AR057753A2 - Derivados de quinazolina, proceso para su preparacion y composiciones farmaceuticas que los contienen - Google Patents
Derivados de quinazolina, proceso para su preparacion y composiciones farmaceuticas que los contienenInfo
- Publication number
- AR057753A2 AR057753A2 ARP070102117A ARP070102117A AR057753A2 AR 057753 A2 AR057753 A2 AR 057753A2 AR P070102117 A ARP070102117 A AR P070102117A AR P070102117 A ARP070102117 A AR P070102117A AR 057753 A2 AR057753 A2 AR 057753A2
- Authority
- AR
- Argentina
- Prior art keywords
- amino
- quinazolin
- acetamide
- pyrazol
- propoxy
- Prior art date
Links
- 239000008194 pharmaceutical composition Substances 0.000 title 1
- JWVCLYRUEFBMGU-UHFFFAOYSA-N quinazoline Chemical class N1=CN=CC2=CC=CC=C21 JWVCLYRUEFBMGU-UHFFFAOYSA-N 0.000 title 1
- -1 2,3-difluorphenyl Chemical group 0.000 abstract 20
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 11
- DLFVBJFMPXGRIB-UHFFFAOYSA-N thioacetamide Natural products CC(N)=O DLFVBJFMPXGRIB-UHFFFAOYSA-N 0.000 abstract 6
- 125000002572 propoxy group Chemical group [*]OC([H])([H])C(C([H])([H])[H])([H])[H] 0.000 abstract 2
- PIJGHCNBBRXNDH-UHFFFAOYSA-N 2-[3-[[7-[3-[cyclopentyl(2-hydroxyethyl)amino]propoxy]quinazolin-4-yl]amino]-1h-pyrazol-5-yl]-n-(3-fluorophenyl)acetamide Chemical compound C1CCCC1N(CCO)CCCOC(C=C1N=CN=2)=CC=C1C=2NC(=NN1)C=C1CC(=O)NC1=CC=CC(F)=C1 PIJGHCNBBRXNDH-UHFFFAOYSA-N 0.000 abstract 1
- UHVRUAQUBZYULG-UHFFFAOYSA-N 2-[3-[[7-[3-[ethyl(3-hydroxypropyl)amino]propoxy]quinazolin-4-yl]amino]-1h-pyrazol-5-yl]-n-(3-fluorophenyl)acetamide Chemical compound N=1C=NC2=CC(OCCCN(CCCO)CC)=CC=C2C=1NC(=NN1)C=C1CC(=O)NC1=CC=CC(F)=C1 UHVRUAQUBZYULG-UHFFFAOYSA-N 0.000 abstract 1
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 abstract 1
- 125000004106 butoxy group Chemical group [*]OC([H])([H])C([H])([H])C(C([H])([H])[H])([H])[H] 0.000 abstract 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
Classifications
-
- 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
- C07F9/645—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having two nitrogen atoms as the only ring hetero atoms
- C07F9/6509—Six-membered rings
- C07F9/6512—Six-membered rings having the nitrogen atoms in positions 1 and 3
-
- 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
- C07F9/6558—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom containing at least two different or differently substituted hetero rings neither condensed among themselves nor condensed with a common carbocyclic ring or ring system
- C07F9/65583—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom containing at least two different or differently substituted hetero rings neither condensed among themselves nor condensed with a common carbocyclic ring or ring system each of the hetero rings containing nitrogen as ring hetero atom
-
- 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
- A61K31/66—Phosphorus compounds
- A61K31/661—Phosphorus acids or esters thereof not having P—C bonds, e.g. fosfosal, dichlorvos, malathion or mevinphos
-
- 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
- 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
- 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
- C07D403/14—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 three or more hetero rings
-
- 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
- C07F9/6558—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom containing at least two different or differently substituted hetero rings neither condensed among themselves nor condensed with a common carbocyclic ring or ring system
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Biochemistry (AREA)
- Molecular Biology (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- Veterinary Medicine (AREA)
- Pharmacology & Pharmacy (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Hematology (AREA)
- Oncology (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
Un compuesto que es cualquiera de los siguientes: N-(2,3-difluorfenil)-2-{3-[(7-{[1-(2-hidroxietil)piperidin-4-il]metoxi}quinazolin-4-il) amino]-1H-pirazol-5-il}acetamida; N-(2,3-difluorfenil)-2-{3-[(7-{3-[(3-hidroxi-1,1- dimetilpropil)amino]propoxi}quinazolin-4-il)amino]-1H- pirazol-5-il}acetamida; N-(2,3-difluorfenil)-2-{3-[(7-{3-[(2S)-2-(2-hidroxietil)pirrolidin-1-il]propoxi}quinazolin-4-il)amino]-1Hpirazol-5-il} acetamida; N-(2,3-difluorfenil)-2-{3-[(7-{3-[(7-{3- [(2-hidroxietil)butil)amino]propoxi}-quinazolin-4-il)amino]-1H-pirazol-5-il}acetamida; 2-{3-[(7-{3-[ciclopentil(2-hidroxietil)amino]propoxi}-quinazolin-4-il)amino]-1H-pirazol-5-il}-N-(2,3-difluorfenil)acetamida; N-(2,3- difluorfenil)-2-{3-[(7-{3- [(2S)-2-(hidroximetil)pirrolidin-2-il]propoxi}-quinazolin-4-il)amino]-1H-pirazol-5-il}acetamida; N-(3- fluorfenil)-2-{3-[(7-{3-[(2S)-2-(hidroximetil)pirrolidin-1-il]propoxi}quinazolin-4-il)amino]-1H-pirazol-5-il}acetamida; 2-{3-[(7-{3-[ciclopentil(2- hidroxietil)amino]propoxi}-quinazolin-4-il)amino]-1H-pirazol-5-il}-N-(3-fluorfenil)acetamida; N-(3-fluorfenil)-2-{3-[(7-{3-[etil(2-hidroxietil)amino] propoxi}-quinazolin-4-il)amino]-1H-pirazol-5-il}acetamida; N-(3-fluorfenil)-2-{3-[(7-{3-[(2-hidroxi- 1,1-dimetietil)amino]propoxi}quinazolin-4-il) amino]-1H-pirazol-5-il}acetamida; N-(3-fluorfenil-2-{3-[(7-{3-[(2-hidroxietil)(propil)amino]propoxi}-quinazolin-4-il)amino]-1H-pirazol-5-il} acetamida; N-(3-fluorfenil)-2-{3-[(7-{3-[(2R)-2- (hidroximetil)pirrolidin-1-il]propoxi}quinazolin-4-il)amino]-1H-pirazol-5-il}acetamida; N-(2,3- difluorfenil)-2-{3-[7-{4-[(2-hidroxietil)(propil)amino]butoxi}-quinazolin-4-il)amino]butoxi}-quinazolin-4-il)amino]-1H-pirazol-5-il}acetamida; N-(3- fluorfenil)-2-{3-[(7-{4-[etil(2-hidroxietil)amino]butoxi}-quinazolin-4-il)amino]-1H-pirazol-5-il}acetamida; N-(2,3- difluorfenil)-2-{3-[(7-{4-[(2R)-2-(hidroximetil)pirrolidin-1-il]butoxi}-quinazolin-4-il)amino]-1H-pirazol-5-il}acetamida; N-(2,3- difluorfenil)-2-{3-[(7-{4-[(2-hidroxietil)(metil)amino]butoxi}quinazolin-4-il)amino]-1H-pirazol-5-il}acetamida; N-(2,3- difluorfenil)-2-{3-[(7-{4-[(2S)-2-(hidroximetil)pirrolidin-1-il]butoxi}-quinazolin-4-il)amino]-1H-pirazol-5-il}acetamida; 2-{3-[(7- {3-[etil(3- hidroxipropil)amino]propoxi}-quinazolin-4-il)amino]-1H-pirazol-5-il}-N-(3-fluorfenil)acetamida; N-(3-fluorfenil)-2-{3-[(7-{3-[(2-hidroxietil)(2- metoxietil)amino]propoxi}quinazolin-4-il)amino]-1H-pirazol-5-il}acetamida y 2-{3-[(7-{3- [etil(2-hidroxietil)amino]propoxi}-6-fluorquinazolin-4-il) amino]-1H-pirazol-5-il}-N-(3-fluorfenil)acetamida; o una sal farmacéuticamente aceptable del mismo.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP02293238 | 2002-12-24 | ||
EP03291315 | 2003-06-02 |
Publications (1)
Publication Number | Publication Date |
---|---|
AR057753A2 true AR057753A2 (es) | 2007-12-19 |
Family
ID=32683824
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ARP030104824A AR042668A1 (es) | 2002-12-24 | 2003-12-23 | Derivados de fosfonoxi quinazolinas y su uso farmaceutico |
ARP070102117A AR057753A2 (es) | 2002-12-24 | 2007-05-16 | Derivados de quinazolina, proceso para su preparacion y composiciones farmaceuticas que los contienen |
Family Applications Before (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ARP030104824A AR042668A1 (es) | 2002-12-24 | 2003-12-23 | Derivados de fosfonoxi quinazolinas y su uso farmaceutico |
Country Status (30)
Country | Link |
---|---|
US (4) | US7528121B2 (es) |
EP (2) | EP1847539B1 (es) |
JP (3) | JP4422102B2 (es) |
KR (1) | KR101010299B1 (es) |
AR (2) | AR042668A1 (es) |
AT (2) | ATE438644T1 (es) |
AU (1) | AU2003290313B2 (es) |
BR (1) | BRPI0317717B8 (es) |
CA (1) | CA2511613C (es) |
CL (1) | CL2003002731A1 (es) |
CY (2) | CY1107775T1 (es) |
DE (2) | DE60315892T2 (es) |
DK (2) | DK1578755T3 (es) |
ES (2) | ES2290529T3 (es) |
HK (2) | HK1080481A1 (es) |
IL (2) | IL169112A (es) |
IS (2) | IS2504B (es) |
MX (1) | MXPA05006918A (es) |
MY (2) | MY136174A (es) |
NO (2) | NO335193B1 (es) |
NZ (1) | NZ540698A (es) |
PL (2) | PL223998B1 (es) |
PT (2) | PT1578755E (es) |
RU (3) | RU2350611C1 (es) |
SA (1) | SA04240504B1 (es) |
SI (2) | SI1847539T1 (es) |
TW (2) | TWI336327B (es) |
UA (1) | UA83814C2 (es) |
UY (1) | UY28149A1 (es) |
WO (1) | WO2004058781A1 (es) |
Families Citing this family (49)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN100491372C (zh) * | 2001-12-24 | 2009-05-27 | 阿斯特拉曾尼卡有限公司 | 作为欧若拉激酶抑制剂的取代喹唑啉衍生物 |
EP1575946A1 (en) * | 2002-12-24 | 2005-09-21 | AstraZeneca AB | Quinazoline compounds |
BRPI0317717B8 (pt) * | 2002-12-24 | 2021-05-25 | Astrazeneca Ab | composto, composição farmacêutica, e uso de um composto |
BRPI0409427A (pt) | 2003-04-16 | 2006-04-18 | Astrazeneca Ab | composto, uso do mesmo, composição farmacêutica, método de tratamento de um humano sofrendo de uma doença hiperproliferativa, e, processo para a preparação de um composto ou de um sal, éster ou pró-droga farmaceuticamente aceitáveis do mesmo |
EP2251343A1 (en) * | 2003-05-15 | 2010-11-17 | Arqule, Inc. | Imidazothiazoles as p38-kinase-inhibitors |
ATE401080T1 (de) * | 2003-06-02 | 2008-08-15 | Astrazeneca Ab | (3-((chinazolin-4-yl)amino)-1h-pyrazol-1- yl)acetamid derivate und verwandte verbindungen als aurora kinase inhibitoren zur behandlung von proliferativen erkrankungen wie krebs |
JP2008515961A (ja) * | 2004-10-12 | 2008-05-15 | アストラゼネカ アクチボラグ | 癌に対する使用のためのキナゾリン誘導体 |
AU2005293336B2 (en) | 2004-10-12 | 2009-05-28 | Astrazeneca Ab | Quinazoline derivatives |
WO2006044687A2 (en) | 2004-10-15 | 2006-04-27 | Takeda San Diego, Inc. | Kinase inhibitors |
JP2008517064A (ja) * | 2004-10-19 | 2008-05-22 | アークル インコーポレイテッド | P38mapキナーゼのイミダゾオキサゾールおよびイミダゾチアゾール阻害剤の合成 |
US8119655B2 (en) | 2005-10-07 | 2012-02-21 | Takeda Pharmaceutical Company Limited | Kinase inhibitors |
UY30183A1 (es) | 2006-03-02 | 2007-10-31 | Astrazeneca Ab | Derivados de quinolina |
WO2007123892A2 (en) * | 2006-04-17 | 2007-11-01 | Arqule Inc. | Raf inhibitors and their uses |
GB0609621D0 (en) * | 2006-05-16 | 2006-06-21 | Astrazeneca Ab | Novel co-crystal |
GB0609619D0 (en) * | 2006-05-16 | 2006-06-21 | Astrazeneca Ab | Combination |
GB0609617D0 (en) | 2006-05-16 | 2006-06-21 | Astrazeneca Ab | Process & intermediate |
US20100120717A1 (en) | 2006-10-09 | 2010-05-13 | Brown Jason W | Kinase inhibitors |
WO2009111028A1 (en) * | 2008-03-04 | 2009-09-11 | Vitae Pharmaceuticals, Inc. | Aurora kinase inhibitors |
US20110033461A1 (en) * | 2008-03-12 | 2011-02-10 | Vladimir Ratushny | Combination Therapy for the Treatment of Cancer |
ES2616255T3 (es) | 2008-04-30 | 2017-06-12 | National Health Research Institutes | Compuestos de pirimidina bicíclicos condensados como inhibidores de las aurora cinasas |
EA201100126A1 (ru) * | 2008-07-03 | 2011-08-30 | Мерк Патент Гмбх | Нафтиридиноны в качестве ингибиторов протеинкиназ |
MX2011005788A (es) * | 2008-12-05 | 2011-06-21 | Arqule Inc | Inhibidores raf y sus usos. |
US7863325B2 (en) | 2008-12-11 | 2011-01-04 | Axcentua Pharmaceuticals Ab | Crystalline genistein sodium salt dihydrate |
US9012495B2 (en) | 2008-12-11 | 2015-04-21 | Axcentua Pharmaceuticals Ab | Crystalline forms of genistein |
CN102264368B (zh) | 2008-12-22 | 2014-09-10 | 米伦纽姆医药公司 | 极光激酶抑制剂与抗cd20抗体的组合 |
US9604963B2 (en) | 2011-03-04 | 2017-03-28 | Glaxosmithkline Intellectual Property Development Limited | Amino-quinolines as kinase inhibitors |
TWI547494B (zh) | 2011-08-18 | 2016-09-01 | 葛蘭素史克智慧財產發展有限公司 | 作為激酶抑制劑之胺基喹唑啉類 |
AR092530A1 (es) | 2012-09-13 | 2015-04-22 | Glaxosmithkline Llc | Compuesto de amino-quinolina, composicion farmaceutica que lo comprende y uso de dicho compuesto para la preparacion de un medicamento |
TWI592417B (zh) | 2012-09-13 | 2017-07-21 | 葛蘭素史克智慧財產發展有限公司 | 胺基喹唑啉激酶抑制劑之前藥 |
AU2014216178B2 (en) | 2013-02-15 | 2018-06-28 | KALA BIO, Inc. | Therapeutic compounds and uses thereof |
CN105189462B (zh) | 2013-02-20 | 2017-11-10 | 卡拉制药公司 | 治疗性化合物和其用途 |
US9688688B2 (en) | 2013-02-20 | 2017-06-27 | Kala Pharmaceuticals, Inc. | Crystalline forms of 4-((4-((4-fluoro-2-methyl-1H-indol-5-yl)oxy)-6-methoxyquinazolin-7-yl)oxy)-1-(2-oxa-7-azaspiro[3.5]nonan-7-yl)butan-1-one and uses thereof |
BR112015019624A2 (pt) * | 2013-02-21 | 2017-07-18 | Glaxosmithkline Ip Dev Ltd | quinazolinas como inibidores de quinase |
SG11201601218PA (en) | 2013-09-16 | 2016-04-28 | Astrazeneca Ab | Therapeutic polymeric nanoparticles and methods of making and using same |
US9890173B2 (en) | 2013-11-01 | 2018-02-13 | Kala Pharmaceuticals, Inc. | Crystalline forms of therapeutic compounds and uses thereof |
KR20160099084A (ko) | 2013-11-01 | 2016-08-19 | 칼라 파마슈티컬스, 인크. | 치료 화합물의 결정질 형태 및 그의 용도 |
EP3076963A4 (en) | 2013-12-06 | 2017-09-13 | Millennium Pharmaceuticals, Inc. | Combination of aurora kinase inhibitors and anti-cd30 antibodies |
JP2018524292A (ja) | 2015-07-21 | 2018-08-30 | ミレニアム ファーマシューティカルズ, インコーポレイテッドMillennium Pharmaceuticals, Inc. | オーロラキナーゼインヒビターと化学療法剤の投与 |
CA3036336A1 (en) | 2016-09-08 | 2018-03-15 | Kala Pharmaceuticals, Inc. | Crystalline forms of therapeutic compounds and uses thereof |
MX2019002629A (es) | 2016-09-08 | 2019-10-07 | Kala Pharmaceuticals Inc | Formas cristalinas de compuestos terapéuticos y usos de los mismos. |
CA3036340A1 (en) | 2016-09-08 | 2018-03-15 | Kala Pharmaceuticals, Inc. | Crystalline forms of therapeutic compounds and uses thereof |
PL3678668T3 (pl) | 2017-09-08 | 2024-06-03 | The Board Of Trustees Of The Leland Stanford Junior University | Inhibitory enpp1 i ich zastosowanie w leczeniu nowotworu |
WO2019195658A1 (en) | 2018-04-05 | 2019-10-10 | Dana-Farber Cancer Institute, Inc. | Sting levels as a biomarker for cancer immunotherapy |
WO2020049208A1 (es) | 2018-09-09 | 2020-03-12 | Fundacio Privada Institut De Recerca De La Sida - Caixa | Aurora cinasa como diana para tratar, prevenir o curar una infección por vih o sida |
WO2021041532A1 (en) | 2019-08-26 | 2021-03-04 | Dana-Farber Cancer Institute, Inc. | Use of heparin to promote type 1 interferon signaling |
WO2021094379A1 (en) | 2019-11-12 | 2021-05-20 | Astrazeneca Ab | Epidermal growth factor receptor tyrosine kinase inhibitors for the treatment of cancer |
CN112939948B (zh) * | 2019-12-11 | 2022-05-17 | 苏州美诺医药科技有限公司 | 新型含喹唑啉类化合物及其中间体与应用 |
WO2021260582A1 (en) | 2020-06-24 | 2021-12-30 | Astrazeneca Uk Limited | Combination of antibody-drug conjugate and aurora b inhibitor |
WO2022192139A1 (en) | 2021-03-10 | 2022-09-15 | Astrazeneca Ab | Aurora kinase b inhibitors for use for treating cancer |
Family Cites Families (33)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
IL89029A (en) | 1988-01-29 | 1993-01-31 | Lilly Co Eli | Fungicidal quinoline and cinnoline derivatives, compositions containing them, and fungicidal methods of using them |
SG64322A1 (en) | 1991-05-10 | 1999-04-27 | Rhone Poulenc Rorer Int | Bis mono and bicyclic aryl and heteroaryl compounds which inhibit egf and/or pdgf receptor tyrosine kinase |
US5710158A (en) | 1991-05-10 | 1998-01-20 | Rhone-Poulenc Rorer Pharmaceuticals Inc. | Aryl and heteroaryl quinazoline compounds which inhibit EGF and/or PDGF receptor tyrosine kinase |
US5480883A (en) | 1991-05-10 | 1996-01-02 | Rhone-Poulenc Rorer Pharmaceuticals Inc. | Bis mono- and bicyclic aryl and heteroaryl compounds which inhibit EGF and/or PDGF receptor tyrosine kinase |
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 |
WO1995033724A1 (en) | 1994-06-09 | 1995-12-14 | Glaxo Group Limited | Phenethanolamine derivatives and their use as atypical beta-adrenoceptor agonists |
GB9510757D0 (en) | 1994-09-19 | 1995-07-19 | Wellcome Found | Therapeuticaly active compounds |
TW321649B (es) | 1994-11-12 | 1997-12-01 | Zeneca Ltd | |
GB9514265D0 (en) | 1995-07-13 | 1995-09-13 | Wellcome Found | Hetrocyclic compounds |
GB9624482D0 (en) | 1995-12-18 | 1997-01-15 | Zeneca Phaema S A | Chemical compounds |
US6716575B2 (en) | 1995-12-18 | 2004-04-06 | Sugen, Inc. | Diagnosis and treatment of AUR1 and/or AUR2 related disorders |
ATE315654T1 (de) | 1995-12-18 | 2006-02-15 | Sugen Inc | Diagnose und behandlung von mit aur-1 und/oder aur-2 assoziierten erkrankungen |
ES2194181T3 (es) | 1996-02-13 | 2003-11-16 | Astrazeneca Ab | Derivados de quinazolina como inhibidores de vegf. |
CA2244897C (en) | 1996-03-05 | 2006-04-11 | Zeneca Limited | 4-anilinoquinazoline derivatives |
GB9718972D0 (en) | 1996-09-25 | 1997-11-12 | Zeneca Ltd | Chemical compounds |
GB9714249D0 (en) | 1997-07-08 | 1997-09-10 | Angiogene Pharm Ltd | Vascular damaging agents |
ZA986732B (en) | 1997-07-29 | 1999-02-02 | Warner Lambert Co | Irreversible inhibitiors of tyrosine kinases |
CN1161352C (zh) * | 1998-10-08 | 2004-08-11 | 阿斯特拉曾尼卡有限公司 | 喹唑啉衍生物 |
GB9900334D0 (en) | 1999-01-07 | 1999-02-24 | Angiogene Pharm Ltd | Tricylic vascular damaging agents |
GB9900752D0 (en) | 1999-01-15 | 1999-03-03 | Angiogene Pharm Ltd | Benzimidazole vascular damaging agents |
SK3822002A3 (en) | 1999-09-21 | 2002-10-08 | Astrazeneca Ab | Quinazoline derivatives, process for the preparation thereof and their use |
GB9922171D0 (en) | 1999-09-21 | 1999-11-17 | Zeneca Ltd | Chemical compounds |
AU2001258628A1 (en) | 2000-05-31 | 2001-12-11 | Astrazeneca Ab | Indole derivatives with vascular damaging activity |
CZ20024120A3 (cs) | 2000-06-28 | 2003-03-12 | Astrazeneca Ab | Substituované chinazolinové deriváty a jejich použití jako inhibitory |
AU6623301A (en) | 2000-07-07 | 2002-01-21 | Angiogene Pharm Ltd | Colchinol derivatives as vascular damaging agents |
WO2002008213A1 (en) | 2000-07-07 | 2002-01-31 | Angiogene Pharmaceuticals Limited | Colchinol derivatives as angiogenesis inhibitors |
US6610677B2 (en) | 2000-09-15 | 2003-08-26 | Vertex Pharmaceuticals Incorporated | Pyrazole compounds useful as protein kinase inhibitors |
US7132427B2 (en) | 2001-06-21 | 2006-11-07 | Ariad Pharmaceuticals, Inc. | Quinazolines and uses thereof |
GB0124299D0 (en) * | 2001-10-10 | 2001-11-28 | Astrazeneca Ab | Crystal structure of enzyme and uses thereof |
CN100491372C (zh) * | 2001-12-24 | 2009-05-27 | 阿斯特拉曾尼卡有限公司 | 作为欧若拉激酶抑制剂的取代喹唑啉衍生物 |
EP1575946A1 (en) * | 2002-12-24 | 2005-09-21 | AstraZeneca AB | Quinazoline compounds |
BRPI0317717B8 (pt) * | 2002-12-24 | 2021-05-25 | Astrazeneca Ab | composto, composição farmacêutica, e uso de um composto |
BRPI0409427A (pt) * | 2003-04-16 | 2006-04-18 | Astrazeneca Ab | composto, uso do mesmo, composição farmacêutica, método de tratamento de um humano sofrendo de uma doença hiperproliferativa, e, processo para a preparação de um composto ou de um sal, éster ou pró-droga farmaceuticamente aceitáveis do mesmo |
-
2003
- 2003-12-22 BR BRPI0317717A patent/BRPI0317717B8/pt not_active IP Right Cessation
- 2003-12-22 AU AU2003290313A patent/AU2003290313B2/en not_active Expired
- 2003-12-22 EP EP07009390A patent/EP1847539B1/en not_active Expired - Lifetime
- 2003-12-22 DE DE60315892T patent/DE60315892T2/de not_active Expired - Lifetime
- 2003-12-22 AT AT07009390T patent/ATE438644T1/de active
- 2003-12-22 MY MYPI20034944A patent/MY136174A/en unknown
- 2003-12-22 CA CA2511613A patent/CA2511613C/en not_active Expired - Lifetime
- 2003-12-22 EP EP03782672A patent/EP1578755B1/en not_active Expired - Lifetime
- 2003-12-22 AT AT03782672T patent/ATE370958T1/de active
- 2003-12-22 WO PCT/GB2003/005613 patent/WO2004058781A1/en active Application Filing
- 2003-12-22 DK DK03782672T patent/DK1578755T3/da active
- 2003-12-22 MY MYPI20071321A patent/MY147761A/en unknown
- 2003-12-22 US US10/539,220 patent/US7528121B2/en active Active
- 2003-12-22 ES ES03782672T patent/ES2290529T3/es not_active Expired - Lifetime
- 2003-12-22 SI SI200331673T patent/SI1847539T1/sl unknown
- 2003-12-22 JP JP2005509716A patent/JP4422102B2/ja not_active Expired - Lifetime
- 2003-12-22 DK DK07009390T patent/DK1847539T3/da active
- 2003-12-22 RU RU2007121850/04A patent/RU2350611C1/ru active
- 2003-12-22 ES ES07009390T patent/ES2329623T3/es not_active Expired - Lifetime
- 2003-12-22 PT PT03782672T patent/PT1578755E/pt unknown
- 2003-12-22 PL PL412704A patent/PL223998B1/pl unknown
- 2003-12-22 RU RU2005123485/04A patent/RU2357971C2/ru active
- 2003-12-22 SI SI200330965T patent/SI1578755T1/sl unknown
- 2003-12-22 PT PT07009390T patent/PT1847539E/pt unknown
- 2003-12-22 MX MXPA05006918A patent/MXPA05006918A/es active IP Right Grant
- 2003-12-22 DE DE60328735T patent/DE60328735D1/de not_active Expired - Lifetime
- 2003-12-22 CL CL200302731A patent/CL2003002731A1/es unknown
- 2003-12-22 NZ NZ540698A patent/NZ540698A/en not_active IP Right Cessation
- 2003-12-22 PL PL377680A patent/PL221490B1/pl unknown
- 2003-12-22 KR KR1020057012015A patent/KR101010299B1/ko active IP Right Grant
- 2003-12-22 UA UAA200507294A patent/UA83814C2/ru unknown
- 2003-12-23 AR ARP030104824A patent/AR042668A1/es active IP Right Grant
- 2003-12-23 TW TW092136601A patent/TWI336327B/zh not_active IP Right Cessation
- 2003-12-23 UY UY28149A patent/UY28149A1/es not_active Application Discontinuation
- 2003-12-23 TW TW099134275A patent/TWI393710B/zh not_active IP Right Cessation
-
2004
- 2004-02-18 SA SA04240504A patent/SA04240504B1/ar unknown
-
2005
- 2005-06-09 IL IL169112A patent/IL169112A/en active IP Right Grant
- 2005-06-13 NO NO20052855A patent/NO335193B1/no not_active IP Right Cessation
- 2005-07-20 IS IS7948A patent/IS2504B/is unknown
-
2006
- 2006-01-10 HK HK06100400A patent/HK1080481A1/xx not_active IP Right Cessation
-
2007
- 2007-05-16 AR ARP070102117A patent/AR057753A2/es not_active Application Discontinuation
- 2007-06-13 RU RU2007121850/04K patent/RU2007121850A/ru unknown
- 2007-06-28 JP JP2007169891A patent/JP4906608B2/ja not_active Expired - Lifetime
- 2007-08-09 IL IL185176A patent/IL185176A/en active IP Right Grant
- 2007-10-24 CY CY20071101369T patent/CY1107775T1/el unknown
-
2008
- 2008-02-13 IS IS8714A patent/IS2884B/is unknown
- 2008-02-27 HK HK08102177.3A patent/HK1111417A1/xx not_active IP Right Cessation
- 2008-10-15 JP JP2008265949A patent/JP4503090B2/ja not_active Expired - Lifetime
-
2009
- 2009-04-28 US US12/431,165 patent/US8268841B2/en active Active
- 2009-10-13 CY CY20091101054T patent/CY1109479T1/el unknown
-
2012
- 2012-08-21 US US13/590,662 patent/US9018191B2/en not_active Expired - Lifetime
-
2013
- 2013-11-01 NO NO20131444A patent/NO335446B1/no not_active IP Right Cessation
-
2015
- 2015-03-18 US US14/661,657 patent/US9567358B2/en not_active Expired - Lifetime
Also Published As
Similar Documents
Publication | Publication Date | Title |
---|---|---|
AR057753A2 (es) | Derivados de quinazolina, proceso para su preparacion y composiciones farmaceuticas que los contienen | |
SE0202463D0 (sv) | Novel compounds | |
BR0007500A (pt) | Composto triazol, fármaco, e, uso do composto | |
GEP20053530B (en) | Tyrosine Kinase Inhibitors, Pharmaceutical Compositions Containing Them and Use Thereof | |
MXPA02005844A (es) | Inhibidores de cinasas de proteina. | |
NO20045434L (no) | En kombinasjon av en NMDA-antagonist og acetylkolinesteraseinhibitorer for behandlingen av Alzheimers sykdom | |
NO20033732L (no) | N-substituerte ikke-aryl-heterosykliske NMDA/NR2B-antagonister, og farmasoytiske preparater som omfatter slike forbindelser. | |
GEP20053659B (en) | Aryl And Heteroaryl Urea CHK1 Inhibitors for Use as Radiosensitizers and Chamosensitizers | |
PL406680A1 (pl) | Inhibitory kinaz tyrozynowych | |
GEP20084571B (en) | Triazole derivatives as vasopressin antagonists | |
NZ517758A (en) | Pyrazolopyrimidines useful as therapeutic agents | |
BR9910583A (pt) | Aminotetralinas n-substituìdas como ligantes para o receptor de neuropeptìdeo y y5 úteis no tratamento de obesidade e outros distúrbios | |
ATE427740T1 (de) | Sedierende und nicht sedierende antihistamine enthaltende zusammensetzungen | |
MA27265A1 (fr) | Formulations d'agoniste opioide a antagoniste liberable et sequestre | |
CY1106240T1 (el) | Αλατα ισοθειαζολο-4-καρβοξαμιδιου και η χρηση αυτων ως αναστολεις του υπερμετρου κυτταρικου πολλαπλασιασμου | |
DE60214198D1 (de) | Isoxazolyl-pyrimidines als inhibitoren von src- und lck-protein-kinasen | |
SG147450A1 (en) | Sustained release pharmaceutical compositions comprising aplindore and derivatives thereof | |
NO20011721D0 (no) | N-aralkylaminotetraliner som ligander for neuropeptid Y Y5 reseptor | |
MXPA05007609A (es) | Antagonista de un receptor sensible al calcio. | |
SE0102055D0 (sv) | New Compounds | |
BR0212353A (pt) | Composto, composição farmacêutica, e, uso de um composto | |
ECSP034795A (es) | "composiciones que contienen imidazotriazinona para administración nasal" | |
PT1268472E (pt) | Inibidores 3-aminopirazolicos de cinases dependentes da ciclina | |
GEP20094801B (en) | Tetrazole derivatives and methods of treatment of metabolic-related disorders thereof | |
EE200100520A (et) | N-(2-fenüül-4-aminobutüül)-1-naftamiidid neurokiniin-1-retseptori antagonistidena |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
FC | Refusal |