JP5032851B2 - キナゾリン誘導体 - Google Patents
キナゾリン誘導体 Download PDFInfo
- Publication number
- JP5032851B2 JP5032851B2 JP2006551898A JP2006551898A JP5032851B2 JP 5032851 B2 JP5032851 B2 JP 5032851B2 JP 2006551898 A JP2006551898 A JP 2006551898A JP 2006551898 A JP2006551898 A JP 2006551898A JP 5032851 B2 JP5032851 B2 JP 5032851B2
- Authority
- JP
- Japan
- Prior art keywords
- alkyl
- formula
- amino
- group
- methyl
- 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.)
- Expired - Fee Related
Links
- 0 CC(C)(CC1*)CN(*)C1=O Chemical compound CC(C)(CC1*)CN(*)C1=O 0.000 description 6
- IWCYLFBJUBISCC-UHFFFAOYSA-N CN(Cc1cc2c(Nc(cccc3Cl)c3F)ncnc2cc1OC)C1(CCNCC1)C(N)=O Chemical compound CN(Cc1cc2c(Nc(cccc3Cl)c3F)ncnc2cc1OC)C1(CCNCC1)C(N)=O IWCYLFBJUBISCC-UHFFFAOYSA-N 0.000 description 2
- GCYWMKNZVNTVIY-UHFFFAOYSA-N CC(C(O)=O)N(Cc(cc1c(Nc(cccc2Cl)c2F)ncnc1c1)c1OC)C(COC)=C Chemical compound CC(C(O)=O)N(Cc(cc1c(Nc(cccc2Cl)c2F)ncnc1c1)c1OC)C(COC)=C GCYWMKNZVNTVIY-UHFFFAOYSA-N 0.000 description 1
- OJGQFAGYVWAAAD-ZDUSSCGKSA-N CC(C)N(Cc(cc1c(Nc(cccc2Cl)c2F)ncnc1c1)c1OC)[C@@H](C)C(N)=O Chemical compound CC(C)N(Cc(cc1c(Nc(cccc2Cl)c2F)ncnc1c1)c1OC)[C@@H](C)C(N)=O OJGQFAGYVWAAAD-ZDUSSCGKSA-N 0.000 description 1
- KPIGRPZFMNNBCP-UHFFFAOYSA-N CC(C)N(Cc(cc1c(Nc2cccc(Cl)c2F)ncnc1c1)c1OC)C(C)C(O)=O Chemical compound CC(C)N(Cc(cc1c(Nc2cccc(Cl)c2F)ncnc1c1)c1OC)C(C)C(O)=O KPIGRPZFMNNBCP-UHFFFAOYSA-N 0.000 description 1
- KPIGRPZFMNNBCP-CYBMUJFWSA-N CC(C)N(Cc1cc2c(Nc(cccc3Cl)c3F)ncnc2cc1OC)[C@H](C)C(O)=O Chemical compound CC(C)N(Cc1cc2c(Nc(cccc3Cl)c3F)ncnc2cc1OC)[C@H](C)C(O)=O KPIGRPZFMNNBCP-CYBMUJFWSA-N 0.000 description 1
- BVJNVOIYPXSNAN-UHFFFAOYSA-N CC(C)OCC(C(N)=O)NC(OCc1ccccc1)=O Chemical compound CC(C)OCC(C(N)=O)NC(OCc1ccccc1)=O BVJNVOIYPXSNAN-UHFFFAOYSA-N 0.000 description 1
- JPPAYRZURRWOMP-UHFFFAOYSA-N CC(C)OCC(C(OC)=O)NC(OCc1ccccc1)=O Chemical compound CC(C)OCC(C(OC)=O)NC(OCc1ccccc1)=O JPPAYRZURRWOMP-UHFFFAOYSA-N 0.000 description 1
- DYMBBDNTXACAEM-LBPRGKRZSA-N CC(C)OC[C@@H](C(O)=O)NC(OCc1ccccc1)=O Chemical compound CC(C)OC[C@@H](C(O)=O)NC(OCc1ccccc1)=O DYMBBDNTXACAEM-LBPRGKRZSA-N 0.000 description 1
- GFTHPCDXSGCQCO-UHFFFAOYSA-N CCN(Cc1cc2c(Nc(cccc3Cl)c3F)ncnc2cc1OC)C(C1)(CN1C(C)CC(N(C)C)=O)C(N)=O Chemical compound CCN(Cc1cc2c(Nc(cccc3Cl)c3F)ncnc2cc1OC)C(C1)(CN1C(C)CC(N(C)C)=O)C(N)=O GFTHPCDXSGCQCO-UHFFFAOYSA-N 0.000 description 1
- RFIFBBFZNIUSCT-UHFFFAOYSA-N CCOc1cc2ncnc(Nc(cccc3Cl)c3F)c2cc1CNC1(CCOCC1)C(O)=O Chemical compound CCOc1cc2ncnc(Nc(cccc3Cl)c3F)c2cc1CNC1(CCOCC1)C(O)=O RFIFBBFZNIUSCT-UHFFFAOYSA-N 0.000 description 1
- OIZPUCAXYYFFJE-UHFFFAOYSA-N CN(Cc1cc2c(Nc(cccc3Cl)c3F)ncnc2cc1OC)C1(CCN(CC2CC2)CC1)C(N)=O Chemical compound CN(Cc1cc2c(Nc(cccc3Cl)c3F)ncnc2cc1OC)C1(CCN(CC2CC2)CC1)C(N)=O OIZPUCAXYYFFJE-UHFFFAOYSA-N 0.000 description 1
- XMWCOOPLQWDGJN-UHFFFAOYSA-N CN(Cc1cc2c(Nc(cccc3Cl)c3F)ncnc2cc1OC)C1(CCOCC1)C(O)=O Chemical compound CN(Cc1cc2c(Nc(cccc3Cl)c3F)ncnc2cc1OC)C1(CCOCC1)C(O)=O XMWCOOPLQWDGJN-UHFFFAOYSA-N 0.000 description 1
- JLFUYZIWZMFTMH-UHFFFAOYSA-N CN(Cc1cc2c(Nc(cccc3Cl)c3F)ncnc2cc1OC)C1(CN(C)CCC1)C(N)=O Chemical compound CN(Cc1cc2c(Nc(cccc3Cl)c3F)ncnc2cc1OC)C1(CN(C)CCC1)C(N)=O JLFUYZIWZMFTMH-UHFFFAOYSA-N 0.000 description 1
- SGTONCVOTKXJAE-UHFFFAOYSA-N CN(Cc1cc2c(Nc(cccc3Cl)c3F)ncnc2cc1OC)C1(CN(C)CCC1)C(O)=O Chemical compound CN(Cc1cc2c(Nc(cccc3Cl)c3F)ncnc2cc1OC)C1(CN(C)CCC1)C(O)=O SGTONCVOTKXJAE-UHFFFAOYSA-N 0.000 description 1
- LJNUYDJKKBIGJB-QGZVFWFLSA-N CN(Cc1cc2c(Nc(cccc3Cl)c3F)ncnc2cc1OC)[C@H](COC)C(N)=O Chemical compound CN(Cc1cc2c(Nc(cccc3Cl)c3F)ncnc2cc1OC)[C@H](COC)C(N)=O LJNUYDJKKBIGJB-QGZVFWFLSA-N 0.000 description 1
- HXRACVFQPLBCAP-UHFFFAOYSA-N CNC(C1(CCOCC1)N(C)Cc1cc2c(Nc3cccc(Cl)c3F)ncnc2cc1OC)=O Chemical compound CNC(C1(CCOCC1)N(C)Cc1cc2c(Nc3cccc(Cl)c3F)ncnc2cc1OC)=O HXRACVFQPLBCAP-UHFFFAOYSA-N 0.000 description 1
- GTZJUBQWCWZING-UHFFFAOYSA-N COC(C(C1)N1C(OCc1ccccc1)=O)=O Chemical compound COC(C(C1)N1C(OCc1ccccc1)=O)=O GTZJUBQWCWZING-UHFFFAOYSA-N 0.000 description 1
- RLQRPFZBWXYXKT-UHFFFAOYSA-N COc1c(CN(CCC#N)CC(N)=O)cc2c(Nc(cccc3Cl)c3F)ncnc2c1 Chemical compound COc1c(CN(CCC#N)CC(N)=O)cc2c(Nc(cccc3Cl)c3F)ncnc2c1 RLQRPFZBWXYXKT-UHFFFAOYSA-N 0.000 description 1
- XWHXIIWBTYYFQA-UHFFFAOYSA-N COc1cc2ncnc(Nc(cccc3Cl)c3F)c2cc1C=O Chemical compound COc1cc2ncnc(Nc(cccc3Cl)c3F)c2cc1C=O XWHXIIWBTYYFQA-UHFFFAOYSA-N 0.000 description 1
- FUNDCHZZVLCUKX-UHFFFAOYSA-N COc1cc2ncnc(Nc(cccc3Cl)c3F)c2cc1CN(CCC#N)CC(O)=O Chemical compound COc1cc2ncnc(Nc(cccc3Cl)c3F)c2cc1CN(CCC#N)CC(O)=O FUNDCHZZVLCUKX-UHFFFAOYSA-N 0.000 description 1
- UKQXEKUEGLPLSV-UHFFFAOYSA-N COc1cc2ncnc(Nc(cccc3Cl)c3F)c2cc1CNC(CCCN1)C1=O Chemical compound COc1cc2ncnc(Nc(cccc3Cl)c3F)c2cc1CNC(CCCN1)C1=O UKQXEKUEGLPLSV-UHFFFAOYSA-N 0.000 description 1
- OFVLVHYPEYCUMY-UHFFFAOYSA-N COc1cc2ncnc(Nc3cccc(Cl)c3F)c2cc1CCCC(CCCN1)C1=O Chemical compound COc1cc2ncnc(Nc3cccc(Cl)c3F)c2cc1CCCC(CCCN1)C1=O OFVLVHYPEYCUMY-UHFFFAOYSA-N 0.000 description 1
- PTZCWFAROOJOMN-HNNXBMFYSA-N C[C@@H](C(N(CC1)CCC1(C(N)=O)N(C)Cc1cc2c(Nc(cccc3Cl)c3F)ncnc2cc1OC)=O)O Chemical compound C[C@@H](C(N(CC1)CCC1(C(N)=O)N(C)Cc1cc2c(Nc(cccc3Cl)c3F)ncnc2cc1OC)=O)O PTZCWFAROOJOMN-HNNXBMFYSA-N 0.000 description 1
- UEUGGJKCZZCQCG-KBPBESRZSA-N C[C@@H](COC)N(Cc(cc1c(Nc(cccc2Cl)c2F)ncnc1c1)c1OC)[C@@H](C)C(N)=O Chemical compound C[C@@H](COC)N(Cc(cc1c(Nc(cccc2Cl)c2F)ncnc1c1)c1OC)[C@@H](C)C(N)=O UEUGGJKCZZCQCG-KBPBESRZSA-N 0.000 description 1
- YCCMTCQQDULIFE-BYPYZUCNSA-N N[C@@H](CCCN1)C1=O Chemical compound N[C@@H](CCCN1)C1=O YCCMTCQQDULIFE-BYPYZUCNSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
- C07D239/32—One oxygen, sulfur or nitrogen atom
- C07D239/42—One nitrogen atom
-
- 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
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- 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
-
- 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
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP04290274 | 2004-02-03 | ||
| EP04290274.2 | 2004-02-03 | ||
| PCT/GB2005/000237 WO2005075439A1 (en) | 2004-02-03 | 2005-01-31 | Quinazoline derivatives |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2007523072A JP2007523072A (ja) | 2007-08-16 |
| JP2007523072A5 JP2007523072A5 (enExample) | 2008-03-21 |
| JP5032851B2 true JP5032851B2 (ja) | 2012-09-26 |
Family
ID=34833782
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2006551898A Expired - Fee Related JP5032851B2 (ja) | 2004-02-03 | 2005-01-31 | キナゾリン誘導体 |
Country Status (11)
| Country | Link |
|---|---|
| US (1) | US7632840B2 (enExample) |
| EP (1) | EP1713781B1 (enExample) |
| JP (1) | JP5032851B2 (enExample) |
| CN (1) | CN1914182B (enExample) |
| AR (1) | AR047703A1 (enExample) |
| AT (1) | ATE413389T1 (enExample) |
| DE (1) | DE602005010824D1 (enExample) |
| ES (1) | ES2315834T3 (enExample) |
| TW (1) | TW200529851A (enExample) |
| UY (1) | UY28736A1 (enExample) |
| WO (1) | WO2005075439A1 (enExample) |
Families Citing this family (27)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB0126433D0 (en) * | 2001-11-03 | 2002-01-02 | Astrazeneca Ab | Compounds |
| JP2005515176A (ja) * | 2001-11-03 | 2005-05-26 | アストラゼネカ アクチボラグ | 抗腫瘍剤としてのキナゾリン誘導体 |
| GB0309009D0 (en) * | 2003-04-22 | 2003-05-28 | Astrazeneca Ab | Quinazoline derivatives |
| GB0309850D0 (en) * | 2003-04-30 | 2003-06-04 | Astrazeneca Ab | Quinazoline derivatives |
| AU2004272350A1 (en) * | 2003-09-16 | 2005-03-24 | Astrazeneca Ab | Quinazoline derivatives as tyrosine kinase inhibitors |
| US7569577B2 (en) * | 2003-09-16 | 2009-08-04 | Astrazeneca Ab | Quinazoline derivatives as tyrosine kinase inhibitors |
| BRPI0414488A (pt) * | 2003-09-16 | 2006-11-14 | Astrazeneca Ab | derivado de quinazolina, composição farmacêutica, uso de um derivado de quinazolina, métodos para produzir um efeito anti - proliferativo em um animal de sangue quente, para prevenção ou tratamento de tumores em um aminal de sangue quente, para fornecer um efeito inibidor da tirosina quinase de egfr seletivo em um animal de sangue quente e para tratar um cáncer em um animal de sangue quente e, processo para a preparação de um derivado de quinazolina |
| EP1664030A1 (en) * | 2003-09-16 | 2006-06-07 | AstraZeneca AB | Quinazoline derivatives |
| GB0321648D0 (en) * | 2003-09-16 | 2003-10-15 | Astrazeneca Ab | Quinazoline derivatives |
| GB0322409D0 (en) * | 2003-09-25 | 2003-10-29 | Astrazeneca Ab | Quinazoline derivatives |
| GB0326459D0 (en) | 2003-11-13 | 2003-12-17 | Astrazeneca Ab | Quinazoline derivatives |
| CA2567832A1 (en) * | 2004-06-04 | 2005-12-15 | Astrazeneca Ab | Quinazoline derivatives as erbb receptor tyrosine kinases |
| GB2418427A (en) | 2004-09-02 | 2006-03-29 | Univ Cambridge Tech | Ligands for G-protein coupled receptors |
| CN101124228B (zh) * | 2004-12-14 | 2011-06-15 | 阿斯利康(瑞典)有限公司 | 用作抗肿瘤药物的吡唑并嘧啶化合物 |
| GB0504474D0 (en) * | 2005-03-04 | 2005-04-13 | Astrazeneca Ab | Chemical compounds |
| GB0508717D0 (en) * | 2005-04-29 | 2005-06-08 | Astrazeneca Ab | Chemical compounds |
| GB0508715D0 (en) * | 2005-04-29 | 2005-06-08 | Astrazeneca Ab | Chemical compounds |
| US7820683B2 (en) * | 2005-09-20 | 2010-10-26 | Astrazeneca Ab | 4-(1H-indazol-5-yl-amino)-quinazoline compounds as erbB receptor tyrosine kinase inhibitors for the treatment of cancer |
| US20090239861A1 (en) * | 2005-09-20 | 2009-09-24 | Robert Hugh Bradbury | Quinazoline derivatives as anticancer agents |
| ATE443053T1 (de) * | 2005-12-02 | 2009-10-15 | Astrazeneca Ab | Als inhibitoren von erbb-tyrosinkinase verwendete chinazoleinderivate |
| WO2007063291A1 (en) * | 2005-12-02 | 2007-06-07 | Astrazeneca Ab | 4-anilino-substituted quinazoline derivatives as tyrosine kinase inhibitors |
| WO2008134048A2 (en) | 2007-04-27 | 2008-11-06 | Paratek Pharmaceuticals, Inc. | Methods for synthesizing and purifying aminoalkyl tetracycline compounds |
| CN101784517A (zh) | 2007-07-06 | 2010-07-21 | 帕拉特克药品公司 | 合成取代的四环素化合物的方法 |
| GB2452696B (en) | 2007-08-02 | 2009-09-23 | Cambridge Entpr Ltd | 3-(2',2'-dimethylpropanoylamino)-tetrahydropyridin-2-one and its use in pharmaceutical compositions |
| US7662967B2 (en) | 2007-08-02 | 2010-02-16 | Cambridge Enterprise Limited | Anti-inflammatory compounds and compositions |
| GB201604329D0 (en) * | 2016-03-14 | 2016-04-27 | Univ Strathclyde | Methods and systems for improving stability of a ship |
| CN111777620A (zh) * | 2019-04-04 | 2020-10-16 | 山东轩竹医药科技有限公司 | 酪氨酸激酶抑制剂的新用途 |
Family Cites Families (98)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4335127A (en) | 1979-01-08 | 1982-06-15 | Janssen Pharmaceutica, N.V. | Piperidinylalkyl quinazoline compounds, composition and method of use |
| KR910006138B1 (ko) | 1986-09-30 | 1991-08-16 | 에자이 가부시끼가이샤 | 환상아민 유도체 |
| US4921863A (en) | 1988-02-17 | 1990-05-01 | Eisai Co., Ltd. | Cyclic amine derivatives |
| US5721237A (en) | 1991-05-10 | 1998-02-24 | Rhone-Poulenc Rorer Pharmaceuticals Inc. | Protein tyrosine kinase aryl and heteroaryl quinazoline compounds having selective inhibition of HER-2 autophosphorylation properties |
| GB9300059D0 (en) | 1992-01-20 | 1993-03-03 | Zeneca Ltd | Quinazoline derivatives |
| GB9510757D0 (en) | 1994-09-19 | 1995-07-19 | Wellcome Found | Therapeuticaly active compounds |
| DE69536015D1 (de) | 1995-03-30 | 2009-12-10 | Pfizer Prod Inc | Chinazolinone Derivate |
| GB9508538D0 (en) | 1995-04-27 | 1995-06-14 | Zeneca Ltd | Quinazoline derivatives |
| WO1996033977A1 (en) | 1995-04-27 | 1996-10-31 | Zeneca Limited | Quinazoline derivatives |
| GB9508565D0 (en) | 1995-04-27 | 1995-06-14 | Zeneca Ltd | Quiazoline derivative |
| GB9508537D0 (en) | 1995-04-27 | 1995-06-14 | Zeneca Ltd | Quinazoline derivatives |
| GB9508535D0 (en) | 1995-04-27 | 1995-06-14 | Zeneca Ltd | Quinazoline derivative |
| US5747498A (en) | 1996-05-28 | 1998-05-05 | Pfizer Inc. | Alkynyl and azido-substituted 4-anilinoquinazolines |
| GB9514265D0 (en) | 1995-07-13 | 1995-09-13 | Wellcome Found | Hetrocyclic compounds |
| WO1997030035A1 (en) | 1996-02-13 | 1997-08-21 | Zeneca Limited | Quinazoline derivatives as vegf inhibitors |
| GB9603095D0 (en) | 1996-02-14 | 1996-04-10 | Zeneca Ltd | Quinazoline derivatives |
| SK284073B6 (sk) | 1996-04-12 | 2004-09-08 | Warner-Lambert Company | Polycyklické zlúčeniny, ich použitie a farmaceutické kompozície na ich báze |
| GB9607729D0 (en) | 1996-04-13 | 1996-06-19 | Zeneca Ltd | Quinazoline derivatives |
| EP0912559B1 (en) | 1996-07-13 | 2002-11-06 | Glaxo Group Limited | Fused heterocyclic compounds as protein tyrosine kinase inhibitors |
| GB9718972D0 (en) | 1996-09-25 | 1997-11-12 | Zeneca Ltd | Chemical compounds |
| EP0837063A1 (en) | 1996-10-17 | 1998-04-22 | Pfizer Inc. | 4-Aminoquinazoline derivatives |
| ZA986732B (en) | 1997-07-29 | 1999-02-02 | Warner Lambert Co | Irreversible inhibitiors of tyrosine kinases |
| GB9800575D0 (en) * | 1998-01-12 | 1998-03-11 | Glaxo Group Ltd | Heterocyclic compounds |
| WO2000009481A1 (en) | 1998-08-11 | 2000-02-24 | Takeda Chemical Industries, Ltd. | Cyclic amide compounds, process for producing the same, intermediates thereof and herbicides |
| US6297258B1 (en) | 1998-09-29 | 2001-10-02 | American Cyanamid Company | Substituted 3-cyanoquinolines |
| HU230728B1 (hu) | 1998-09-29 | 2017-12-28 | Wyeth Holdings Llc | Szubsztituált 3-cianokinolinok mint protein tirozin kinázok inhibitorai |
| BR9914162A (pt) | 1998-10-01 | 2001-06-26 | Astrazeneca Ab | Derivado de amida, processo para preparar um derivado de amida, ou um sal farmaceuticamente aceitável ou éster clivável in vivo do mesmo, composição farmacêutica e uso de um derivado de amida, ou um sal farmaceuticamente aceitável ou éster clivável in vivo do mesmo |
| TW575567B (en) | 1998-10-23 | 2004-02-11 | Akzo Nobel Nv | Serine protease inhibitor |
| UA71945C2 (en) | 1999-01-27 | 2005-01-17 | Pfizer Prod Inc | Substituted bicyclic derivatives being used as anticancer agents |
| AU3281600A (en) | 1999-02-27 | 2000-09-21 | Boehringer Ingelheim Pharma Gmbh & Co. Kg | 4-amino-quinazoline and quinoline derivatives having an inhibitory effect on signal transsduction mediated by tyrosine kinases |
| DE19911509A1 (de) | 1999-03-15 | 2000-09-21 | Boehringer Ingelheim Pharma | Bicyclische Heterocyclen, diese Verbindungen enthaltende Arzneimittel, deren Verwendung und Verfahren zu ihrer Herstellung |
| US6258820B1 (en) | 1999-03-19 | 2001-07-10 | Parker Hughes Institute | Synthesis and anti-tumor activity of 6,7-dialkoxy-4-phenylamino-quinazolines |
| WO2000078735A1 (de) | 1999-06-21 | 2000-12-28 | Boehringer Ingelheim Pharma Kg | Bicyclische heterocyclen, diese verbindungen enthaltende arzneimittel, deren verwendung und verfahren zu ihrer herstellung |
| KR20020029419A (ko) | 1999-07-07 | 2002-04-18 | 다비드 에 질레스 | 퀴나졸린 유도체 |
| GB9917408D0 (en) | 1999-07-23 | 1999-09-22 | Smithkline Beecham Plc | Compounds |
| CZ20021009A3 (cs) | 1999-09-21 | 2002-06-12 | Astrazeneca Ab | Deriváty chinazolinu, způsob jejich přípravy a jejich pouľití jako léčiv |
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-
2005
- 2005-01-31 AT AT05701999T patent/ATE413389T1/de not_active IP Right Cessation
- 2005-01-31 CN CN2005800038578A patent/CN1914182B/zh not_active Expired - Fee Related
- 2005-01-31 ES ES05701999T patent/ES2315834T3/es not_active Expired - Lifetime
- 2005-01-31 WO PCT/GB2005/000237 patent/WO2005075439A1/en not_active Ceased
- 2005-01-31 EP EP05701999A patent/EP1713781B1/en not_active Expired - Lifetime
- 2005-01-31 US US10/586,965 patent/US7632840B2/en not_active Expired - Fee Related
- 2005-01-31 DE DE602005010824T patent/DE602005010824D1/de not_active Expired - Lifetime
- 2005-01-31 JP JP2006551898A patent/JP5032851B2/ja not_active Expired - Fee Related
- 2005-02-02 UY UY28736A patent/UY28736A1/es unknown
- 2005-02-03 AR ARP050100415A patent/AR047703A1/es unknown
- 2005-02-03 TW TW094103412A patent/TW200529851A/zh unknown
Also Published As
| Publication number | Publication date |
|---|---|
| UY28736A1 (es) | 2005-09-30 |
| AR047703A1 (es) | 2006-02-08 |
| JP2007523072A (ja) | 2007-08-16 |
| ATE413389T1 (de) | 2008-11-15 |
| TW200529851A (en) | 2005-09-16 |
| ES2315834T3 (es) | 2009-04-01 |
| HK1095590A1 (en) | 2007-05-11 |
| CN1914182A (zh) | 2007-02-14 |
| CN1914182B (zh) | 2011-09-07 |
| EP1713781B1 (en) | 2008-11-05 |
| US7632840B2 (en) | 2009-12-15 |
| US20070293490A1 (en) | 2007-12-20 |
| EP1713781A1 (en) | 2006-10-25 |
| DE602005010824D1 (de) | 2008-12-18 |
| WO2005075439A1 (en) | 2005-08-18 |
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