts of 3,5-diaminopyrazole kinase inhibitors |
| HUE049801T2 (hu) | 2014-12-23 | 2020-10-28 | Sma Therapeutics Inc | 3,5-diaminopirazol kináz inhibitorok |
| CN104892514A (zh) * | 2015-05-19 | 2015-09-09 | 广州诺威生物技术有限公司 | 一种咪唑类新化合物 |
| US20170071970A1 (en) | 2015-09-15 | 2017-03-16 | Janssen Pharmaceutica Nv | Co-therapy comprising canagliflozin and phentermine for the treatment of obesity and obesity related disorders |
| GB202011068D0 (en) * | 2020-07-17 | 2020-09-02 | Syngenta Crop Protection Ag | Improvements in or relating to organic compounds |
| CN119930520A (zh) * | 2023-11-03 | 2025-05-06 | 中国药科大学 | N-芳基吡唑类化合物及其药物组合物和应用 |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0178035B1 (en) * | 1984-05-12 | 1990-01-03 | FISONS plc | Anti-inflammatory 1,n-diarylpyrazol-3-amines, compositions containing them and processes for their preparation |
| FI855180A7 (fi) * | 1985-01-18 | 1986-07-19 | Nissan Chemical Ind Ltd | Pyratsolisulfonamidijohdannainen, menetelmä sen valmistamiseksi ja sitä sisältävä rikkaruohomyrkky. |
| US4881985A (en) * | 1988-08-05 | 1989-11-21 | General Motors Corporation | Method for producing anisotropic RE-FE-B type magnetically aligned material |
| PH27357A (en) * | 1989-09-22 | 1993-06-21 | Fujisawa Pharmaceutical Co | Pyrazole derivatives and pharmaceutical compositions comprising the same |
| FR2652352A1 (fr) * | 1989-09-28 | 1991-03-29 | Jouveinal Sa | Benzodiazepines, leur procede et intermediaires de preparation et leurs applications en therapeutique. |
| US5434178A (en) * | 1993-11-30 | 1995-07-18 | G.D. Searle & Co. | 1,3,5 trisubstituted pyrazole compounds for treatment of inflammation |
| US5466823A (en) * | 1993-11-30 | 1995-11-14 | G.D. Searle & Co. | Substituted pyrazolyl benzenesulfonamides |
| FR2725719B1 (fr) * | 1994-10-14 | 1996-12-06 | Jouveinal Inst Rech | Diazepino-indoles inhibiteurs de phosphodiesterases iv |
| US5700816A (en) * | 1995-06-12 | 1997-12-23 | Isakson; Peter C. | Treatment of inflammation and inflammation-related disorders with a combination of a cyclooxygenase-2 inhibitor and a leukotriene A4 hydrolase inhibitor |
| FR2746800B1 (fr) * | 1996-03-29 | 1998-06-05 | Jouveinal Inst Rech | Diazepino-indoles inhibiteurs de phosphodiesterases 4 |
| DK0892791T3 (da) * | 1996-04-12 | 2003-06-23 | Searle & Co | N-[[4-(5-methyl-3-phenylisoxazol-4-yl]-phenyl]-sulfonylpropylamid og dets natriumsalt som prodrugs for COX-2-inhibitorer |
| FR2762841B1 (fr) * | 1997-04-30 | 1999-07-02 | Jouveinal Inst Rech | Diazepino-indolones inhibitrices de phosphodiesterases iv |
| SK4202000A3 (en) | 1997-09-24 | 2000-10-09 | Merck & Co Inc | Process of making 3-aryloxy-4-aryl furan-2-ones useful as inhibitors of cox-2 |
| EP1028951A1 (en) | 1997-10-30 | 2000-08-23 | Merck Frosst Canada Inc. | Diaryl-5-alkyl-5-methyl-2(5h)-furanones as selective cyclooxygenase-2 inhibitors |
| YU67600A (sh) * | 1998-05-05 | 2003-07-07 | F.Hofmann - La Roche Ag. | Derivati pirazola kao inhibitori p-38 map kinaze |
| JP2000169453A (ja) * | 1998-09-30 | 2000-06-20 | Mitsubishi Chemicals Corp | 1―フェニルピラゾ―ル―3―カルボキサミド誘導体、その中間体およびこれを有効成分とする農薬 |
| AU2001232175B2 (en) * | 2000-03-03 | 2005-07-07 | Pfizer Products Inc. | Pyrazole ether derivatives as anti-inflammatory/analgesic agents |
-
2001
- 2001-02-22 AU AU2001232175A patent/AU2001232175B2/en not_active Ceased
- 2001-02-22 AU AU3217501A patent/AU3217501A/xx active Pending
- 2001-02-22 BR BR0108908-0A patent/BR0108908A/pt not_active IP Right Cessation
- 2001-02-22 MX MXPA02008627A patent/MXPA02008627A/es unknown
- 2001-02-22 JP JP2001563509A patent/JP2003525288A/ja active Pending
- 2001-02-22 EP EP01904263A patent/EP1259504A1/en not_active Withdrawn
- 2001-02-22 CA CA002401697A patent/CA2401697A1/en not_active Abandoned
- 2001-02-22 WO PCT/IB2001/000237 patent/WO2001064669A1/en not_active Ceased
- 2001-03-01 PE PE2001000213A patent/PE20011164A1/es not_active Application Discontinuation
- 2001-03-01 AR ARP010100978A patent/AR027967A1/es not_active Application Discontinuation
- 2001-03-02 HN HN2001000037A patent/HN2001000037A/es unknown
- 2001-03-02 TN TNTNSN01035A patent/TNSN01035A1/fr unknown
- 2001-03-02 US US09/798,752 patent/US6878726B2/en not_active Expired - Fee Related
- 2001-03-02 PA PA20018513101A patent/PA8513101A1/es unknown
- 2001-03-02 GT GT200100036A patent/GT200100036A/es unknown
- 2001-03-02 CO CO01016923A patent/CO5271651A1/es not_active Application Discontinuation
-
2002
- 2002-09-02 ZA ZA200207015A patent/ZA200207015B/en unknown
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2004
- 2004-07-16 US US10/893,521 patent/US20050004135A1/en not_active Abandoned
- 2004-07-16 US US10/893,520 patent/US20040259879A1/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| AU2001232175B2 (en) | 2005-07-07 |
| ZA200207015B (en) | 2003-09-02 |
| WO2001064669A1 (en) | 2001-09-07 |
| AU3217501A (en) | 2001-09-12 |
| CO5271651A1 (es) | 2003-04-30 |
| US20020058681A1 (en) | 2002-05-16 |
| US20050004135A1 (en) | 2005-01-06 |
| CA2401697A1 (en) | 2001-09-07 |
| EP1259504A1 (en) | 2002-11-27 |
| JP2003525288A (ja) | 2003-08-26 |
| AR027967A1 (es) | 2003-04-16 |
| US20040259879A1 (en) | 2004-12-23 |
| PE20011164A1 (es) | 2001-11-13 |
| US6878726B2 (en) | 2005-04-12 |
| PA8513101A1 (es) | 2003-06-30 |
| MXPA02008627A (es) | 2003-02-24 |
| TNSN01035A1 (fr) | 2005-11-10 |
| BR0108908A (pt) | 2002-12-24 |
| HN2001000037A (es) | 2001-06-18 |
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