BRPI0410714A - derivados de quinazolina - Google Patents
derivados de quinazolinaInfo
- Publication number
- BRPI0410714A BRPI0410714A BRPI0410714-4A BRPI0410714A BRPI0410714A BR PI0410714 A BRPI0410714 A BR PI0410714A BR PI0410714 A BRPI0410714 A BR PI0410714A BR PI0410714 A BRPI0410714 A BR PI0410714A
- Authority
- BR
- Brazil
- Prior art keywords
- alkyl
- independently represent
- het
- represent hydrogen
- optionally substituted
- Prior art date
Links
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D498/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D498/06—Peri-condensed systems
-
- 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
- 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
-
- 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
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C229/00—Compounds containing amino and carboxyl groups bound to the same carbon skeleton
- C07C229/02—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton
- C07C229/04—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated
- C07C229/06—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated having only one amino and one carboxyl group bound to the carbon skeleton
- C07C229/10—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated having only one amino and one carboxyl group bound to the carbon skeleton the nitrogen atom of the amino group being further bound to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings
- C07C229/16—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated having only one amino and one carboxyl group bound to the carbon skeleton the nitrogen atom of the amino group being further bound to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings to carbon atoms of hydrocarbon radicals substituted by amino or carboxyl groups, e.g. ethylenediamine-tetra-acetic acid, iminodiacetic acids
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C229/00—Compounds containing amino and carboxyl groups bound to the same carbon skeleton
- C07C229/40—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino groups bound to carbon atoms of at least one six-membered aromatic ring and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton
-
- 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
- C07D239/86—Quinazolines; Hydrogenated quinazolines with hetero atoms directly attached in position 4
- C07D239/88—Oxygen atoms
-
- 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
- C07D239/86—Quinazolines; Hydrogenated quinazolines with hetero atoms directly attached in position 4
- C07D239/93—Sulfur atoms
-
- 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
- C07D239/86—Quinazolines; Hydrogenated quinazolines with hetero atoms directly attached in position 4
- C07D239/94—Nitrogen atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Engineering & Computer Science (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Heart & Thoracic Surgery (AREA)
- Cardiology (AREA)
- Vascular Medicine (AREA)
- Urology & Nephrology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Abstract
"DERIVADOS DE QUINAZOLINA". A presente invenção se refere a compostos da fórmula: as formas de N-óxido, os sais de adição farmaceuticamente aceitáveis e as formas estereoquimicamente isoméricas do mesmo, em que: Z representa NH; Y representa -C~ 3-9~ alquila-, -C~ 2-9~ alquenila-, -C~ 3-7~alquil-CO-NH opcionalmente substituída por amino, mono - ou di(C~ 1-4~alquil)amino ou C~ 1-4~ alquilóxicarbonilamino-, -C~ 3-7~alquenil-CO-NH- opcionalmente substituído por amino, mono- ou di(C~ 1~-4~alquil)amino- ou C~ 1-4~ alquilóxicarbonilamino-, C~ 1-5~alquil-NR~ 13~-C~ 1-5~ alquila-, C~ 1-5~alquil-NR¬ 14¬-CO-C~ 1-5~ alquila-, -C~ 1-6~alquil-CO-NH-, -C~ 1-5~alquil-CO NR¬ 15¬-C~ 1-5~ alquila-, -C~ 1-3~alquil-NH-CO-Het¬ 20¬-, -C~ 1-2~alquil-CO-Het¬ 21¬CO-, -C~ 1-2~alquil-NH-CO-CR¬ 16¬R¬ 17¬-NH-, -C~ 1-2~alquiL-CO-NH-CR¬ 18¬R¬ 19¬-CO-, -C~ 1-2~alquiL-CO-Nr¬ 20¬-C~ 1-3~alquil-CO- ou -NR¬ 22¬-CO-C~ 1-3~alquil-NH-; X¬ 1¬ representa uma ligação direta, O ou -O-C~ 1-2~ alquila-; X¬ 2¬ representa uma ligação direta, -CO-C~ 1-2~ alquila-, NR¬ 12¬,-NR¬ 12¬-C~ 1-2~ alquila-, -O-N=CH- ou -C~ 1-2~ alquila-; R¬ 1¬ e R¬ 2¬ representam, cada um independentemente, hidrogênio ou halo; R¬ 3¬ representa hidrogênio; R¬ 4¬ representa hidrogênio ou C~ 1-4~ alquilóxi; R¬ 12¬ e R¬ 13¬ representam, cada um independentemente, hidrogênio OU C~ 1-4~ alquila; R¬ 14¬ e R¬ 15¬ representa hidrogênio; R¬ 16¬ e R~ 17¬ representam, cada um independentemente, hidrogênio ou C~ 1-4~ alquila; R¬ 18¬ e R¬ 19¬ representam, cada um independentemente, hidrogênio ou C~ 1-4~ alquila opcionalmente substituída por fenila ou hidróxi; R¬ 20¬ e R¬ 21¬ representam, cada um independentemente, hidrogênio OU C~ 1-4~ alquila opcionalmente substituída por C~ 1-4~ alquilóxi; Het¬ 20¬, Het¬ 21¬ e Het¬ 22¬ representam, cada um independentemente, um heterociclo selecionado do grupo consistindo de pirrolidinila, 2-pirrolidinonila ou piperidinila opcionalmente substituída por hidróxi.
Applications Claiming Priority (7)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP0305723 | 2003-05-27 | ||
| EPPCT/EP03/05723 | 2003-05-27 | ||
| EPPCT/EP03/10266 | 2003-09-15 | ||
| EP0310266 | 2003-09-15 | ||
| EP0351061 | 2003-12-18 | ||
| EPPCT/EP03/51061 | 2003-12-18 | ||
| PCT/EP2004/005621 WO2004105765A1 (en) | 2003-05-27 | 2004-05-25 | Macrocyclic quinazoline derivatives as antiproliferative agents |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| BRPI0410714A true BRPI0410714A (pt) | 2006-06-13 |
| BRPI0410714B1 BRPI0410714B1 (pt) | 2019-09-24 |
| BRPI0410714B8 BRPI0410714B8 (pt) | 2021-05-25 |
Family
ID=33493782
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| BRPI0410714A BRPI0410714B8 (pt) | 2003-05-27 | 2004-05-25 | derivados de quinazolina macrocíclicos, seu processo de preparação, composição farmacêutica que os compreende e uso |
Country Status (31)
| Country | Link |
|---|---|
| US (4) | US7648975B2 (pt) |
| EP (2) | EP2305687A1 (pt) |
| JP (1) | JP4887151B2 (pt) |
| KR (1) | KR101143878B1 (pt) |
| CN (1) | CN102718775B (pt) |
| AR (2) | AR045687A1 (pt) |
| AT (1) | ATE544454T1 (pt) |
| AU (1) | AU2004243487B2 (pt) |
| BR (1) | BRPI0410714B8 (pt) |
| CA (1) | CA2525214C (pt) |
| CL (1) | CL2004001267A1 (pt) |
| CO (1) | CO5640038A2 (pt) |
| CY (1) | CY1113002T1 (pt) |
| DK (1) | DK1633365T3 (pt) |
| EA (1) | EA009064B1 (pt) |
| ES (1) | ES2381976T3 (pt) |
| HR (1) | HRP20120351T1 (pt) |
| IL (3) | IL172154A0 (pt) |
| IS (1) | IS3030B (pt) |
| JO (1) | JO2785B1 (pt) |
| MX (1) | MXPA05012762A (pt) |
| MY (1) | MY148633A (pt) |
| NO (1) | NO334209B1 (pt) |
| NZ (1) | NZ544154A (pt) |
| PA (1) | PA8603801A1 (pt) |
| PL (1) | PL1633365T3 (pt) |
| PT (1) | PT1633365E (pt) |
| SI (1) | SI1633365T1 (pt) |
| TW (3) | TWI379835B (pt) |
| UA (1) | UA84010C2 (pt) |
| WO (1) | WO2004105765A1 (pt) |
Families Citing this family (53)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JO2785B1 (en) * | 2003-05-27 | 2014-03-15 | شركة جانسين فارماسوتيكا ان. في | Quinazoline derivatives |
| EP1684762A4 (en) * | 2003-11-13 | 2009-06-17 | Ambit Biosciences Corp | UREA DERIVATIVES AS MODULATORS OF KINASE |
| MXPA06007018A (es) * | 2003-12-18 | 2006-08-31 | Janssen Pharmaceutica Nv | Derivados de 3-ciano-quinolino con actividad anti-proliferativa. |
| MXPA06007017A (es) | 2003-12-18 | 2006-08-31 | Janssen Pharmaceutica Nv | Derivados de pirido y pirimidopirimidina como agentes antiproliferativos. |
| NI200700147A (es) | 2004-12-08 | 2019-05-10 | Janssen Pharmaceutica Nv | Derivados de quinazolina inhibidores de cinasas dirigidos a multip |
| JO3088B1 (ar) * | 2004-12-08 | 2017-03-15 | Janssen Pharmaceutica Nv | مشتقات كوينازولين كبيرة الحلقات و استعمالها بصفتها موانع كينيز متعددة الاهداف |
| MY169441A (en) | 2004-12-08 | 2019-04-11 | Janssen Pharmaceutica Nv | 2,4, (4,6) pyrimidine derivatives |
| DK1854789T3 (da) | 2005-02-23 | 2013-10-21 | Shionogi & Co | Quinazolinderivat med tyrosin-kinase inhibitorisk aktivitet |
| GB0509227D0 (en) * | 2005-05-05 | 2005-06-15 | Chroma Therapeutics Ltd | Intracellular enzyme inhibitors |
| US8778919B2 (en) * | 2005-06-30 | 2014-07-15 | Janssen Pharmaceutica Nv | Cyclic anilino—pyridinotriazines |
| JP2009542778A (ja) * | 2006-07-13 | 2009-12-03 | ジヤンセン・フアーマシユーチカ・ナームローゼ・フエンノートシヤツプ | Mtkiキナゾリン誘導体 |
| JP2009242240A (ja) * | 2006-08-04 | 2009-10-22 | Mebiopharm Co Ltd | 含ホウ素キナゾリン誘導体 |
| EP2061469B8 (en) * | 2006-09-11 | 2014-02-26 | Curis, Inc. | Quinazoline based egfr inhibitors |
| US7547781B2 (en) | 2006-09-11 | 2009-06-16 | Curis, Inc. | Quinazoline based EGFR inhibitors containing a zinc binding moiety |
| AU2007296746B2 (en) | 2006-09-11 | 2012-07-05 | Curis, Inc. | Quinazoline based EGFR inhibitors containing a zinc binding moiety |
| AU2007310842A1 (en) * | 2006-10-27 | 2008-05-02 | Janssen Pharmaceutica Nv | Use of a MT kinase inhibitor for treating or preventing brain cancer |
| JP2010507384A (ja) * | 2006-10-27 | 2010-03-11 | ジヤンセン・フアーマシユーチカ・ナームローゼ・フエンノートシヤツプ | キナーゼ阻害剤のプロファイリング方法 |
| CA2664148A1 (en) * | 2006-10-27 | 2008-05-02 | Janssen Pharmaceutica Nv | Vegfr3 inhibitors |
| JP2010507628A (ja) * | 2006-10-27 | 2010-03-11 | ジヤンセン・フアーマシユーチカ・ナームローゼ・フエンノートシヤツプ | 骨ガンの処置又は予防のためのmtki1の使用 |
| EP2123627B1 (en) * | 2007-01-19 | 2013-11-20 | Ube Industries, Ltd. | Process for producing aromatic amine having aralkyloxy or heteroaralkyloxy group |
| US8642067B2 (en) | 2007-04-02 | 2014-02-04 | Allergen, Inc. | Methods and compositions for intraocular administration to treat ocular conditions |
| AU2008281849B2 (en) | 2007-07-27 | 2013-11-28 | Janssen Pharmaceutica Nv | Pyrrolopyrimidines |
| US8119616B2 (en) | 2007-09-10 | 2012-02-21 | Curis, Inc. | Formulation of quinazoline based EGFR inhibitors containing a zinc binding moiety |
| CL2008003384A1 (es) * | 2007-11-14 | 2009-12-11 | Enanta Pharm Inc | Compuestos derivados de quinoxalina macrocíclica, inhibidores de serina proteasa; composicion farmaceutica que los comprende; y su uso en el tratamiento de la hepatitis c. |
| US8426430B2 (en) | 2008-06-30 | 2013-04-23 | Hutchison Medipharma Enterprises Limited | Quinazoline derivatives |
| WO2010033941A1 (en) | 2008-09-22 | 2010-03-25 | Array Biopharma Inc. | Substituted imidazo[1,2b]pyridazine compounds as trk kinase inhibitors |
| MY169791A (en) | 2008-10-22 | 2019-05-15 | Array Biopharma Inc | Substituted pyrazolo [1,5-a] pyrimidine compounds as trk kinase inhibitors |
| WO2010085597A1 (en) * | 2009-01-23 | 2010-07-29 | Incyte Corporation | Macrocyclic compounds and their use as kinase inhibitors |
| AR077468A1 (es) | 2009-07-09 | 2011-08-31 | Array Biopharma Inc | Compuestos de pirazolo (1,5 -a) pirimidina sustituidos como inhibidores de trk- quinasa |
| TWI406853B (zh) * | 2010-04-07 | 2013-09-01 | Dev Center Biotechnology | Egfr與vegfr-2雙重抑制劑及其用途與製法 |
| ME03376B (me) | 2010-05-20 | 2020-01-20 | Array Biopharma Inc | Makrociklička jedinjenja kао inhibiтori trk kinaze |
| WO2013126015A1 (en) | 2012-02-23 | 2013-08-29 | N. V. Nutricia | Composition comprising non- digestible oligosaccharides |
| DK2822953T5 (en) * | 2012-03-06 | 2017-09-11 | Pfizer | Macrocyclic derivatives for the treatment of proliferative diseases |
| CN104513253A (zh) * | 2013-10-01 | 2015-04-15 | 南京波尔泰药业科技有限公司 | 用于治疗增殖性疾病的大环化合物 |
| RU2733405C2 (ru) * | 2014-02-07 | 2020-10-01 | Экзитера Фармасьютикалз Инк. | Терапевтические соединения и композиции |
| MA39822A (fr) | 2014-04-03 | 2018-02-06 | Janssen Pharmaceutica Nv | Dérivés de pyrimidine bicycle |
| MA39823A (fr) | 2014-04-03 | 2018-01-09 | Janssen Pharmaceutica Nv | Dérivés de pyridine macrocyclique |
| CN113354649B (zh) | 2014-11-16 | 2024-12-10 | 阵列生物制药公司 | 一种新的晶型 |
| JP6740354B2 (ja) | 2015-10-05 | 2020-08-12 | ザ トラスティーズ オブ コロンビア ユニバーシティー イン ザ シティー オブ ニューヨーク | オートファジーの流れ及びホスホリパーゼd及びタウを含むタンパク質凝集体のクリアランスの活性化剤ならびにタンパク質症の治療方法 |
| EP3368039A1 (en) | 2015-10-26 | 2018-09-05 | The Regents of The University of Colorado, A Body Corporate | Point mutations in trk inhibitor-resistant cancer and methods relating to the same |
| EP3423113B1 (en) | 2016-02-29 | 2020-09-02 | Oncodesign S.A. | Radiolabeled macrocyclic egfr inhibitor |
| US10045991B2 (en) | 2016-04-04 | 2018-08-14 | Loxo Oncology, Inc. | Methods of treating pediatric cancers |
| FI3439662T3 (fi) | 2016-04-04 | 2024-09-04 | Loxo Oncology Inc | (s)-n-(5-((r)-2-(2,5-difluorifenyyli)pyrrolidin-1-yyli)pyratsolo[1,5-a]pyrimidin-3-yyli)-3-hydroksipyrrolidiini-1-karboksamidin nesteformulaatioita |
| EP3458456B1 (en) | 2016-05-18 | 2020-11-25 | Loxo Oncology Inc. | Preparation of (s)-n-(5-((r)-2-(2,5-difluorophenyl)pyrrolidin-1-yl)pyrazolo[1,5-a]pyrimidin-3-yl)-3-hydroxypyrrolidine-1-carboxamide |
| JOP20190092A1 (ar) | 2016-10-26 | 2019-04-25 | Array Biopharma Inc | عملية لتحضير مركبات بيرازولو[1، 5-a]بيريميدين وأملاح منها |
| JOP20190213A1 (ar) | 2017-03-16 | 2019-09-16 | Array Biopharma Inc | مركبات حلقية ضخمة كمثبطات لكيناز ros1 |
| IL275121B2 (en) | 2017-12-07 | 2025-11-01 | Amplyx Pharmaceuticals Inc | Heterocycle substituted pyridine derivative antifungal agents |
| KR20210023984A (ko) | 2018-06-25 | 2021-03-04 | 앰플릭스 파마슈티컬스, 인크. | 헤테로환형 고리 및 아미노기로 치환된 피리딘 유도체 |
| US20230126352A1 (en) * | 2020-01-31 | 2023-04-27 | Oncodesign Sa | Macrocyclic rip2-kinase inhibitors |
| US20230159556A1 (en) * | 2020-04-20 | 2023-05-25 | Tenova Pharmaceuticals Inc. | Novel protein kinase inhibitors |
| WO2023114809A1 (en) | 2021-12-16 | 2023-06-22 | Kinnate Biopharma Inc. | Inhibitors of met kinase |
| WO2024017258A1 (zh) * | 2022-07-19 | 2024-01-25 | 百极弘烨(南通)医药科技有限公司 | Egfr小分子抑制剂、含其的药物组合物及其用途 |
| WO2026008023A1 (zh) * | 2024-07-04 | 2026-01-08 | 正大天晴药业集团股份有限公司 | 哒嗪胺类化合物及其医药用途 |
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| BE558251A (pt) * | 1956-06-11 | |||
| DE2423536A1 (de) | 1974-05-15 | 1975-11-27 | Bayer Ag | 3-amino-phenylessigsaeure-derivate, verfahren zu ihrer herstellung sowie ihre verwendung als herbizide |
| US4066772A (en) * | 1975-07-21 | 1978-01-03 | Janssen Pharmaceutica N.V. | 1,3-Dihydro-1-[3-(1-piperidinyl)propyl]-2H-benzimidazol-2-ones and related compounds |
| NZ181256A (en) * | 1975-07-21 | 1978-04-28 | Janssen Pharmaceutica Nv | 1-(w-benzazol-11-ylalkyl)-piperidine derivatives and pharmaceutical compositions containing certain of these derivatives |
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| FR2809400B1 (fr) * | 2000-05-25 | 2004-04-09 | Inst Francais Du Petrole | Materiaux comportant des groupements organiques contenant du soufre et du phosphore lie par l'intermediaire d'atomes d'oxygenes a un oxyde mineral |
| JO2785B1 (en) | 2003-05-27 | 2014-03-15 | شركة جانسين فارماسوتيكا ان. في | Quinazoline derivatives |
| JO3088B1 (ar) * | 2004-12-08 | 2017-03-15 | Janssen Pharmaceutica Nv | مشتقات كوينازولين كبيرة الحلقات و استعمالها بصفتها موانع كينيز متعددة الاهداف |
-
2004
- 2004-05-24 JO JO200466A patent/JO2785B1/en active
- 2004-05-24 PA PA20048603801A patent/PA8603801A1/es unknown
- 2004-05-25 CA CA2525214A patent/CA2525214C/en not_active Expired - Lifetime
- 2004-05-25 CN CN201210144221.7A patent/CN102718775B/zh not_active Expired - Lifetime
- 2004-05-25 US US10/558,007 patent/US7648975B2/en not_active Expired - Lifetime
- 2004-05-25 EA EA200501866A patent/EA009064B1/ru unknown
- 2004-05-25 EP EP10192741A patent/EP2305687A1/en not_active Withdrawn
- 2004-05-25 MX MXPA05012762A patent/MXPA05012762A/es active IP Right Grant
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- 2004-05-25 WO PCT/EP2004/005621 patent/WO2004105765A1/en not_active Ceased
- 2004-05-25 PT PT04739341T patent/PT1633365E/pt unknown
- 2004-05-25 JP JP2006529915A patent/JP4887151B2/ja not_active Expired - Lifetime
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- 2004-05-25 EP EP04739341A patent/EP1633365B1/en not_active Expired - Lifetime
- 2004-05-25 SI SI200431864T patent/SI1633365T1/sl unknown
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- 2004-05-25 DK DK04739341.8T patent/DK1633365T3/da active
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- 2004-05-26 AR ARP040101806A patent/AR045687A1/es active IP Right Grant
- 2004-05-26 TW TW101115205A patent/TWI468397B/zh not_active IP Right Cessation
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2005
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- 2005-11-24 IL IL172154A patent/IL172154A0/en active IP Right Grant
- 2005-11-24 CO CO05119403A patent/CO5640038A2/es active IP Right Grant
- 2005-12-27 NO NO20056196A patent/NO334209B1/no unknown
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2009
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2012
- 2012-05-08 CY CY20121100428T patent/CY1113002T1/el unknown
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2013
- 2013-01-18 US US13/744,878 patent/US9273013B2/en not_active Expired - Lifetime
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2014
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2016
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