PE20030333A1 - Compuestos biciclicos aromaticos sustituidos con amino-alquilo, procedimiento para su preparacion y su utilizacion como medicamentos - Google Patents
Compuestos biciclicos aromaticos sustituidos con amino-alquilo, procedimiento para su preparacion y su utilizacion como medicamentosInfo
- Publication number
- PE20030333A1 PE20030333A1 PE2002000743A PE2002000743A PE20030333A1 PE 20030333 A1 PE20030333 A1 PE 20030333A1 PE 2002000743 A PE2002000743 A PE 2002000743A PE 2002000743 A PE2002000743 A PE 2002000743A PE 20030333 A1 PE20030333 A1 PE 20030333A1
- Authority
- PE
- Peru
- Prior art keywords
- alkyl
- aryl
- amino
- medicines
- procedure
- Prior art date
Links
- 150000001875 compounds Chemical group 0.000 title abstract 4
- 239000003814 drug Substances 0.000 title 1
- -1 AMINO Chemical group 0.000 abstract 2
- 208000008589 Obesity Diseases 0.000 abstract 1
- 230000000578 anorexic effect Effects 0.000 abstract 1
- 239000004202 carbamide Substances 0.000 abstract 1
- 206010061428 decreased appetite Diseases 0.000 abstract 1
- 206010012601 diabetes mellitus Diseases 0.000 abstract 1
- 230000001729 effect on metabolism Effects 0.000 abstract 1
- 235000020824 obesity Nutrition 0.000 abstract 1
- 229910052760 oxygen Inorganic materials 0.000 abstract 1
- 229910052717 sulfur Inorganic materials 0.000 abstract 1
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 abstract 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D235/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
- C07D235/02—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
- C07D235/04—Benzimidazoles; Hydrogenated benzimidazoles
- C07D235/06—Benzimidazoles; Hydrogenated benzimidazoles with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached in position 2
-
- 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
- A61P25/18—Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
-
- 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
- A61P25/22—Anxiolytics
-
- 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
- A61P25/24—Antidepressants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/04—Anorexiants; Antiobesity agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/06—Antihyperlipidemics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- 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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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/12—Antihypertensives
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/04—Indoles; Hydrogenated indoles
- C07D209/08—Indoles; Hydrogenated indoles with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, directly attached to carbon atoms of the hetero ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D235/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
- C07D235/02—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
- C07D235/04—Benzimidazoles; Hydrogenated benzimidazoles
- C07D235/06—Benzimidazoles; Hydrogenated benzimidazoles with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached in position 2
- C07D235/08—Radicals containing only hydrogen and carbon atoms
-
- 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
- C07D401/12—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 linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/06—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur 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)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Veterinary Medicine (AREA)
- General Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Diabetes (AREA)
- Obesity (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Hematology (AREA)
- Biomedical Technology (AREA)
- Psychiatry (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Endocrinology (AREA)
- Emergency Medicine (AREA)
- Vascular Medicine (AREA)
- Urology & Nephrology (AREA)
- Pain & Pain Management (AREA)
- Child & Adolescent Psychology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (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)
- Furan Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Indole Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Abstract
SE REFIERE A COMPUESTOS BICICLICOS AROMATICOS SUSTITUIDOS CON AMINO ALQUILO DE FORMULA I, A ES ALQUILO C1-C8, ALQUILEN C0-C8-ARILO, ANILLO MONOCICLICO, BICICLICO DE 3-12 MIEMBROS, O-ALQUILO C1-C6, S-ALQUILO C1-C6, NHCO-ALQUILO C1-C6; X ES ENLACE, C(R8)(R9), C(OR10)(R11), O, NR12, S, SO, SO2, CO; X ES C(R8)(R9), C(OR10)(R11), O, NR12, S, SO, SO2, CO; R8, R9, R10, R11, R12 SON H, ALQUILO C1-C6; D ES N, CR41; E ES N, CR42, G ES N, CR43; L ES N, CR44; R1, R2, R3, R41, R43, R44 SON H, F, Br, I, OH, CF3, NO2, CN, OCF3, O-ALQUILO C1-C6, ALCOXI-ALQUILO C1-C4, ENTRE OTROS; R13, R14, R15, R16, R17, R19, R24, R5 SON H, ALQUILO C1-C6 O R13 Y R14 O R15 Y R16 JUNTO A N FORMAN UN ANILLO DE 5-6 MIEMBROS, ENTRE OTROS; R18, R20, R21 SON ALQUILO C1-C6, ARILO; B ES NR24, O; W ES N, CR25; R25 ES H, ALQUILO C1-C6, ARILO, UN ENLACE CON Y; T ES N, CR26; R26 ES H, ALQUILO C1-C6, ARILO, ALQUILEN C0-C8-ARILO, U ES O, S, NR27, C(R30)=N, N=CR31; R27, R30, R31 SON H, ALQUILO C1-C6, UN ENLACE CON Y; Y ES ALQUILENO C1-C8; R6 Y R7 SON H, ALQUILO C1-C6, CICLOALQUILO C3-C7 O R6 E Y O R6 Y R7 FORMAN JUNTO A N UN ANILLO DE 3-8 MIEMBROS. SON COMPUESTOS PREFERIDOS 1-[1-(2-DIMETILAMINO-ETIL)-1H-INDOL-5-IL]-3-(4-FENOXI-FENIL)-UREA; 1-(4-BUTOXI-FENIL)-3-[1-(2-DIMETILAMINO-ETIL)-1H-INDOL-5-IL]-UREA; 1-(1-METIL-2-PIRROLIDIN-1-IL-METIL)-1H-INDOL-5-IL)-3-(4-FENOXI-FENIL)-UREA, ENTRE OTROS. LOS COMPUESTOS SON ANOREXICOS, TIENEN EFECTO SOBRE EL METABOLISMO Y PUEDEN SER UTILES PARA TRATAMIENTO DE OBESIDAD, DIABETES
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE10139416A DE10139416A1 (de) | 2001-08-17 | 2001-08-17 | Aminoalkyl substituierte aromatische Bicyclen, Verfahren zu ihrer Herstellung und ihre Verwendung als Arzneimittel |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PE20030333A1 true PE20030333A1 (es) | 2003-04-24 |
Family
ID=7695086
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PE2002000743A PE20030333A1 (es) | 2001-08-17 | 2002-08-16 | Compuestos biciclicos aromaticos sustituidos con amino-alquilo, procedimiento para su preparacion y su utilizacion como medicamentos |
Country Status (23)
| Country | Link |
|---|---|
| US (5) | US20030212070A1 (es) |
| EP (1) | EP1418906A1 (es) |
| JP (1) | JP2005505530A (es) |
| KR (1) | KR20040043197A (es) |
| CN (1) | CN1555260A (es) |
| AR (1) | AR043477A1 (es) |
| BR (1) | BR0211989A (es) |
| CA (1) | CA2457037A1 (es) |
| DE (1) | DE10139416A1 (es) |
| EE (1) | EE200400055A (es) |
| GT (1) | GT200200165A (es) |
| HR (1) | HRP20040149A2 (es) |
| HU (1) | HUP0401329A2 (es) |
| IL (1) | IL160424A0 (es) |
| MX (1) | MXPA04001307A (es) |
| NO (1) | NO20040678L (es) |
| PA (1) | PA8553001A1 (es) |
| PE (1) | PE20030333A1 (es) |
| PL (1) | PL366794A1 (es) |
| RU (1) | RU2004107654A (es) |
| UY (1) | UY27417A1 (es) |
| WO (1) | WO2003015769A1 (es) |
| ZA (1) | ZA200401221B (es) |
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| IL161478A0 (en) | 2001-10-25 | 2004-09-27 | Takeda Chemical Industries Ltd | Quinoline compound |
| US7084156B2 (en) | 2001-11-27 | 2006-08-01 | Merck & Co., Inc. | 2-Aminoquinoline compounds |
| AU2003252715B2 (en) | 2002-07-30 | 2009-06-04 | Banyu Pharmaceutical Co., Ltd. | Antagonist of melanin-concentrating hormone receptor comprising benzimidazole derivative as active ingredient |
| US20050101542A1 (en) * | 2002-08-20 | 2005-05-12 | Regents Of The University Of California | Combination therapy for controlling appetites |
| US7772188B2 (en) | 2003-01-28 | 2010-08-10 | Ironwood Pharmaceuticals, Inc. | Methods and compositions for the treatment of gastrointestinal disorders |
| AU2004209505B2 (en) * | 2003-02-10 | 2009-07-23 | Banyu Pharmaceutical Co., Ltd. | Melanin-concentrating hormone receptor antagonists containing piperidine derivatives as the active ingredient |
| DE10314610A1 (de) | 2003-04-01 | 2004-11-04 | Aventis Pharma Deutschland Gmbh | Neues Diphenylazetidinon mit verbesserten physiologischen Eigenschaften, Verfahren zu dessen Herstellung, diese Verbindungen enthaltende Arzneimittel und dessen Verwendung |
| US7514438B2 (en) | 2003-08-13 | 2009-04-07 | Amgen, Inc. | Melanin concentrating hormone receptor antagonist |
| WO2005019240A2 (en) * | 2003-08-13 | 2005-03-03 | Amgen, Inc. | Melanin concentrating hormone receptor antagonists |
| WO2005016928A1 (ja) | 2003-08-15 | 2005-02-24 | Banyu Pharmaceutical Co., Ltd. | イミダゾピリジン誘導体 |
| FR2859472A1 (fr) * | 2003-09-04 | 2005-03-11 | Oreal | Utilisation, pour la teinture des fibres keratiniques, d'un derive de para-phenylenediamine substituee par un noyau homopiperidine |
| ES2326980T3 (es) * | 2003-10-02 | 2009-10-22 | Schering Corporation | Aminobenzimidazoles utiles como antagonistas selectivos del receptor de la hormona concentrada de melamina (mch) para el tratamiento de la obesidad y desordenes asociados. |
| WO2005035534A1 (ja) * | 2003-10-08 | 2005-04-21 | Ono Pharmaceutical Co., Ltd. | 複素ビシクロ環および複素トリシクロ環化合物およびその医薬 |
| SE0303480D0 (sv) * | 2003-12-19 | 2003-12-19 | Biovitrum Ab | Benzofuranes |
| US7049307B2 (en) | 2003-12-23 | 2006-05-23 | Abbott Laboratories | Antagonists of melanin concentrating hormone effects on the melanin concentrating hormone receptor |
| US7071182B2 (en) | 2003-12-23 | 2006-07-04 | Abbott Laboratories | Antagonists of melanin concentrating hormone effects on the melanin concentrating hormone receptor |
| FR2864957A1 (fr) * | 2004-01-09 | 2005-07-15 | Oreal | Composition pour la teinture des fibres keratiniques comprenant au moins un derive de para-phenylenediamine substitue par un noyau heptamethylenediamine |
| US8519158B2 (en) * | 2004-03-12 | 2013-08-27 | Ligand Pharmaceuticals Incorporated | Androgen receptor modulator compounds and methods |
| US20080125403A1 (en) | 2004-04-02 | 2008-05-29 | Merck & Co., Inc. | Method of Treating Men with Metabolic and Anthropometric Disorders |
| DE102004017932A1 (de) * | 2004-04-14 | 2005-11-03 | Boehringer Ingelheim Pharma Gmbh & Co. Kg | Neue Alkin-Verbindungen mit MCH-antagonistischer Wirkung und diese Verbindungen enthaltende Arzneimittel |
| WO2005123714A1 (en) * | 2004-06-16 | 2005-12-29 | 7Tm Pharma A/S | Quinazoline compounds and their use in mch-related disease |
| DE102004039789A1 (de) | 2004-08-16 | 2006-03-02 | Sanofi-Aventis Deutschland Gmbh | Arylsubstituierte polycyclische Amine, Verfahren zu ihrer Herstellung und ihre Verwendung als Arzneimittel |
| EP1632491A1 (en) | 2004-08-30 | 2006-03-08 | Laboratorios Del Dr. Esteve, S.A. | Substituted indole compounds and their use as 5-HT6 receptor modulators |
| CA2589274A1 (en) * | 2004-12-07 | 2006-06-15 | Locus Pharmaceuticals, Inc. | Inhibitors of protein kinases |
| WO2006062982A2 (en) * | 2004-12-07 | 2006-06-15 | Locus Pharmaceuticals, Inc. | Urea inhibitors of map kinases |
| DK1828177T3 (da) * | 2004-12-17 | 2008-11-17 | Lilly Co Eli | Hidtil ukendte MCH-receptorantagonister |
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| KR20090047458A (ko) | 2006-08-08 | 2009-05-12 | 사노피-아벤티스 | 아릴아미노아릴-알킬-치환된 이미다졸리딘-2,4-디온, 이의 제조방법, 이들 화합물을 포함하는 약제 및 이의 용도 |
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| US8969514B2 (en) | 2007-06-04 | 2015-03-03 | Synergy Pharmaceuticals, Inc. | Agonists of guanylate cyclase useful for the treatment of hypercholesterolemia, atherosclerosis, coronary heart disease, gallstone, obesity and other cardiovascular diseases |
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| UY31968A (es) | 2008-07-09 | 2010-01-29 | Sanofi Aventis | Nuevos derivados heterocíclicos, sus procesos para su preparación, y sus usos terapéuticos |
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| DE2928485A1 (de) * | 1979-07-14 | 1981-01-29 | Bayer Ag | Verwendung von harnstoffderivaten als arzneimittel bei der behandlung von fettstoffwechselstoerungen |
| US5599930A (en) * | 1991-07-03 | 1997-02-04 | The Upjohn Company | Substituted indoles as anti-AIDS pharmaceuticals |
| JPH10500960A (ja) * | 1994-05-28 | 1998-01-27 | スミスクライン・ビーチャム・パブリック・リミテッド・カンパニー | 5ht1d−アンタゴニスト活性を有するアミド誘導体 |
| ATE236137T1 (de) * | 1996-02-02 | 2003-04-15 | Merck & Co Inc | Heterocyclische verbindungen als antidiabetische mittel und für die behandlung von fettleibigkeit |
| DK0971878T3 (da) * | 1997-02-27 | 2008-06-30 | Takeda Pharmaceutical | Aminforbindelser, fremstillingen og anvendelsen deraf som inhibitorer af amyloid-beta-produktion |
| WO1998047868A1 (en) * | 1997-04-18 | 1998-10-29 | Smithkline Beecham Plc | Heterocycle-containing urea derivatives as 5ht1a, 5ht1b and 5ht1d receptor antagonists |
| JP2002508366A (ja) * | 1997-12-12 | 2002-03-19 | スミスクライン・ビーチャム・パブリック・リミテッド・カンパニー | キノリンピペラジンおよびキノリンピペリジン誘導体、それらの製造方法、ならびに複合的5−ht1a、5−ht1bおよび5−ht1d受容体アンタゴニストとしてのそれらの用途 |
| WO2001021577A2 (en) * | 1999-09-20 | 2001-03-29 | Takeda Chemical Industries, Ltd. | Melanin concentrating hormone antagonist |
| TR200401029T4 (tr) * | 2000-06-09 | 2004-06-21 | Aventis Pharma Deutschland Gmbh | Asilfenil-üre türevleri, imalat yöntemleri ve ilaç maddesi olarak kullanımları |
| FR2810979B1 (fr) * | 2000-06-29 | 2002-08-23 | Adir | Nouveaux derives de diphenyluree, leur procede de preparation et les compositions pharmaceutiques qui les contiennent |
-
2001
- 2001-08-17 DE DE10139416A patent/DE10139416A1/de not_active Withdrawn
-
2002
- 2002-08-03 HR HR20040149A patent/HRP20040149A2/hr not_active Application Discontinuation
- 2002-08-03 HU HU0401329A patent/HUP0401329A2/hu unknown
- 2002-08-03 CA CA002457037A patent/CA2457037A1/en not_active Abandoned
- 2002-08-03 IL IL16042402A patent/IL160424A0/xx unknown
- 2002-08-03 MX MXPA04001307A patent/MXPA04001307A/es unknown
- 2002-08-03 PL PL02366794A patent/PL366794A1/xx unknown
- 2002-08-03 JP JP2003520728A patent/JP2005505530A/ja not_active Withdrawn
- 2002-08-03 EP EP02774498A patent/EP1418906A1/de not_active Withdrawn
- 2002-08-03 RU RU2004107654/04A patent/RU2004107654A/ru not_active Application Discontinuation
- 2002-08-03 BR BR0211989-7A patent/BR0211989A/pt not_active Application Discontinuation
- 2002-08-03 KR KR10-2004-7002348A patent/KR20040043197A/ko not_active Withdrawn
- 2002-08-03 WO PCT/EP2002/008686 patent/WO2003015769A1/de not_active Ceased
- 2002-08-03 CN CNA02818162XA patent/CN1555260A/zh active Pending
- 2002-08-14 US US10/218,034 patent/US20030212070A1/en not_active Abandoned
- 2002-08-15 AR ARP020103080A patent/AR043477A1/es not_active Application Discontinuation
- 2002-08-15 UY UY27417A patent/UY27417A1/es unknown
- 2002-08-16 PA PA20028553001A patent/PA8553001A1/es unknown
- 2002-08-16 GT GT200200165A patent/GT200200165A/es unknown
- 2002-08-16 PE PE2002000743A patent/PE20030333A1/es not_active Application Discontinuation
-
2003
- 2003-08-03 EE EEP200400055A patent/EE200400055A/xx unknown
-
2004
- 2004-02-16 ZA ZA200401221A patent/ZA200401221B/en unknown
- 2004-02-16 NO NO20040678A patent/NO20040678L/no not_active Application Discontinuation
- 2004-04-09 US US10/820,703 patent/US20040198731A1/en not_active Abandoned
- 2004-04-09 US US10/820,706 patent/US20040192693A1/en not_active Abandoned
- 2004-04-09 US US10/820,736 patent/US20040198732A1/en not_active Abandoned
- 2004-04-09 US US10/820,883 patent/US20040198733A1/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| ZA200401221B (en) | 2004-10-27 |
| PL366794A1 (en) | 2005-02-07 |
| HRP20040149A2 (en) | 2004-08-31 |
| EP1418906A1 (de) | 2004-05-19 |
| CN1555260A (zh) | 2004-12-15 |
| KR20040043197A (ko) | 2004-05-22 |
| US20040192693A1 (en) | 2004-09-30 |
| DE10139416A1 (de) | 2003-03-06 |
| HUP0401329A2 (hu) | 2004-12-28 |
| WO2003015769A1 (de) | 2003-02-27 |
| US20040198731A1 (en) | 2004-10-07 |
| US20040198733A1 (en) | 2004-10-07 |
| GT200200165A (es) | 2003-05-22 |
| JP2005505530A (ja) | 2005-02-24 |
| IL160424A0 (en) | 2004-07-25 |
| BR0211989A (pt) | 2004-09-28 |
| AR043477A1 (es) | 2005-08-03 |
| US20040198732A1 (en) | 2004-10-07 |
| NO20040678L (no) | 2004-05-13 |
| MXPA04001307A (es) | 2004-05-20 |
| PA8553001A1 (es) | 2003-02-28 |
| EE200400055A (et) | 2004-04-15 |
| RU2004107654A (ru) | 2005-09-10 |
| US20030212070A1 (en) | 2003-11-13 |
| UY27417A1 (es) | 2002-11-29 |
| CA2457037A1 (en) | 2003-02-27 |
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