AR049578A1 - Derivados de hidantoina, procesos de obtencion y composiciones farmaceuticas - Google Patents
Derivados de hidantoina, procesos de obtencion y composiciones farmaceuticasInfo
- Publication number
- AR049578A1 AR049578A1 ARP050102793A ARP050102793A AR049578A1 AR 049578 A1 AR049578 A1 AR 049578A1 AR P050102793 A ARP050102793 A AR P050102793A AR P050102793 A ARP050102793 A AR P050102793A AR 049578 A1 AR049578 A1 AR 049578A1
- Authority
- AR
- Argentina
- Prior art keywords
- pharmaceutical compositions
- hydantoin derivatives
- alkyl
- obtaining processes
- obtaining
- Prior art date
Links
- 229940053195 antiepileptics hydantoin derivative Drugs 0.000 title abstract 3
- 238000000034 method Methods 0.000 title abstract 3
- 239000008194 pharmaceutical composition Substances 0.000 title abstract 3
- WJRBRSLFGCUECM-UHFFFAOYSA-N hydantoin Chemical class O=C1CNC(=O)N1 WJRBRSLFGCUECM-UHFFFAOYSA-N 0.000 title 1
- 125000000217 alkyl group Chemical group 0.000 abstract 3
- 150000001875 compounds Chemical class 0.000 abstract 2
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 abstract 2
- 150000001469 hydantoins Chemical class 0.000 abstract 2
- 102000002013 Transforming Protein 3 Src Homology 2 Domain-Containing Human genes 0.000 abstract 1
- 108010040633 Transforming Protein 3 Src Homology 2 Domain-Containing Proteins 0.000 abstract 1
- 125000001153 fluoro group Chemical group F* 0.000 abstract 1
- 239000003475 metalloproteinase inhibitor Substances 0.000 abstract 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 abstract 1
Classifications
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/06—Antiasthmatics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/08—Bronchodilators
-
- 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
- A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
-
- 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
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Engineering & Computer Science (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pulmonology (AREA)
- Immunology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Rheumatology (AREA)
- Physical Education & Sports Medicine (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Derivados de hidantoína, procesos de obtencion y composiciones farmacéuticas. Los compuestos pertenecen a la categoría de derivados de hidantoína utilizados como inhibidores de metaloproteinasa. Procedimientos de obtencion de los mismos. Composiciones farmacéuticas que los contienen. Reivindicacion 1: Un compuesto caracterizado porque responde a la formula (1) o una sal de éste aceptable para el uso farmacéutico, donde R1 representa C1 a 2 alquilo, ciclopropilo, OCH3, SHC3 o OCF3; donde dicho grupo alquilo o ciclopropilo está opcionalmente sustituido adicionalmente con uno o más átomos de fluor; y R2 representa C1 a 3 alquilo.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| SE0401762A SE0401762D0 (sv) | 2004-07-05 | 2004-07-05 | Novel compounds |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR049578A1 true AR049578A1 (es) | 2006-08-16 |
Family
ID=32768773
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP050102793A AR049578A1 (es) | 2004-07-05 | 2005-07-05 | Derivados de hidantoina, procesos de obtencion y composiciones farmaceuticas |
Country Status (32)
| Country | Link |
|---|---|
| US (1) | US7989620B2 (es) |
| EP (1) | EP1778673B1 (es) |
| JP (1) | JP4390833B2 (es) |
| KR (1) | KR101222736B1 (es) |
| CN (1) | CN100543024C (es) |
| AR (1) | AR049578A1 (es) |
| AT (1) | ATE448219T1 (es) |
| AU (1) | AU2005260142B2 (es) |
| BR (1) | BRPI0512974A (es) |
| CA (1) | CA2569716C (es) |
| CY (1) | CY1109728T1 (es) |
| DE (1) | DE602005017636D1 (es) |
| DK (1) | DK1778673T3 (es) |
| ES (1) | ES2335424T3 (es) |
| HR (1) | HRP20100020T1 (es) |
| IL (1) | IL179906A (es) |
| MX (1) | MXPA06014661A (es) |
| MY (1) | MY145613A (es) |
| NO (1) | NO20070576L (es) |
| NZ (1) | NZ552101A (es) |
| PL (1) | PL1778673T3 (es) |
| PT (1) | PT1778673E (es) |
| RS (1) | RS51280B (es) |
| RU (1) | RU2386629C2 (es) |
| SA (1) | SA05260192B1 (es) |
| SE (1) | SE0401762D0 (es) |
| SI (1) | SI1778673T1 (es) |
| TW (1) | TWI353985B (es) |
| UA (1) | UA86977C2 (es) |
| UY (1) | UY29002A1 (es) |
| WO (1) | WO2006004532A1 (es) |
| ZA (1) | ZA200610698B (es) |
Families Citing this family (28)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| SE0100902D0 (sv) | 2001-03-15 | 2001-03-15 | Astrazeneca Ab | Compounds |
| SE0202539D0 (sv) | 2002-08-27 | 2002-08-27 | Astrazeneca Ab | Compounds |
| SE0401763D0 (sv) * | 2004-07-05 | 2004-07-05 | Astrazeneca Ab | Compounds |
| US7648992B2 (en) | 2004-07-05 | 2010-01-19 | Astrazeneca Ab | Hydantoin derivatives for the treatment of obstructive airway diseases |
| SE0401762D0 (sv) | 2004-07-05 | 2004-07-05 | Astrazeneca Ab | Novel compounds |
| US7776869B2 (en) * | 2004-10-18 | 2010-08-17 | Amgen Inc. | Heteroaryl-substituted alkyne compounds and method of use |
| SE0403086D0 (sv) | 2004-12-17 | 2004-12-17 | Astrazeneca Ab | Compounds |
| SE0403085D0 (sv) | 2004-12-17 | 2004-12-17 | Astrazeneca Ab | Novel componds |
| TW200740769A (en) | 2006-03-16 | 2007-11-01 | Astrazeneca Ab | Novel process |
| TW200831488A (en) * | 2006-11-29 | 2008-08-01 | Astrazeneca Ab | Novel compounds |
| GB0702456D0 (en) | 2007-02-08 | 2007-03-21 | Astrazeneca Ab | New combination |
| WO2009007747A2 (en) * | 2007-07-11 | 2009-01-15 | Astrazeneca Ab | Hydantoin derivatives used as mmp12 inhibitors |
| GB0913345D0 (en) | 2009-07-31 | 2009-09-16 | Astrazeneca Ab | New combination 802 |
| WO2011061527A1 (en) | 2009-11-17 | 2011-05-26 | Astrazeneca Ab | Combinations comprising a glucocorticoid receptor modulator for the treatment of respiratory diseases |
| WO2011073662A1 (en) | 2009-12-17 | 2011-06-23 | Astrazeneca Ab | Combination of a benzoxazinone and a further agent for treating respiratory diseases |
| GB201021979D0 (en) | 2010-12-23 | 2011-02-02 | Astrazeneca Ab | New compound |
| GB201021992D0 (en) | 2010-12-23 | 2011-02-02 | Astrazeneca Ab | Compound |
| EP2907512A1 (en) | 2014-02-14 | 2015-08-19 | Commissariat A L'energie Atomique Et Aux Energies Alternatives | Inhibitors of MMP-12 as antiviral Agents |
| RU2555341C1 (ru) * | 2014-04-29 | 2015-07-10 | Федеральное бюджетное учреждение науки "Федеральный научный центр медико-профилактических технологий управления рисками здоровью населения" (ФБУН "ФНЦ медико-профилактических технологий управления рисками здоровью населения") | Способ профилактики развития у детей старше 5 лет неконтролируемых форм бронхиальной астмы, обусловленных воздействием марганца и ванадия |
| WO2016120355A2 (en) * | 2015-01-30 | 2016-08-04 | Basf Se | Herbicidal phenylpyrimidines |
| CN109561685A (zh) | 2016-07-25 | 2019-04-02 | 巴斯夫欧洲公司 | 除草的嘧啶化合物 |
| EP3487848B1 (en) | 2016-07-25 | 2020-09-30 | Basf Se | Herbicidal pyrimidine compounds |
| AU2018283422A1 (en) | 2017-06-14 | 2019-12-19 | Basf Se | Herbicidal pyrimidine compounds |
| WO2019121408A1 (en) | 2017-12-20 | 2019-06-27 | Basf Se | Herbicidal pyrimidine compounds |
| CA3104246A1 (en) | 2018-07-16 | 2020-01-23 | Heparegenix Gmbh | Protein kinase inhibitors for promoting liver regeneration or reducing or preventing hepatocyte death |
| JP7472109B2 (ja) | 2018-09-19 | 2024-04-22 | バイエル・アクチエンゲゼルシヤフト | 除草活性を有する置換フェニルピリミジンヒドラジド類 |
| EP4171553A1 (en) * | 2020-06-26 | 2023-05-03 | The University Of Birmingham | Mmp-9 and mmp-12 inhibition for treating spinal cord injury or related injury to neurological tissue |
| GB202403774D0 (en) | 2024-03-15 | 2024-05-01 | Univ Sheffield | Treatment of stroke |
Family Cites Families (74)
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|---|---|---|---|---|
| US2327890A (en) | 1940-04-17 | 1943-08-24 | Parke Davis & Co | Substituted phenoxyalkyl ethers |
| US2745875A (en) | 1953-06-30 | 1956-05-15 | Hoechst Ag | Preparation of nu-acylamino-phenylpropane diols |
| US3452040A (en) | 1966-01-05 | 1969-06-24 | American Home Prod | 5,5-disubstituted hydantoins |
| US3529019A (en) | 1968-04-23 | 1970-09-15 | Colgate Palmolive Co | Alkylaryloxy alanines |
| US3849574A (en) | 1971-05-24 | 1974-11-19 | Colgate Palmolive Co | Alpha-substituted-beta-arylthioalkyl amino-acids,for increasing heart rate |
| US4315031A (en) | 1977-09-01 | 1982-02-09 | Science Union Et Cie | Thiosubstituted amino acids |
| GB1601310A (en) | 1978-05-23 | 1981-10-28 | Lilly Industries Ltd | Aryl hydantoins |
| JPS6172762A (ja) | 1984-09-17 | 1986-04-14 | Kanegafuchi Chem Ind Co Ltd | 光学活性ヒダントイン類の製造法 |
| JPS61212292A (ja) | 1985-03-19 | 1986-09-20 | Mitsui Toatsu Chem Inc | D−α−アミノ酸の製造方法 |
| CA1325222C (en) | 1985-08-23 | 1993-12-14 | Lederle (Japan), Ltd. | Process for producing 4-biphenylylacetic acid |
| GB8618559D0 (en) | 1986-07-30 | 1986-09-10 | Genetics Int Inc | Rhodococcus bacterium |
| US4983771A (en) | 1989-09-18 | 1991-01-08 | Hexcel Corporation | Method for resolution of D,L-alpha-phenethylamine with D(-)mandelic acid |
| NL9000386A (nl) | 1990-02-16 | 1991-09-16 | Stamicarbon | Werkwijze voor de bereiding van optisch aktief aminozuuramide. |
| DK161690D0 (da) | 1990-07-05 | 1990-07-05 | Novo Nordisk As | Fremgangsmaade til fremstilling af enantiomere forbindelser |
| IL99957A0 (en) | 1990-11-13 | 1992-08-18 | Merck & Co Inc | Piperidinylcamphorsulfonyl oxytocin antagonists and pharmaceutical compositions containing them |
| PH31245A (en) | 1991-10-30 | 1998-06-18 | Janssen Pharmaceutica Nv | 1,3-Dihydro-2H-imidazoÄ4,5-BÜ-quinolin-2-one derivatives. |
| US5308853A (en) | 1991-12-20 | 1994-05-03 | Warner-Lambert Company | Substituted-5-methylidene hydantoins with AT1 receptor antagonist properties |
| US5246943A (en) | 1992-05-19 | 1993-09-21 | Warner-Lambert Company | Substituted 1,2,3,4-tetahydroisoquinolines with angiotensin II receptor antagonist properties |
| NL9201230A (nl) | 1992-07-09 | 1994-02-01 | Dsm Nv | Werkwijze voor de bereiding van optisch aktief methionineamide. |
| EP0640594A1 (en) | 1993-08-23 | 1995-03-01 | Fujirebio Inc. | Hydantoin derivative as metalloprotease inhibitor |
| AU687953B2 (en) | 1993-11-16 | 1998-03-05 | Merck & Co., Inc. | Piperidinylcamphorsulfonyl oxytocin antagonists |
| DE69534213T2 (de) | 1994-10-25 | 2006-01-12 | Astrazeneca Ab | Therapeutisch wirksame Heterocyclen |
| ZA96211B (en) | 1995-01-12 | 1996-07-26 | Teva Pharma | Compositions containing and methods of using 1- aminoindan and derivatives thereof and process for preparing optically active 1-aminoindan derivatives |
| US5863949A (en) | 1995-03-08 | 1999-01-26 | Pfizer Inc | Arylsulfonylamino hydroxamic acid derivatives |
| US6166041A (en) | 1995-10-11 | 2000-12-26 | Euro-Celtique, S.A. | 2-heteroaryl and 2-heterocyclic benzoxazoles as PDE IV inhibitors for the treatment of asthma |
| AU711907B2 (en) | 1995-11-22 | 1999-10-21 | Darwin Discovery Limited | Mercaptoalkylpeptidyl compounds having an imidazole substituent and their use as inhibitors of matrix metalloproteinases (MMP) and/or tumor necrosis factor (TNF) |
| GB9616643D0 (en) | 1996-08-08 | 1996-09-25 | Chiroscience Ltd | Compounds |
| US5919790A (en) | 1996-10-11 | 1999-07-06 | Warner-Lambert Company | Hydroxamate inhibitors of interleukin-1β converting enzyme |
| ATE212619T1 (de) | 1996-10-22 | 2002-02-15 | Upjohn Co | Alpha-amino sulfonyl hydroxamsäure als matrix metalloproteinase inhibitoren |
| HUP0003362A3 (en) | 1997-05-06 | 2001-04-28 | Novo Nordisk As | Piperidine derivatives and pharmaceutical compositions containing them |
| DE59802394D1 (de) | 1997-05-09 | 2002-01-24 | Hoechst Ag | Substituierte Diaminocarbonsäuren |
| BR9810760A (pt) | 1997-07-31 | 2001-11-27 | Abbott Lab | Inibidores de hidroxamato reverso demetaloproteinases de matriz |
| TW514634B (en) | 1997-10-14 | 2002-12-21 | Lilly Co Eli | Process to make chiral compounds |
| RU2210567C2 (ru) | 1997-11-12 | 2003-08-20 | Дарвин Дискавери Лимитед | Производные гидроксамовой и карбоновой кислоты, имеющие mmp ингибирующую активность, и фармацевтическая композиция на их основе |
| CN1195735C (zh) | 1998-02-04 | 2005-04-06 | 诺瓦提斯公司 | 抑制使基质退化的金属蛋白酶的磺酰氨基衍生物 |
| US6329418B1 (en) | 1998-04-14 | 2001-12-11 | The Procter & Gamble Company | Substituted pyrrolidine hydroxamate metalloprotease inhibitors |
| CA2330095A1 (en) | 1998-05-14 | 1999-11-18 | Dupont Pharmaceuticals Company | Substituted aryl hydroxamic acids as metalloproteinase inhibitors |
| CA2334002A1 (en) | 1998-06-03 | 1999-12-09 | Mark H. Norman | N-linked sulphonamides of n-heterocyclic carboxylic acids or carboxylic acid isosteres |
| US6429213B1 (en) | 1998-06-17 | 2002-08-06 | Bristol Myers Squibb Pharma Co | Cyclic hydroxamic acids as metalloproteinase inhibitors |
| FR2782082B3 (fr) | 1998-08-05 | 2000-09-22 | Sanofi Sa | Formes cristallines de (r)-(+)-n-[[3-[1-benzoyl-3-(3,4- dichlorophenyl)piperidin-3-yl]prop-1-yl]-4-phenylpiperidin-4 -yl]-n-methylacetamide (osanetant) et procede pour la preparation dudit compose |
| US6339101B1 (en) | 1998-08-14 | 2002-01-15 | Gpi Nil Holdings, Inc. | N-linked sulfonamides of N-heterocyclic carboxylic acids or isosteres for vision and memory disorders |
| JP2002526370A (ja) | 1998-10-07 | 2002-08-20 | 矢崎総業株式会社 | 多孔質型を用いたゾル・ゲル法 |
| DE69915004T2 (de) | 1998-11-05 | 2004-09-09 | Pfizer Products Inc., Groton | 5-Oxo-pyrrolidine-2-Carbonsäure-Hydroxamidderivate |
| US6340691B1 (en) | 1999-01-27 | 2002-01-22 | American Cyanamid Company | Alkynyl containing hydroxamic acid compounds as matrix metalloproteinase and tace inhibitors |
| WO2000044770A1 (en) | 1999-01-28 | 2000-08-03 | Chugai Seiyaku Kabushiki Kaisha | Substituted phenethylamine derivatives |
| US20020006920A1 (en) | 1999-07-22 | 2002-01-17 | Robinson Ralph Pelton | Arylsulfonylamino hydroxamic acid derivatives |
| EP1078923B1 (en) | 1999-08-02 | 2006-03-08 | F. Hoffmann-La Roche Ag | Process for the preparation of benzothiophene derivatives |
| HUP0203542A3 (en) | 1999-08-12 | 2003-07-28 | Upjohn Co | 3(5)-amino-pyrazole derivatives, process for their preparation, their use and pharmaceutical compositions containing the same |
| US6283379B1 (en) * | 2000-02-14 | 2001-09-04 | Kic Thermal Profiling | Method for correlating processor and part temperatures using an air temperature sensor for a conveyorized thermal processor |
| IL150806A0 (en) * | 2000-02-21 | 2003-02-12 | Astrazeneca Ab | Piperidine-and piperazine substituted n-hydroxyformamides as inhibitors of metalloproteinases |
| US6525202B2 (en) | 2000-07-17 | 2003-02-25 | Wyeth | Cyclic amine phenyl beta-3 adrenergic receptor agonists |
| US20020065219A1 (en) | 2000-08-15 | 2002-05-30 | Naidu B. Narasimhulu | Water soluble thiazolyl peptide derivatives |
| US20020091107A1 (en) | 2000-09-08 | 2002-07-11 | Madar David J. | Oxazolidinone antibacterial agents |
| EP1191024A1 (en) | 2000-09-22 | 2002-03-27 | Harald Tschesche | Thiadiazines and their use as inhibitors of metalloproteinases |
| SE0100902D0 (sv) | 2001-03-15 | 2001-03-15 | Astrazeneca Ab | Compounds |
| SE0100903D0 (sv) | 2001-03-15 | 2001-03-15 | Astrazeneca Ab | Compounds |
| US20040147573A1 (en) * | 2001-03-15 | 2004-07-29 | Anders Eriksson | Metalloproteinase inhibitors |
| ES2333412T3 (es) | 2001-05-25 | 2010-02-22 | Bristol-Myers Squibb Company | Derivados de hidantoina como inhibidores de metaloproteinasas de matriz. |
| GB0114004D0 (en) | 2001-06-08 | 2001-08-01 | Glaxo Group Ltd | Chemical compounds |
| SE0103710D0 (sv) | 2001-11-07 | 2001-11-07 | Astrazeneca Ab | Compounds |
| EP1550725A4 (en) | 2002-06-05 | 2010-08-25 | Kaneka Corp | PROCESS FOR PRODUCING OPTICALLY ACTIVE alpha-METHYLCYSTEINE DERIVATIVE |
| SE0202539D0 (sv) | 2002-08-27 | 2002-08-27 | Astrazeneca Ab | Compounds |
| GB0221250D0 (en) | 2002-09-13 | 2002-10-23 | Astrazeneca Ab | Compounds |
| GB0221246D0 (en) | 2002-09-13 | 2002-10-23 | Astrazeneca Ab | Compounds |
| US20040266832A1 (en) | 2003-06-26 | 2004-12-30 | Li Zheng J. | Crystal forms of 2-(3-difluoromethyl-5-phenyl-pyrazol-1-yl)-5-methanesulfonyl pyridine |
| TWI220073B (en) | 2003-07-24 | 2004-08-01 | Au Optronics Corp | Method for manufacturing polysilicon film |
| US7648992B2 (en) | 2004-07-05 | 2010-01-19 | Astrazeneca Ab | Hydantoin derivatives for the treatment of obstructive airway diseases |
| SE0401763D0 (sv) | 2004-07-05 | 2004-07-05 | Astrazeneca Ab | Compounds |
| SE0401762D0 (sv) | 2004-07-05 | 2004-07-05 | Astrazeneca Ab | Novel compounds |
| SE0403086D0 (sv) | 2004-12-17 | 2004-12-17 | Astrazeneca Ab | Compounds |
| SE0403085D0 (sv) | 2004-12-17 | 2004-12-17 | Astrazeneca Ab | Novel componds |
| TW200740769A (en) | 2006-03-16 | 2007-11-01 | Astrazeneca Ab | Novel process |
| TW200800954A (en) | 2006-03-16 | 2008-01-01 | Astrazeneca Ab | Novel crystal modifications |
| TW200831488A (en) | 2006-11-29 | 2008-08-01 | Astrazeneca Ab | Novel compounds |
-
2004
- 2004-07-05 SE SE0401762A patent/SE0401762D0/xx unknown
-
2005
- 2005-04-07 UA UAA200613009A patent/UA86977C2/ru unknown
- 2005-06-29 SA SA05260192A patent/SA05260192B1/ar unknown
- 2005-06-29 TW TW094121763A patent/TWI353985B/zh not_active IP Right Cessation
- 2005-07-01 MY MYPI20053029A patent/MY145613A/en unknown
- 2005-07-04 EP EP05756403A patent/EP1778673B1/en not_active Expired - Lifetime
- 2005-07-04 KR KR1020077000186A patent/KR101222736B1/ko not_active Expired - Fee Related
- 2005-07-04 RU RU2007101236/04A patent/RU2386629C2/ru not_active IP Right Cessation
- 2005-07-04 RS RSP-2010/0038A patent/RS51280B/sr unknown
- 2005-07-04 PL PL05756403T patent/PL1778673T3/pl unknown
- 2005-07-04 ES ES05756403T patent/ES2335424T3/es not_active Expired - Lifetime
- 2005-07-04 AT AT05756403T patent/ATE448219T1/de active
- 2005-07-04 CA CA2569716A patent/CA2569716C/en not_active Expired - Fee Related
- 2005-07-04 NZ NZ552101A patent/NZ552101A/en not_active IP Right Cessation
- 2005-07-04 SI SI200530892T patent/SI1778673T1/sl unknown
- 2005-07-04 MX MXPA06014661A patent/MXPA06014661A/es active IP Right Grant
- 2005-07-04 DE DE602005017636T patent/DE602005017636D1/de not_active Expired - Lifetime
- 2005-07-04 WO PCT/SE2005/001092 patent/WO2006004532A1/en not_active Ceased
- 2005-07-04 CN CNB2005800228017A patent/CN100543024C/zh not_active Expired - Lifetime
- 2005-07-04 PT PT05756403T patent/PT1778673E/pt unknown
- 2005-07-04 HR HR20100020T patent/HRP20100020T1/hr unknown
- 2005-07-04 JP JP2007520267A patent/JP4390833B2/ja not_active Expired - Lifetime
- 2005-07-04 BR BRPI0512974-5A patent/BRPI0512974A/pt active Search and Examination
- 2005-07-04 AU AU2005260142A patent/AU2005260142B2/en not_active Ceased
- 2005-07-04 DK DK05756403.1T patent/DK1778673T3/da active
- 2005-07-05 AR ARP050102793A patent/AR049578A1/es not_active Application Discontinuation
- 2005-07-05 UY UY29002A patent/UY29002A1/es not_active Application Discontinuation
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2006
- 2006-12-07 IL IL179906A patent/IL179906A/en not_active IP Right Cessation
- 2006-12-19 ZA ZA200610698A patent/ZA200610698B/en unknown
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2007
- 2007-01-30 NO NO20070576A patent/NO20070576L/no not_active Application Discontinuation
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2009
- 2009-12-02 US US12/629,630 patent/US7989620B2/en not_active Expired - Lifetime
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2010
- 2010-01-11 CY CY20101100026T patent/CY1109728T1/el unknown
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