SI2297115T1 - Dialkoksikinazolinski derivati kot inhibitorji kdr - Google Patents
Dialkoksikinazolinski derivati kot inhibitorji kdrInfo
- Publication number
- SI2297115T1 SI2297115T1 SI200931257T SI200931257T SI2297115T1 SI 2297115 T1 SI2297115 T1 SI 2297115T1 SI 200931257 T SI200931257 T SI 200931257T SI 200931257 T SI200931257 T SI 200931257T SI 2297115 T1 SI2297115 T1 SI 2297115T1
- Authority
- SI
- Slovenia
- Prior art keywords
- dialkoxyquinazoline
- derivatives
- kdr inhibitors
- kdr
- inhibitors
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/517—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with carbocyclic ring systems, e.g. quinazoline, perimidine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/06—Antipsoriatics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P27/00—Drugs for disorders of the senses
- A61P27/02—Ophthalmic agents
-
- 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
- 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
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/04—Antineoplastic agents specific for metastasis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
-
- 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
- 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
-
- 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
- A61P9/14—Vasoprotectives; Antihaemorrhoidals; Drugs for varicose therapy; Capillary stabilisers
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Immunology (AREA)
- Diabetes (AREA)
- Oncology (AREA)
- Vascular Medicine (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Rheumatology (AREA)
- Hematology (AREA)
- Epidemiology (AREA)
- Obesity (AREA)
- Urology & Nephrology (AREA)
- Pain & Pain Management (AREA)
- Endocrinology (AREA)
- Ophthalmology & Optometry (AREA)
- Dermatology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Emergency Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US12/118,019 US7829574B2 (en) | 2008-05-09 | 2008-05-09 | Substituted quinazoline compounds and their use in treating angiogenesis-related diseases |
PCT/US2009/043347 WO2009137797A2 (en) | 2008-05-09 | 2009-05-08 | Quinazoline derivatives |
EP09743783.4A EP2297115B1 (en) | 2008-05-09 | 2009-05-08 | Dialkoxyquinazoline derivatives as kdr inhibitors |
Publications (1)
Publication Number | Publication Date |
---|---|
SI2297115T1 true SI2297115T1 (sl) | 2015-10-30 |
Family
ID=41265455
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SI200931257T SI2297115T1 (sl) | 2008-05-09 | 2009-05-08 | Dialkoksikinazolinski derivati kot inhibitorji kdr |
Country Status (22)
Country | Link |
---|---|
US (3) | US7829574B2 (sl) |
EP (1) | EP2297115B1 (sl) |
JP (2) | JP5856842B2 (sl) |
KR (2) | KR20160045925A (sl) |
AU (1) | AU2009244130B2 (sl) |
BR (1) | BRPI0908675B1 (sl) |
CA (1) | CA2723148C (sl) |
CY (1) | CY1117222T1 (sl) |
DK (1) | DK2297115T3 (sl) |
ES (1) | ES2550245T3 (sl) |
HR (1) | HRP20150954T1 (sl) |
HU (1) | HUE025723T2 (sl) |
MX (2) | MX340021B (sl) |
MY (1) | MY155566A (sl) |
NZ (1) | NZ588900A (sl) |
PH (1) | PH12013500363A1 (sl) |
PL (1) | PL2297115T3 (sl) |
PT (1) | PT2297115E (sl) |
RU (1) | RU2506261C2 (sl) |
SI (1) | SI2297115T1 (sl) |
TW (1) | TWI458724B (sl) |
WO (1) | WO2009137797A2 (sl) |
Families Citing this family (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7829574B2 (en) * | 2008-05-09 | 2010-11-09 | Hutchison Medipharma Enterprises Limited | Substituted quinazoline compounds and their use in treating angiogenesis-related diseases |
CN102317269B (zh) * | 2009-02-11 | 2015-06-17 | 默克专利有限公司 | 新氨基氮杂杂环甲酰胺类 |
CA2772642C (en) | 2009-09-03 | 2017-08-29 | Bristol-Myers Squibb Company | Quinazolines as potassium ion channel inhibitors |
CN105461702A (zh) * | 2014-09-10 | 2016-04-06 | 和记黄埔医药(上海)有限公司 | 6-(6,7-二甲氧基喹唑啉-4-基氧基)-n,2-二甲基苯并呋喃-3-甲酰胺晶型 |
KR20180086187A (ko) | 2015-10-05 | 2018-07-30 | 더 트러스티이스 오브 콜롬비아 유니버시티 인 더 시티 오브 뉴욕 | 자가포식 유동의 활성체 및 포스포리파제 d 및 타우를 포함하는 단백질 응집물의 클리어런스 및 단백질질환의 치료 |
WO2017189483A1 (en) * | 2016-04-25 | 2017-11-02 | The Johns Hopkins University | Znt8 assays for drug development and pharmaceutical compositions |
US11892457B2 (en) | 2017-07-12 | 2024-02-06 | The Johns Hopkins University | Proteoliposome-based ZnT8 self-antigen for type 1 diabetes diagnosis |
CN116987070A (zh) * | 2018-03-30 | 2023-11-03 | 杭州领业医药科技有限公司 | 呋喹替尼的共晶、其制备方法、组合物和用途 |
CN113166241B (zh) | 2018-08-16 | 2025-02-25 | 约翰霍普金斯大学 | 人类znt8抗体 |
CN111184698A (zh) * | 2018-11-15 | 2020-05-22 | 和记黄埔医药(上海)有限公司 | 呋喹替尼制剂及其应用 |
CN110898065A (zh) * | 2019-11-25 | 2020-03-24 | 南通大学 | 呋喹替尼或其盐在制备治疗脉络膜新生血管药物中的用途 |
KR20230170039A (ko) | 2021-04-13 | 2023-12-18 | 뉴베일런트, 아이엔씨. | Egfr 돌연변이를 지니는 암을 치료하기 위한 아미노-치환된 헤테로사이클 |
Family Cites Families (33)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB9300059D0 (en) | 1992-01-20 | 1993-03-03 | Zeneca Ltd | Quinazoline derivatives |
HRP970371A2 (en) | 1996-07-13 | 1998-08-31 | Kathryn Jane Smith | Heterocyclic compounds |
US6235741B1 (en) | 1997-05-30 | 2001-05-22 | Merck & Co., Inc. | Angiogenesis inhibitors |
CA2362715C (en) * | 1999-02-10 | 2010-10-19 | Astrazeneca Ab | Quinazoline derivatives as angiogenesis inhibitors |
US6943161B2 (en) | 1999-12-28 | 2005-09-13 | Pharmacopela Drug Discovery, Inc. | Pyrimidine and triazine kinase inhibitors |
DE10009267A1 (de) | 2000-02-26 | 2001-08-30 | Goedecke Ag | Verfahren zur einfachen Herstellung von (3-Chlor-4-fluor-phenyl)-[7-(3-morpholin-4-yl-propoxy)-6-nitro-quinazolin-4-yl]-amin bzw. (3-Chlor-4-fluor-phenyl)-[7-(3-morpholin-4-yl-propoxy)-6-amino-quinazolin-4-yl]-amin |
AR035851A1 (es) * | 2000-03-28 | 2004-07-21 | Wyeth Corp | 3-cianoquinolinas, 3-ciano-1,6-naftiridinas y 3-ciano-1,7-naftiridinas como inhibidoras de proteina quinasas |
UA73993C2 (uk) * | 2000-06-06 | 2005-10-17 | Астразенека Аб | Хіназолінові похідні для лікування пухлин та фармацевтична композиція |
AU2001292137A1 (en) * | 2000-10-13 | 2002-04-22 | Astrazeneca Ab | Quinazoline derivatives |
EP1326859A1 (en) * | 2000-10-13 | 2003-07-16 | AstraZeneca AB | Quinazoline derivatives with anti-tumour activity |
EP1367050A4 (en) | 2001-03-01 | 2005-09-21 | Ono Pharmaceutical Co | 2-METHYLINDOLE-4-ACETIC ACID, PROCESS FOR PRODUCING THE SAME, AND PROCESS FOR PRODUCING INTERMEDIATE PRODUCT THEREOF |
WO2003048159A1 (en) * | 2001-12-05 | 2003-06-12 | Astrazeneca Ab | Quinoline derivatives |
TWI329105B (en) | 2002-02-01 | 2010-08-21 | Rigel Pharmaceuticals Inc | 2,4-pyrimidinediamine compounds and their uses |
GB0206215D0 (en) | 2002-03-15 | 2002-05-01 | Novartis Ag | Organic compounds |
UA77303C2 (en) * | 2002-06-14 | 2006-11-15 | Pfizer | Derivatives of thienopyridines substituted by benzocondensed heteroarylamide useful as therapeutic agents, pharmaceutical compositions and methods for their use |
WO2004014382A1 (en) | 2002-07-29 | 2004-02-19 | Rigel Pharmaceuticals | Methods of treating or preventing autoimmune diseases with 2,4-pyrimidinediamine compounds |
KR100802856B1 (ko) * | 2003-07-02 | 2008-02-12 | 에프. 호프만-라 로슈 아게 | 아릴아민-치환된 퀴나졸린온 화합물 |
US7442698B2 (en) | 2003-07-24 | 2008-10-28 | Amgen Inc. | Substituted heterocyclic compounds and methods of use |
GB0318423D0 (en) | 2003-08-06 | 2003-09-10 | Astrazeneca Ab | Chemical compounds |
GB0321710D0 (en) | 2003-09-16 | 2003-10-15 | Novartis Ag | Organic compounds |
EP1699780A1 (en) * | 2003-12-23 | 2006-09-13 | Pfizer, Inc. | Novel quinoline derivatives |
WO2005097134A2 (en) * | 2004-03-31 | 2005-10-20 | The Scripps Research Institute | Quinazoline based protein kinase inhibitors |
US20080268460A1 (en) * | 2004-05-20 | 2008-10-30 | Wyeth | Assays to Identify Irreversibly Binding Inhibitors of Receptor Tyrosine Kinases |
WO2005115145A2 (en) | 2004-05-20 | 2005-12-08 | Wyeth | Quinone substituted quinazoline and quinoline kinase inhibitors |
WO2006071079A1 (en) | 2004-12-29 | 2006-07-06 | Hanmi Pharm. Co., Ltd. | Quinazoline derivatives for inhibiting cancer cell growth and method for the preparation thereof |
KR100735639B1 (ko) | 2004-12-29 | 2007-07-04 | 한미약품 주식회사 | 암세포 성장 억제 효과를 갖는 퀴나졸린 유도체 및 이의제조방법 |
EP1890703B1 (en) | 2005-06-14 | 2016-05-11 | Taigen Biotechnology | Pyrimidine compounds as chemokine receptors inhibitors |
WO2007066181A2 (en) | 2005-12-05 | 2007-06-14 | Pfizer Products Inc. | Methods of preparing a vegf-r inhibitor |
US7601844B2 (en) * | 2006-01-27 | 2009-10-13 | Bristol-Myers Squibb Company | Piperidinyl derivatives as modulators of chemokine receptor activity |
GB0604937D0 (en) * | 2006-03-10 | 2006-04-19 | Novartis Ag | Organic compounds |
CA2652341A1 (en) * | 2006-05-15 | 2007-11-22 | Senex Biotechnology, Inc. | Identification of cdki pathway inhibitors |
TW200922590A (en) * | 2007-09-10 | 2009-06-01 | Curis Inc | VEGFR inhibitors containing a zinc binding moiety |
US7829574B2 (en) * | 2008-05-09 | 2010-11-09 | Hutchison Medipharma Enterprises Limited | Substituted quinazoline compounds and their use in treating angiogenesis-related diseases |
-
2008
- 2008-05-09 US US12/118,019 patent/US7829574B2/en active Active
- 2008-07-04 TW TW097125278A patent/TWI458724B/zh active
-
2009
- 2009-05-08 BR BRPI0908675-7A patent/BRPI0908675B1/pt active IP Right Grant
- 2009-05-08 CA CA2723148A patent/CA2723148C/en active Active
- 2009-05-08 PT PT97437834T patent/PT2297115E/pt unknown
- 2009-05-08 SI SI200931257T patent/SI2297115T1/sl unknown
- 2009-05-08 MX MX2014001023A patent/MX340021B/es active IP Right Grant
- 2009-05-08 KR KR1020167009777A patent/KR20160045925A/ko not_active Application Discontinuation
- 2009-05-08 AU AU2009244130A patent/AU2009244130B2/en active Active
- 2009-05-08 JP JP2011508714A patent/JP5856842B2/ja active Active
- 2009-05-08 NZ NZ588900A patent/NZ588900A/xx unknown
- 2009-05-08 EP EP09743783.4A patent/EP2297115B1/en active Active
- 2009-05-08 PL PL09743783T patent/PL2297115T3/pl unknown
- 2009-05-08 HU HUE09743783A patent/HUE025723T2/en unknown
- 2009-05-08 RU RU2010150345/04A patent/RU2506261C2/ru active
- 2009-05-08 KR KR1020107024889A patent/KR101686679B1/ko active IP Right Grant
- 2009-05-08 WO PCT/US2009/043347 patent/WO2009137797A2/en active Application Filing
- 2009-05-08 PH PH1/2013/500363A patent/PH12013500363A1/en unknown
- 2009-05-08 ES ES09743783.4T patent/ES2550245T3/es active Active
- 2009-05-08 MX MX2010012168A patent/MX2010012168A/es active IP Right Grant
- 2009-05-08 DK DK09743783.4T patent/DK2297115T3/en active
- 2009-05-08 MY MYPI2010005148A patent/MY155566A/en unknown
-
2010
- 2010-09-29 US US12/893,872 patent/US8212033B2/en active Active
-
2012
- 2012-06-04 US US13/487,434 patent/US8497372B2/en active Active
-
2014
- 2014-07-04 JP JP2014138608A patent/JP2014177499A/ja active Pending
-
2015
- 2015-08-06 CY CY20151100689T patent/CY1117222T1/el unknown
- 2015-09-09 HR HRP20150954TT patent/HRP20150954T1/hr unknown
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