AR049769A1 - DERIVATIVES OF PIRAZOLO (1,5-A) PIRIMIDIN 7-IL-AMINA TO BE USED IN THE TREATMENT OF DEPENDENT DISEASES OF PROTEIN KINASE - Google Patents
DERIVATIVES OF PIRAZOLO (1,5-A) PIRIMIDIN 7-IL-AMINA TO BE USED IN THE TREATMENT OF DEPENDENT DISEASES OF PROTEIN KINASEInfo
- Publication number
- AR049769A1 AR049769A1 ARP050100208A ARP050100208A AR049769A1 AR 049769 A1 AR049769 A1 AR 049769A1 AR P050100208 A ARP050100208 A AR P050100208A AR P050100208 A ARP050100208 A AR P050100208A AR 049769 A1 AR049769 A1 AR 049769A1
- Authority
- AR
- Argentina
- Prior art keywords
- substituted
- unsubstituted
- treatment
- unsubstituted aryl
- unsubstituted heteroaryl
- Prior art date
Links
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—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
-
- 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
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/16—Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/08—Drugs for disorders of the urinary system of the prostate
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/12—Drugs for disorders of the urinary system of the kidneys
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P15/00—Drugs for genital or sexual disorders; Contraceptives
-
- 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
-
- 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
- A61P17/02—Drugs for dermatological disorders for treating wounds, ulcers, burns, scars, keloids, or the like
-
- 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
- A61P27/00—Drugs for disorders of the senses
- A61P27/02—Ophthalmic agents
- A61P27/06—Antiglaucoma agents or miotics
-
- 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
- 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
- A61P37/02—Immunomodulators
- A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
-
- 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
-
- 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
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Veterinary Medicine (AREA)
- Life Sciences & Earth Sciences (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Immunology (AREA)
- Dermatology (AREA)
- Ophthalmology & Optometry (AREA)
- Urology & Nephrology (AREA)
- Rheumatology (AREA)
- Cardiology (AREA)
- Epidemiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Vascular Medicine (AREA)
- Pain & Pain Management (AREA)
- Hematology (AREA)
- Oncology (AREA)
- Endocrinology (AREA)
- Reproductive Health (AREA)
- Gastroenterology & Hepatology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Transplantation (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
Uso en el tratamiento de enfermedades dependientes de quinasa, y para la fabricacion de preparaciones farmacéuticas para el tratamiento de estas enfermedades. Reivindicacion 1: El uso de un compuesto de la formula (1), en donde: R2 es H; arilo sustituido o insustituido; heteroarilo sustituido o insustituido; un residuo alifático sustituido o insustituido; un grupo funcional; o un arilo sustituido o insustituido, heteroarilo sustituido o insustituido, o un residuo alifático sustituido o insustituido que se conecta mediante un grupo o átomo conector con el anillo de pirazolo[1,5-a]pirimidinilo; y R3 puede ser H, arilo sustituido o insustituido, heteroarilo sustituido o insustituido, un residuo alifático sustituido o insustituido, un grupo funcional, o un residuo alifático sustituido o instituido que se puede conectar mediante un grupo o átomo conector con el anillo de pirazolo[1,5-a]pirimidinilo; cuando menos uno de R2 o R3 es arilo sustituido o insustituido; heteroarilo sustituido o insustituido; o heteroarilo sustituido o insustituido, o un residuo de arilo sustituido o insustituido que se conecta mediante un grupo o átomo conector con el anillo de pirazolo[1,5-a]pirimidinilo; A es H, halogeno (tal como bromo), una fraccion alifática, un grupo funcional, arilo sustituido o insustituido, o heteroarilo sustituido o insustituido; y R1 es H, halogeno, o alquilo inferior; o sales farmacéuticamente aceptables del mismo, para el tratamiento de una enfermedad dependiente de la quinasa de proteína.Use in the treatment of kinase dependent diseases, and for the manufacture of pharmaceutical preparations for the treatment of these diseases. Claim 1: The use of a compound of the formula (1), wherein: R2 is H; substituted or unsubstituted aryl; substituted or unsubstituted heteroaryl; a substituted or unsubstituted aliphatic residue; a functional group; or a substituted or unsubstituted aryl, substituted or unsubstituted heteroaryl, or a substituted or unsubstituted aliphatic residue that is connected by a group or atom connected to the pyrazolo [1,5-a] pyrimidinyl ring; and R3 may be H, substituted or unsubstituted aryl, substituted or unsubstituted heteroaryl, a substituted or unsubstituted aliphatic residue, a functional group, or a substituted or instituted aliphatic residue that can be connected by a linker group or atom with the pyrazolo ring [ 1,5-a] pyrimidinyl; at least one of R2 or R3 is substituted or unsubstituted aryl; substituted or unsubstituted heteroaryl; or substituted or unsubstituted heteroaryl, or a substituted or unsubstituted aryl residue that is connected by a group or atom connecting with the pyrazolo [1,5-a] pyrimidinyl ring; A is H, halogen (such as bromine), an aliphatic fraction, a functional group, substituted or unsubstituted aryl, or substituted or unsubstituted heteroaryl; and R1 is H, halogen, or lower alkyl; or pharmaceutically acceptable salts thereof, for the treatment of a protein kinase dependent disease.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US53822004P | 2004-01-22 | 2004-01-22 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR049769A1 true AR049769A1 (en) | 2006-09-06 |
Family
ID=34807167
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP050100208A AR049769A1 (en) | 2004-01-22 | 2005-01-20 | DERIVATIVES OF PIRAZOLO (1,5-A) PIRIMIDIN 7-IL-AMINA TO BE USED IN THE TREATMENT OF DEPENDENT DISEASES OF PROTEIN KINASE |
Country Status (17)
| Country | Link |
|---|---|
| EP (1) | EP1708710A1 (en) |
| JP (1) | JP2007519662A (en) |
| KR (1) | KR20070009546A (en) |
| CN (1) | CN1909908A (en) |
| AR (1) | AR049769A1 (en) |
| AU (1) | AU2005205915B2 (en) |
| BR (1) | BRPI0507071A (en) |
| CA (1) | CA2552885A1 (en) |
| EC (1) | ECSP066718A (en) |
| IL (1) | IL176737A0 (en) |
| MA (1) | MA28400B1 (en) |
| NO (1) | NO20063758L (en) |
| PE (1) | PE20051089A1 (en) |
| RU (1) | RU2006130003A (en) |
| TN (1) | TNSN06226A1 (en) |
| TW (1) | TW200528103A (en) |
| WO (1) | WO2005070431A1 (en) |
Families Citing this family (44)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7605155B2 (en) * | 2002-09-04 | 2009-10-20 | Schering Corporation | Substituted pyrazolo[1,5-a]pyrimidines as protein kinase inhibitors |
| US7196078B2 (en) | 2002-09-04 | 2007-03-27 | Schering Corpoartion | Trisubstituted and tetrasubstituted pyrazolopyrimidines as cyclin dependent kinase inhibitors |
| US7563798B2 (en) * | 2002-09-04 | 2009-07-21 | Schering Corporation | Substituted pyrazolo[1,5-a]pyrimidines as protein kinase inhibitors |
| GB0515026D0 (en) * | 2005-07-21 | 2005-08-31 | Novartis Ag | Organic compounds |
| WO2007044441A2 (en) * | 2005-10-06 | 2007-04-19 | Schering Corporation | Use of pyrazolo [1 , 5 -a] pyrimidine derivatives for inhibiting protein kinases methods for inhibiting protein kinases |
| KR20080063806A (en) * | 2005-10-06 | 2008-07-07 | 쉐링 코포레이션 | Pyrazolopyrimidines as Protein Kinase Inhibitors |
| SI2495016T1 (en) | 2005-12-23 | 2020-04-30 | Ariad Pharmaceuticals, Inc. | Bicyclic Heteroaryl Compounds |
| WO2007103432A2 (en) * | 2006-03-08 | 2007-09-13 | Novartis Ag | Use of pyrazolo[1,5a]pyrimidin-7-yl amine derivatives in the treatment of neurological disorders |
| WO2007109183A2 (en) * | 2006-03-20 | 2007-09-27 | Novartis Ag | Mutations and polymorphisms of fms-related tyrosine kinase 1 |
| GB0606805D0 (en) * | 2006-04-04 | 2006-05-17 | Novartis Ag | Organic compounds |
| GB0606804D0 (en) * | 2006-04-04 | 2006-05-17 | Novartis Ag | Organic Compounds |
| CA2664375A1 (en) * | 2006-09-28 | 2008-04-03 | Novartis Ag | Pyrazolo [1, 5-a] pyrimidine derivatives and their therapeutic use |
| KR20090073121A (en) | 2006-09-29 | 2009-07-02 | 노파르티스 아게 | Pyrazolopyrimidines as PI3 'Lipid Kinase Inhibitors |
| EP1918291A1 (en) * | 2006-10-30 | 2008-05-07 | Novartis AG | 3-Aminocarbonyl-substituted fused pyrazolo-derivatives as protein kinase modulators |
| WO2008153870A1 (en) * | 2007-06-07 | 2008-12-18 | Schering Corporation | Synthesis of substituted-3-aminopyrazoles |
| US8591943B2 (en) | 2009-04-09 | 2013-11-26 | Merck Sharp & Dohme Corp. | Pyrazolo[1,5-a]pyrimidine derivatives as mTOR inhibitors |
| US8658651B2 (en) | 2009-09-30 | 2014-02-25 | Merck Sharp & Dohme Corp. | Compounds that are ERK inhibitors |
| UY33227A (en) * | 2010-02-19 | 2011-09-30 | Novartis Ag | PIRROLOPIRIMIDINE COMPOUNDS AS INHIBITORS OF THE CDK4 / 6 |
| WO2011146336A1 (en) | 2010-05-20 | 2011-11-24 | Array Biopharma Inc. | Macrocyclic compounds as trk kinase inhibitors |
| KR101856266B1 (en) * | 2010-08-09 | 2018-05-09 | 가부시키가이샤 에누비 켄코우겡큐쇼 | INHIBITOR OF CASEIN KINASE 1δ AND CASEIN KINASE 1ε |
| WO2012023143A1 (en) | 2010-08-19 | 2012-02-23 | E. I. Du Pont De Nemours And Company | Fungicidal pyrazoles |
| US9242981B2 (en) | 2010-09-16 | 2016-01-26 | Merck Sharp & Dohme Corp. | Fused pyrazole derivatives as novel ERK inhibitors |
| KR101404151B1 (en) * | 2011-11-25 | 2014-06-05 | 가톨릭대학교 산학협력단 | Composition for preventing and treating ocular diseases |
| CN105906630B (en) * | 2015-04-06 | 2018-10-23 | 四川百利药业有限责任公司 | Two substitutional amine-group compounds of N- (1H- pyrazoles -5- bases) pyrimido pyrazoles -4,6- as FGFR inhibitor |
| JP6816100B2 (en) | 2015-07-16 | 2021-01-20 | アレイ バイオファーマ、インコーポレイテッド | Substituted pyrazolo [1,5-a] pyridine compound as a RET kinase inhibitor |
| TWI704148B (en) | 2016-10-10 | 2020-09-11 | 美商亞雷生物製藥股份有限公司 | Substituted pyrazolo[1,5-a]pyridine compounds as ret kinase inhibitors |
| JOP20190077A1 (en) | 2016-10-10 | 2019-04-09 | Array Biopharma Inc | Substituted pyrazolo[1,5-a]pyridine compounds as ret kinase inhibitors |
| CN106588893A (en) * | 2016-12-01 | 2017-04-26 | 北京万全德众医药生物技术有限公司 | Preparation of vilazodone double oxide |
| CN110267960B (en) | 2017-01-18 | 2022-04-26 | 阿雷生物药品公司 | Substituted pyrazolo [1,5-a ] pyrazine compounds as RET kinase inhibitors |
| WO2018136663A1 (en) | 2017-01-18 | 2018-07-26 | Array Biopharma, Inc. | Ret inhibitors |
| JOP20190213A1 (en) | 2017-03-16 | 2019-09-16 | Array Biopharma Inc | Macrocyclic compounds as ros1 kinase inhibitors |
| TWI812649B (en) | 2017-10-10 | 2023-08-21 | 美商絡速藥業公司 | Formulations of 6-(2-hydroxy-2-methylpropoxy)-4-(6-(6-((6-methoxypyridin-3-yl)methyl)-3,6-diazabicyclo[3.1.1]heptan-3-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile |
| TWI791053B (en) | 2017-10-10 | 2023-02-01 | 美商亞雷生物製藥股份有限公司 | Crystalline forms of 6-(2-hydroxy-2-methylpropoxy)-4-(6-(6-((6-methoxypyridin-3-yl)methyl)-3,6-diazabicyclo[3.1.1]heptan-3-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile and pharmaceutical composition thereof |
| WO2019143977A1 (en) | 2018-01-18 | 2019-07-25 | Array Biopharma Inc. | Substituted pyrrolo[2,3-d]pyrimidines compounds as ret kinase inhibitors |
| CA3087578C (en) | 2018-01-18 | 2023-08-08 | Array Biopharma Inc. | Substituted pyrazolo[3,4-d]pyrimidine compounds as ret kinase inhibitors |
| EP3740486A1 (en) | 2018-01-18 | 2020-11-25 | Array Biopharma, Inc. | Substituted pyrazolyl[4,3-c]pyridinecompounds as ret kinase inhibitors |
| KR20200116481A (en) * | 2018-01-29 | 2020-10-12 | 메르크 파텐트 게엠베하 | GCN2 inhibitors and uses thereof |
| SG11202006832YA (en) | 2018-01-29 | 2020-08-28 | Merck Patent Gmbh | Gcn2 inhibitors and uses thereof |
| EP3849986B1 (en) | 2018-09-10 | 2022-06-08 | Array Biopharma, Inc. | Fused heterocyclic compounds as ret kinase inhibitors |
| CN109836428A (en) * | 2019-02-27 | 2019-06-04 | 华东师范大学 | Pyrazoles [4,3-d] pyrimidine derivatives and purposes with immunosuppressive activity |
| WO2021007094A1 (en) * | 2019-07-10 | 2021-01-14 | Musc Foundation For Research Development | Endostatin peptides for the treatment of tumors, fibrosis and acute lung injury |
| JOP20220125A1 (en) | 2019-11-25 | 2023-01-30 | Amgen Inc | Heterocyclic compounds as delta-5 dysaturase inhibitors and methods for their use |
| EP4476204A1 (en) * | 2022-02-08 | 2024-12-18 | Theras, Inc. | Compounds having a t-structure formed by at least four cycles for use in the treatment of cancer and other indications |
| CN114751910B (en) * | 2022-05-17 | 2023-02-24 | 重庆文理学院 | Compound capable of inducing cell megalophage death and preparation method and application thereof |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3130633A1 (en) * | 1981-08-01 | 1983-02-17 | Basf Ag, 6700 Ludwigshafen | 7-AMINO-AZOLO (1,5-A) PYRIMIDINE AND FUNGICIDES CONTAINING THEM |
| ATE174917T1 (en) * | 1991-04-22 | 1999-01-15 | Otsuka Pharma Co Ltd | PYRAZOLO(1,5-A>PYRIMIDINE DERIVATIVES AND ANTI-INFLAMMATORY AGENTS CONTAINING SAME |
| JP3163413B2 (en) * | 1994-06-21 | 2001-05-08 | 株式会社大塚製薬工場 | Painkillers |
| AU680370B2 (en) * | 1994-06-21 | 1997-07-24 | Otsuka Pharmaceutical Factory, Inc. | Pyrazolo(1,5-a)pyrimidine derivative |
| WO1998010590A1 (en) * | 1996-09-02 | 1998-03-12 | Sony Corporation | Device and method for transmitting video signal |
| US7074924B2 (en) * | 2002-09-04 | 2006-07-11 | Schering Corporation | Pyrazolopyrimidines as cyclin dependent kinase inhibitors |
| TW200412966A (en) * | 2002-09-04 | 2004-08-01 | Schering Corp | Novel pyrazolopyrimidines as cyclin dependent kinase inhibitors |
-
2005
- 2005-01-20 AR ARP050100208A patent/AR049769A1/en unknown
- 2005-01-20 PE PE2005000080A patent/PE20051089A1/en not_active Application Discontinuation
- 2005-01-21 EP EP05706961A patent/EP1708710A1/en not_active Withdrawn
- 2005-01-21 CA CA002552885A patent/CA2552885A1/en not_active Abandoned
- 2005-01-21 BR BRPI0507071-6A patent/BRPI0507071A/en not_active IP Right Cessation
- 2005-01-21 CN CNA2005800030379A patent/CN1909908A/en active Pending
- 2005-01-21 WO PCT/EP2005/000602 patent/WO2005070431A1/en not_active Ceased
- 2005-01-21 RU RU2006130003/15A patent/RU2006130003A/en not_active Application Discontinuation
- 2005-01-21 TW TW094101852A patent/TW200528103A/en unknown
- 2005-01-21 AU AU2005205915A patent/AU2005205915B2/en not_active Ceased
- 2005-01-21 KR KR1020067014683A patent/KR20070009546A/en not_active Withdrawn
- 2005-01-21 JP JP2006550056A patent/JP2007519662A/en active Pending
-
2006
- 2006-07-06 IL IL176737A patent/IL176737A0/en unknown
- 2006-07-10 MA MA29182A patent/MA28400B1/en unknown
- 2006-07-21 EC EC2006006718A patent/ECSP066718A/en unknown
- 2006-07-21 TN TNP2006000226A patent/TNSN06226A1/en unknown
- 2006-08-22 NO NO20063758A patent/NO20063758L/en not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| AU2005205915A1 (en) | 2005-08-04 |
| BRPI0507071A (en) | 2007-06-19 |
| CA2552885A1 (en) | 2005-08-04 |
| MA28400B1 (en) | 2007-01-02 |
| PE20051089A1 (en) | 2006-01-25 |
| IL176737A0 (en) | 2006-10-31 |
| EP1708710A1 (en) | 2006-10-11 |
| AU2005205915B2 (en) | 2009-05-21 |
| TNSN06226A1 (en) | 2007-12-03 |
| ECSP066718A (en) | 2006-10-31 |
| JP2007519662A (en) | 2007-07-19 |
| TW200528103A (en) | 2005-09-01 |
| NO20063758L (en) | 2006-10-23 |
| CN1909908A (en) | 2007-02-07 |
| WO2005070431A1 (en) | 2005-08-04 |
| KR20070009546A (en) | 2007-01-18 |
| RU2006130003A (en) | 2008-04-10 |
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