ATE489370T1 - Herstellung und verwendung von verbindungen als aspartylproteasehemmer - Google Patents
Herstellung und verwendung von verbindungen als aspartylproteasehemmerInfo
- Publication number
- ATE489370T1 ATE489370T1 AT06784809T AT06784809T ATE489370T1 AT E489370 T1 ATE489370 T1 AT E489370T1 AT 06784809 T AT06784809 T AT 06784809T AT 06784809 T AT06784809 T AT 06784809T AT E489370 T1 ATE489370 T1 AT E489370T1
- Authority
- AT
- Austria
- Prior art keywords
- compounds
- preparation
- protease inhibitors
- aspartyl protease
- aspartyl
- Prior art date
Links
- 239000003696 aspartic proteinase inhibitor Substances 0.000 title 1
- 150000001875 compounds Chemical class 0.000 title 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D251/00—Heterocyclic compounds containing 1,3,5-triazine rings
- C07D251/02—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings
- C07D251/10—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D251/00—Heterocyclic compounds containing 1,3,5-triazine rings
- C07D251/72—Heterocyclic compounds containing 1,3,5-triazine rings condensed with carbocyclic rings or ring systems
-
- 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
- A61K31/53—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with three nitrogens as the only ring hetero atoms, e.g. chlorazanil, melamine
-
- 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
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
- A61P31/14—Antivirals for RNA viruses
- A61P31/18—Antivirals for RNA viruses for HIV
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P33/00—Antiparasitic agents
-
- 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
-
- 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
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/6564—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms
- C07F9/6581—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms having phosphorus and nitrogen atoms with or without oxygen or sulfur atoms, as ring hetero atoms
- C07F9/6584—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms having phosphorus and nitrogen atoms with or without oxygen or sulfur atoms, as ring hetero atoms having one phosphorus atom as ring hetero atom
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Diabetes (AREA)
- Molecular Biology (AREA)
- Biochemistry (AREA)
- Virology (AREA)
- Neurosurgery (AREA)
- Tropical Medicine & Parasitology (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- Oncology (AREA)
- Emergency Medicine (AREA)
- Endocrinology (AREA)
- Hematology (AREA)
- Obesity (AREA)
- Heart & Thoracic Surgery (AREA)
- Hospice & Palliative Care (AREA)
- Cardiology (AREA)
- Communicable Diseases (AREA)
- Psychiatry (AREA)
- AIDS & HIV (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen- Or Sulfur-Containing Heterocyclic Ring Compounds With Rings Of Six Or More Members (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US69041305P | 2005-06-14 | 2005-06-14 | |
| PCT/US2006/022920 WO2006138266A2 (en) | 2005-06-14 | 2006-06-12 | The preparation and use of compounds as aspartyl protease inhibitors |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ATE489370T1 true ATE489370T1 (de) | 2010-12-15 |
Family
ID=37388420
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AT06784809T ATE489370T1 (de) | 2005-06-14 | 2006-06-12 | Herstellung und verwendung von verbindungen als aspartylproteasehemmer |
Country Status (16)
| Country | Link |
|---|---|
| US (1) | US8110682B2 (de) |
| EP (2) | EP1896430B1 (de) |
| JP (1) | JP4859922B2 (de) |
| KR (1) | KR20080015861A (de) |
| CN (1) | CN101198597B (de) |
| AR (1) | AR054510A1 (de) |
| AT (1) | ATE489370T1 (de) |
| AU (1) | AU2006259574A1 (de) |
| CA (1) | CA2610829A1 (de) |
| DE (1) | DE602006018456D1 (de) |
| IL (1) | IL187453A0 (de) |
| MX (1) | MX2007016177A (de) |
| PE (1) | PE20070115A1 (de) |
| TW (1) | TW200716574A (de) |
| WO (1) | WO2006138266A2 (de) |
| ZA (1) | ZA200710342B (de) |
Families Citing this family (42)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7700603B2 (en) | 2003-12-15 | 2010-04-20 | Schering Corporation | Heterocyclic aspartyl protease inhibitors |
| US7763609B2 (en) * | 2003-12-15 | 2010-07-27 | Schering Corporation | Heterocyclic aspartyl protease inhibitors |
| US7592348B2 (en) | 2003-12-15 | 2009-09-22 | Schering Corporation | Heterocyclic aspartyl protease inhibitors |
| ATE482214T1 (de) * | 2005-06-14 | 2010-10-15 | Schering Corp | Aspartylproteasehemmer |
| SG162790A1 (en) | 2005-06-14 | 2010-07-29 | Schering Corp | Aspartyl protease inhibitors |
| EP1896032B1 (de) | 2005-06-14 | 2012-10-31 | Merck Sharp & Dohme Corp. | Herstellung und verwendung von verbindungen als proteasehemmer |
| ATE478070T1 (de) | 2005-10-27 | 2010-09-15 | Schering Corp | Heterozyklische aspartyl-proteasehemmer |
| US8168641B2 (en) | 2006-06-12 | 2012-05-01 | Schering Corporation | Aspartyl protease inhibitors |
| TW200815349A (en) | 2006-06-22 | 2008-04-01 | Astrazeneca Ab | New compounds |
| MX2009006228A (es) | 2006-12-12 | 2009-06-22 | Schering Corp | Inhibidores de aspartil proteasa. |
| TW200902499A (en) | 2007-05-15 | 2009-01-16 | Astrazeneca Ab | New compounds |
| CN101848897A (zh) | 2007-09-06 | 2010-09-29 | 先灵公司 | γ分泌酶调节剂 |
| WO2009061699A1 (en) | 2007-11-05 | 2009-05-14 | Schering Corporation | Gamma secretase modulators |
| CA2708300A1 (en) | 2007-12-11 | 2009-06-18 | Schering Corporation | Gamma secretase modulators |
| AU2009314049B2 (en) | 2008-11-13 | 2015-03-05 | Merck Sharp & Dohme Corp. | Gamma secretase modulators |
| TW201020244A (en) | 2008-11-14 | 2010-06-01 | Astrazeneca Ab | New compounds |
| JP2012513399A (ja) | 2008-12-22 | 2012-06-14 | シェーリング コーポレイション | γ−セクレターゼ調節剤 |
| EP2379566A2 (de) | 2008-12-22 | 2011-10-26 | Schering Corporation | Modulatoren von gamma-sekretase |
| WO2010147969A2 (en) | 2009-06-16 | 2010-12-23 | Schering Corporation | Gamma secretase modulators |
| WO2010147975A1 (en) | 2009-06-16 | 2010-12-23 | Schering Corporation | Gamma secretase modulators |
| EP2443118A1 (de) | 2009-06-16 | 2012-04-25 | Schering Corporation | Gammasekretasemodulatoren |
| EP2281824A1 (de) | 2009-08-07 | 2011-02-09 | Noscira, S.A. | Furan-Imidazolon-Derivate zur Behandlung von kognitiven, neurodegenerativen oder neuronalen Erkrankungen oder Funktionsstörungen |
| US8557826B2 (en) | 2009-10-08 | 2013-10-15 | Merck Sharp & Dohme Corp. | Pentafluorosulfur imino heterocyclic compounds as BACE-1 inhibitors, compositions, and their use |
| EP2485920B1 (de) | 2009-10-08 | 2016-04-27 | Merck Sharp & Dohme Corp. | Heterozyklische pentafluorsulfur-imin-verbindungen als bace-1-hemmer sowie zusammensetzungen damit und ihre verwendung |
| UA108363C2 (uk) * | 2009-10-08 | 2015-04-27 | Похідні імінотіадіазиндіоксиду як інгібітори bace, композиція на їх основі і їх застосування | |
| EP2485591B1 (de) | 2009-10-08 | 2016-03-23 | Merck Sharp & Dohme Corp. | Iminothiadiazindioxinverbindungen als bace-hemmer, zusammensetzungen und ihre verwendung |
| EP2643299B1 (de) | 2010-11-22 | 2016-06-22 | Noscira, S.A. | Bipyridinsulfonamidderivate zur behandlung von neurodegenerativen erkrankungen oder zuständen |
| US9145426B2 (en) | 2011-04-07 | 2015-09-29 | Merck Sharp & Dohme Corp. | Pyrrolidine-fused thiadiazine dioxide compounds as BACE inhibitors, compositions, and their use |
| EP2694489B1 (de) | 2011-04-07 | 2017-09-06 | Merck Sharp & Dohme Corp. | C5-c6-oxacyclus-fusionierte thiadiazindioxidverbindungen als bace-hemmer sowie zusammensetzungen daraus und ihre verwendung |
| US9181236B2 (en) | 2011-08-22 | 2015-11-10 | Merck Sharp & Dohme Corp. | 2-spiro-substituted iminothiazines and their mono-and dioxides as bace inhibitors, compositions and their use |
| CN104270945B (zh) | 2012-03-19 | 2017-03-29 | 巴克老龄化研究所 | App特异性bace抑制剂(asbi)及其用途 |
| WO2014062549A1 (en) | 2012-10-17 | 2014-04-24 | Merck Sharp & Dohme Corp. | Tricyclic substituted thiadiazine dioxide compounds as bace inhibitors, compositions, and their use |
| EP2908824B1 (de) | 2012-10-17 | 2018-05-02 | Merck Sharp & Dohme Corp. | Tricyclische substituierte thiadiazindioxidverbindungen als bace-hemmer, zusammensetzungen und deren verwendung |
| CA2899938C (en) | 2013-02-12 | 2021-10-19 | Buck Institute For Research On Aging | Hydantoins that modulate bace-mediated app processing |
| EP2781919A1 (de) | 2013-03-19 | 2014-09-24 | Roche Diagniostics GmbH | Verfahren/Vorrichtung zur Erzeugung eines korrigierten Werts einer Analytenkonzentration in einer Körperflüssigkeitsprobe |
| US9745324B2 (en) | 2013-12-18 | 2017-08-29 | Merck Sharp & Dohme Corp. | Iminothiadiazepane dioxide compounds as BACE inhibitors, compositions, and their use |
| AU2017275657B2 (en) | 2016-06-02 | 2021-08-19 | Novartis Ag | Potassium channel modulators |
| UA123810C2 (uk) | 2017-01-23 | 2021-06-02 | Цадент Терапеутікс, Інк. | Модулятори калієвих каналів |
| JP7368856B2 (ja) | 2017-07-25 | 2023-10-25 | トゥルーバインディング,インコーポレイテッド | Tim-3とそのリガンドとの相互作用の遮断によるがん治療 |
| MX2021004647A (es) | 2018-10-22 | 2021-08-16 | Novartis Ag | Formas cristalinas de moduladores de los canales de potasio. |
| CN120058944A (zh) | 2019-01-30 | 2025-05-30 | 真和制药有限公司 | 抗gal3抗体及其用途 |
| JP2023528797A (ja) | 2020-05-26 | 2023-07-06 | トゥルーバインディング,インコーポレイテッド | ガレクチン-3を遮断することにより炎症性疾患を処置する方法 |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US1077204A (en) | 1912-11-20 | 1913-10-28 | John Bonner Semple | Tracer for projectiles. |
| US3287366A (en) * | 1963-12-24 | 1966-11-22 | American Cyanamid Co | Novel 1, 2-dihydro-s-triazines |
| US3287365A (en) * | 1963-12-24 | 1966-11-22 | American Cyanamid Co | Novel dihydro-s-triazines and method of preparation |
| US3876785A (en) * | 1967-12-06 | 1975-04-08 | Beecham Group Ltd | 4,6-diamino-1,2-dihydro-arylmethoxy-1,3,5-triazines for combating plasmodium parasites |
| GB1217415A (en) * | 1968-07-04 | 1970-12-31 | Vitamins Ltd | Triazine derivatives and pharmaceutical formulation and processes for making same |
| US3723429A (en) * | 1969-11-06 | 1973-03-27 | Beecham Group Ltd | Di-hydro triazine derivatives |
| US3682912A (en) * | 1969-12-18 | 1972-08-08 | Beecham Group Ltd | Di-hydro triazine derivatives |
| US6232309B1 (en) * | 1989-03-09 | 2001-05-15 | Nihon Bayer Agrochem K.K. | Insecticidal heterocyclic compounds |
| WO1993004047A1 (en) | 1991-08-16 | 1993-03-04 | Merck & Co., Inc. | Quinazoline derivatives as inhibitors of hiv reverse transcriptase |
| US5723490A (en) * | 1992-09-08 | 1998-03-03 | Vertex Pharmaceuticals Incorporated | THF-containing sulfonamide inhibitors of aspartyl protease |
| US5565451A (en) * | 1994-09-15 | 1996-10-15 | Fmc Corporation | 1-substituted-2, 4-diamino-6, 6-dialkyl-1, 6-dihydro-1, 3, 5-triazines as insecticides |
| US5889006A (en) | 1995-02-23 | 1999-03-30 | Schering Corporation | Muscarinic antagonists |
| IL117149A0 (en) | 1995-02-23 | 1996-06-18 | Schering Corp | Muscarinic antagonists |
| US5935958A (en) | 1996-07-01 | 1999-08-10 | Schering Corporation | Muscarinic antagonists |
| US5952349A (en) | 1996-07-10 | 1999-09-14 | Schering Corporation | Muscarinic antagonists for treating memory loss |
| US5977138A (en) | 1996-08-15 | 1999-11-02 | Schering Corporation | Ether muscarinic antagonists |
| US6066636A (en) | 1998-06-30 | 2000-05-23 | Schering Corporation | Muscarinic antagonists |
| CN1165528C (zh) * | 1998-12-01 | 2004-09-08 | 日本拜耳农药株式会社 | 取代的1,3,5-三嗪 |
| US6294554B1 (en) | 1999-09-22 | 2001-09-25 | Schering Corporation | Muscarinic antagonists |
| GB0001565D0 (en) * | 2000-01-24 | 2000-03-15 | Isis Innovation | Dihydrofolate reductase inhibitors |
| FR2804113B1 (fr) * | 2000-01-26 | 2004-06-18 | Lipha | Derives animes de dihydro-1,3,5-triazine et leurs applications en therapeutique |
| WO2002004464A1 (en) * | 2000-07-07 | 2002-01-17 | Lg Life Sciences Ltd | Novel cephalosporin compounds and process for preparing the same |
| US6458812B1 (en) | 2000-12-22 | 2002-10-01 | Schering Corporation | Muscarinic antagonists |
| AU2002306734A1 (en) | 2001-03-15 | 2002-10-03 | The Johns Hopkins University | Inhibitors of plasmepsins |
| GB0123467D0 (en) * | 2001-09-28 | 2001-11-21 | Hoffmann La Roche | Carbocyclic HIV Protease inhibitors |
| ES2269774T3 (es) | 2001-10-10 | 2007-04-01 | Schering Corporation | Compuestos de piperidina como antagonistas muscarinicos. |
| AU2002335607A1 (en) * | 2002-09-06 | 2004-03-29 | Infineon Technologies Ag | Method and system for determining conformance of a data key with rules by means of memory lookups |
| US7772197B2 (en) * | 2002-09-24 | 2010-08-10 | 1,3,5-Triazines for Treatment of Viral Diseases | 1,3,5-triazines for treatment of viral diseases |
| US7256218B2 (en) * | 2002-11-22 | 2007-08-14 | Jacobus Pharmaceutical Company, Inc. | Biguanide and dihydrotriazine derivatives |
| CA2510468C (en) * | 2002-12-17 | 2011-01-04 | Hamari Chemicals, Ltd. | Novel 2,4-diamino-1,3,5-triazine derivative |
| EP1670787B1 (de) * | 2003-09-11 | 2012-05-30 | iTherX Pharma, Inc. | Cytokininhibitoren |
| DE10348023A1 (de) * | 2003-10-15 | 2005-05-19 | Imtm Gmbh | Neue Alanyl-Aminopeptidasen-Inhibitoren zur funktionellen Beeinflussung unterschiedlicher Zellen und zur Behandlung immunologischer, entzündlicher, neuronaler und anderer Erkrankungen |
| US20050123906A1 (en) * | 2003-11-06 | 2005-06-09 | Rana Tariq M. | Protein modulation |
| US7592348B2 (en) | 2003-12-15 | 2009-09-22 | Schering Corporation | Heterocyclic aspartyl protease inhibitors |
| US7763609B2 (en) * | 2003-12-15 | 2010-07-27 | Schering Corporation | Heterocyclic aspartyl protease inhibitors |
| EP1740563A2 (de) * | 2004-04-27 | 2007-01-10 | Teva Gyógyszergyár Zártköruen Muködo Részvenytarsaság | Mykophenolatmofetilverunreinigung |
| JP2008503460A (ja) | 2004-06-16 | 2008-02-07 | ワイス | β−セクレターゼのインヒビターとしてのジフェニルイミダゾピリミジンおよびイミダゾールアミン |
| ATE444962T1 (de) | 2004-06-16 | 2009-10-15 | Wyeth Corp | Amino-5,5-diphenylimidazolon-derivate zur beta- sekretase-hemmung |
| WO2006044497A2 (en) | 2004-10-13 | 2006-04-27 | Merck & Co., Inc. | Spiropiperidine compounds useful as beta-secretase inhibitors for the treatment of alzhermer’s disease |
| WO2006044492A2 (en) | 2004-10-14 | 2006-04-27 | Ingenious Targeting Laboratory, Inc. | Methods for generating rat embryo-derived cell lines and genetic modification of rat genome |
| EP1802587A4 (de) | 2004-10-15 | 2010-02-17 | Astrazeneca Ab | Substituierte aminoverbindungen und deren anwendungen |
-
2006
- 2006-06-12 AU AU2006259574A patent/AU2006259574A1/en not_active Abandoned
- 2006-06-12 EP EP06784809A patent/EP1896430B1/de active Active
- 2006-06-12 CA CA002610829A patent/CA2610829A1/en not_active Abandoned
- 2006-06-12 CN CN200680021093XA patent/CN101198597B/zh not_active Expired - Fee Related
- 2006-06-12 US US11/451,262 patent/US8110682B2/en active Active
- 2006-06-12 AT AT06784809T patent/ATE489370T1/de not_active IP Right Cessation
- 2006-06-12 EP EP10152202A patent/EP2194047A1/de not_active Withdrawn
- 2006-06-12 AR ARP060102464A patent/AR054510A1/es not_active Application Discontinuation
- 2006-06-12 MX MX2007016177A patent/MX2007016177A/es active IP Right Grant
- 2006-06-12 JP JP2008516999A patent/JP4859922B2/ja not_active Expired - Fee Related
- 2006-06-12 KR KR1020077029471A patent/KR20080015861A/ko not_active Withdrawn
- 2006-06-12 DE DE602006018456T patent/DE602006018456D1/de active Active
- 2006-06-12 WO PCT/US2006/022920 patent/WO2006138266A2/en not_active Ceased
- 2006-06-13 TW TW095120995A patent/TW200716574A/zh unknown
- 2006-06-13 PE PE2006000662A patent/PE20070115A1/es not_active Application Discontinuation
-
2007
- 2007-11-18 IL IL187453A patent/IL187453A0/en unknown
- 2007-11-28 ZA ZA200710342A patent/ZA200710342B/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| PE20070115A1 (es) | 2007-02-13 |
| AR054510A1 (es) | 2007-06-27 |
| EP1896430A2 (de) | 2008-03-12 |
| EP1896430B1 (de) | 2010-11-24 |
| US20070010667A1 (en) | 2007-01-11 |
| CN101198597A (zh) | 2008-06-11 |
| JP4859922B2 (ja) | 2012-01-25 |
| MX2007016177A (es) | 2008-03-07 |
| EP2194047A1 (de) | 2010-06-09 |
| US8110682B2 (en) | 2012-02-07 |
| JP2008546697A (ja) | 2008-12-25 |
| WO2006138266A2 (en) | 2006-12-28 |
| CA2610829A1 (en) | 2006-12-28 |
| DE602006018456D1 (de) | 2011-01-05 |
| TW200716574A (en) | 2007-05-01 |
| CN101198597B (zh) | 2011-11-16 |
| WO2006138266A3 (en) | 2007-03-08 |
| IL187453A0 (en) | 2008-02-09 |
| AU2006259574A1 (en) | 2006-12-28 |
| ZA200710342B (en) | 2008-12-31 |
| KR20080015861A (ko) | 2008-02-20 |
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