MA29439B1 - Derives d'uree d'heteroaryle utilises pour inhiber chk1 - Google Patents
Derives d'uree d'heteroaryle utilises pour inhiber chk1Info
- Publication number
- MA29439B1 MA29439B1 MA30325A MA30325A MA29439B1 MA 29439 B1 MA29439 B1 MA 29439B1 MA 30325 A MA30325 A MA 30325A MA 30325 A MA30325 A MA 30325A MA 29439 B1 MA29439 B1 MA 29439B1
- Authority
- MA
- Morocco
- Prior art keywords
- heteroaryle
- urea derivatives
- derivatives used
- inhibit chk1
- treatment
- Prior art date
Links
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical class NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 title abstract 2
- 101000777293 Homo sapiens Serine/threonine-protein kinase Chk1 Proteins 0.000 title 1
- 102100031081 Serine/threonine-protein kinase Chk1 Human genes 0.000 title 1
- 230000004543 DNA replication Effects 0.000 abstract 2
- 230000006378 damage Effects 0.000 abstract 2
- 206010028980 Neoplasm Diseases 0.000 abstract 1
- 201000011510 cancer Diseases 0.000 abstract 1
- 230000032823 cell division Effects 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 201000010099 disease Diseases 0.000 abstract 1
- 208000037765 diseases and disorders Diseases 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
- 239000003814 drug Substances 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 238000005204 segregation Methods 0.000 abstract 1
- 229940124597 therapeutic agent Drugs 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- 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
- A61K31/4965—Non-condensed pyrazines
- A61K31/497—Non-condensed pyrazines containing further heterocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/02—Drugs for dermatological disorders for treating wounds, ulcers, burns, scars, keloids, or the like
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/06—Antipsoriatics
-
- 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
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/04—Antineoplastic agents specific for metastasis
-
- 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
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Immunology (AREA)
- Dermatology (AREA)
- Oncology (AREA)
- Rheumatology (AREA)
- Pain & Pain Management (AREA)
- Hematology (AREA)
- Transplantation (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Plural Heterocyclic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Pyridine Compounds (AREA)
Abstract
L'INVENTION CONCERNE DES COMPOSÉS D'URÉE SUBSTITUÉS UTILISÉS DANS LE TRAITEMENT DE MALADIES ET DE TROUBLES LIÉS À DES DOMMAGES À L'ADN OU DES LÉSIONS DANS LA RÉPLICATION DE L'ADN. CETTE INVENTION A AUSSI POUR OBJET DES MÉTHODES DE CONCEPTION DES COMPOSÉS ET LEUR UTILISATION EN TANT QU'AGENTS THÉRAPEUTIQUES, PAR EXEMPLE, DANS LE TRAITEMENT DE CANCER ET D'AUTRES MALADIES CARACTÉRISÉES PAR DES DÉFAUTS DANS LA RÉPLICATION DE L'ADN, LA SÉGRÉGATION CHROMOSOMIQUE OU LA DIVISION CELLULAIRE.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US66602605P | 2005-03-29 | 2005-03-29 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MA29439B1 true MA29439B1 (fr) | 2008-05-02 |
Family
ID=36677174
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MA30325A MA29439B1 (fr) | 2005-03-29 | 2007-10-26 | Derives d'uree d'heteroaryle utilises pour inhiber chk1 |
Country Status (31)
| Country | Link |
|---|---|
| US (1) | US8093244B2 (fr) |
| EP (2) | EP1869020B1 (fr) |
| JP (2) | JP5117374B2 (fr) |
| KR (2) | KR20090031459A (fr) |
| CN (2) | CN102219784A (fr) |
| AR (1) | AR056645A1 (fr) |
| AT (1) | ATE490248T1 (fr) |
| AU (1) | AU2006230337B2 (fr) |
| BR (1) | BRPI0609667A2 (fr) |
| CA (1) | CA2602199C (fr) |
| CR (1) | CR9395A (fr) |
| CY (1) | CY1111240T1 (fr) |
| DE (1) | DE602006018590D1 (fr) |
| DK (1) | DK1869020T3 (fr) |
| EA (1) | EA011287B1 (fr) |
| ES (1) | ES2356068T3 (fr) |
| HR (1) | HRP20100678T1 (fr) |
| IL (1) | IL185481A0 (fr) |
| MA (1) | MA29439B1 (fr) |
| MX (1) | MX2007012116A (fr) |
| NO (1) | NO20074944L (fr) |
| NZ (1) | NZ561458A (fr) |
| PL (1) | PL1869020T3 (fr) |
| PT (1) | PT1869020E (fr) |
| RS (1) | RS51616B (fr) |
| SI (1) | SI1869020T1 (fr) |
| TN (1) | TNSN07369A1 (fr) |
| TW (1) | TWI375559B (fr) |
| UA (1) | UA92164C2 (fr) |
| WO (1) | WO2006105262A1 (fr) |
| ZA (1) | ZA200707715B (fr) |
Families Citing this family (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5221367A (en) | 1988-08-03 | 1993-06-22 | International Business Machines, Corp. | Strained defect-free epitaxial mismatched heterostructures and method of fabrication |
| UA95310C2 (ru) * | 2006-10-20 | 2011-07-25 | Айкос Корпорейшен | Композиция, содержащая ингибитор chk1 и циклодекстрин, для лечения рака |
| CN101200429B (zh) * | 2006-12-13 | 2012-08-22 | 上海睿智化学研究有限公司 | 2-硝基-4,5-二卤代苯酚类和2-氨基-4,5-二卤代苯酚类及其盐及其合成方法 |
| GB201008005D0 (en) | 2010-05-13 | 2010-06-30 | Sentinel Oncology Ltd | Pharmaceutical compounds |
| CA2928568A1 (fr) | 2013-07-26 | 2015-01-29 | Update Pharma Inc. | Procedes combinatoires permettant d'ameliorer l'avantage therapeutique du bisantrene |
| PL3157566T3 (pl) | 2014-06-17 | 2019-10-31 | Vertex Pharma | Metoda leczenia nowotworu przy użyciu kombinacji inhibitorów chk1 i atr |
| TW201702218A (zh) | 2014-12-12 | 2017-01-16 | 美國杰克森實驗室 | 關於治療癌症、自體免疫疾病及神經退化性疾病之組合物及方法 |
| KR102678021B1 (ko) | 2015-09-30 | 2024-06-26 | 버텍스 파마슈티칼스 인코포레이티드 | Dna 손상제와 병용되는, atr 저해제를 포함하는 암 치료용 약제학적 조성물 |
| CN108601781B (zh) | 2016-02-04 | 2019-11-22 | 广州必贝特医药技术有限公司 | 作为检测点激酶1(chk1)抑制剂的3,5-二取代吡唑及其制备及应用 |
| ES3057783T3 (en) | 2016-03-15 | 2026-03-04 | Oryzon Genomics Sa | Combinations of lsd1 inhibitors for use in the treatment of neoplastic diseases |
| US20200108074A1 (en) * | 2017-03-31 | 2020-04-09 | Seattle Genetics, Inc. | Combinations of chk1- and wee1- inhibitors |
| EP3461480A1 (fr) | 2017-09-27 | 2019-04-03 | Onxeo | Combinaison d'inhibiteurs de point de contrôle du cycle cellulaire de réponse à un dommage à l'adn et de belinostat pour traiter le cancer |
| CN112457306A (zh) | 2019-09-06 | 2021-03-09 | 上海瑛派药业有限公司 | 3,5-二取代吡唑化合物作为激酶抑制剂及其应用 |
| WO2021183973A1 (fr) * | 2020-03-13 | 2021-09-16 | Research Development Foundation | Méthodes de diagnostic et de traitement de cancers |
Family Cites Families (33)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4293552A (en) | 1978-02-27 | 1981-10-06 | Eli Lilly And Company | Novel 1-(mono-o-substituted benzoyl)-3-(substituted pyrazinyl) ureas |
| US6174993B1 (en) | 1997-05-21 | 2001-01-16 | The Children's Medical Center Corp. | Short peptides which selectively modulate the activity of serine/threonine kinases |
| US6218109B1 (en) | 1997-09-05 | 2001-04-17 | Baylor College Of Medicine | Mammalian checkpoint genes and proteins |
| GB9718952D0 (en) | 1997-09-05 | 1997-11-12 | Medical Res Council | Mammalian chk1 effector cell cycle checkpoint protein kinase materials and methods |
| CA2304565A1 (fr) | 1997-10-06 | 1999-04-15 | Basf Aktiengesellschaft | Derives d'indeno(1,2-c)-, de naphto(1,2-c)-, et de benzo(6,7)cyclohepta(1,2-c)pyrazole |
| JP2002526450A (ja) | 1998-09-18 | 2002-08-20 | スミスクライン・ビーチャム・コーポレイション | Chk1キナーゼ阻害物質 |
| YU54202A (sh) | 2000-01-18 | 2006-01-16 | Agouron Pharmaceuticals Inc. | Jedinjenja indazola, farmaceutske smeše i postupci za stimulisanje i inhibiranje ćelijske proliferacije |
| HN2001000008A (es) | 2000-01-21 | 2003-12-11 | Inc Agouron Pharmaceuticals | Compuesto de amida y composiciones farmaceuticas para inhibir proteinquinasas, y su modo de empleo |
| AU3974001A (en) | 2000-02-03 | 2001-08-14 | Ali R. Fattaey | Method and reagent for the inhibition of checkpoint kinase-1 (chk 1) enzyme |
| WO2001062900A1 (fr) | 2000-02-25 | 2001-08-30 | The Regents Of The University Of California. | Scytonemine et ses procedes d'utilisation |
| US6211164B1 (en) | 2000-03-10 | 2001-04-03 | Abbott Laboratories | Antisense oligonucleotides of the human chk1 gene and uses thereof |
| US6534691B2 (en) | 2000-07-18 | 2003-03-18 | E. I. Du Pont De Nemours And Company | Manufacturing process for α-olefins |
| WO2002016326A1 (fr) | 2000-08-18 | 2002-02-28 | Agouron Pharmaceuticals, Inc. | Hydroxyimino-fluorenes heterocycliques et leur utilisation pour inhiber des proteines kinases |
| CA2434066A1 (fr) | 2001-01-26 | 2002-09-12 | Pharmacia Italia S.P.A. | Derives de chromane, procede de preparation et d'utilisation de ces derives en tant qu'agents antitumoraux |
| UA76977C2 (en) | 2001-03-02 | 2006-10-16 | Icos Corp | Aryl- and heteroaryl substituted chk1 inhibitors and their use as radiosensitizers and chemosensitizers |
| US7064215B2 (en) | 2001-07-03 | 2006-06-20 | Chiron Corporation | Indazole benzimidazole compounds |
| WO2003028731A1 (fr) | 2001-10-04 | 2003-04-10 | Smithkline Beecham Corporation | Inhibiteurs de kinase chk1 |
| WO2003029241A1 (fr) | 2001-10-04 | 2003-04-10 | Smithkline Beecham Corporation | Inhibiteurs de chk1 kinase |
| EP1448545B1 (fr) | 2001-10-04 | 2008-11-19 | Smithkline Beecham Corporation | Inhibiteurs du facteur de transcription nf-kb |
| WO2003028724A1 (fr) | 2001-10-04 | 2003-04-10 | Smithkline Beecham Corporation | Inhibiteurs de la kinase chk1 |
| AU2002356871A1 (en) | 2001-10-30 | 2003-05-12 | Pharmacia Corporation | Heteroaromatic carboxamide derivatives for the treatment of inflammation |
| US20030187026A1 (en) | 2001-12-13 | 2003-10-02 | Qun Li | Kinase inhibitors |
| US20030119839A1 (en) | 2001-12-13 | 2003-06-26 | Nan-Horng Lin | Protein kinase inhibitors |
| CA2483496A1 (fr) | 2002-04-26 | 2003-11-06 | Warner-Lambert Company Llc | Inhibiteurs de checkpoint kinases (wee1 et chk1) |
| US7202244B2 (en) * | 2002-05-29 | 2007-04-10 | Millennium Pharmaceuticals, Inc. | Chk-1 inhibitors |
| US20040034038A1 (en) | 2002-08-13 | 2004-02-19 | Goaquan Li | Urea kinase inhibitors |
| US7056925B2 (en) * | 2002-08-13 | 2006-06-06 | Abbott Laboratories | Urea kinase inhibitors |
| CA2496164C (fr) | 2002-08-23 | 2010-11-09 | Chiron Corporation | Quinolinones de benzimidazole et leurs utilisations |
| KR20050084027A (ko) | 2002-11-28 | 2005-08-26 | 쉐링 악티엔게젤샤프트 | Chk-, pdk- 및 akt-억제성 피리미딘, 그의제조방법 및 약제로서의 그의 용도 |
| PL378372A1 (pl) | 2003-01-09 | 2006-04-03 | Pfizer Inc. | Tricykliczne związki jako inhibitory kinaz białkowych do wzmacniania skuteczności środków przeciwnowotworowych i radioterapii |
| CA2571424A1 (fr) | 2004-06-25 | 2006-02-02 | Icos Corporation | Derives de bisaryluree utiles pour inhiber chk1 |
| CA2679908A1 (fr) | 2009-09-23 | 2011-03-23 | Shell Internationale Research Maatschappij B.V. | Processus d'extraction de solvant en boucle fermee pour les sables bitumineux |
| CN104407475B (zh) | 2014-12-04 | 2017-04-05 | 厦门天马微电子有限公司 | 液晶显示面板 |
-
2006
- 2006-03-29 HR HR20100678T patent/HRP20100678T1/hr unknown
- 2006-03-29 KR KR1020097002925A patent/KR20090031459A/ko not_active Ceased
- 2006-03-29 ES ES06748900T patent/ES2356068T3/es not_active Expired - Lifetime
- 2006-03-29 UA UAA200710711A patent/UA92164C2/ru unknown
- 2006-03-29 MX MX2007012116A patent/MX2007012116A/es active IP Right Grant
- 2006-03-29 CA CA2602199A patent/CA2602199C/fr not_active Expired - Fee Related
- 2006-03-29 AU AU2006230337A patent/AU2006230337B2/en not_active Ceased
- 2006-03-29 JP JP2008504337A patent/JP5117374B2/ja not_active Expired - Fee Related
- 2006-03-29 SI SI200630870T patent/SI1869020T1/sl unknown
- 2006-03-29 AT AT06748900T patent/ATE490248T1/de active
- 2006-03-29 PT PT06748900T patent/PT1869020E/pt unknown
- 2006-03-29 US US11/908,416 patent/US8093244B2/en not_active Expired - Fee Related
- 2006-03-29 RS RS20110053A patent/RS51616B/sr unknown
- 2006-03-29 CN CN2011101022112A patent/CN102219784A/zh active Pending
- 2006-03-29 CN CN2006800101504A patent/CN101151259B/zh not_active Expired - Fee Related
- 2006-03-29 EP EP06748900A patent/EP1869020B1/fr not_active Expired - Lifetime
- 2006-03-29 BR BRPI0609667-0A patent/BRPI0609667A2/pt not_active IP Right Cessation
- 2006-03-29 NZ NZ561458A patent/NZ561458A/en not_active IP Right Cessation
- 2006-03-29 DK DK06748900.5T patent/DK1869020T3/da active
- 2006-03-29 PL PL06748900T patent/PL1869020T3/pl unknown
- 2006-03-29 EP EP10189889A patent/EP2330105A1/fr not_active Withdrawn
- 2006-03-29 WO PCT/US2006/011584 patent/WO2006105262A1/fr not_active Ceased
- 2006-03-29 AR ARP060101226A patent/AR056645A1/es unknown
- 2006-03-29 TW TW095110859A patent/TWI375559B/zh not_active IP Right Cessation
- 2006-03-29 DE DE602006018590T patent/DE602006018590D1/de not_active Expired - Lifetime
- 2006-03-29 EA EA200702094A patent/EA011287B1/ru not_active IP Right Cessation
- 2006-03-29 KR KR1020077022281A patent/KR100912998B1/ko not_active Expired - Fee Related
-
2007
- 2007-08-23 IL IL185481A patent/IL185481A0/en unknown
- 2007-09-07 ZA ZA200707715A patent/ZA200707715B/xx unknown
- 2007-09-26 CR CR9395A patent/CR9395A/es unknown
- 2007-09-28 TN TNP2007000369A patent/TNSN07369A1/en unknown
- 2007-10-01 NO NO20074944A patent/NO20074944L/no not_active Application Discontinuation
- 2007-10-26 MA MA30325A patent/MA29439B1/fr unknown
-
2009
- 2009-05-20 JP JP2009122107A patent/JP2009227682A/ja active Pending
-
2011
- 2011-02-03 CY CY20111100117T patent/CY1111240T1/el unknown
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| MA29692B1 (fr) | Derives de la xanthine en tant qu'agonistes selectifs du hm74a | |
| MA32300B1 (fr) | Anticorps anti-facteur d humanises et utilisations de ceux-ci | |
| MA31260B1 (fr) | 3-imidazolyl-indoles pour le traitement de maladies proliferatives | |
| EP1841426A4 (fr) | Carbinamines tertiaires incluant des heterocycles substitues, agissant en tant qu'inhibiteurs de la beta-secretase et utilisees dans le traitement de la maladie d'alzheimer | |
| MA29568B1 (fr) | Composes d'azaindazole et methodes d'utilisation desdits composes | |
| EP1651623A4 (fr) | Hexahydrodiazepinones utilises en tant qu'inhibiteurs de la dipeptidyl peptidase iv pour le traitement ou la prevention du diabete | |
| TN2009000551A1 (fr) | Nouveaux composes chimiques | |
| ATE440087T1 (de) | 2,4-diaminopyrimidinderivate, die sich als inhibitoren von pkc-theta eignen | |
| MA30340B1 (fr) | Nouveaux composes | |
| EP1673078A4 (fr) | Inhibiteurs de type benzylether et benzylamino de beta-secretase pour le traitement de la maladie d'alzheimer | |
| MA27675A1 (fr) | Derives de piperazine et leur utilisation dans le traitement de maladies neurologiques et psychiatriques | |
| MA30333B1 (fr) | Aminotetrahydropyranes utiles en tant qu'inhibiteurs de la dipeptidyle peptidase-iv pour le traitement ou la prevention du diabete. | |
| NO20064726L (no) | Imidazolforbindelser for behandling av neurodegenerative forstyrrelser | |
| MA33606B1 (fr) | Dérivés de pyrimidine en tant qu'inhibiteurs de protéine tyrosine kinase 2 | |
| MA31283B1 (fr) | Produits dérivés de 2,3-dihydroimidazo[1,2-c]quinazoline substitués, utiles pour le traitement de troubles hyperlifératifs et de maladies associées à une angiogénèse | |
| MA27482A1 (fr) | Piperazines, (1,4) diazepines, et 2,5-diazabicyclo (2.2.1) heptanes substitues en tant qu'antagonistes de l'histamine h1 et/ou h3 ou antagonistes inverses de l'histamine h3 | |
| EP1888066A4 (fr) | Aminocyclohexanes en tant qu'inhibiteurs de dipeptidyle peptidase-iv pour le traitement ou la prevention du diabete | |
| EP1624874A4 (fr) | Derives d'acide 3-amino-4-phenylbutanoique en tant qu'inhibiteurs de dipeptidyl peptidase dans le cadre du traitement ou de la prevention du diabete | |
| CY1111086T1 (el) | Παραγωγα 2-αμινο-κιναζολινης χρησιμα ως αναστολεις της βητα-σεκρετασης (bace) | |
| EP1784188A4 (fr) | Derives de triazole accoles inhibiteurs de la dipeptidyl peptidase-iv utilises dans le traitement ou la prevention du diabete | |
| MA30041B1 (fr) | Immunoglobulines | |
| MA34655B1 (fr) | Dérivés de 2,3- dihydroimidazo[1,2-c]quinazoléine substitués par un aminoalcool utiles pour traiter des troubles hyperprolifératifs et des maladies associées à l'angiogenèse | |
| BRPI0509391A (pt) | piridonas substituìdos como inibidores de poli(adp-ribose) polimerase (parp) | |
| CL2007002899A1 (es) | Compuestos derivados de azaciclilaminas n-sustituidas, inhibidores del receptor de histamina 3; proceso de preparacion; composicion farmaceutica que comprende los compuestos, y usopara el tratamiento de trastornos cognitivos, esquizofre nia y enfermedad de alzheimer entre otros. | |
| EP2091328A4 (fr) | Composés de spiropipéridine inhibiteurs de la bêta-sécrétase pour le traitement de la maladie d'alzheimer |