AR041875A1 - Compuesto de fenilo, composicion farmaceutica que lo comprende, su uso para preparar un medicamento y procedimiento para preparar dicho compuesto - Google Patents
Compuesto de fenilo, composicion farmaceutica que lo comprende, su uso para preparar un medicamento y procedimiento para preparar dicho compuestoInfo
- Publication number
- AR041875A1 AR041875A1 ARP030103972A ARP030103972A AR041875A1 AR 041875 A1 AR041875 A1 AR 041875A1 AR P030103972 A ARP030103972 A AR P030103972A AR P030103972 A ARP030103972 A AR P030103972A AR 041875 A1 AR041875 A1 AR 041875A1
- Authority
- AR
- Argentina
- Prior art keywords
- optionally substituted
- alkyl
- heterocyclyl
- compound
- phenyl
- Prior art date
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- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D333/00—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
- C07D333/02—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings
- C07D333/04—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom
- C07D333/26—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom 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
- C07D333/38—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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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/12—Drugs for disorders of the urinary system of the kidneys
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/08—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
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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
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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
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
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- 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]
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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
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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
- A61P37/02—Immunomodulators
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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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- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C229/00—Compounds containing amino and carboxyl groups bound to the same carbon skeleton
- C07C229/52—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to carbon atoms of six-membered aromatic rings of the same carbon skeleton
- C07C229/54—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to carbon atoms of six-membered aromatic rings of the same carbon skeleton with amino and carboxyl groups bound to carbon atoms of the same non-condensed six-membered aromatic ring
- C07C229/64—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to carbon atoms of six-membered aromatic rings of the same carbon skeleton with amino and carboxyl groups bound to carbon atoms of the same non-condensed six-membered aromatic ring the carbon skeleton being further substituted by singly-bound oxygen atoms
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- C07C233/01—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms
- C07C233/45—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by carboxyl groups
- C07C233/53—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by carboxyl groups with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by a carbon atom of a six-membered aromatic ring
- C07C233/54—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by carboxyl groups with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by a carbon atom of a six-membered aromatic ring having the carbon atom of the carboxamide group bound to a hydrogen atom or to a carbon atom of a saturated carbon skeleton
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- C07C235/00—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms
- C07C235/42—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings and singly-bound oxygen atoms bound to the same carbon skeleton
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- C07C311/00—Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
- C07C311/01—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms
- C07C311/02—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton
- C07C311/08—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton 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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- C07C311/50—Compounds containing any of the groups, X being a hetero atom, Y being any atom
- C07C311/51—Y being a hydrogen or a carbon atom
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- C07C65/00—Compounds having carboxyl groups bound to carbon atoms of six—membered aromatic rings and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups
- C07C65/01—Compounds having carboxyl groups bound to carbon atoms of six—membered aromatic rings and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups containing hydroxy or O-metal groups
- C07C65/03—Compounds having carboxyl groups bound to carbon atoms of six—membered aromatic rings and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups containing hydroxy or O-metal groups monocyclic and having all hydroxy or O-metal groups bound to the ring
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- C07C65/00—Compounds having carboxyl groups bound to carbon atoms of six—membered aromatic rings and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups
- C07C65/21—Compounds having carboxyl groups bound to carbon atoms of six—membered aromatic rings and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups containing ether groups, groups, groups, or groups
- C07C65/24—Compounds having carboxyl groups bound to carbon atoms of six—membered aromatic rings and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups containing ether groups, groups, groups, or groups polycyclic
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- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/66—Esters of carboxylic acids having esterified carboxylic groups bound to acyclic carbon atoms and having any of the groups OH, O—metal, —CHO, keto, ether, acyloxy, groups, groups, or in the acid moiety
- C07C69/73—Esters of carboxylic acids having esterified carboxylic groups bound to acyclic carbon atoms and having any of the groups OH, O—metal, —CHO, keto, ether, acyloxy, groups, groups, or in the acid moiety of unsaturated acids
- C07C69/734—Ethers
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- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/76—Esters of carboxylic acids having a carboxyl group bound to a carbon atom of a six-membered aromatic ring
- C07C69/94—Esters of carboxylic acids having a carboxyl group bound to a carbon atom of a six-membered aromatic ring of polycyclic hydroxy carboxylic acids, the hydroxy groups and the carboxyl groups of which are bound to carbon atoms of six-membered aromatic rings
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- 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
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- 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
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- C07D211/62—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals attached in position 4
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- C07D213/00—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
- C07D213/02—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
- 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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- C07D213/02—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
- 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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- C07D213/02—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
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- C07D213/02—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
- 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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- C07D213/63—One oxygen atom
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- C07D213/02—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
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- C07D213/60—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 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
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- C07D261/10—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more 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
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- C07D333/14—Radicals substituted by singly bound hetero atoms other than halogen
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Abstract
Un compuesto de fenilo que tiene la fórmula (1), en la que: A representa un arilo opcionalmente sustituido, o un anillo de heterociclilo de 5 ó 6 miembros opcionalmente sustituido, o un grupo heterociclilo bicíclico opcionalmente sustituido; B representa un anillo de fenilo o piridilo; Z representa O, S, SO, o SO2; R1 representa CO2R4, CN, CONR5R6, CH2CO2R4, alquilo opcionalmente sustituido, alquenilo opcionalmente sustituido, SO2alquilo opcionalmente sustituido, SO2NR5R6, NR5CONR5R6, Coalquilo, 2H-tetrazol-5-il-metilo, heterociclo bicíclico opcionalmente sustituido o heterociclilo opcionalmente sustituido; R2a y R2b representan independientemente hidrógeno, halógeno, alquilo opcionalmente sustituido, alcoxi opcionalmente sustituido, CN, SO2alquilo, SR5, NO2, arilo opcionalmente sustituido, CONR5R6 o heteroarilo opcionalmente sustituido; Rx representa alquilo opcionalmente sustituido en el que 1 ó 2 de los átomos de carbono no terminales se sustituyen opcionalmente por un grupo independientemente seleccionado de NR4, O y Som, en el que n es 0, 1 ó 2; o Rx representa CQaQb-heterociclilo opcionalmente sustituido, CQaQb-heterociclilo bicíclico opcionalmente sustituido; R5 representa hidrógeno o un alquilo opcionalmente sustituido; R6 representa hidrógeno o alquilo opcionalmente sustituido, heteroarilo opcionalmente sustituido, SO2arilo opcionalmente sustituido, SO2alquilo opcionalmente sustituido, SO2heteroarilo opcionalmente sustituido, CN, CQaQbarilo opcionalmente sustituido, CQaQbheteroarilo opcionalmente sustituido o COR7; R7 representa hidrógeno, alquilo opcionalmente sustituido, heteroarilo opcionalmente sustituido o arilo opcionalmente sustituido; R8 y R9 representan independientemente hidrógeno, cloro, flúor, CF3, alcoxi C1-3 o alquilo C1-3; Qa y Qb se seleccionan independientemente de hidrógeno y CH3; en la que cuando A es un anillo de 6 miembros, el sustituyente R1 y el anillo de fenilo están unidos a los átomos de carbono 1,2- 1,3- o 1,4- uno respecto a otro, y cuando A es un anillo de cinco miembros o grupo heterociclilo bicíclico, el sustituyente R1 y el anillo de fenilo están unidos a los átomos de carbono sustituibles, 1,2- o 1,3- uno respecto a otro; y sus derivados; con la condición de que el compuesto no sea el ácido 2-benciloxi[1,1';2',1'']terfenil-4''-carboxílico. Un procedimiento para preparar dichos compuestos, composiciones farmacéuticas que los comprenden, y el uso de dichos compuestos de fórmula (1) para preparar medicamentos de utilidad para tratar a un sujeto humano o animal que padece un estado que es mediado por la acción de la PGE2 en los receptores de Ep1. Los estados mencionados pueden ser un dolor, o un trastorno inflamatorio, inmunológico, óseo, neurodegenerativo o renal.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GBGB0225548.7A GB0225548D0 (en) | 2002-11-01 | 2002-11-01 | Compounds |
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| AR041875A1 true AR041875A1 (es) | 2005-06-01 |
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
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| ARP030103972A AR041875A1 (es) | 2002-11-01 | 2003-10-30 | Compuesto de fenilo, composicion farmaceutica que lo comprende, su uso para preparar un medicamento y procedimiento para preparar dicho compuesto |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US7446222B2 (es) |
| EP (1) | EP1556330A2 (es) |
| JP (1) | JP2006504767A (es) |
| AR (1) | AR041875A1 (es) |
| AU (1) | AU2003287979A1 (es) |
| GB (1) | GB0225548D0 (es) |
| TW (1) | TW200503998A (es) |
| WO (1) | WO2004039753A2 (es) |
Families Citing this family (30)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB0225548D0 (en) | 2002-11-01 | 2002-12-11 | Glaxo Group Ltd | Compounds |
| US20070043512A1 (en) * | 2003-03-26 | 2007-02-22 | Michael Rolph | Therapeutic and prophylactic compositions and uses therefor |
| DE602004011966T2 (de) * | 2003-10-24 | 2009-02-12 | Glaxo Group Ltd., Greenford | Heterocyclylverbindungen |
| GB0410121D0 (en) * | 2004-05-06 | 2004-06-09 | Glaxo Group Ltd | Compounds |
| GB0416508D0 (en) * | 2004-07-23 | 2004-08-25 | Merck Sharp & Dohme | Therapeutic agents |
| EA200801909A1 (ru) | 2004-12-23 | 2009-06-30 | Глэксо Груп Лимитед | Соединения пиридина для лечения заболеваний, опосредованных действием простагландина |
| ES2259909B1 (es) * | 2005-02-28 | 2007-06-16 | Inke, S.A. | Procedimiento para la obtencion de un compuesto farmaceuticamente activo y de su intermedio de sintesis. |
| EP1868980B1 (en) * | 2005-04-08 | 2010-07-28 | Galderma Research & Development | New method for the preparation of 6-(3-(1-adamantyl)-4-methoxphenyl)-2-naphthoic acid |
| WO2009110985A2 (en) | 2008-02-29 | 2009-09-11 | Renovis, Inc. | Amide compounds, compositions and uses thereof |
| JPWO2009151069A1 (ja) | 2008-06-12 | 2011-11-17 | 第一三共株式会社 | 4,7−ジアザスピロ[2.5]オクタン環構造を有するイミダゾチアゾール誘導体 |
| CA2728095A1 (en) | 2008-07-17 | 2010-01-21 | Asahi Kasei Pharma Corporation | Pyrazole-containing tricyclic compounds as antagonists of an ep1 receptor |
| EP2298767A4 (en) * | 2008-07-17 | 2011-10-19 | Asahi Kasei Pharma Corp | NITROGENATED BICYCLIC AND HETEROCYCLIC COMPOUND |
| EP2570125A1 (en) * | 2011-09-16 | 2013-03-20 | Almirall, S.A. | Ep1 receptor ligands |
| SMT202000540T1 (it) | 2014-10-06 | 2020-11-10 | Vertex Pharma | Modulatori di regolatore di conduttanza transmembrana di fibrosi cistica |
| US10738030B2 (en) | 2016-03-31 | 2020-08-11 | Vertex Pharmaceuticals Incorporated | Modulators of cystic fibrosis transmembrane conductance regulator |
| JOP20190042B1 (ar) | 2016-09-30 | 2021-08-17 | Vertex Pharma | مُعدِّل لمنظم موصلية التليف الكيسي عبر الغشاء، وتركيبات صيدلانية، وطرق للعلاج، وعملية لتصنيع المُعدِّل |
| UY37513A (es) | 2016-12-09 | 2018-07-31 | Vertex Pharma | Modulador del regulador de conductancia transmembrana de fibrosis quística, composiciones farmacéuticas, métodos de tratamiento y proceso para producir el modulador |
| US11253509B2 (en) | 2017-06-08 | 2022-02-22 | Vertex Pharmaceuticals Incorporated | Methods of treatment for cystic fibrosis |
| BR112020000941A2 (pt) | 2017-07-17 | 2020-07-21 | Vertex Pharmaceuticals Incorporated | métodos de tratamento para fibrose cística |
| AU2018309043B2 (en) | 2017-08-02 | 2022-03-31 | Vertex Pharmaceuticals Incorporated | Processes for preparing pyrrolidine compounds |
| CA3078893A1 (en) | 2017-10-19 | 2019-04-25 | Vertex Pharmaceuticals Incorporated | Crystalline forms and compositions of cftr modulators |
| US11465985B2 (en) | 2017-12-08 | 2022-10-11 | Vertex Pharmaceuticals Incorporated | Processes for making modulators of cystic fibrosis transmembrane conductance regulator |
| KR20250086795A (ko) * | 2017-12-15 | 2025-06-13 | 메르크 파텐트 게엠베하 | 유기 전계 발광 디바이스용 치환된 방향족 아민 |
| TWI810243B (zh) | 2018-02-05 | 2023-08-01 | 美商維泰克斯製藥公司 | 用於治療囊腫纖化症之醫藥組合物 |
| CN108314656B (zh) | 2018-02-27 | 2020-10-27 | 浙江工业大学 | 不饱和烃嘧啶硫醚类化合物及其制备方法与应用 |
| EP3774825A1 (en) | 2018-04-13 | 2021-02-17 | Vertex Pharmaceuticals Incorporated | Modulators of cystic fibrosis transmembrane conductance regulator, pharmaceutical compositions, methods of treatment, and process for making the modulator |
| US11654996B2 (en) | 2018-04-27 | 2023-05-23 | FUELL Inc. | Electric saddle type vehicle |
| US11753101B2 (en) | 2018-04-27 | 2023-09-12 | FUELL Inc. | Electric saddle type vehicle with storage areas |
| US11299229B2 (en) | 2018-04-27 | 2022-04-12 | FUELL Inc. | Electric saddle type vehicle chassis |
| CN115466195B (zh) * | 2022-09-15 | 2024-04-19 | 中国科学院成都生物研究所 | 一类联苯类酰胺化合物及其制备方法和应用 |
Family Cites Families (110)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BE611179A (es) | ||||
| AR206796A1 (es) | 1973-02-19 | 1976-08-23 | Ciba Geigy Ag | Procedimiento para la elaboracion de nuevos compuestos derivados de cicloalquil-fenilalcanoilpiridinas |
| DE3042769A1 (de) | 1980-11-13 | 1982-06-09 | Bayer Ag, 5090 Leverkusen | C-3 verknuepfte 1,4-dihydropyridine, ihre verwendung in arzneimitteln und verfahren zu ihrer herstellung |
| US4581370A (en) | 1983-07-12 | 1986-04-08 | Schering A.G. | Antiarrhythmic imidazoliums |
| US5663180A (en) * | 1983-10-29 | 1997-09-02 | G.D. Searle & Co. | Substituted cyclopentenes for the treatment of inflammation |
| EP0733366B1 (en) | 1988-01-07 | 1998-04-01 | E.I. Du Pont De Nemours And Company | Pharmaceutical compositions comprising angiotensin II receptor blocking imidazoles and diuretics |
| CA2079343A1 (en) | 1990-03-30 | 1991-10-01 | Eric E. Allen | Substituted pyrazoles, isoxazoles and isothiazoles |
| JP3064343B2 (ja) | 1990-07-17 | 2000-07-12 | 東レ株式会社 | フォトクロミック材料 |
| GB9017480D0 (en) | 1990-08-09 | 1990-09-26 | Ici Plc | Chemical process |
| WO1992002257A2 (en) | 1990-08-10 | 1992-02-20 | G.D. Searle & Co. | Renal-selective angiotensin ii antagonists for treatment of hypertension |
| DE4032522A1 (de) | 1990-10-11 | 1992-04-16 | Schering Ag | Neue thienoimidazolderivate, verfahren zu ihrer herstellung und ihre phamazeutische verwendung |
| US5470975A (en) * | 1990-10-16 | 1995-11-28 | E.R. Squibb & Sons, Inc. | Dihydropyrimidine derivatives |
| DE4034728A1 (de) | 1990-10-30 | 1992-05-07 | Schering Ag | Neue thienoimidazolderivate, verfahren zu ihrer herstellung und ihre pharmazeutische verwendung |
| JPH04235933A (ja) | 1991-01-18 | 1992-08-25 | Fuji Photo Film Co Ltd | 1−m−ヒドロキシアリール−1−シクロアルケン |
| IE920175A1 (en) | 1991-02-11 | 1992-08-12 | Zeneca Ltd | Nitrogen heterocycles |
| GB9102803D0 (en) | 1991-02-11 | 1991-03-27 | Ici Plc | Pyridine compounds |
| EP0584222B1 (en) | 1991-05-10 | 1997-10-08 | Rhone-Poulenc Rorer International (Holdings) Inc. | Bis mono-and bicyclic aryl and heteroaryl compounds which inhibit egf and/or pdgf receptor tyrosine kinase |
| CZ36394A3 (en) | 1991-08-19 | 1994-07-13 | Du Pont | Substituted imidazilonone derivatives and pharmaceutical preparations based thereon |
| AU2496492A (en) | 1991-08-19 | 1993-03-16 | E.I. Du Pont De Nemours And Company | Angiotensin ii receptor blocking imidazolinone derivatives |
| CA2081507C (en) | 1991-10-30 | 2004-04-06 | Shun-Ichi Murahashi | Process for producing epoxide |
| JPH05224442A (ja) | 1992-02-12 | 1993-09-03 | Kao Corp | 電子写真感光体 |
| US5219856A (en) * | 1992-04-06 | 1993-06-15 | E. I. Du Pont De Nemours And Company | Angiotensin-II receptor blocking, heterocycle substituted imidazoles |
| US6048859A (en) * | 1992-06-29 | 2000-04-11 | Merck & Co., Inc. | Morpholine and thiomorpholine tachykinin receptor antagonists |
| US5232945A (en) * | 1992-07-20 | 1993-08-03 | Pfizer Inc. | 3-aryl-2-hydroxypropionic acid derivatives and analogs as antihypertensives |
| JPH0665213A (ja) | 1992-08-18 | 1994-03-08 | Nippon Soda Co Ltd | ジシアノピラジン誘導体及びその製造方法 |
| US5428060A (en) | 1992-08-27 | 1995-06-27 | Merck Frosst Canada, Inc. | Heteroarylnaphthalene lactones as inhibitors of leukotriene biosynthesis |
| GB2272899A (en) | 1992-11-30 | 1994-06-01 | Du Pont Merck Pharma | Angiotensin-11 receptor blocking cycloalkylbenzylimidazoles |
| GB9420616D0 (en) | 1994-10-12 | 1994-11-30 | Merck Sharp & Dohme | Method, compositions and use |
| US6613804B2 (en) * | 1993-05-20 | 2003-09-02 | Encysive Pharmaceuticals, Inc. | Biphenylsulfonamides and derivatives thereof that modulate the activity of endothelin |
| US5840746A (en) * | 1993-06-24 | 1998-11-24 | Merck Frosst Canada, Inc. | Use of inhibitors of cyclooxygenase in the treatment of neurodegenerative diseases |
| US5474995A (en) * | 1993-06-24 | 1995-12-12 | Merck Frosst Canada, Inc. | Phenyl heterocycles as cox-2 inhibitors |
| WO1995005372A1 (en) | 1993-08-13 | 1995-02-23 | Banyu Pharmaceutical Co., Ltd. | Endothelin-antagonistic cyclopentane derivative |
| FR2711140B1 (fr) | 1993-10-12 | 1996-01-05 | Sanofi Sa | 1-Naphtylpyrazole-3-carboxamides substitués actifs sur la neurotensine, leur préparation, les compositions pharmaceutiques en contenant. |
| US5344991A (en) * | 1993-10-29 | 1994-09-06 | G.D. Searle & Co. | 1,2 diarylcyclopentenyl compounds for the treatment of inflammation |
| US6492411B1 (en) * | 1993-11-30 | 2002-12-10 | G. D. Searle & Co. | Substituted pyrazolyl benzenesulfonamides for the treatment of inflammation |
| DK0736018T3 (da) | 1993-12-20 | 2000-09-18 | Fujisawa Pharmaceutical Co | 4,5-Diaryloxazolderivater |
| DE4407488A1 (de) | 1994-03-07 | 1995-09-14 | Bayer Ag | Verwendung von Biphenyl- und Pyridylmethylpyridonen |
| GB9406573D0 (en) | 1994-03-31 | 1994-05-25 | Merck Sharp & Dohme | Medicaments |
| WO1995027692A1 (en) | 1994-04-08 | 1995-10-19 | Smithkline Beecham Corporation | Subtituted biphenyl tnf inhibitors |
| US5441946A (en) * | 1994-04-14 | 1995-08-15 | Rhone-Poulenc-Rorer Pharmaceuticals, Inc. | Phosphonate derivatives of lipophilic amines |
| US20010020100A1 (en) * | 1994-06-14 | 2001-09-06 | G.D. Searle & Co. | N-substituted-1, 2, 4-triazolone compounds for treatment of cardiovascular disorders |
| DE4430213A1 (de) * | 1994-08-28 | 1996-02-29 | Merck Patent Gmbh | Arylbenzoylguanidine |
| US5563143A (en) | 1994-09-21 | 1996-10-08 | Pfizer Inc. | Catechol diether compounds as inhibitors of TNF release |
| US5593994A (en) | 1994-09-29 | 1997-01-14 | The Dupont Merck Pharmaceutical Company | Prostaglandin synthase inhibitors |
| GB9420557D0 (en) * | 1994-10-12 | 1994-11-30 | Zeneca Ltd | Aromatic compounds |
| DE69524528T2 (de) | 1994-10-14 | 2002-08-01 | Merck Patent Gmbh | ZNS wirksames (R)-(-)-2-[5-(4-Fluorophenyl)-3-pyridylmethylaminomethyl]chroman |
| US5739166A (en) | 1994-11-29 | 1998-04-14 | G.D. Searle & Co. | Substituted terphenyl compounds for the treatment of inflammation |
| FR2732967B1 (fr) * | 1995-04-11 | 1997-07-04 | Sanofi Sa | 1-phenylpyrazole-3-carboxamides substitues, actifs sur la neurotensine, leur preparation, les compositions pharmaceutiques en contenant |
| US5691374A (en) | 1995-05-18 | 1997-11-25 | Merck Frosst Canada Inc. | Diaryl-5-oxygenated-2-(5H) -furanones as COX-2 inhibitors |
| GB9510716D0 (en) | 1995-05-26 | 1995-07-19 | Pharmacia Spa | Substituted camptothecin derivatives and process for their preparation |
| EP0833664A1 (en) * | 1995-06-12 | 1998-04-08 | G.D. SEARLE & CO. | Combination of a cyclooxygenase-2 inhibitor and a leukotriene b 4? receptor antagonist for the treatment of inflammations |
| ES2247604T3 (es) * | 1995-06-12 | 2006-03-01 | G.D. SEARLE & CO. | Composiciones que comprenden un inhibidor de ciclooxigenasa-2 y un inhibidor de 5-lipoxigenasa. |
| DE69635254T2 (de) | 1995-07-07 | 2006-07-13 | Astrazeneca Ab | Ortho-substituierte aromatische Verbindungen, die drei (Het)aryl-Ringe enthalten, deren Herstellung und deren Verwendung als Prostaglandin-E2-(PGE2)-Antagonisten |
| HU225506B1 (en) | 1995-07-19 | 2007-01-29 | Merck & Co Inc | Use of 4-(4-methylsulfonyl-phenyl)-3-phenyl-2-(5h)-furanone for the preparation of medicaments treating colonic adenomas |
| US6593361B2 (en) * | 1995-07-19 | 2003-07-15 | Merck & Co Inc | Method of treating colonic adenomas |
| US5846990A (en) | 1995-07-24 | 1998-12-08 | Bristol-Myers Squibb Co. | Substituted biphenyl isoxazole sulfonamides |
| EP0783502A1 (en) | 1995-08-02 | 1997-07-16 | J. URIACH & CIA. S.A. | New carboxamides with antifungal activity |
| EP0853481A1 (en) | 1995-09-27 | 1998-07-22 | Merck Frosst Canada Inc. | Compositions for treating inflammation containing certain prostaglandins and a selective cyclooxygenase-2 inhibitor |
| JP3337477B2 (ja) | 1995-10-30 | 2002-10-21 | メルク フロスト カナダ アンド カンパニー | Cox−2阻害剤のプロドラッグとしての3,4−ジアリール−2−ヒドロキシ−2,5−ジヒドロフラン |
| DE19612101A1 (de) | 1996-03-27 | 1997-10-02 | Merck Patent Gmbh | Endothelin-Rezeptor-Antagonisten |
| US5908858A (en) | 1996-04-05 | 1999-06-01 | Sankyo Company, Limited | 1,2-diphenylpyrrole derivatives, their preparation and their therapeutic uses |
| TR199802049T2 (xx) | 1996-04-12 | 1999-01-18 | G.D.Searle & Co. | COX-2 Inhibit�rlerinin �nilac� olarak s�bstit�e edilmi� benzens�lfonamid t�revleri. |
| DE69738815D1 (de) | 1996-10-15 | 2008-08-14 | Searle Llc | Verwendung von Cyclooxygenase-2 Inhibitoren zur Behandlung und Vorbeugung von Neoplasia |
| US5935990A (en) | 1996-12-10 | 1999-08-10 | G.D. Searle & Co. | Substituted pyrrolyl compounds for the treatment of inflammation |
| WO1998028257A1 (en) | 1996-12-24 | 1998-07-02 | Chugai Seiyaku Kabushiki Kaisha | Aromatic amine derivatives having nos inhibitory effect |
| AUPO713297A0 (en) | 1997-06-02 | 1997-06-26 | Fujisawa Pharmaceutical Co., Ltd. | Oxazole compound |
| CA2306077A1 (en) | 1997-10-08 | 1999-04-15 | Smithkline Beecham Corporation | Novel cycloalkenyl substituted compounds |
| US5972986A (en) * | 1997-10-14 | 1999-10-26 | G.D. Searle & Co. | Method of using cyclooxygenase-2 inhibitors in the treatment and prevention of neoplasia |
| US6433012B1 (en) | 1998-03-25 | 2002-08-13 | Large Scale Biology Corp. | Method for inhibiting inflammatory disease |
| DE19813354A1 (de) * | 1998-03-26 | 1999-09-30 | Bayer Ag | Arylphenylsubstituierte cyclische Ketoenole |
| DE19818732A1 (de) * | 1998-04-27 | 1999-10-28 | Bayer Ag | Arylphenylsubstituierte cyclische Ketoenole |
| WO1999058487A1 (en) | 1998-05-11 | 1999-11-18 | Novo Nordisk A/S | New compounds, their preparation and use |
| CA2336691C (en) | 1998-07-10 | 2009-02-10 | Massachusetts Institute Of Technology | Ligands for metals and metal-catalyzed processes |
| DE19836470A1 (de) * | 1998-08-12 | 2000-02-17 | Clariant Gmbh | Verfahren zur Herstellung von 4-Chlorbiphenylen |
| EP1159264A2 (en) | 1999-02-11 | 2001-12-05 | Cor Therapeutics, Inc. | INHIBITORS OF FACTOR Xa |
| ATE306263T1 (de) | 1999-03-10 | 2005-10-15 | Searle Llc | Zusammensetzungen zur verabreichung eines cyclooxygenase-2-hemmers an tiere |
| US6548529B1 (en) | 1999-04-05 | 2003-04-15 | Bristol-Myers Squibb Company | Heterocyclic containing biphenyl aP2 inhibitors and method |
| CN1378446A (zh) | 1999-06-10 | 2002-11-06 | 华纳一兰伯特公司 | 抑制淀粉样蛋白聚集和使淀粉样沉积物成象的方法 |
| ATE259795T1 (de) * | 1999-09-14 | 2004-03-15 | Merck Frosst Canada Inc | Carbonsäuren und acylsulfonamide, solche verbindungen enthaltende zubereitungen und behandlungsmethoden |
| DE19945302A1 (de) | 1999-09-22 | 2001-03-29 | Merck Patent Gmbh | Biphenylderivate als NHE-3-Inhibitoren |
| WO2001055146A1 (en) | 2000-01-29 | 2001-08-02 | Lg Chem Investment Ltd. | FACTOR Xa INHIBITORS WITH ARYL-AMIDINES AND DERIVATIVES, AND PRODRUGS THEREOF |
| US6605615B2 (en) | 2000-03-01 | 2003-08-12 | Tularik Inc. | Hydrazones and analogs as cholesterol lowering agents |
| ES2159489B1 (es) | 2000-03-23 | 2002-04-16 | Uriach & Cia Sa J | Nuevos derivados de imidazol con actividad antiinflamatoria. |
| JP2003531201A (ja) | 2000-04-25 | 2003-10-21 | ファルマシア・コーポレーション | 炎症を治療するための2−フルオロベンゼンスルホニル化合物 |
| FR2812876B1 (fr) | 2000-08-08 | 2002-09-27 | Galderma Res & Dev | Nouveaux composes bi-aromatiques activateurs des recepteurs de type ppar-gamma et leur utilisation dans des compositions cosmetiques ou pharmaceutiques |
| AU2002215155A1 (en) | 2000-12-20 | 2002-07-01 | Warner-Lambert Company Llc | Non-halogenated phenyl substituted phenols, antimicrobial compositions containing the same, and methods of using the same |
| JP2002275064A (ja) | 2001-01-15 | 2002-09-25 | Sankyo Co Ltd | クロマン類縁体を含有する医薬 |
| ITMI20010733A1 (it) * | 2001-04-05 | 2002-10-05 | Recordati Chem Pharm | Uso di inibitori dell'isoenzina cox-2 per il trattamento dell'incontinenza urinaria |
| US6673818B2 (en) | 2001-04-20 | 2004-01-06 | Pharmacia Corporation | Fluoro-substituted benzenesulfonyl compounds for the treatment of inflammation |
| EP1264847A1 (fr) | 2001-06-06 | 2002-12-11 | SOLVAY POLYOLEFINS EUROPE - BELGIUM (Société Anonyme) | Procédé pour la polymérisation des alpha-oléfines |
| US7163803B2 (en) | 2001-06-07 | 2007-01-16 | Electrophoretics Limited | Method for characterizing polypeptides |
| JP3965028B2 (ja) | 2001-06-08 | 2007-08-22 | 大日本印刷株式会社 | 酸化珪素膜の製造方法 |
| HRP20031096A2 (en) | 2001-06-12 | 2005-08-31 | Neurogen Corporation | 2,5-diarylpyrazines, 2,5-diarylpyridines and 2,5-diarylpyrimidines as crf1 receptor modulators |
| US6608216B2 (en) * | 2001-06-29 | 2003-08-19 | Abbott Laboratories | Process for the preparation of chiral glucocorticoid receptor agents |
| WO2003002548A1 (en) | 2001-06-29 | 2003-01-09 | Abbott Laboratories | A process for the preparation of chiral glucocorticoid receptor agents |
| EP1578898A2 (en) | 2001-07-13 | 2005-09-28 | Virtual Drug Development, Inc. | Nad synthetase inhibitors and uses thereof |
| DE10135466A1 (de) | 2001-07-20 | 2003-02-06 | Bayer Cropscience Ag | Biphenylsubstituierte 4-Hydroxy-chinolone |
| US6495149B1 (en) * | 2001-08-10 | 2002-12-17 | The Procter & Gamble Company | Topical leave-on compositions containing selected pantothenic acid derivatives |
| DE10143353A1 (de) | 2001-09-04 | 2003-03-20 | Covion Organic Semiconductors | Konjugierte Polymere enthaltend Spirobifluoren-Einheiten und deren Verwendung |
| DE60219746T2 (de) | 2001-11-19 | 2008-01-17 | Sumitomo Chemical Co., Ltd. | Verfahren zur Herstellung von Biarylverbindungen |
| US6660876B2 (en) | 2001-11-26 | 2003-12-09 | E. I. Du Pont De Nemours And Company | Phosphorus-containing compositions and their use in hydrocyanation, isomerization and hydroformylation reactions |
| KR20050044696A (ko) | 2001-12-05 | 2005-05-12 | 시바 스페셜티 케미칼스 홀딩 인크. | 유기 용매없이 2-(2-니트로페닐아조)페놀을 제조하는 방법 |
| US6774248B2 (en) | 2001-12-18 | 2004-08-10 | Wyeth | Substituted 2-phenyl benzofurans as estrogenic agents |
| MXPA04005999A (es) | 2001-12-21 | 2005-07-13 | Taisho Pharma Co Ltd | Derivado de piperazina. |
| JP2003192659A (ja) | 2001-12-26 | 2003-07-09 | Bayer Ag | フェニル尿素誘導体 |
| TW200408621A (en) * | 2002-04-08 | 2004-06-01 | Glaxo Group Ltd | Compounds |
| GB0212785D0 (en) | 2002-05-31 | 2002-07-10 | Glaxo Group Ltd | Compounds |
| DE20211496U1 (de) | 2002-07-13 | 2002-10-10 | Wella Ag, 64295 Darmstadt | Mittel zum Färben von Keratinfasern |
| GB0225548D0 (en) | 2002-11-01 | 2002-12-11 | Glaxo Group Ltd | Compounds |
| GB0306329D0 (en) | 2003-03-19 | 2003-04-23 | Glaxo Group Ltd | Compounds |
-
2002
- 2002-11-01 GB GBGB0225548.7A patent/GB0225548D0/en not_active Ceased
-
2003
- 2003-10-30 AR ARP030103972A patent/AR041875A1/es not_active Application Discontinuation
- 2003-10-30 EP EP03779828A patent/EP1556330A2/en not_active Withdrawn
- 2003-10-30 US US10/533,036 patent/US7446222B2/en not_active Expired - Fee Related
- 2003-10-30 JP JP2004547644A patent/JP2006504767A/ja not_active Withdrawn
- 2003-10-30 WO PCT/EP2003/012181 patent/WO2004039753A2/en not_active Ceased
- 2003-10-30 TW TW092130184A patent/TW200503998A/zh unknown
- 2003-10-30 AU AU2003287979A patent/AU2003287979A1/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| TW200503998A (en) | 2005-02-01 |
| AU2003287979A1 (en) | 2004-05-25 |
| WO2004039753A2 (en) | 2004-05-13 |
| GB0225548D0 (en) | 2002-12-11 |
| EP1556330A2 (en) | 2005-07-27 |
| US20060235057A1 (en) | 2006-10-19 |
| AU2003287979A8 (en) | 2004-05-25 |
| JP2006504767A (ja) | 2006-02-09 |
| WO2004039753A3 (en) | 2004-07-15 |
| US7446222B2 (en) | 2008-11-04 |
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