AR046062A1 - Derivados de tetrahidronaftaleno procedimiento para su preparacion y su uso antiinflamatorio - Google Patents
Derivados de tetrahidronaftaleno procedimiento para su preparacion y su uso antiinflamatorioInfo
- Publication number
- AR046062A1 AR046062A1 ARP040103651A ARP040103651A AR046062A1 AR 046062 A1 AR046062 A1 AR 046062A1 AR P040103651 A ARP040103651 A AR P040103651A AR P040103651 A ARP040103651 A AR P040103651A AR 046062 A1 AR046062 A1 AR 046062A1
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- 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
- C07D209/30—Indoles; Hydrogenated indoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to carbon atoms of the hetero ring
- C07D209/32—Oxygen atoms
- C07D209/34—Oxygen atoms in position 2
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- 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
- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
- A61K31/403—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
- A61K31/4035—Isoindoles, e.g. phthalimide
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- 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
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/47—Quinolines; Isoquinolines
- A61K31/4709—Non-condensed quinolines and containing further heterocyclic rings
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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
- A61P1/04—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
- 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
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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
- A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
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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
- A61P35/00—Antineoplastic agents
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
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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
- A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
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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
- A61P37/08—Antiallergic agents
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C211/00—Compounds containing amino groups bound to a carbon skeleton
- C07C211/43—Compounds containing amino groups bound to a carbon skeleton having amino groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton
- C07C211/57—Compounds containing amino groups bound to a carbon skeleton having amino groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton having amino groups bound to carbon atoms of six-membered aromatic rings being part of condensed ring systems of the carbon skeleton
- C07C211/58—Naphthylamines; N-substituted derivatives thereof
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- 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
- C07D209/44—Iso-indoles; Hydrogenated iso-indoles
- C07D209/46—Iso-indoles; Hydrogenated iso-indoles with an oxygen atom in position 1
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
- C07D215/02—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
- C07D215/16—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms 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
- C07D215/38—Nitrogen atoms
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D217/00—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems
- C07D217/22—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems 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 carbon atoms of the nitrogen-containing ring
- C07D217/24—Oxygen atoms
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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
- C07D231/54—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings condensed with carbocyclic rings or ring systems
- C07D231/56—Benzopyrazoles; Hydrogenated benzopyrazoles
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D237/00—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings
- C07D237/26—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings condensed with carbocyclic rings or ring systems
- C07D237/30—Phthalazines
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/70—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings condensed with carbocyclic rings or ring systems
- C07D239/72—Quinazolines; Hydrogenated quinazolines
- C07D239/74—Quinazolines; Hydrogenated quinazolines with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, attached to ring carbon atoms of the hetero ring
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/60—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings condensed with carbocyclic rings or ring systems
- C07D277/62—Benzothiazoles
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Immunology (AREA)
- Epidemiology (AREA)
- Pulmonology (AREA)
- Rheumatology (AREA)
- Hematology (AREA)
- Transplantation (AREA)
- Pain & Pain Management (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Oncology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Quinoline Compounds (AREA)
- Furan Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Indole Compounds (AREA)
- Other In-Based Heterocyclic Compounds (AREA)
- Pyridine Compounds (AREA)
Abstract
El presente se refiere a uso como antiinflamatorios. Reivindicación 1: Compuestos de la fórmula general (1), donde: R1 y R2 son, independientemente entre sí, un átomo de hidrógeno, un grupo hidrozoo, un átomo de halógeno, un grupo alquilo-(C1-10) que puede ser sustituido, un grupo Alcoy-(C1-10) que puede ser sustituido, un grupo alquiltio-(C1-10), un grupo perfluoralquilo-(C1-5), un grupo ciano, un grupo nitro; o R1 y R2 juntos son un grupo seleccionados de los grupos -O-(CH2)n-O-, -O-(CH2)n- CH2, -O-CH=CH-, -(CH2)n+2, -NH-(CH2)n+1, -N(alquilo-C1-3)-(CH2)n+1, -NH-N=CH-, donde n es = 1 ó 2 y los átomos de oxígeno en posición final y/o átomos de carbono y/o átomos de nitrógeno están unidos con átomos de carbono del anillo directamente adyacentes, o son NR8R9, donde R8 y R9 pueden ser independientemente entre sí, hidrógeno, -alquilo-(C1-5) o (CO)-alquilo-(C1-5); R11 es un átomo de hidrógeno, un grupo hidroxi, un átomo de halógeno, un grupo ciano, un grupo alquilo-(C1-10) que puede ser sustituido, un grupo alcoxi-(C1-10), un grupo alquiltio-(C1-10), un grupo perfluoralquilo-(C1-5); R12 es un átomo de hidrógeno, un grupo hidroxi, un átomo de halógeno, un grupo ciano, un grupo alquilo-(C1-10) que puede ser sustituido, un grupo alcoxi-(C1-10); R3 es un grupo alquilo-(C1-10) que puede ser sustituido por 1-3 grupos hidroxi, átomos de halógeno, 1-3 grupos alcoxi-(C1-5); un grupo cicloalquilo-(C3-7) que puede ser sustituido; un grupo heterociclilo que puede ser sustituido; un grupo arilo que puede ser sustituido, un grupo heteroarilo mono- o bicíclico que puede ser sustituido independientemente entre si por uno o varios grupos seleccionados de entre grupos alquilo-(C1-5) que a su vez puede ser sustituido por 1-3 grupos hidroxi o 1-3 grupos COOR13, donde R13 significa hidrógeno o alquilo-(C1-5); grupos alcoxi-(C1-5); átomos de halógeno; grupos hidroxi; grupos NR8R9; grupos exometileno, oxígeno, que pueden contener 1-4 átomos de nitrógeno, y/o 1-2 átomos de oxígeno y/o 1-2 átomos de azufre y/o 1-2 grupos ceto, donde este grupo puede estar unido en cualquier posición con la amina del sistema tetrahidronaftaleno y pueden ser hidrogenados en uno o varios lugares; R4 es un grupo hidroxi, un grupo OR10 o un grupo O(CO)R10, donde R10 significa cualquier grupo protector hidroxi o un grupo alquilo-(C1-10); R5 es un grupo alquilo-(C1-10), o un grupo alquilo-(C1-10) que puede ser parcial o totalmente fluorado, un grupo cicloalquilo-(C3-7), un grupo alquil-(C1- 8)cicloalquilo(C3-7), un grupo alquenilo-(C2-8)cicloalquilo(C3-7), un grupo heterociclilo, un grupo alquilheterociclilo-(C1-8), un grupo alquenilheterociclilo-(C2-8), un grupo arilo, un grupo alquilarilo-(C1-8), un grupo alquenilarilo-(C2-8), grupos alquinilarilo-(C2-8); un grupo heteroarilo mono- o bicíclico, un grupo alquilheteroarilo-(C1-8) o un grupo alquenilheteroarilo-(C2-8); un grupo alquinilheteroarilo-(C2-8) que puede ser sustituido por 1-2 grupos ceto, 1-2 grupos alquilo-(C1-5), 1-2 grupos alcoxi-(C1-5), 1-3 átomos de halógeno, 1-2 grupos exometileno, que contiene 1-3 átomos de nitrógeno y/o 1-2 átomos de oxígeno y/o 1-2 átomos de azufre, donde estos grupos pueden estar unidos en cualquier posición con el sistema tetrahidronaftaleno y que pueden estar hidrogenados en uno o varios lugares; R6 y R7 son, independientemente entre sí, un átomo de hidrógeno, un grupo metilo o etilo o junto con el átomo de carbono del sistema tetrahidronaftaleno, un anillo cicloalquilo-(C3-6).
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE10347386A DE10347386B4 (de) | 2003-10-08 | 2003-10-08 | Tetrahydronaphthalinderivate, Verfahren zu ihrer Herstellung und ihre Verwendung als Entzündungshemmer |
DE10347383A DE10347383A1 (de) | 2003-10-08 | 2003-10-08 | Tetrahydronaphthalinderivate, Verfahren zu ihrer Herstellung und ihre Verwendung als Entzündungshemmer |
DE102004017662A DE102004017662B3 (de) | 2004-04-05 | 2004-04-05 | Mehrfach substituierte Tetrahydronaphthalinderivate, Verfahren zu ihrer Herstellung und ihre Verwendung als Entzündungshemmer |
Publications (1)
Publication Number | Publication Date |
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AR046062A1 true AR046062A1 (es) | 2005-11-23 |
Family
ID=34437487
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ARP040103651A AR046062A1 (es) | 2003-10-08 | 2004-10-08 | Derivados de tetrahidronaftaleno procedimiento para su preparacion y su uso antiinflamatorio |
Country Status (30)
Country | Link |
---|---|
US (1) | US7659297B2 (es) |
EP (1) | EP1670458B1 (es) |
JP (1) | JP4638438B2 (es) |
KR (1) | KR20070000395A (es) |
AR (1) | AR046062A1 (es) |
AT (1) | ATE348609T1 (es) |
AU (1) | AU2004280088B2 (es) |
BR (1) | BRPI0415209A (es) |
CA (1) | CA2539587A1 (es) |
CR (1) | CR8357A (es) |
CY (1) | CY1107596T1 (es) |
DE (1) | DE502004002403D1 (es) |
DK (1) | DK1670458T3 (es) |
EA (1) | EA010186B1 (es) |
EC (1) | ECSP066539A (es) |
ES (1) | ES2279454T3 (es) |
HK (1) | HK1097734A1 (es) |
HN (1) | HN2004000446A (es) |
IL (1) | IL174405A (es) |
ME (1) | MEP15908A (es) |
MY (1) | MY141853A (es) |
NO (1) | NO20062020L (es) |
NZ (1) | NZ546473A (es) |
PE (1) | PE20060604A1 (es) |
PL (1) | PL1670458T3 (es) |
PT (1) | PT1670458E (es) |
RS (1) | RS20060250A (es) |
SI (1) | SI1670458T1 (es) |
TW (1) | TWI306455B (es) |
WO (1) | WO2005034939A1 (es) |
Families Citing this family (28)
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US7662821B2 (en) | 2003-10-08 | 2010-02-16 | Bayer Schering Pharma Ag | Tetrahydronaphthalene derivatives, process for their production and their use as anti-inflammatory agents |
US7638515B2 (en) | 2003-10-08 | 2009-12-29 | Bayer Schering Pharma Aktiengesellschaft | Tetrahydronaphthalene derivatives, process for their production and their use as anti-inflammatory agents |
JP4638438B2 (ja) | 2003-10-08 | 2011-02-23 | バイエル・シエーリング・ファーマ アクチエンゲゼルシャフト | テトラヒドロナフタレン誘導体類、それらの生成方法及び抗−炎症剤としてのそれらの使用 |
US20080153859A1 (en) * | 2004-04-05 | 2008-06-26 | Hartmut Rehwinkel | Multiply-substituted tetrahydronaphthalene derivatives, process for their production and their use as anti-inflammatory agents |
US20060084652A1 (en) * | 2004-09-09 | 2006-04-20 | Stefan Baeurle | Alkylidene-tetrahydronaphthalene derivatives, process for their production and their use as anti-inflammatory agents |
DE102004044680B3 (de) * | 2004-09-09 | 2006-06-08 | Schering Ag | Alkyliden-Tetrahydronaphthalinderivate, Verfahren zu ihrer Herstellung und ihre Verwendung als Entzündungshemmer sowie diese enthaltende pharmazeutische Präparate |
DE102004063227A1 (de) * | 2004-12-22 | 2006-07-06 | Schering Ag | Tricylische Aminoalkohole, Verfahren zu ihrer Herstellung und ihre Verwendung als Entzündungshemmer |
US20060167025A1 (en) * | 2004-12-22 | 2006-07-27 | Markus Berger | Tricyclic amino alcohols, processes for synthesis of same and use of same as anti-inflammatory drugs |
US20060247292A1 (en) * | 2005-03-22 | 2006-11-02 | Hartmut Rehwinkel | Benzocycloheptene derivatives, process for their production and their use as anti-inflammatory agents |
US20060229305A1 (en) * | 2005-03-22 | 2006-10-12 | Markus Berger | Tetrahydronaphthalene derivatives, process for their production and their use as anti-inflammatory agents |
US7297700B2 (en) | 2005-03-24 | 2007-11-20 | Renovis, Inc. | Bicycloheteroaryl compounds as P2X7 modulators and uses thereof |
DE102005017286B3 (de) * | 2005-04-14 | 2006-12-28 | Schering Ag | Tetrahydronaphthalinderivate, Verfahren zu ihrer Herstellung und ihre Verwendung als Entzündungshemmer |
EP1834948A1 (de) | 2006-03-15 | 2007-09-19 | Bayer Schering Pharma Aktiengesellschaft | Tetrahydronaphthalinderivate, Verfahren zu ihrer Herstellung und ihre Verwendung als Entzündungshemmer |
TWI464148B (zh) | 2006-03-16 | 2014-12-11 | Evotec Us Inc | 作為p2x7調節劑之雙環雜芳基化合物與其用途 |
AR060536A1 (es) | 2006-04-20 | 2008-06-25 | Glaxo Group Ltd | Agonista del receptor de glucocorticoides y composiciones farmaceuticas |
EP1917963A1 (en) * | 2006-10-31 | 2008-05-07 | Bayer Schering Pharma Aktiengesellschaft | Cyclic phenyl-substituted indazols, a process for their production and their use as anti-inflammatory agents |
EP1958934A1 (en) * | 2007-02-16 | 2008-08-20 | Bayer Schering Pharma Aktiengesellschaft | Tetrahydronaphthalenylamides, a process for their production and their use as anti-inflammatory agents |
EP2072509A1 (en) | 2007-12-18 | 2009-06-24 | Bayer Schering Pharma Aktiengesellschaft | 1-Aryl-1H-quinoline-2-ones: process for their production and their use as anti-inflammatory agents |
US8236786B2 (en) | 2008-08-07 | 2012-08-07 | Pulmagen Therapeutics (Inflammation) Limited | Respiratory disease treatment |
ES2442343T3 (es) | 2008-12-30 | 2014-02-11 | Pulmagen Therapeutics (Inflammation) Limited | Compuestos de sulfonamida para el tratamiento de trastornos respiratorios |
WO2010150014A1 (en) | 2009-06-24 | 2010-12-29 | Pulmagen Therapeutics (Inflammation) Limited | 5r- 5 -deuterated glitazones for respiratory disease treatment |
CA2769563A1 (en) | 2009-07-31 | 2011-02-10 | Cadila Healthcare Limited | Novel compounds as modulators of glucocorticoid receptors |
WO2011098746A1 (en) | 2010-02-09 | 2011-08-18 | Pulmagen Therapeutics (Inflammation) Limited | Crystalline acid addition salts of ( 5r) -enanti0mer of pioglitazone |
GB201002224D0 (en) | 2010-02-10 | 2010-03-31 | Argenta Therapeutics Ltd | Respiratory disease treatment |
GB201002243D0 (en) | 2010-02-10 | 2010-03-31 | Argenta Therapeutics Ltd | Respiratory disease treatment |
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2004
- 2004-10-06 JP JP2006530142A patent/JP4638438B2/ja not_active Expired - Fee Related
- 2004-10-06 CA CA002539587A patent/CA2539587A1/en not_active Abandoned
- 2004-10-06 DE DE502004002403T patent/DE502004002403D1/de not_active Expired - Lifetime
- 2004-10-06 RS YUP-2006/0250A patent/RS20060250A/sr unknown
- 2004-10-06 ME MEP-159/08A patent/MEP15908A/xx unknown
- 2004-10-06 ES ES04790271T patent/ES2279454T3/es not_active Expired - Lifetime
- 2004-10-06 NZ NZ546473A patent/NZ546473A/en not_active IP Right Cessation
- 2004-10-06 EA EA200600621A patent/EA010186B1/ru not_active IP Right Cessation
- 2004-10-06 EP EP04790271A patent/EP1670458B1/de not_active Expired - Lifetime
- 2004-10-06 KR KR1020067006768A patent/KR20070000395A/ko active IP Right Grant
- 2004-10-06 DK DK04790271T patent/DK1670458T3/da active
- 2004-10-06 PT PT04790271T patent/PT1670458E/pt unknown
- 2004-10-06 SI SI200430231T patent/SI1670458T1/sl unknown
- 2004-10-06 PL PL04790271T patent/PL1670458T3/pl unknown
- 2004-10-06 BR BRPI0415209-3A patent/BRPI0415209A/pt not_active IP Right Cessation
- 2004-10-06 AT AT04790271T patent/ATE348609T1/de active
- 2004-10-06 AU AU2004280088A patent/AU2004280088B2/en not_active Ceased
- 2004-10-06 WO PCT/EP2004/011370 patent/WO2005034939A1/de active IP Right Grant
- 2004-10-08 MY MYPI20044145A patent/MY141853A/en unknown
- 2004-10-08 US US10/960,754 patent/US7659297B2/en not_active Expired - Fee Related
- 2004-10-08 TW TW093130577A patent/TWI306455B/zh not_active IP Right Cessation
- 2004-10-08 AR ARP040103651A patent/AR046062A1/es not_active Application Discontinuation
- 2004-11-03 HN HN2004000446A patent/HN2004000446A/es unknown
- 2004-11-11 PE PE2004001100A patent/PE20060604A1/es not_active Application Discontinuation
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2006
- 2006-03-20 IL IL174405A patent/IL174405A/en not_active IP Right Cessation
- 2006-04-24 CR CR8357A patent/CR8357A/es not_active Application Discontinuation
- 2006-05-02 EC EC2006006539A patent/ECSP066539A/es unknown
- 2006-05-05 NO NO20062020A patent/NO20062020L/no not_active Application Discontinuation
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2007
- 2007-02-15 HK HK07101854.6A patent/HK1097734A1/xx not_active IP Right Cessation
- 2007-03-20 CY CY20071100384T patent/CY1107596T1/el unknown
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