TW200716651A - Thienopyrimidine and thienopyridine kinase modulators - Google Patents
Thienopyrimidine and thienopyridine kinase modulatorsInfo
- Publication number
- TW200716651A TW200716651A TW095120482A TW95120482A TW200716651A TW 200716651 A TW200716651 A TW 200716651A TW 095120482 A TW095120482 A TW 095120482A TW 95120482 A TW95120482 A TW 95120482A TW 200716651 A TW200716651 A TW 200716651A
- Authority
- TW
- Taiwan
- Prior art keywords
- compounds
- flt3
- thienopyrimidine
- thienopyridine
- kinase modulators
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
- C07D495/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D495/04—Ortho-condensed systems
-
- 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
- A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
-
- 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
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US68971005P | 2005-06-10 | 2005-06-10 | |
US74694106P | 2006-05-10 | 2006-05-10 |
Publications (1)
Publication Number | Publication Date |
---|---|
TW200716651A true TW200716651A (en) | 2007-05-01 |
Family
ID=37074647
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
TW095120482A TW200716651A (en) | 2005-06-10 | 2006-06-09 | Thienopyrimidine and thienopyridine kinase modulators |
Country Status (19)
Country | Link |
---|---|
US (3) | US20060281768A1 (zh) |
EP (1) | EP1899355A1 (zh) |
JP (1) | JP2008543759A (zh) |
KR (1) | KR20080021126A (zh) |
AR (1) | AR057063A1 (zh) |
AU (1) | AU2006258049A1 (zh) |
BR (1) | BRPI0613644A2 (zh) |
CA (1) | CA2611587A1 (zh) |
CR (1) | CR9650A (zh) |
EA (1) | EA200800011A1 (zh) |
EC (1) | ECSP077992A (zh) |
IL (1) | IL187689A0 (zh) |
MX (1) | MX2007015741A (zh) |
NI (1) | NI200700311A (zh) |
NO (1) | NO20080162L (zh) |
PE (1) | PE20070070A1 (zh) |
TW (1) | TW200716651A (zh) |
UY (1) | UY29590A1 (zh) |
WO (1) | WO2006135639A1 (zh) |
Families Citing this family (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
MY179032A (en) | 2004-10-25 | 2020-10-26 | Cancer Research Tech Ltd | Ortho-condensed pyridine and pyrimidine derivatives (e.g.purines) as protein kinase inhibitors |
JP5606734B2 (ja) | 2006-04-25 | 2014-10-15 | アステックス、セラピューティックス、リミテッド | 医薬化合物 |
US20090124610A1 (en) * | 2006-04-25 | 2009-05-14 | Gordon Saxty | Pharmaceutical compounds |
WO2008039794A1 (en) * | 2006-09-25 | 2008-04-03 | Arete Therapeutics, Inc. | Soluble epoxide hydrolase inhibitors |
US8193178B2 (en) | 2007-09-14 | 2012-06-05 | Janssen Pharmaceutica Nv | Thieno- and furo-pyrimidine modulators of the histamine H4 receptor |
CN101861321B (zh) | 2007-10-11 | 2013-02-06 | 阿斯利康(瑞典)有限公司 | 作为蛋白激酶b抑制剂的吡咯并[2,3-d]嘧啶衍生物 |
US9402847B2 (en) | 2011-04-01 | 2016-08-02 | Astrazeneca Ab | Combinations comprising (S)-4-amino-N-(1-(4-chlorophenyl)-3-hydroxypropyl)-1-(7H-pyrrolo[2,3-d]pyrimidin-4-yl)piperidine-4-carboxamide |
JP5933902B2 (ja) | 2011-05-13 | 2016-06-15 | アレイ バイオファーマ、インコーポレイテッド | Trkaキナーゼ阻害剤としてのピロリジニル尿素およびピロリジニルチオ尿素化合物 |
AR090037A1 (es) * | 2011-11-15 | 2014-10-15 | Xention Ltd | Derivados de tieno y/o furo-pirimidinas y piridinas inhibidores de los canales de potasio |
CA2856646C (en) | 2011-11-30 | 2020-01-14 | Astrazeneca Ab | Combination treatment of cancer |
AU2013204533B2 (en) | 2012-04-17 | 2017-02-02 | Astrazeneca Ab | Crystalline forms |
RS59286B1 (sr) | 2014-05-15 | 2019-10-31 | Array Biopharma Inc | 1-((3s,4r)-4-(3-fluorofenil)-1-(2-metoksietil)pirolidin-3-il)-3-(4-metil-3-(2-metilpirimidin-5-il)-1-fenil-1h-pirazol-5-il)urea kao inhibitor trka kinaze |
EP3559006A4 (en) * | 2016-12-23 | 2021-03-03 | Arvinas Operations, Inc. | COMPOUNDS AND METHODS FOR TARGETED DEGRADATION OF FETAL LIVER KINASE POLYPEPTIDES |
CN113874015A (zh) | 2018-12-21 | 2021-12-31 | 细胞基因公司 | Ripk2的噻吩并吡啶抑制剂 |
Family Cites Families (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0627940B1 (en) * | 1992-03-05 | 2003-05-07 | Board of Regents, The University of Texas System | Use of immunoconjugates for the diagnosis and/or therapy of vascularized tumors |
US5474765A (en) * | 1992-03-23 | 1995-12-12 | Ut Sw Medical Ctr At Dallas | Preparation and use of steroid-polyanionic polymer-based conjugates targeted to vascular endothelial cells |
US5932765A (en) * | 1997-05-23 | 1999-08-03 | Merck Patent Gesellschaft Mit | Nitromethyl ketones, process for preparing them and compositions containing them |
CN1280580A (zh) * | 1997-11-11 | 2001-01-17 | 辉瑞产品公司 | 用作抗癌药的噻吩并嘧啶和噻吩并吡啶衍生物 |
ZA99607B (en) * | 1998-01-27 | 1999-07-27 | Rhone Poulenc Rorer Pharma | Substituted oxoazaheterocyclyl factor xa inhibitors. |
WO2000064946A2 (en) * | 1999-04-28 | 2000-11-02 | Board Of Regents, The University Of Texas System | Compositions and methods for cancer treatment by selectively inhibiting vegf |
US6776796B2 (en) * | 2000-05-12 | 2004-08-17 | Cordis Corportation | Antiinflammatory drug and delivery device |
DE10110750A1 (de) * | 2001-03-07 | 2002-09-12 | Bayer Ag | Neuartige Aminodicarbonsäurederivate mit pharmazeutischen Eigenschaften |
AR035885A1 (es) * | 2001-05-14 | 2004-07-21 | Novartis Ag | Derivados de 4-amino-5-fenil-7-ciclobutilpirrolo (2,3-d)pirimidina, un proceso para su preparacion, una composicion farmaceutica y el uso de dichos derivados para la preparacion de una composicion farmaceutica |
US7105505B2 (en) * | 2002-04-18 | 2006-09-12 | Schering Corporation | Benzimidazole derivatives useful as histamine H3 antagonists |
MY141867A (en) * | 2002-06-20 | 2010-07-16 | Vertex Pharma | Substituted pyrimidines useful as protein kinase inhibitors |
MXPA05001631A (es) * | 2002-08-12 | 2005-08-19 | Takeda Pharmaceutical | Derivado de benceno fusionado y su uso. |
JPWO2004039782A1 (ja) * | 2002-10-29 | 2006-03-02 | 麒麟麦酒株式会社 | Flt3自己リン酸化を阻害するキノリン誘導体およびキナゾリン誘導体並びにそれらを含有する医薬組成物 |
US20050026944A1 (en) * | 2003-07-24 | 2005-02-03 | Patrick Betschmann | Thienopyridine and furopyridine kinase inhibitors |
US20060281769A1 (en) * | 2005-06-10 | 2006-12-14 | Baumann Christian A | Synergistic modulation of flt3 kinase using thienopyrimidine and thienopyridine kinase modulators |
-
2006
- 2006-06-06 US US11/422,359 patent/US20060281768A1/en not_active Abandoned
- 2006-06-07 NI NI200700311A patent/NI200700311A/es unknown
- 2006-06-07 EA EA200800011A patent/EA200800011A1/ru unknown
- 2006-06-07 EP EP06772445A patent/EP1899355A1/en not_active Withdrawn
- 2006-06-07 WO PCT/US2006/022151 patent/WO2006135639A1/en active Application Filing
- 2006-06-07 KR KR1020087000618A patent/KR20080021126A/ko not_active Application Discontinuation
- 2006-06-07 AU AU2006258049A patent/AU2006258049A1/en not_active Abandoned
- 2006-06-07 MX MX2007015741A patent/MX2007015741A/es unknown
- 2006-06-07 CA CA002611587A patent/CA2611587A1/en not_active Abandoned
- 2006-06-07 BR BRPI0613644-3A patent/BRPI0613644A2/pt not_active Application Discontinuation
- 2006-06-07 JP JP2008515879A patent/JP2008543759A/ja not_active Withdrawn
- 2006-06-08 UY UY29590A patent/UY29590A1/es unknown
- 2006-06-08 PE PE2006000640A patent/PE20070070A1/es not_active Application Discontinuation
- 2006-06-09 AR ARP060102425A patent/AR057063A1/es not_active Application Discontinuation
- 2006-06-09 TW TW095120482A patent/TW200716651A/zh unknown
-
2007
- 2007-11-27 IL IL187689A patent/IL187689A0/en unknown
- 2007-12-10 EC EC2007007992A patent/ECSP077992A/es unknown
-
2008
- 2008-01-09 NO NO20080162A patent/NO20080162L/no not_active Application Discontinuation
- 2008-01-09 CR CR9650A patent/CR9650A/es not_active Application Discontinuation
-
2009
- 2009-01-30 US US12/362,933 patent/US20090143378A1/en not_active Abandoned
- 2009-01-30 US US12/363,043 patent/US20090163710A1/en not_active Abandoned
Also Published As
Publication number | Publication date |
---|---|
NI200700311A (es) | 2009-03-03 |
KR20080021126A (ko) | 2008-03-06 |
AU2006258049A1 (en) | 2006-12-21 |
JP2008543759A (ja) | 2008-12-04 |
CA2611587A1 (en) | 2006-12-21 |
WO2006135639A1 (en) | 2006-12-21 |
UY29590A1 (es) | 2006-10-02 |
NO20080162L (no) | 2008-03-07 |
ECSP077992A (es) | 2008-01-23 |
MX2007015741A (es) | 2008-04-29 |
US20060281768A1 (en) | 2006-12-14 |
PE20070070A1 (es) | 2007-03-08 |
CR9650A (es) | 2008-09-09 |
BRPI0613644A2 (pt) | 2011-01-25 |
EP1899355A1 (en) | 2008-03-19 |
US20090163710A1 (en) | 2009-06-25 |
US20090143378A1 (en) | 2009-06-04 |
AU2006258049A8 (en) | 2006-12-21 |
EA200800011A1 (ru) | 2008-06-30 |
IL187689A0 (en) | 2008-08-07 |
AR057063A1 (es) | 2007-11-14 |
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