AU2003215325B8 - Purine derivatives as kinase inhibitors - Google Patents
Purine derivatives as kinase inhibitors Download PDFInfo
- Publication number
- AU2003215325B8 AU2003215325B8 AU2003215325A AU2003215325A AU2003215325B8 AU 2003215325 B8 AU2003215325 B8 AU 2003215325B8 AU 2003215325 A AU2003215325 A AU 2003215325A AU 2003215325 A AU2003215325 A AU 2003215325A AU 2003215325 B8 AU2003215325 B8 AU 2003215325B8
- Authority
- AU
- Australia
- Prior art keywords
- dihydro
- dioxopyrrole
- indol
- diazepino
- mmol
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Ceased
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/06—Peri-condensed systems
-
- 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
-
- 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
- A61P19/10—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease for osteoporosis
-
- 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
- A61P25/08—Antiepileptics; Anticonvulsants
-
- 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
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/06—Peri-condensed systems
Landscapes
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Physical Education & Sports Medicine (AREA)
- Diabetes (AREA)
- Rheumatology (AREA)
- Neurology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Biomedical Technology (AREA)
- Neurosurgery (AREA)
- Emergency Medicine (AREA)
- Hospice & Palliative Care (AREA)
- Psychiatry (AREA)
- Pain & Pain Management (AREA)
- Obesity (AREA)
- Hematology (AREA)
- Endocrinology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Enzymes And Modification Thereof (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US36224502P | 2002-03-05 | 2002-03-05 | |
| US60/362,245 | 2002-03-05 | ||
| PCT/US2003/005050 WO2003076442A1 (en) | 2002-03-05 | 2003-03-04 | Purine derivatives as kinase inhibitors |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| AU2003215325A1 AU2003215325A1 (en) | 2003-09-22 |
| AU2003215325B2 AU2003215325B2 (en) | 2008-09-18 |
| AU2003215325B8 true AU2003215325B8 (en) | 2008-10-09 |
Family
ID=27805149
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AU2003215325A Ceased AU2003215325B8 (en) | 2002-03-05 | 2003-03-04 | Purine derivatives as kinase inhibitors |
Country Status (16)
| Country | Link |
|---|---|
| US (4) | US7491716B2 (https=) |
| EP (1) | EP1483265B1 (https=) |
| JP (1) | JP4414232B2 (https=) |
| KR (1) | KR100974770B1 (https=) |
| CN (1) | CN1312154C (https=) |
| AT (1) | ATE346070T1 (https=) |
| AU (1) | AU2003215325B8 (https=) |
| BR (1) | BR0308243B1 (https=) |
| CA (1) | CA2477967C (https=) |
| CY (1) | CY1109006T1 (https=) |
| DE (1) | DE60309848T2 (https=) |
| DK (1) | DK1483265T3 (https=) |
| ES (1) | ES2276048T3 (https=) |
| IL (2) | IL163781A0 (https=) |
| PT (1) | PT1483265E (https=) |
| WO (1) | WO2003076442A1 (https=) |
Families Citing this family (68)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ES2289274T3 (es) * | 2002-03-08 | 2008-02-01 | Eli Lilly And Company | Derivados de pirrol-2,5-diona y su uso como inhibidores de gsk-3. |
| GB0212049D0 (en) * | 2002-05-24 | 2002-07-03 | Merck Sharp & Dohme | Therapeutic agents |
| KR100941205B1 (ko) | 2005-02-09 | 2010-02-10 | 아르퀼 인코포레이티드 | 말레이미드 유도체, 약제학적 조성물 및 암을 치료하는방법 |
| US20080207594A1 (en) * | 2005-05-04 | 2008-08-28 | Davelogen Aktiengesellschaft | Use of Gsk-3 Inhibitors for Preventing and Treating Pancreatic Autoimmune Disorders |
| EP1879591B8 (en) * | 2005-05-04 | 2012-04-04 | DeveloGen Aktiengesellschaft | Use of azapaullones for preventing and treating pancreatic autoimmune disorders |
| EP2275095A3 (en) | 2005-08-26 | 2011-08-17 | Braincells, Inc. | Neurogenesis by muscarinic receptor modulation |
| EP2258358A3 (en) | 2005-08-26 | 2011-09-07 | Braincells, Inc. | Neurogenesis with acetylcholinesterase inhibitor |
| EP1940389A2 (en) | 2005-10-21 | 2008-07-09 | Braincells, Inc. | Modulation of neurogenesis by pde inhibition |
| AU2006308889A1 (en) | 2005-10-31 | 2007-05-10 | Braincells, Inc. | GABA receptor mediated modulation of neurogenesis |
| TW200800203A (en) | 2006-03-08 | 2008-01-01 | Astrazeneca Ab | New use |
| US20100216734A1 (en) | 2006-03-08 | 2010-08-26 | Braincells, Inc. | Modulation of neurogenesis by nootropic agents |
| CA2645376C (en) * | 2006-03-13 | 2017-06-20 | Activx Biosciences, Inc. | Aminoquinolones as gsk-3 inhibitors |
| EP1845098A1 (en) | 2006-03-29 | 2007-10-17 | Ferrer Internacional, S.A. | Imidazo[1,2-b]pyridazines, their processes of preparation and their use as GABA receptor ligands |
| EP2382975A3 (en) | 2006-05-09 | 2012-02-29 | Braincells, Inc. | Neurogenesis by modulating angiotensin |
| EP2061767B1 (de) | 2006-08-08 | 2014-12-17 | Sanofi | Arylaminoaryl-alkyl-substituierte Imidazolidin-2,4-dione, Verfahren zu ihrer Herstellung, diese Verbindungen enthaltende Arzneimittel und ihre Verwendung |
| US20100184806A1 (en) | 2006-09-19 | 2010-07-22 | Braincells, Inc. | Modulation of neurogenesis by ppar agents |
| CN101302216B (zh) * | 2007-05-11 | 2011-08-10 | 上海睿智化学研究有限公司 | 稠环吲哚类化合物的制备方法 |
| CA2912546A1 (en) | 2007-06-22 | 2008-12-31 | Arqule, Inc. | Compositions and methods for treatment of cancer |
| EP2170870B1 (en) | 2007-06-22 | 2014-03-05 | ArQule, Inc. | Pyrrolidinone, pyrrolidine-2, 5-dione, pyrrolidine and thiosuccinimide derivatives, compositions and methods for treatment of cancer |
| KR20100024494A (ko) | 2007-06-22 | 2010-03-05 | 아르퀼 인코포레이티드 | 퀴나졸리논 화합물 및 이의 사용 방법 |
| TWI428132B (zh) * | 2007-07-02 | 2014-03-01 | Lilly Co Eli | 癌症化療效果之強化 |
| EP2025674A1 (de) | 2007-08-15 | 2009-02-18 | sanofi-aventis | Substituierte Tetrahydronaphthaline, Verfahren zu ihrer Herstellung und ihre Verwendung als Arzneimittel |
| JP5465720B2 (ja) * | 2008-07-08 | 2014-04-09 | インサイト・コーポレイション | インドールアミン2,3−ジオキシゲナーゼの阻害剤としての1,2,5−オキサジアゾール |
| UY31968A (es) | 2008-07-09 | 2010-01-29 | Sanofi Aventis | Nuevos derivados heterocíclicos, sus procesos para su preparación, y sus usos terapéuticos |
| WO2010068601A1 (en) | 2008-12-08 | 2010-06-17 | Sanofi-Aventis | A crystalline heteroaromatic fluoroglycoside hydrate, processes for making, methods of use and pharmaceutical compositions thereof |
| WO2010099217A1 (en) | 2009-02-25 | 2010-09-02 | Braincells, Inc. | Modulation of neurogenesis using d-cycloserine combinations |
| SG175207A1 (en) | 2009-04-14 | 2011-11-28 | Lilly Co Eli | Benzodiazepine derivative for the treatment of hematopoietic neoplasm and leukemia |
| KR20120060207A (ko) | 2009-08-26 | 2012-06-11 | 사노피 | 신규한 결정성 헤테로방향족 플루오로글리코시드 수화물, 이들 화합물을 포함하는 약제 및 이들의 용도 |
| KR101774035B1 (ko) | 2009-10-30 | 2017-09-01 | 얀센 파마슈티카 엔.브이. | 이미다조[1,2―b]피리다진 유도체 및 PDE10 저해제로서의 그의 용도 |
| WO2011082266A2 (en) | 2009-12-30 | 2011-07-07 | Arqule, Inc. | Substituted heterocyclic compounds |
| KR20120120307A (ko) | 2010-01-19 | 2012-11-01 | 아스트라제네카 아베 | 피라진 유도체 |
| WO2011107494A1 (de) | 2010-03-03 | 2011-09-09 | Sanofi | Neue aromatische glykosidderivate, diese verbindungen enthaltende arzneimittel und deren verwendung |
| AR080754A1 (es) | 2010-03-09 | 2012-05-09 | Janssen Pharmaceutica Nv | Derivados de imidazo (1,2-a) pirazina y su uso como inhibidores de pde10 |
| EP2582709B1 (de) | 2010-06-18 | 2018-01-24 | Sanofi | Azolopyridin-3-on-derivate als inhibitoren von lipasen und phospholipasen |
| US8530413B2 (en) | 2010-06-21 | 2013-09-10 | Sanofi | Heterocyclically substituted methoxyphenyl derivatives with an oxo group, processes for preparation thereof and use thereof as medicaments |
| TW201221505A (en) | 2010-07-05 | 2012-06-01 | Sanofi Sa | Aryloxyalkylene-substituted hydroxyphenylhexynoic acids, process for preparation thereof and use thereof as a medicament |
| TW201215387A (en) | 2010-07-05 | 2012-04-16 | Sanofi Aventis | Spirocyclically substituted 1,3-propane dioxide derivatives, processes for preparation thereof and use thereof as a medicament |
| TW201215388A (en) | 2010-07-05 | 2012-04-16 | Sanofi Sa | (2-aryloxyacetylamino)phenylpropionic acid derivatives, processes for preparation thereof and use thereof as medicaments |
| JP5984837B2 (ja) * | 2010-12-23 | 2016-09-06 | アークル インコーポレイテッド | ピロロキノリニル−ピロリジン−2,5−ジオン組成物ならびにそれを調製および使用する方法 |
| EP2683702B1 (de) | 2011-03-08 | 2014-12-24 | Sanofi | Neue substituierte phenyl-oxathiazinderivate, verfahren zu deren herstellung, diese verbindungen enthaltende arzneimittel und deren verwendung |
| US8828994B2 (en) | 2011-03-08 | 2014-09-09 | Sanofi | Di- and tri-substituted oxathiazine derivatives, method for the production thereof, use thereof as medicine and drug containing said derivatives and use thereof |
| EP2683704B1 (de) | 2011-03-08 | 2014-12-17 | Sanofi | Verzweigte oxathiazinderivate, verfahren zu deren herstellung, ihre verwendung als medikament sowie sie enthaltendes arzneimittel und deren verwendung |
| WO2012120051A1 (de) | 2011-03-08 | 2012-09-13 | Sanofi | Mit adamantan- oder noradamantan substituierte benzyl-oxathiazinderivate, diese verbindungen enthaltende arzneimittel und deren verwendung |
| WO2012120056A1 (de) | 2011-03-08 | 2012-09-13 | Sanofi | Tetrasubstituierte oxathiazinderivate, verfahren zu deren herstellung, ihre verwendung als medikament sowie sie enthaltendes arzneimittel und deren verwendung |
| EP2683699B1 (de) | 2011-03-08 | 2015-06-24 | Sanofi | Di- und trisubstituierte oxathiazinderivate, verfahren zu deren herstellung, ihre verwendung als medikament sowie sie enthaltendes arzneimittel und deren verwendung |
| EP2766349B1 (de) | 2011-03-08 | 2016-06-01 | Sanofi | Mit carbozyklen oder heterozyklen substituierte oxathiazinderivate, verfahren zu deren herstellung, diese verbindungen enthaltende arzneimittel und deren verwendung |
| WO2012120058A1 (de) | 2011-03-08 | 2012-09-13 | Sanofi | Mit benzyl- oder heteromethylengruppen substituierte oxathiazinderivate, verfahren zu deren herstellung, ihre verwendung als medikament sowie sie enthaltendes arzneimittel und deren verwendung |
| US8895547B2 (en) | 2011-03-08 | 2014-11-25 | Sanofi | Substituted phenyl-oxathiazine derivatives, method for producing them, drugs containing said compounds and the use thereof |
| WO2013000924A1 (en) | 2011-06-27 | 2013-01-03 | Janssen Pharmaceutica Nv | 1-ARYL-4-METHYL-[1,2,4]TRIAZOLO[4,3-a]QUINOXALINE DERIVATIVES |
| WO2013037390A1 (en) | 2011-09-12 | 2013-03-21 | Sanofi | 6-(4-hydroxy-phenyl)-3-styryl-1h-pyrazolo[3,4-b]pyridine-4-carboxylic acid amide derivatives as kinase inhibitors |
| WO2013045413A1 (en) | 2011-09-27 | 2013-04-04 | Sanofi | 6-(4-hydroxy-phenyl)-3-alkyl-1h-pyrazolo[3,4-b]pyridine-4-carboxylic acid amide derivatives as kinase inhibitors |
| WO2014001314A1 (en) | 2012-06-26 | 2014-01-03 | Janssen Pharmaceutica Nv | Combinations comprising pde 2 inhibitors such as 1-aryl-4-methyl- [1,2,4] triazolo [4,3-a] quinoxaline compounds and pde 10 inhibitors for use in the treatment of neurological or metabolic disorders |
| AU2013289284B2 (en) | 2012-07-09 | 2017-03-30 | Janssen Pharmaceutica Nv | Inhibitors of phosphodiesterase 10 enzyme |
| WO2014098000A1 (en) * | 2012-12-17 | 2014-06-26 | Daiichi Sankyo Company, Limited | Process for preparation of a tricyclic heterocycle |
| EP3015468A4 (en) | 2013-06-26 | 2017-02-22 | Daiichi Sankyo Co., Ltd. | Method for producing tricyclic heterocyclic compound |
| EP2818471A1 (en) * | 2013-06-27 | 2014-12-31 | Max-Planck-Gesellschaft zur Förderung der Wissenschaften e.V. | Nitrogen bicyclic compounds as inhibitors for Scyl1 and Grk5 |
| EP3562827A1 (en) * | 2016-12-30 | 2019-11-06 | Frequency Therapeutics, Inc. | 1h-pyrrole-2,5-dione compounds and methods of using them to induce self-renewal of stem/progenitor supporting cells |
| WO2018191350A1 (en) | 2017-04-11 | 2018-10-18 | Frequency Therapeutics, Inc. | Methods for hair follicle stem cell proliferation |
| WO2019126686A1 (en) * | 2017-12-21 | 2019-06-27 | Frequency Therapeutics, Inc. | 1,2-dihydro-3h-pyrazol-3-one compounds and methods of using same |
| US10526343B2 (en) | 2018-03-26 | 2020-01-07 | University Of Sharjah | Heterocyclic systems and pharmaceutical applications thereof |
| CN112839648B (zh) | 2018-06-07 | 2025-04-04 | 达萨玛治疗公司 | Sarm1抑制剂 |
| AU2019318209B2 (en) | 2018-08-10 | 2025-09-25 | Diapin Therapeutics, Llc | Tri-peptides and treatment of metabolic, cardiovascular and inflammatory disorders |
| WO2020081838A1 (en) | 2018-10-17 | 2020-04-23 | Frequency Therapeutics, Inc. | Methods for hair follicle stem cell proliferation |
| EP3897670A4 (en) | 2018-12-19 | 2022-09-07 | Disarm Therapeutics, Inc. | MRSA1 INHIBITORS IN COMBINATION WITH NEUROPROTECTIVE AGENTS |
| EP3920885A1 (en) | 2019-02-08 | 2021-12-15 | Frequency Therapeutics, Inc. | Valproic acid compounds and wnt agonists for treating ear disorders |
| CN112390794B (zh) * | 2019-08-19 | 2023-05-26 | 鲁南制药集团股份有限公司 | 一种米诺膦酸关键中间体的制备方法 |
| CN115925622B (zh) * | 2023-02-10 | 2025-04-22 | 山西永津集团有限公司 | 一种3-氰基吡啶-2-基氨基甲酸叔丁酯的合成方法 |
| CN115974850B (zh) * | 2023-02-16 | 2024-08-06 | 中国药科大学 | 一类作为akr1c3抑制剂的化合物及其制备方法与用途 |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NZ227850A (en) * | 1988-02-10 | 1991-11-26 | Hoffmann La Roche | Indole substituted pyrrole derivatives; preparatory process and medicaments for use against inflammatory immunological, bronchopulmonary or vascular disorders |
| GB8904161D0 (en) * | 1989-02-23 | 1989-04-05 | Hoffmann La Roche | Substituted pyrroles |
| WO1998016528A1 (en) | 1996-10-11 | 1998-04-23 | Chiron Corporation | Purine inhibitors of glycogen synthase kinase 3 (gsk3) |
| GB9828640D0 (en) | 1998-12-23 | 1999-02-17 | Smithkline Beecham Plc | Novel method and compounds |
| AU2576901A (en) * | 1999-12-16 | 2001-06-25 | Eli Lilly And Company | Agents and methods for the treatment of proliferative diseases |
| EP1242420A2 (en) | 1999-12-16 | 2002-09-25 | Eli Lilly And Company | Agents and methods for the treatment of proliferative diseases |
| CA2417277A1 (en) | 2000-07-27 | 2002-02-07 | F. Hoffmann-La Roche Ag | 3-indolyl-4-phenyl-1h-pyrrole-2,5-dione derivatives as inhibitors of glycogen synthase kinase-3.beta. |
| ATE301661T1 (de) | 2000-12-08 | 2005-08-15 | Ortho Mcneil Pharm Inc | Makroheterocyclische verbindungen als kinase inhibitoren |
| BR0116468A (pt) | 2000-12-08 | 2004-06-29 | Ortho Mcneil Pharm Inc | Compostos de pirrolina substituìda por indazolila como inibidores de cinase |
-
2003
- 2003-03-04 WO PCT/US2003/005050 patent/WO2003076442A1/en not_active Ceased
- 2003-03-04 CN CNB03805292XA patent/CN1312154C/zh not_active Expired - Fee Related
- 2003-03-04 IL IL16378103A patent/IL163781A0/xx unknown
- 2003-03-04 KR KR1020047013828A patent/KR100974770B1/ko not_active Expired - Fee Related
- 2003-03-04 CA CA2477967A patent/CA2477967C/en not_active Expired - Fee Related
- 2003-03-04 DE DE60309848T patent/DE60309848T2/de not_active Expired - Lifetime
- 2003-03-04 AT AT03711146T patent/ATE346070T1/de active
- 2003-03-04 AU AU2003215325A patent/AU2003215325B8/en not_active Ceased
- 2003-03-04 DK DK03711146T patent/DK1483265T3/da active
- 2003-03-04 JP JP2003574659A patent/JP4414232B2/ja not_active Expired - Fee Related
- 2003-03-04 EP EP03711146A patent/EP1483265B1/en not_active Expired - Lifetime
- 2003-03-04 BR BRPI0308243-1A patent/BR0308243B1/pt not_active IP Right Cessation
- 2003-03-04 ES ES03711146T patent/ES2276048T3/es not_active Expired - Lifetime
- 2003-03-04 US US10/506,459 patent/US7491716B2/en not_active Expired - Fee Related
- 2003-03-04 PT PT03711146T patent/PT1483265E/pt unknown
-
2004
- 2004-08-26 IL IL163781A patent/IL163781A/en not_active IP Right Cessation
-
2007
- 2007-01-18 CY CY20071100071T patent/CY1109006T1/el unknown
-
2008
- 2008-12-12 US US12/333,775 patent/US8022065B2/en not_active Expired - Fee Related
-
2011
- 2011-05-04 US US13/100,618 patent/US8058425B2/en not_active Expired - Fee Related
- 2011-08-09 US US13/206,057 patent/US20110294792A1/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| US8058425B2 (en) | 2011-11-15 |
| IL163781A0 (en) | 2005-12-18 |
| EP1483265B1 (en) | 2006-11-22 |
| AU2003215325B2 (en) | 2008-09-18 |
| CA2477967C (en) | 2010-08-10 |
| EP1483265A1 (en) | 2004-12-08 |
| CA2477967A1 (en) | 2003-09-18 |
| PT1483265E (pt) | 2007-01-31 |
| JP4414232B2 (ja) | 2010-02-10 |
| US20110294792A1 (en) | 2011-12-01 |
| CN1639165A (zh) | 2005-07-13 |
| US8022065B2 (en) | 2011-09-20 |
| KR20040087338A (ko) | 2004-10-13 |
| US20050090483A1 (en) | 2005-04-28 |
| JP2005526072A (ja) | 2005-09-02 |
| DE60309848T2 (de) | 2007-05-16 |
| BR0308243B1 (pt) | 2014-08-26 |
| KR100974770B1 (ko) | 2010-08-06 |
| CN1312154C (zh) | 2007-04-25 |
| DE60309848D1 (de) | 2007-01-04 |
| US20110207721A1 (en) | 2011-08-25 |
| BR0308243A (pt) | 2005-01-11 |
| IL163781A (en) | 2010-04-15 |
| DK1483265T3 (da) | 2007-03-19 |
| AU2003215325A1 (en) | 2003-09-22 |
| WO2003076442A1 (en) | 2003-09-18 |
| CY1109006T1 (el) | 2014-07-02 |
| ATE346070T1 (de) | 2006-12-15 |
| US20090105229A1 (en) | 2009-04-23 |
| US7491716B2 (en) | 2009-02-17 |
| ES2276048T3 (es) | 2007-06-16 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| AU2003215325B8 (en) | Purine derivatives as kinase inhibitors | |
| AU2007209689B2 (en) | Pyrrolo [3,2-c] pyridine-4-one 2-indolinone protein kinase inhibitors | |
| KR101793807B1 (ko) | 단백질 키나제 억제제로서의 융합된 헤테로시클릭 화합물 | |
| CN111867590B (zh) | Atr激酶的杂环抑制剂 | |
| US20210393623A1 (en) | Novel Heterocyclic Derivatives Useful as SHP2 Inhibitors | |
| CZ301751B6 (cs) | Bicyklický pyrrolový derivát, farmaceutická kompozice obsahující tento derivát, tato kompozice pro použití pri lécení a použití uvedeného derivátu pri výrobe léciva | |
| AU2023501A (en) | Fused heterotricyclic compounds, process for preparing the compounds and drugs containing the same | |
| TW202246266A (zh) | 作為parp7抑制劑的三環衍生物 | |
| WO2022167682A1 (en) | Azabicyclic shp2 inhibitors | |
| CN101243087A (zh) | 1,4-二氢吡啶-稠合杂环、其制备方法、应用以及含有其的组合物 | |
| WO2024067694A1 (zh) | 含氮杂环类化合物及其医药用途 | |
| EP1250334B1 (en) | Medicaments useful for the treatment of proliferative diseases | |
| US6743785B2 (en) | Agents and methods for the treatment of proliferative diseases | |
| CN101203516A (zh) | 用于免疫抑制的嘌呤及咪唑并吡啶衍生物 |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| TH | Corrigenda |
Free format text: IN VOL 22, NO 37, PAGE(S) 4433 UNDER THE HEADING APPLICATIONS ACCEPTED -NAME INDEX UNDER THE NAME ELI LILLY AND COMPANY, APPLICATION NO. 2003215325, U NDER INID(72), CORRECT THE CO INVENTOR NAME TO BERRIDGE, BRIAN RAYMOND, RUEGG, CHARLES EDWARDS AND SULLIVAN, JOHN MORRIS |
|
| FGA | Letters patent sealed or granted (standard patent) | ||
| MK14 | Patent ceased section 143(a) (annual fees not paid) or expired |