AR059505A1 - Dihidrodiazepinas utiles como inhibidores de proteina quinasas - Google Patents
Dihidrodiazepinas utiles como inhibidores de proteina quinasasInfo
- Publication number
- AR059505A1 AR059505A1 ARP070100633A ARP070100633A AR059505A1 AR 059505 A1 AR059505 A1 AR 059505A1 AR P070100633 A ARP070100633 A AR P070100633A AR P070100633 A ARP070100633 A AR P070100633A AR 059505 A1 AR059505 A1 AR 059505A1
- Authority
- AR
- Argentina
- Prior art keywords
- aliphatic
- monocyclic ring
- so2r2
- optionally substituted
- cycloaliphatic
- Prior art date
Links
- 229940045988 antineoplastic drug protein kinase inhibitors Drugs 0.000 title 1
- 239000003909 protein kinase inhibitor Substances 0.000 title 1
- 125000001931 aliphatic group Chemical group 0.000 abstract 26
- 125000002950 monocyclic group Chemical group 0.000 abstract 12
- 125000005842 heteroatom Chemical group 0.000 abstract 9
- 229910052757 nitrogen Inorganic materials 0.000 abstract 9
- 229910052717 sulfur Inorganic materials 0.000 abstract 9
- 125000005843 halogen group Chemical group 0.000 abstract 8
- 229910052760 oxygen Inorganic materials 0.000 abstract 8
- 229920006395 saturated elastomer Polymers 0.000 abstract 6
- -1 C3-10 cycloaliphatic Chemical group 0.000 abstract 5
- 125000004429 atom Chemical group 0.000 abstract 5
- 125000000041 C6-C10 aryl group Chemical group 0.000 abstract 4
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 4
- 125000001313 C5-C10 heteroaryl group Chemical group 0.000 abstract 3
- 125000003118 aryl group Chemical group 0.000 abstract 3
- 229910052799 carbon Inorganic materials 0.000 abstract 3
- 125000004432 carbon atom Chemical group C* 0.000 abstract 3
- 125000006714 (C3-C10) heterocyclyl group Chemical group 0.000 abstract 2
- JCXJVPUVTGWSNB-UHFFFAOYSA-N Nitrogen dioxide Chemical compound O=[N]=O JCXJVPUVTGWSNB-UHFFFAOYSA-N 0.000 abstract 2
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 abstract 2
- 125000004122 cyclic group Chemical group 0.000 abstract 2
- 125000000623 heterocyclic group Chemical group 0.000 abstract 2
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 1
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 abstract 1
- 125000006570 (C5-C6) heteroaryl group Chemical group 0.000 abstract 1
- 229910006074 SO2NH2 Inorganic materials 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 125000001072 heteroaryl group Chemical group 0.000 abstract 1
- 229910052739 hydrogen Inorganic materials 0.000 abstract 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 1
- 125000000565 sulfonamide group Chemical group 0.000 abstract 1
Classifications
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- 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
- 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
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- 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
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/445—Non condensed piperidines, e.g. piperocaine
- A61K31/4523—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
- A61K31/4545—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring hetero atom, e.g. pipamperone, anabasine
-
- 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
- A61K31/55—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
- A61K31/551—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having two nitrogen atoms, e.g. dilazep
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory 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
-
- 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
- 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
- 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
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/08—Antiallergic agents
-
- 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
- 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
- C07D487/12—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 three hetero rings
- C07D487/14—Ortho-condensed systems
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Immunology (AREA)
- Epidemiology (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- Neurosurgery (AREA)
- Pulmonology (AREA)
- Hematology (AREA)
- Oncology (AREA)
- Hospice & Palliative Care (AREA)
- Transplantation (AREA)
- Psychiatry (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Abstract
Reivindicacion 1: Un compuesto de formula (1) en donde X1 es un enlace, O, NR8, S, SO o SO2; Y1 es O o NR9; R1 es H, alifático C1-10, arilo C6-10, heteroarilo de 5-10 miembros o heterociclilo de 3-10 miembros; en donde dicho R1 está opcionalmente sustituido con 0-5 J1, con la condicion de que, cuando X1 es un enlace, R1 no sea H; R2 es H, alifático C1-10, -(alifático C1-10)-(cicloalifático C3-10), cicloalifático C3-8, haloalifático C1-4; en donde dicho R2 está opcionalmente sustituido con 0- 4 J2; cada R3, R4, R5 y R6 es, de modo independiente, H, alifático C1-10, cicloalifático C3-10, arilo C6-10 o heteroarilo de 5-10 miembros; en donde cada R3, R4, R5 y R6 está sustituido, de modo opcional e independiente, con 0-5 J3, J4, J5 y J6 respectivamente; y R7es H, C(O)R, C(O)OR o C(O)NRR', alifático C1-10,cicloalifático C3-10, arilo C6-10, heteroarilo de 5-10miembros, heterociclilo de 3-10 miembros, -(alifático C1-6)-(cicloalifático C3-10), -(alifático C1-6)-(arilo C6-10) o - (alifático C1-6)-(heteroarilo de 5-10 miembros); en dicho R7 está opcionalmente sustituido con 0-5 J7; o R3 y R4, junto con el átomo de carbono al que están unidos, forman opcionalmente un anillo monocíclico saturado o parcialmente insaturado de 3-8 miembros que contiene 0-4 heteroátomos seleccionados, de modo independiente, de O, N y S; dicho anillo monocíclico formado por R3 y R4 está opcionalmente sustituido con 0-4 J34; R5 y R6, junto con el átomo de carbono al que están unidos forman opcionalmente un anillo monocíclico saturado o parcialmente insaturado de 3-8 miembros que contiene 0-4 heteroátomos seleccionados, de modo independiente, de O, N y S; dicho anillo monocíclico formado por R5 y R6 está opcionalmente sustituido con 0- 4 J56; R3 y R5, junto con los átomos de carbono a los que están unidos, forman opcionalmente un anillo monocíclico saturado o parcialmente insaturado de 3-8 miembros que contiene 0-4 heteroátomos seleccionados, de modo independiente, de O, N y S; dicho anillo monocíclico formado por R3 y R5 está opcionalmente sustituido con 0-4 J35; R3 y R7, junto con los átomos a los que están unidos, forman opcionalmente un anillo monocíclico saturado o parcialmente insaturado de 4-8 miembros que contiene 0-4 heteroátomos seleccionados, de modo independiente, de O, N y S; dicho anillo monocíclico formado por R3 y R7 está opcionalmente sustituido con 0-4 J37; R5 y R7, junto con los átomos a los que están unidos, forman opcionalmente un anillo monocíclico saturado o parcialmente insaturado de 3-8 miembros que contiene 0-4 heteroátomos seleccionados, de modo independiente, de O, N y S; dicho anillo monocíclico formado por R5 y R7 está opcionalmente substituido con 0-4 J57; R8 es H, alifático C1-6, cicloalifático C3-8, C(o)R, C(O)OR o C(O)NRR'; R9 es H o alifático C1-6 no sustituido; o R2 y R9, junto con los átomos a los que están unidos, forman opcionalmente un anillo monocíclico aromático o no aromático de 5-8 miembros que contiene 2-4 heteroátomos seleccionados, de modo independiente, de O, N y S; dicho anillo monocíclico formado por R2 y R9 está opcionalmente sustituido con 0-4 J29; cada J1 es, de modo independiente, haloalquilo C1-6, halo, NO2, CN, Q o -Z-Q; o, dos J1 juntos pueden formar opcionalmente =O; Z es alifático C1-6 opcionalmente reemplazado por 0-3 apariciones de -NR-, -O-, -S-, -C(O)-, --C(=NR)-, -C(=NOR)-, -SO- o -SO2-; cada Z está opcionalmente sustituido con 0-2 Jz; Q es H; alifático C1-6, un anillo monocíclico aromático o no aromático de 3-8 miembros que tiene 0-3 heteroátomos seleccionados, de modo independiente, de O, N y S; o un sistema de anillos bicíclicos aromáticos o no aromáticos de 8-12 miembros que tiene 0-5 heteroátomos seleccionados, de modo independiente, de O, N y S; cada Q está opcionalmente sustituido con 0-5 JQ; cada J2 es halo o haloalifático C1-4; cada J3, J4, J5 y J6 es, de modo independiente, alifático C1-6, cicloalifático C3-6 o -(alquil C1-4)n-V1; en donde n es 0 o 1; V1 es halo(alifático C1-4), -O(haloalifático C1-4), halo, NO2, CN, OH, ORö, SH, SRö, NH2, NHRö, N(Rö)2, COH, CORö, CO2H, CO2Rö, CONH2, CONHRö, CONRö2, OCORö, OCONH2, OCONHRö, OCON(Rö)2, NHCORö, NRöCORö, NHCO2Rö, NRöCO2Rö, NHCO2H, NRöCO2H, NHCONH2, NHCONHRö, NHCON(Rö)2, SO2NH2, SO2NHRö, SO2N(Rö)2, NHSO2Rö, NRöSO2Rö; o V1 es un grupo cíclico seleccionado de cicloalifático C3-6, fenilo, heteroarilo de 5-6 miembros o heterociclilo de 3-6 miembros; en donde dicho grupo cíclico está opcionalmente sustituido con 0-3 Jv; Rö es alifático C1-4 no sustituido; o dos de los mismos J3, J4, J5 o J6, unidos al mismo átomo, pueden formar juntos opcionalmente =O; cada 'Jz y Jv es de modo independiente, halo, alifático C16, cicloalifático C3-6, NO2, CN, -NH2, -NH(alifático C1-4), -N(alifático C1-4)2, -OH, -O(alifático C1-4), -CO2H, -CO2(alifático C1-4), -O(haloalifático C1-4) o halo(alifático C1-4); cada JQ, J7, J29, J34, J56, J35, J37 y J57 es, de modo independiente, M o -Y-M; cada Y es, de modo independiente, un alifático C1-6 no sustituido opcionalmente reemplazado por 0-3 apariciones de -NR-, -O-, -S-, -C(O)-, -SO- o -SO2-; cada M es de modo independiente H, alifático C1-6, cicloalifático C3-6, halo(alifático C1-4), -O(haloalifático C1-4), heterociclilo de 3-6 miembros, halo, NO2, CN, OH, OR', SH, SR', NH2, NHR', N(R')2, COH, COR', CO2H, CO2R', CONH2, CONHR', CONR'2, OCOR', OCONH2, OCONHR', OCON(R')2, NHCOR', NR'COR', NHCO2R', NR'CO2R', NHCO2H, NR'CO2H, NHCONH2, NHCONHR', NHCON(R')2, SO2NH2, SO2NHR', SO2N(R')2, NHSO2R' o NR'SO2R'; R es H o alifático C1-6 no sustituido; R' es alifático C1-6 no sustituido; o dos grupos R', junto con el átomo al que están unidos, forman un anillo monocíclico saturado o parcialmente insaturado no sustituido de 3-8 miembros que tiene 0-1 heteroátomos seleccionados, de modo independiente, de O, N y S.
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US77299206P | 2006-02-14 | 2006-02-14 | |
| US83137106P | 2006-07-17 | 2006-07-17 | |
| US84935306P | 2006-10-04 | 2006-10-04 | |
| US87620606P | 2006-12-21 | 2006-12-21 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR059505A1 true AR059505A1 (es) | 2008-04-09 |
Family
ID=38330249
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP070100633A AR059505A1 (es) | 2006-02-14 | 2007-02-14 | Dihidrodiazepinas utiles como inhibidores de proteina quinasas |
Country Status (15)
| Country | Link |
|---|---|
| US (4) | US7622463B2 (es) |
| EP (1) | EP1983987B1 (es) |
| JP (2) | JP5243970B2 (es) |
| KR (1) | KR20080095902A (es) |
| AR (1) | AR059505A1 (es) |
| AT (1) | ATE479434T1 (es) |
| AU (1) | AU2007215221C1 (es) |
| CA (1) | CA2652648C (es) |
| DE (1) | DE602007008837D1 (es) |
| IL (1) | IL193240A0 (es) |
| NO (1) | NO20083918L (es) |
| NZ (1) | NZ570530A (es) |
| RU (1) | RU2475488C2 (es) |
| TW (1) | TW200804389A (es) |
| WO (1) | WO2007095188A2 (es) |
Families Citing this family (55)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TW200808325A (en) * | 2006-07-06 | 2008-02-16 | Astrazeneca Ab | Novel compounds |
| HRP20110807T1 (hr) * | 2007-03-22 | 2011-12-31 | Takeda Pharmaceutical Company Limited | Supstituirani pirimidodiazepini korisni kao plk1 inhibitori |
| TW200914457A (en) * | 2007-05-31 | 2009-04-01 | Kyowa Hakko Kogyo Kk | Pyrimidodiazepinone derivative |
| SI2168966T1 (sl) | 2007-06-15 | 2017-03-31 | Msd K.K. | Derivat biciklo anilina |
| CN101952291A (zh) | 2007-08-15 | 2011-01-19 | 弗特克斯药品有限公司 | 用作人蛋白激酶plk1至plk4的抑制剂以治疗增殖疾病的4-(9-(3,3-二氟环戊基)-5,7,7-三甲基-6-氧代-6,7,8,9-四氢-5h-嘧啶并[4,5-b][1,4]二氮杂䓬-2-基氨基)-3-甲氧基苯甲酰胺衍生物 |
| ES2488966T3 (es) * | 2007-09-25 | 2014-09-01 | Takeda Pharmaceutical Company Limited | Inhibidores de cinasa de tipo Polo |
| CA2700979C (en) | 2007-09-28 | 2017-06-20 | Cyclacel Limited | Pyrimidine derivatives as protein kinase inhibitors |
| WO2009067547A1 (en) * | 2007-11-19 | 2009-05-28 | Takeda Pharmaceutical Company Limited | Polo-like kinase inhibitors |
| US8598172B2 (en) | 2007-12-04 | 2013-12-03 | Nerviano Medical Sciences S.R.L. | Substituted dihydropteridin-6-one derivatives, process for their preparation and their use as kinase inhibitors |
| EP2303889A1 (en) | 2008-06-18 | 2011-04-06 | F. Hoffmann-La Roche AG | Halo-substituted pyrimidodiazepines as plkl inhibitors |
| AU2009271658B2 (en) * | 2008-06-23 | 2014-04-10 | Vertex Pharmaceuticals Incorporated | Protein kinase inhibitors |
| AU2009271663B2 (en) | 2008-06-23 | 2014-04-17 | Vertex Pharmaceuticals Incorporated | Protein kinase inhibitors |
| TW201639852A (zh) | 2008-12-09 | 2016-11-16 | 吉李德科學股份有限公司 | 用於製備可用作類鐸受體調節劑之化合物的中間體化合物 |
| WO2010080712A2 (en) | 2009-01-06 | 2010-07-15 | Dana Farber Cancer Institute | Pyrimido-diazepinone kinase scaffold compounds and methods of treating disorders |
| US8049005B2 (en) | 2009-03-31 | 2011-11-01 | Arqule, Inc. | Substituted tetrahydropyrazolo-pyrido-azepine compounds |
| KR102050712B1 (ko) | 2009-06-17 | 2019-12-02 | 버텍스 파마슈티칼스 인코포레이티드 | 인플루엔자 바이러스 복제의 억제제 |
| AU2010299579A1 (en) * | 2009-09-25 | 2012-05-03 | Vertex Pharmaceuticals Incorporated | Methods for preparing pyrimidine derivatives useful as protein kinase inhibitors |
| SG179207A1 (en) | 2009-09-25 | 2012-04-27 | Vertex Pharma | Methods for preparing pyrimidine derivatives useful as protein kinase inhibitors |
| TW201201813A (en) | 2010-03-31 | 2012-01-16 | Arqule Inc | Substituted benzo-pyrido-triazolo-diazepine compounds |
| MX373121B (es) | 2010-05-14 | 2020-04-30 | Dana Farber Cancer Inst Inc | Composiciones y metodos para el tratamiento de leucemia. |
| CN103037865B (zh) | 2010-05-14 | 2014-10-29 | 达那-法伯癌症研究所 | 用于治疗瘤形成、炎性疾病和其他失调的化合物 |
| JP6022442B2 (ja) | 2010-05-14 | 2016-11-09 | ダナ−ファーバー キャンサー インスティテュート, インコーポレイテッド | 男性用避妊組成物および使用方法 |
| US8933070B2 (en) | 2010-07-02 | 2015-01-13 | University Health Network | Methods of targeting PTEN mutant diseases and compositions therefor |
| WO2012083117A1 (en) | 2010-12-16 | 2012-06-21 | Vertex Pharmaceuticals Incorporated | Inhibitors of influenza viruses replication |
| UA118010C2 (uk) | 2011-08-01 | 2018-11-12 | Вертекс Фармасьютікалз Інкорпорейтед | Інгібітори реплікації вірусів грипу |
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-
2007
- 2007-02-13 NZ NZ570530A patent/NZ570530A/en unknown
- 2007-02-13 WO PCT/US2007/003699 patent/WO2007095188A2/en not_active Ceased
- 2007-02-13 JP JP2008555299A patent/JP5243970B2/ja active Active
- 2007-02-13 RU RU2008136854/04A patent/RU2475488C2/ru not_active IP Right Cessation
- 2007-02-13 KR KR1020087022521A patent/KR20080095902A/ko not_active Abandoned
- 2007-02-13 US US11/706,070 patent/US7622463B2/en active Active
- 2007-02-13 EP EP07750530A patent/EP1983987B1/en active Active
- 2007-02-13 AT AT07750530T patent/ATE479434T1/de active
- 2007-02-13 TW TW096105339A patent/TW200804389A/zh unknown
- 2007-02-13 CA CA2652648A patent/CA2652648C/en active Active
- 2007-02-13 DE DE602007008837T patent/DE602007008837D1/de active Active
- 2007-02-13 AU AU2007215221A patent/AU2007215221C1/en not_active Ceased
- 2007-02-14 AR ARP070100633A patent/AR059505A1/es unknown
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2008
- 2008-08-05 IL IL193240A patent/IL193240A0/en unknown
- 2008-09-15 NO NO20083918A patent/NO20083918L/no not_active Application Discontinuation
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2009
- 2009-09-29 US US12/569,237 patent/US8022202B2/en active Active
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2011
- 2011-08-10 US US13/206,638 patent/US8394952B2/en active Active
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2013
- 2013-01-21 US US13/745,968 patent/US20140038935A1/en not_active Abandoned
- 2013-01-23 JP JP2013009857A patent/JP2013067666A/ja not_active Withdrawn
Also Published As
| Publication number | Publication date |
|---|---|
| RU2008136854A (ru) | 2010-03-20 |
| RU2475488C2 (ru) | 2013-02-20 |
| KR20080095902A (ko) | 2008-10-29 |
| JP2013067666A (ja) | 2013-04-18 |
| WO2007095188A2 (en) | 2007-08-23 |
| NO20083918L (no) | 2008-11-12 |
| IL193240A0 (en) | 2009-08-03 |
| CA2652648C (en) | 2016-10-25 |
| US8394952B2 (en) | 2013-03-12 |
| NZ570530A (en) | 2011-09-30 |
| AU2007215221B2 (en) | 2013-01-17 |
| US8022202B2 (en) | 2011-09-20 |
| US20080167289A1 (en) | 2008-07-10 |
| JP5243970B2 (ja) | 2013-07-24 |
| HK1129298A1 (en) | 2009-11-27 |
| ATE479434T1 (de) | 2010-09-15 |
| CA2652648A1 (en) | 2007-08-23 |
| US20120149898A1 (en) | 2012-06-14 |
| EP1983987B1 (en) | 2010-09-01 |
| US20100190765A1 (en) | 2010-07-29 |
| US7622463B2 (en) | 2009-11-24 |
| AU2007215221A1 (en) | 2007-08-23 |
| JP2009526849A (ja) | 2009-07-23 |
| WO2007095188A3 (en) | 2007-10-25 |
| DE602007008837D1 (de) | 2010-10-14 |
| EP1983987A2 (en) | 2008-10-29 |
| AU2007215221C1 (en) | 2013-05-30 |
| TW200804389A (en) | 2008-01-16 |
| US20140038935A1 (en) | 2014-02-06 |
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