AR041134A1 - Pirazolopirimidinas como inhibidores de la quinasa dependiente de ciclina - Google Patents
Pirazolopirimidinas como inhibidores de la quinasa dependiente de ciclinaInfo
- Publication number
- AR041134A1 AR041134A1 ARP030103189A ARP030103189A AR041134A1 AR 041134 A1 AR041134 A1 AR 041134A1 AR P030103189 A ARP030103189 A AR P030103189A AR P030103189 A ARP030103189 A AR P030103189A AR 041134 A1 AR041134 A1 AR 041134A1
- Authority
- AR
- Argentina
- Prior art keywords
- nr5r6
- cycloalkyl
- alkyl
- aryl
- group
- Prior art date
Links
- 108091000080 Phosphotransferase Proteins 0.000 title 1
- 239000003112 inhibitor Substances 0.000 title 1
- 102000020233 phosphotransferase Human genes 0.000 title 1
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 17
- 125000000217 alkyl group Chemical group 0.000 abstract 16
- 125000003118 aryl group Chemical group 0.000 abstract 15
- 125000001072 heteroaryl group Chemical group 0.000 abstract 13
- 125000000623 heterocyclic group Chemical group 0.000 abstract 9
- 125000003710 aryl alkyl group Chemical group 0.000 abstract 8
- 229910052736 halogen Inorganic materials 0.000 abstract 8
- 125000004415 heterocyclylalkyl group Chemical group 0.000 abstract 7
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 abstract 7
- 125000005843 halogen group Chemical group 0.000 abstract 6
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 abstract 6
- 125000004446 heteroarylalkyl group Chemical group 0.000 abstract 5
- 150000001875 compounds Chemical class 0.000 abstract 4
- 229910006069 SO3H Inorganic materials 0.000 abstract 3
- -1 compounds compounds Chemical class 0.000 abstract 3
- 150000002367 halogens Chemical class 0.000 abstract 3
- 238000000034 method Methods 0.000 abstract 3
- 239000008194 pharmaceutical composition Substances 0.000 abstract 3
- 125000000304 alkynyl group Chemical group 0.000 abstract 2
- 108091007914 CDKs Proteins 0.000 abstract 1
- 239000002875 cyclin dependent kinase inhibitor Substances 0.000 abstract 1
- 229940043378 cyclin-dependent kinase inhibitor Drugs 0.000 abstract 1
- 125000001316 cycloalkyl alkyl group Chemical group 0.000 abstract 1
- 201000010099 disease Diseases 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
- 230000005764 inhibitory process Effects 0.000 abstract 1
- KIWSYRHAAPLJFJ-DNZSEPECSA-N n-[(e,2z)-4-ethyl-2-hydroxyimino-5-nitrohex-3-enyl]pyridine-3-carboxamide Chemical compound [O-][N+](=O)C(C)C(/CC)=C/C(=N/O)/CNC(=O)C1=CC=CN=C1 KIWSYRHAAPLJFJ-DNZSEPECSA-N 0.000 abstract 1
- 230000002265 prevention Effects 0.000 abstract 1
- LDIJKUBTLZTFRG-UHFFFAOYSA-N pyrazolo[1,5-a]pyrimidine Chemical class N1=CC=CN2N=CC=C21 LDIJKUBTLZTFRG-UHFFFAOYSA-N 0.000 abstract 1
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
- 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
- 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
- A61P25/00—Drugs for disorders of the nervous system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
-
- 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
- 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
- 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
- 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
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Oncology (AREA)
- Neurosurgery (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- Rheumatology (AREA)
- Communicable Diseases (AREA)
- Heart & Thoracic Surgery (AREA)
- Immunology (AREA)
- Hematology (AREA)
- Cardiology (AREA)
- Virology (AREA)
- Hospice & Palliative Care (AREA)
- Psychiatry (AREA)
- Pain & Pain Management (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Abstract
Compuestos de pirazolo[1,5-a]pirimidina, inhibidores de quinasas dependientes de ciclina, métodos de preparación de dichos compuestos, composiciones farmacéuticas que contienen uno o más de dichos compuestos, métodos de preparación de formulaciones farmacéuticas que comprenden uno o más de dichos compuestos, y métodos de tratamiento, prevención, inhibición, o alivio de una o más enfermedades asociadas con las CDKs a través del uso de dichos compuestos o composiciones farmacéuticas. Reivindicación 1: Un compuesto representado por la fórmula estructural (1), en el cual: R es heteroarilo, donde dicho heteroarilo puede estar no sustituido o sustituido en forma opcional e independiente con uno o más restos que pueden ser iguales o diferentes, cada resto se selecciona en forma independiente del grupo formado por halógeno, arilo, cicloalquilo, CF3, OCF3, CN, -OR5, -NR5R6, C(R4R5)nOR5, -C(O)R5, -C(O)NR5R6, -SR6, -S(O2)R7, -S(O2)NR5R6, -N(R5)S(O)R7, -N(R5)C(O)R7 y -N(R5)C(O)NR5R6; R2 se selecciona del grupo formado por R9, alquilo, alquinilo, arilo, heteroarilo, CF3, heterociclilalquilo, alquinilalquilo, cicloalquilo, -C(O)OR4, alquilo sustituido con 1-6 grupos R9 que pueden ser iguales o diferentes y se seleccionan en forma independiente del listado de R9 que se muestra más adelante o es un resto del grupo de fórmula (2), donde el arilo en las definiciones indicadas precedentemente para R2 puede estar sustituido o sustituido en forma opcional con uno o más restos que pueden ser iguales o diferentes, cada resto se selecciona en forma del grupo formado por halógeno, CN, -OR5, SR5, -CH2OR5, -C(O)R5, -SO3H, -S(O2)R6, -S(O2)NR5R6, -NR5R6, -C(O)NR5R6, -CF3 y -OCF3; R3 se seleccionan del grupo formado por H, halógeno, -NR5R6, -C(O)OR4, -C(O)NR5R6, alquilo, alquinilo, cicloalquilo, cicloalquilalquilo, arilo, arilalquilo, heterociclilo, heterociclilalquilo, heteroarilo, o es un resto del grupo de fórmula (3), donde cada uno de dicho alquilo, cicloalquilo, arilo, arilalquilo, heterociclilo, heterociclilalquilo, heteroarilo y heteroarilalquilo para R3 y los restos heterociclilo cuyas estructuras se mostraron precedentemente para R3 pueden estar sustituidos o sustituidos en forma opcional e independiente con uno o más restos que pueden ser iguales o diferentes, cada resto se selecciona en forma independiente del grupo formado por halógeno, alquilo, arilo, cicloalquilo, CF3, CN, -OCF3,-(CR4R5)nOR5, -OR5, -NR5R6, -(CR4R5)nNR5R6, -C(O2)R5, -C(O)R5, -C(O)NR5R6, -SR6, -S(O2)R6, -S(O2)NR5R6, -N(R5)S(O2)R7, -N(R5)C(O)R7 y -N(R5)C(O)NR5R6; R4 es H, halo o alquilo; R5 es H o alquilo; R6 se selecciona del grupo formado por H, alquilo, arilo, arilalquilo, cicloalquilo, heterociclilo, heterociclilalquilo, heteroarilo, y heteroarilalquilo, donde cada uno de dichos alquilo, arilo, arilalquilo, cicloalquilo, heterociclilo, heterociclilalquilo, heteroarilo, y heteroarilalquilo puede estar sustituido o sustituido en forma opcional con uno o más restos que pueden ser iguales o diferentes, cada resto se selecciona en forma independiente del grupo formado por halógeno, alquilo, arilo, cicloalquilo, CF3, OCF3, CN, -OR5, -NR5R10, -N(R5)Boc, -(CR4R5)nOR5, -C(O2)R5, -C(O)R5, -C(O)NR5R10, -SO3H, -SR10, -S(O2)R7, -S(O2)NR5R10, -N(R5)S(O2)R7, -N(R5)C(O)R7 y -N(R5)C(O)NR5R10; R10 se selecciona del grupo formado por H, alquilo, arilo, arilalquilo, cicloalquilo, heterociclilo, heterociclilalquilo, heteroarilo, y heteroarilalquilo, donde cada uno de dichos alquilo, arilo, arilalquilo, cicloalquilo, heterociclilo, heterociclilalquilo, heteroarilo, y heteroarilalquilo puede estar no sustituido o sustituido en forma opcional con uno o más restos que pueden ser iguales o diferentes, cada resto se selecciona en forma independiente del grupo formado por halógeno, alquilo, arilo, cicloalquilo, CF3, OCF3, CN, -OR5, -NR4R5, -N(R5)Boc, -(CR4R5)nOR5, -C(O2)R5, -C(O)NR4R5, -C(O)R5, -SO3H, -SR5, -S(O2)R7, -S(O2)NR4R5, -N(R5)S(02)R7, -N(R5)C(O)R7 y -N(R5)C(O)NR4R5; o en forma opcional (i) R5 y R10 en el resto -NR5R10, o (ii) R5 y R6 en el resto -NR5R6, pueden estar unidos para formar un resto cicloalquilo o heterociclilo, con cada uno de dichos resto cicloalquilo o heterociclilo, con cada uno de dichos resto cicloalquilos o heterociclilos sustituidos o sustituido en forma opcional e independiente con uno o más grupos R9; R7 se selecciona del grupo formado por alquilo, cicloalquilo, arilo, heteroarilo, arilalquilo y heteroarilalquilo, donde cada uno de dichos alquilo, cicloalquilo, heteroarilalquilo, arilo, heteroarilo y arilalquilo para R7 puede ser no sustituido o sustituido en forma opcional e independiente con uno o más restos que pueden ser iguales o diferentes, cada resto se selecciona en forma independiente del grupo formado por halógeno, alquilo, arilo, cicloalquilo, CF3, OCF3, CN, -OR5, -NR5R10, -CH2OR5, -C(O2)R5, -C(O)NR5R10, -C(O)R5, -SR10, -S(O2)R10, -S(O2)NR5R10, -N(R5)S(02)R10, -N(R5)C(O)R10 y -N(R5)C(O)NR5R10; R8 se selecciona del grupo formado por R6, -C(O)NR5R10, -CH2OR4, -C(O)OR6, -C(O)R7 y -S(O2)R7; R9 se selecciona del grupo formado por, halógeno, -CN, -NR5R6, -(CH2)nOR4, -C(O2)R6, -C(O)NR5R6, -OR6, -SR6, -S(O2)R7, -S(O2)NR5R6, -N(R5)S(O2)R7, -N(R5)C(O)R7 y -N(R5)C(O)NR5R6; m es 0 hasta 4; y n es 1 hasta 4.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US40803002P | 2002-09-04 | 2002-09-04 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR041134A1 true AR041134A1 (es) | 2005-05-04 |
Family
ID=31978549
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP030103189A AR041134A1 (es) | 2002-09-04 | 2003-09-03 | Pirazolopirimidinas como inhibidores de la quinasa dependiente de ciclina |
Country Status (17)
| Country | Link |
|---|---|
| US (2) | US7078525B2 (es) |
| EP (1) | EP1534709B1 (es) |
| JP (2) | JP2006501260A (es) |
| KR (1) | KR20050058507A (es) |
| CN (1) | CN1310918C (es) |
| AR (1) | AR041134A1 (es) |
| AT (1) | ATE364608T1 (es) |
| CA (1) | CA2497444C (es) |
| DE (1) | DE60314427T2 (es) |
| ES (1) | ES2285164T3 (es) |
| MX (1) | MXPA05002573A (es) |
| MY (1) | MY139336A (es) |
| NZ (1) | NZ539162A (es) |
| PE (1) | PE20041076A1 (es) |
| TW (1) | TW200413377A (es) |
| WO (1) | WO2004022559A1 (es) |
| ZA (1) | ZA200501851B (es) |
Families Citing this family (59)
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|---|---|---|---|---|
| WO1999001124A1 (en) * | 1996-12-03 | 1999-01-14 | Sloan-Kettering Institute For Cancer Research | Synthesis of epothilones, intermediates thereto, analogues and uses thereof |
| US20020058286A1 (en) * | 1999-02-24 | 2002-05-16 | Danishefsky Samuel J. | Synthesis of epothilones, intermediates thereto and analogues thereof |
| US7649006B2 (en) | 2002-08-23 | 2010-01-19 | Sloan-Kettering Institute For Cancer Research | Synthesis of epothilones, intermediates thereto and analogues thereof |
| US6921769B2 (en) | 2002-08-23 | 2005-07-26 | Sloan-Kettering Institute For Cancer Research | Synthesis of epothilones, intermediates thereto and analogues thereof |
| ATE450534T1 (de) | 2002-08-23 | 2009-12-15 | Sloan Kettering Inst Cancer | Synthese von epothilonen, zwischenprodukte davon, analoga und ihre verwendung |
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| US7119200B2 (en) * | 2002-09-04 | 2006-10-10 | Schering Corporation | Pyrazolopyrimidines as cyclin dependent kinase inhibitors |
| MXPA05002572A (es) | 2002-09-04 | 2005-09-08 | Schering Corp | Compuestos pirazolo[1,5-a]pirimidinas como inhibidores de cinasa depentes de ciclina. |
| US7196092B2 (en) * | 2002-09-04 | 2007-03-27 | Schering Corporation | N-heteroaryl pyrazolopyrimidines as cyclin dependent kinase inhibitors |
| US7205308B2 (en) * | 2002-09-04 | 2007-04-17 | Schering Corporation | Trisubstituted 7-aminopyrazolopyrimidines as cyclin dependent kinase inhibitors |
| US7605155B2 (en) * | 2002-09-04 | 2009-10-20 | Schering Corporation | Substituted pyrazolo[1,5-a]pyrimidines as protein kinase inhibitors |
| US7563798B2 (en) * | 2002-09-04 | 2009-07-21 | Schering Corporation | Substituted pyrazolo[1,5-a]pyrimidines as protein kinase inhibitors |
| ATE364608T1 (de) * | 2002-09-04 | 2007-07-15 | Schering Corp | Pyrazolopyrimidine als hemmstoffe cyclin- abhängiger kinasen |
| WO2004076458A1 (en) * | 2003-02-28 | 2004-09-10 | Teijin Pharma Limited | Pyrazolo[1,5-a]pyrimidine derivatives |
| GB0305559D0 (en) * | 2003-03-11 | 2003-04-16 | Teijin Ltd | Compounds |
| US20070179161A1 (en) * | 2003-03-31 | 2007-08-02 | Vernalis (Cambridge) Limited. | Pyrazolopyrimidine compounds and their use in medicine |
| EP1644003A1 (en) * | 2003-06-04 | 2006-04-12 | Vernalis (Cambridge) Limited | Triazolo ´1,5-a!pyrimidines and their use in medicine |
| CA2538026A1 (en) * | 2003-09-09 | 2005-03-24 | Ono Pharmaceutical Co., Ltd. | Crf antagonists and heterobicyclic compounds |
| AU2005286793A1 (en) | 2004-09-20 | 2006-03-30 | Xenon Pharmaceuticals Inc. | Heterocyclic derivatives for the treatment of diseases mediated by stearoyl-CoA desaturase enzymes |
| MX2007003325A (es) | 2004-09-20 | 2007-06-05 | Xenon Pharmaceuticals Inc | Derivados heterociclicos y su uso como inhibidores estearoil-coa-desaturasa. |
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| AU2005286648A1 (en) | 2004-09-20 | 2006-03-30 | Xenon Pharmaceuticals Inc. | Heterocyclic derivatives and their use as stearoyl-CoA desaturase inhibitors |
| EP2316458A1 (en) | 2004-09-20 | 2011-05-04 | Xenon Pharmaceuticals Inc. | Pyridazine derivatives for inhibiting human stearoyl-coa-desaturase |
| CN101084212A (zh) | 2004-09-20 | 2007-12-05 | 泽农医药公司 | 杂环衍生物及其作为硬脂酰CoA去饱和酶介导剂的用途 |
| US7777036B2 (en) | 2004-09-20 | 2010-08-17 | Xenon Pharmaceuticals Inc. | Heterocyclic derivatives and their use as therapeutic agents |
| BRPI0611187A2 (pt) | 2005-06-03 | 2010-08-24 | Xenon Pharmaceuticals Inc | derivados aminotiazàis como inibidores da estearoil-coa desaturase humana |
| CA2621983A1 (en) | 2005-09-09 | 2007-03-22 | Schering Corporation | Azafused cyclin dependent kinase inhibitors |
| TWI421078B (zh) * | 2005-10-06 | 2014-01-01 | Merck Sharp & Dohme | 關卡激酶抑制劑及其用途 |
| JP2009511484A (ja) * | 2005-10-06 | 2009-03-19 | シェーリング コーポレイション | プロテインキナーゼインヒビターとしてのピラゾロピリミジン |
| TWI403320B (zh) * | 2005-12-16 | 2013-08-01 | Infinity Discovery Inc | 用於抑制bcl蛋白和結合夥伴間之交互作用的化合物及方法 |
| US8008307B2 (en) | 2006-08-08 | 2011-08-30 | Millennium Pharmaceuticals, Inc. | Heteroaryl compounds useful as inhibitors of E1 activating enzymes |
| GB0704652D0 (en) * | 2007-03-09 | 2007-04-18 | Syngenta Participations Ag | Novel herbicides |
| EP2155725A1 (en) * | 2007-06-07 | 2010-02-24 | Schering Corporation | Synthesis of substituted-3-aminopyrazoles |
| DE102008022221A1 (de) * | 2008-05-06 | 2009-11-12 | Universität des Saarlandes | Inhibitoren der humanen Aldosteronsynthase CYP11B2 |
| WO2010087467A1 (en) | 2009-01-27 | 2010-08-05 | Takeda Pharmaceutical Company Limited | Delta-5-desaturase inhibitors |
| US8993535B2 (en) | 2009-09-04 | 2015-03-31 | Merck Sharp & Dohme Corp. | Modulators of cell cycle checkpoints and their use in combination with checkpoint kinase inhibitors |
| US10953012B2 (en) | 2011-04-26 | 2021-03-23 | Bioenergenix Llc | Heterocyclic compounds for the inhibition of pask |
| WO2012178125A1 (en) | 2011-06-22 | 2012-12-27 | Vertex Pharmaceuticals Incorporated | Compounds useful as inhibitors of atr kinase |
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| US9663519B2 (en) | 2013-03-15 | 2017-05-30 | Vertex Pharmaceuticals Incorporated | Compounds useful as inhibitors of ATR kinase |
| EP2970288A1 (en) | 2013-03-15 | 2016-01-20 | Vertex Pharmaceuticals Incorporated | Compounds useful as inhibitors of atr kinase |
| CA2916468C (en) | 2013-07-02 | 2019-07-23 | Millennium Pharmaceuticals, Inc. | Heteroaryl compounds useful as inhibitors of sumo activating enzyme |
| PT3077397T (pt) | 2013-12-06 | 2020-01-22 | Vertex Pharma | Composto de 2-amino-6-fluoro-n-[5-fluoro-piridin-3-il]pirazolo[1,5-a]pirimidin-3-carboxamida útil como inibidor da atr quinase, a sua preparação, diferentes formas sólidas e derivados radiomarcados do mesmo |
| JP6568111B2 (ja) | 2014-06-05 | 2019-08-28 | バーテックス ファーマシューティカルズ インコーポレイテッドVertex Pharmaceuticals Incorporated | ATRキナーゼ阻害剤として有用な2−アミノ−6−フルオロ−N−[5−フルオロ−ピリジン−3−イル]ピラゾロ[1,5−a]ピリミジン−3−カルボキサミド化合物の放射性標識された誘導体、この化合物およびその異なる固体形態の調製 |
| HRP20191375T1 (hr) | 2014-06-17 | 2019-11-01 | Vertex Pharma | Postupak liječenja raka upotrebom kombinacije chk1 i atr inhibitora |
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| EP0628559B1 (en) | 1993-06-10 | 2002-04-03 | Beiersdorf-Lilly GmbH | Pyrimidine compounds and their use as pharmaceuticals |
| US5571813A (en) * | 1993-06-10 | 1996-11-05 | Beiersdorf-Lilly Gmbh | Fused pyrimidine compounds and their use as pharmaceuticals |
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| FR2805160B1 (fr) | 2000-02-23 | 2002-04-05 | Oreal | Compositions pour la teinture d'oxydation des fibres keratiniques comprenant un n(2-hydroxybenzene)-carbramate ou un n-(2-hydroxybenzene)-uree et une pyrazolopyrimidine, et procedes de teinture |
| US6282096B1 (en) * | 2000-04-28 | 2001-08-28 | Siliconware Precision Industries Co., Ltd. | Integration of heat conducting apparatus and chip carrier in IC package |
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| ATE364608T1 (de) * | 2002-09-04 | 2007-07-15 | Schering Corp | Pyrazolopyrimidine als hemmstoffe cyclin- abhängiger kinasen |
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-
2003
- 2003-09-03 AT AT03749317T patent/ATE364608T1/de not_active IP Right Cessation
- 2003-09-03 US US10/654,157 patent/US7078525B2/en not_active Expired - Lifetime
- 2003-09-03 ES ES03749317T patent/ES2285164T3/es not_active Expired - Lifetime
- 2003-09-03 CN CNB038244489A patent/CN1310918C/zh not_active Expired - Fee Related
- 2003-09-03 TW TW092124349A patent/TW200413377A/zh unknown
- 2003-09-03 MX MXPA05002573A patent/MXPA05002573A/es active IP Right Grant
- 2003-09-03 KR KR1020057003150A patent/KR20050058507A/ko not_active Ceased
- 2003-09-03 AR ARP030103189A patent/AR041134A1/es unknown
- 2003-09-03 JP JP2004534424A patent/JP2006501260A/ja not_active Withdrawn
- 2003-09-03 DE DE60314427T patent/DE60314427T2/de not_active Expired - Lifetime
- 2003-09-03 EP EP03749317A patent/EP1534709B1/en not_active Expired - Lifetime
- 2003-09-03 CA CA2497444A patent/CA2497444C/en not_active Expired - Fee Related
- 2003-09-03 WO PCT/US2003/027405 patent/WO2004022559A1/en not_active Ceased
- 2003-09-03 NZ NZ539162A patent/NZ539162A/en not_active IP Right Cessation
- 2003-09-03 MY MYPI20033320A patent/MY139336A/en unknown
- 2003-09-04 PE PE2003000901A patent/PE20041076A1/es not_active Application Discontinuation
-
2005
- 2005-03-03 ZA ZA200501851A patent/ZA200501851B/en unknown
-
2006
- 2006-03-31 US US11/395,974 patent/US7470695B2/en not_active Expired - Lifetime
-
2010
- 2010-03-02 JP JP2010045900A patent/JP2010132704A/ja active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| HK1071570A1 (en) | 2005-07-22 |
| TW200413377A (en) | 2004-08-01 |
| AU2003268357A1 (en) | 2004-03-29 |
| CN1310918C (zh) | 2007-04-18 |
| US20040102451A1 (en) | 2004-05-27 |
| US20060235025A1 (en) | 2006-10-19 |
| CN1738821A (zh) | 2006-02-22 |
| JP2006501260A (ja) | 2006-01-12 |
| DE60314427T2 (de) | 2008-06-12 |
| MY139336A (en) | 2009-09-30 |
| EP1534709B1 (en) | 2007-06-13 |
| ZA200501851B (en) | 2005-09-08 |
| WO2004022559A1 (en) | 2004-03-18 |
| DE60314427D1 (de) | 2007-07-26 |
| ES2285164T3 (es) | 2007-11-16 |
| US7078525B2 (en) | 2006-07-18 |
| US7470695B2 (en) | 2008-12-30 |
| CA2497444A1 (en) | 2004-03-18 |
| ATE364608T1 (de) | 2007-07-15 |
| EP1534709A1 (en) | 2005-06-01 |
| PE20041076A1 (es) | 2005-01-22 |
| KR20050058507A (ko) | 2005-06-16 |
| JP2010132704A (ja) | 2010-06-17 |
| MXPA05002573A (es) | 2005-09-08 |
| NZ539162A (en) | 2006-07-28 |
| CA2497444C (en) | 2010-11-30 |
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