TN2011000259A1 - Substituted pyrimidines for the treatment of diseases such as cancer - Google Patents
Substituted pyrimidines for the treatment of diseases such as cancerInfo
- Publication number
- TN2011000259A1 TN2011000259A1 TN2011000259A TN2011000259A TN2011000259A1 TN 2011000259 A1 TN2011000259 A1 TN 2011000259A1 TN 2011000259 A TN2011000259 A TN 2011000259A TN 2011000259 A TN2011000259 A TN 2011000259A TN 2011000259 A1 TN2011000259 A1 TN 2011000259A1
- Authority
- TN
- Tunisia
- Prior art keywords
- treatment
- diseases
- cancer
- substituted pyrimidines
- medicament
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
-
- 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
- A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
-
- 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
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/04—Antibacterial agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/10—Antimycotics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
-
- 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
- A61P37/00—Drugs for immunological or allergic disorders
-
- 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
-
- 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
- C07D239/46—Two or more oxygen, sulphur or nitrogen atoms
- C07D239/47—One nitrogen atom and one oxygen or sulfur atom, e.g. cytosine
-
- 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
- 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
- C07D401/14—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 three or more hetero rings
-
- 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
- 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
-
- 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
- C07D405/14—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 three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D419/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen, oxygen, and sulfur atoms as the only ring hetero atoms
- C07D419/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen, oxygen, and sulfur atoms as the only ring hetero atoms containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D493/00—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system
- C07D493/02—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system in which the condensed system contains two hetero rings
- C07D493/04—Ortho-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Immunology (AREA)
- Virology (AREA)
- Hematology (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP08169807 | 2008-11-24 | ||
EP09169654 | 2009-09-07 | ||
PCT/EP2009/065768 WO2010058032A2 (fr) | 2008-11-24 | 2009-11-24 | Nouveaux composés |
Publications (1)
Publication Number | Publication Date |
---|---|
TN2011000259A1 true TN2011000259A1 (en) | 2012-12-17 |
Family
ID=42115425
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
TN2011000259A TN2011000259A1 (en) | 2008-11-24 | 2011-05-20 | Substituted pyrimidines for the treatment of diseases such as cancer |
Country Status (27)
Country | Link |
---|---|
US (4) | US8846689B2 (fr) |
EP (1) | EP2367800B9 (fr) |
JP (1) | JP5622740B2 (fr) |
KR (1) | KR101710058B1 (fr) |
CN (2) | CN102292322B (fr) |
AP (1) | AP2960A (fr) |
AR (1) | AR074210A1 (fr) |
AU (1) | AU2009317170B2 (fr) |
BR (1) | BRPI0922801B1 (fr) |
CA (1) | CA2744351C (fr) |
CL (1) | CL2011001215A1 (fr) |
CO (1) | CO6511283A2 (fr) |
EA (1) | EA021997B1 (fr) |
EC (1) | ECSP11011079A (fr) |
ES (1) | ES2664499T3 (fr) |
GE (1) | GEP20146072B (fr) |
HK (1) | HK1160841A1 (fr) |
IL (1) | IL212814B (fr) |
MA (1) | MA32811B1 (fr) |
MX (1) | MX337116B (fr) |
MY (1) | MY176944A (fr) |
NZ (1) | NZ592925A (fr) |
PE (1) | PE20120034A1 (fr) |
TN (1) | TN2011000259A1 (fr) |
TW (1) | TWI491605B (fr) |
UY (1) | UY32259A (fr) |
WO (1) | WO2010058032A2 (fr) |
Families Citing this family (28)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AR074210A1 (es) | 2008-11-24 | 2010-12-29 | Boehringer Ingelheim Int | Derivados de pirimidina como inhibidores de ptk2-quinasa |
TW201024281A (en) | 2008-11-24 | 2010-07-01 | Boehringer Ingelheim Int | New compounds |
US8933227B2 (en) | 2009-08-14 | 2015-01-13 | Boehringer Ingelheim International Gmbh | Selective synthesis of functionalized pyrimidines |
EP2464633A1 (fr) | 2009-08-14 | 2012-06-20 | Boehringer Ingelheim International GmbH | Préparation régiosélective de dérivés de 2-amino-5-trifluorométhylpyrimidine |
US20120244141A1 (en) | 2010-09-28 | 2012-09-27 | Boehringer Ingelheim International Gmbh | Stratification of cancer patients for susceptibility to therapy with PTK2 inhibitors |
ES2724525T3 (es) | 2011-02-17 | 2019-09-11 | Cancer Therapeutics Crc Pty Ltd | Inhibidores selectivos de FAK |
WO2012110773A1 (fr) | 2011-02-17 | 2012-08-23 | Cancer Therapeutics Crc Pty Limited | Inhibiteurs de fak |
WO2013146963A1 (fr) * | 2012-03-28 | 2013-10-03 | 武田薬品工業株式会社 | Composé hétérocyclique |
HUE045462T2 (hu) | 2013-09-09 | 2019-12-30 | Peloton Therapeutics Inc | Aril-éterek és alkalmazásaik |
US10155726B2 (en) | 2015-03-11 | 2018-12-18 | Peloton Therapeutics, Inc. | Substituted pyridines and uses thereof |
US10512626B2 (en) | 2015-03-11 | 2019-12-24 | Peloton Therapeautics, Inc. | Compositions for use in treating glioblastoma |
WO2016145032A1 (fr) | 2015-03-11 | 2016-09-15 | Peloton Therapeutics, Inc. | Compositions utilisées pour traiter l'hypertension artérielle pulmonaire |
US10807948B2 (en) | 2015-03-11 | 2020-10-20 | Peloton Therapeutics, Inc. | Aromatic compounds and uses thereof |
US10335388B2 (en) | 2015-04-17 | 2019-07-02 | Peloton Therapeutics, Inc. | Combination therapy of a HIF-2-alpha inhibitor and an immunotherapeutic agent and uses thereof |
US20170066778A1 (en) * | 2015-09-04 | 2017-03-09 | Aunova Medchem LLC | Solubility for target compounds |
MX2022005994A (es) * | 2019-11-18 | 2022-06-17 | Inxmed Nanjing Co Ltd | Uso del inhibidor de fak en la preparacion de un farmaco para el tratamiento contra tumores con mutacion nras. |
US12121519B2 (en) * | 2019-11-28 | 2024-10-22 | Inxmed (Nanjing) Co., Ltd. | Use of BI853520 in cancer treatment |
JP2023515765A (ja) | 2020-02-05 | 2023-04-14 | ▲應▼世生物科技(南京)有限公司 | Bi853520と化学療法薬の併用 |
CN116096713A (zh) * | 2020-08-03 | 2023-05-09 | 应世生物科技(南京)有限公司 | 化合物的固体形式 |
TW202313044A (zh) | 2021-08-16 | 2023-04-01 | 大陸商應世生物科技(南京)有限公司 | In10018與pld的聯用 |
TW202339755A (zh) | 2021-12-10 | 2023-10-16 | 大陸商應世生物科技(南京)有限公司 | 治療腫瘤的藥物組合及用途 |
US12084453B2 (en) | 2021-12-10 | 2024-09-10 | Incyte Corporation | Bicyclic amines as CDK12 inhibitors |
EP4455139A1 (fr) | 2021-12-21 | 2024-10-30 | Wigen Biomedicine Technology (Shanghai) Co., Ltd. | Composé utilisé comme inhibiteur de fak et son utilisation |
AU2023224815A1 (en) * | 2022-02-28 | 2024-09-26 | Wigen Biomedicine Technology (shanghai) Co., Ltd. | Compound as fak inhibitor and use thereof |
TW202408528A (zh) | 2022-06-24 | 2024-03-01 | 大陸商應世生物科技(南京)有限公司 | 治療腫瘤的藥物組合及用途 |
CN117462553A (zh) * | 2022-07-20 | 2024-01-30 | 益方生物科技(上海)股份有限公司 | 药物组合产品以及组合疗法 |
WO2024041527A1 (fr) * | 2022-08-24 | 2024-02-29 | 应世生物科技(南京)有限公司 | Association pharmaceutique d'inhibiteur de fak et d'inhibiteur de microtubule et utilisation associée |
CN118580221A (zh) * | 2023-03-02 | 2024-09-03 | 应世生物科技(南京)有限公司 | 化合物的固体形式 |
Family Cites Families (37)
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GB9705361D0 (en) | 1997-03-14 | 1997-04-30 | Celltech Therapeutics Ltd | Chemical compounds |
DE69933680T2 (de) | 1998-08-29 | 2007-08-23 | Astrazeneca Ab | Pyrimidine verbindungen |
US6906067B2 (en) * | 1999-12-28 | 2005-06-14 | Bristol-Myers Squibb Company | N-heterocyclic inhibitors of TNF-α expression |
GB0004888D0 (en) | 2000-03-01 | 2000-04-19 | Astrazeneca Uk Ltd | Chemical compounds |
GB0004890D0 (en) | 2000-03-01 | 2000-04-19 | Astrazeneca Uk Ltd | Chemical compounds |
GB0004886D0 (en) | 2000-03-01 | 2000-04-19 | Astrazeneca Uk Ltd | Chemical compounds |
GB0016877D0 (en) | 2000-07-11 | 2000-08-30 | Astrazeneca Ab | Chemical compounds |
EP2332924A1 (fr) | 2001-10-17 | 2011-06-15 | Boehringer Ingelheim Pharma GmbH & Co. KG | Derivés pyrimidine, agent pharmaceutique contenant ces composés, utilisation et procédé de fabrication de ces composés |
MY141867A (en) | 2002-06-20 | 2010-07-16 | Vertex Pharma | Substituted pyrimidines useful as protein kinase inhibitors |
PL377795A1 (pl) | 2002-11-28 | 2006-02-20 | Schering Aktiengesellschaft | Pirymidyny będące inhibitorami Chk, Pdk i Akt, sposób ich wytwarzania oraz ich zastosowanie jako środków farmaceutycznych |
US7514446B2 (en) | 2003-02-20 | 2009-04-07 | Smithkline Beecham Corporation | Pyrimidine compounds |
CL2004000306A1 (es) * | 2003-02-20 | 2005-04-08 | Tibotec Pharm Ltd | Compuestos derivados de pirimidina sustituidas con indano; proceso para su preparacion; composicion farmaceutica que lo comprende; combinacion farmaceutica; y su uso para el tratamiento o profilaxis de una enfermedad infecciosa. |
GB0305929D0 (en) | 2003-03-14 | 2003-04-23 | Novartis Ag | Organic compounds |
US7504396B2 (en) * | 2003-06-24 | 2009-03-17 | Amgen Inc. | Substituted heterocyclic compounds and methods of use |
MXPA06001759A (es) | 2003-08-15 | 2006-05-12 | Novartis Ag | 2,4-pirimidinadiaminas utiles en el tratamiento de enfermedades neoplasticas, desordenes del sistema inmune e inflamatorios. |
EP1598343A1 (fr) | 2004-05-19 | 2005-11-23 | Boehringer Ingelheim International GmbH | Dérivés de 2-arylaminopyrimidines comme des inhibiteurs de PLK |
US7521457B2 (en) * | 2004-08-20 | 2009-04-21 | Boehringer Ingelheim International Gmbh | Pyrimidines as PLK inhibitors |
GB0419160D0 (en) * | 2004-08-27 | 2004-09-29 | Novartis Ag | Organic compounds |
WO2006035068A2 (fr) | 2004-09-30 | 2006-04-06 | Tibotec Pharmaceuticals Ltd. | 5-carbo- ou heterocycliques pyrimidines substituees inhibitrices de vih |
CN101103028A (zh) | 2005-01-14 | 2008-01-09 | 神经能质公司 | 经杂芳基取代的喹啉-4-基氨类似物 |
US20070032514A1 (en) | 2005-07-01 | 2007-02-08 | Zahn Stephan K | 2,4-diamino-pyrimidines as aurora inhibitors |
WO2007035309A1 (fr) | 2005-09-15 | 2007-03-29 | Merck & Co., Inc. | Inhibiteurs de la tyrosine kinase |
EP1968950A4 (fr) * | 2005-12-19 | 2010-04-28 | Genentech Inc | Inhibiteurs de pyrimidine kinase |
FR2896503B1 (fr) | 2006-01-23 | 2012-07-13 | Aventis Pharma Sa | Nouveaux derives soufres d'uree cyclique, leur preparation et leur utilisation pharmaceutique comme inhibiteurs de kinases |
TW200804364A (en) | 2006-02-22 | 2008-01-16 | Boehringer Ingelheim Int | New compounds |
CA2648036C (fr) | 2006-03-31 | 2012-05-22 | Janssen Pharmaceutica N.V. | Benzoimidazol-2-yl pyrimidines et pyrazines modulatrices du recepteur de l'histamine h4 |
GB0619343D0 (en) | 2006-09-30 | 2006-11-08 | Vernalis R&D Ltd | New chemical compounds |
WO2008040951A1 (fr) | 2006-10-03 | 2008-04-10 | Astrazeneca Ab | Composés |
WO2008071587A2 (fr) | 2006-12-13 | 2008-06-19 | F. Hoffmann-La Roche Ag | Inhibiteurs non nucléosidiques de la transcriptase inverse |
CA2670645A1 (fr) | 2006-12-19 | 2008-07-03 | Genentech, Inc. | Inhibiteurs de pyrimidine kinase |
AU2008210266B2 (en) | 2007-01-31 | 2013-09-05 | Ym Biosciences Australia Pty Ltd | Thiopyrimidine-based compounds and uses thereof |
PT2154967E (pt) * | 2007-04-16 | 2014-06-05 | Hutchison Medipharma Entpr Ltd | Derivados de pirimidina |
CA2718858A1 (fr) | 2008-03-20 | 2009-09-24 | Boehringer Ingelheim International Gmbh | Elaboration regioselective de pyrimidines substituees |
NZ589843A (en) | 2008-06-27 | 2012-12-21 | Avila Therapeutics Inc | Pyrimidine heteroaryl compounds and uses thereof as protein kinase inhibitors |
AR074210A1 (es) | 2008-11-24 | 2010-12-29 | Boehringer Ingelheim Int | Derivados de pirimidina como inhibidores de ptk2-quinasa |
TW201024281A (en) | 2008-11-24 | 2010-07-01 | Boehringer Ingelheim Int | New compounds |
CA2760794C (fr) | 2009-05-05 | 2017-07-25 | Dana Farber Cancer Institute | Inhibiteurs d'egfr et procedes de traitement de troubles |
-
2009
- 2009-11-23 AR ARP090104511A patent/AR074210A1/es not_active Application Discontinuation
- 2009-11-23 TW TW098139766A patent/TWI491605B/zh active
- 2009-11-24 AU AU2009317170A patent/AU2009317170B2/en active Active
- 2009-11-24 EP EP09756513.9A patent/EP2367800B9/fr active Active
- 2009-11-24 CA CA2744351A patent/CA2744351C/fr active Active
- 2009-11-24 AP AP2011005706A patent/AP2960A/xx active
- 2009-11-24 WO PCT/EP2009/065768 patent/WO2010058032A2/fr active Application Filing
- 2009-11-24 NZ NZ592925A patent/NZ592925A/xx unknown
- 2009-11-24 US US13/130,669 patent/US8846689B2/en active Active
- 2009-11-24 MX MX2011005420A patent/MX337116B/es active IP Right Grant
- 2009-11-24 ES ES09756513.9T patent/ES2664499T3/es active Active
- 2009-11-24 EA EA201100794A patent/EA021997B1/ru not_active IP Right Cessation
- 2009-11-24 JP JP2011536901A patent/JP5622740B2/ja active Active
- 2009-11-24 PE PE2011001080A patent/PE20120034A1/es active IP Right Grant
- 2009-11-24 KR KR1020117014264A patent/KR101710058B1/ko active IP Right Grant
- 2009-11-24 CN CN200980155031.1A patent/CN102292322B/zh active Active
- 2009-11-24 UY UY0001032259A patent/UY32259A/es not_active Application Discontinuation
- 2009-11-24 BR BRPI0922801-2A patent/BRPI0922801B1/pt active IP Right Grant
- 2009-11-24 GE GEAP200912270A patent/GEP20146072B/en unknown
- 2009-11-24 CN CN201410635154.8A patent/CN104478865B/zh active Active
- 2009-11-24 MY MYPI2011002290A patent/MY176944A/en unknown
-
2011
- 2011-05-11 IL IL212814A patent/IL212814B/en active IP Right Grant
- 2011-05-20 TN TN2011000259A patent/TN2011000259A1/fr unknown
- 2011-05-20 MA MA33866A patent/MA32811B1/fr unknown
- 2011-05-24 CO CO11063881A patent/CO6511283A2/es not_active Application Discontinuation
- 2011-05-24 CL CL2011001215A patent/CL2011001215A1/es unknown
- 2011-05-24 EC EC2011011079A patent/ECSP11011079A/es unknown
-
2012
- 2012-02-07 HK HK12101136.9A patent/HK1160841A1/zh unknown
-
2014
- 2014-08-29 US US14/472,627 patent/US20140371205A1/en not_active Abandoned
-
2015
- 2015-09-04 US US14/845,529 patent/US20150376141A1/en not_active Abandoned
-
2016
- 2016-08-24 US US15/245,854 patent/US9676762B2/en not_active Expired - Fee Related
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