AR060432A1 - Tetrahidropteridinas utiles como inhibidores de las proteinas quinasas - Google Patents
Tetrahidropteridinas utiles como inhibidores de las proteinas quinasasInfo
- Publication number
- AR060432A1 AR060432A1 ARP070101560A ARP070101560A AR060432A1 AR 060432 A1 AR060432 A1 AR 060432A1 AR P070101560 A ARP070101560 A AR P070101560A AR P070101560 A ARP070101560 A AR P070101560A AR 060432 A1 AR060432 A1 AR 060432A1
- Authority
- AR
- Argentina
- Prior art keywords
- aliphatic
- independently
- cycloaliphatic
- halo
- optionally substituted
- 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
- C07D487/12—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
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/12—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains three hetero rings
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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
- A61K31/495—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
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- 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
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/06—Antiasthmatics
-
- 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
- A61P19/08—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
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- 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
- A61P3/00—Drugs for disorders of the metabolism
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
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- 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
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
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- 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
-
- 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
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- 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
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- 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
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P5/00—Drugs for disorders of the endocrine system
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
-
- 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)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Diabetes (AREA)
- Immunology (AREA)
- Hematology (AREA)
- Neurosurgery (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Pulmonology (AREA)
- Obesity (AREA)
- Physical Education & Sports Medicine (AREA)
- Oncology (AREA)
- Endocrinology (AREA)
- Rheumatology (AREA)
- Psychiatry (AREA)
- Heart & Thoracic Surgery (AREA)
- Cardiology (AREA)
- Emergency Medicine (AREA)
- Pain & Pain Management (AREA)
- Transplantation (AREA)
- Hospice & Palliative Care (AREA)
- Virology (AREA)
- Gastroenterology & Hepatology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Communicable Diseases (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
Se refiere a compuestos utiles como inhibidores de la proteína quinasa. Además provee composiciones farmacéuticamente aceptables que comprenden dichos compuestos y métodos para la utilizacion de las composiciones en el tratamiento de varias enfermedades, condiciones o trastornos. Como antiproliferativo, antiinflamatorio, inmunomodulador o inmunosupresor, neurodegenerativo. Reivindicacion 1:Un compuesto de la formula 1: caracterizado porque el anillo A es un anillo heteroarilo de 5 miembros donde el anillo está opcionalmente sustituido con haloalquilo C1-6, halo, NO2, -OH, -CN o un alquilo C1-6opcionalmente sustituido; X1 es un enlace, -O-, -NR8-, -S-, -S(O)-, o -S(O)2; R1 es H, alifático C1-10, cicloalifático C3-10, arilo C6- 10, heteroarilo de 5-10 miembros, o heterociclilo de 3-10, donde dicha R1 está opcionalmente sustituida con 0-5 J1 Cada R2 y R3 es independientemente H, un alifático C1-10, o cicloalifático C3-10, donde cada R2 y R3 está opcional e independientemente sustituido con 0-5 J2 y J3 respectivamente, o R2 y R3, junto con el átomo de carbono al que está ligados, forman un anillo monocíclico de 3-8 miembros, saturado o parcialmente insaturado que contiene 0-4 heteroátomos seleccionados independientemente entre O, N y S, donde dicho anillo monocíclico formado por R2 y R3 está opcionalmente sustituido con 0-4 J23; R4 es H, -C(O)R, -C(O)OR, -C(O)NRR', un alifático C1-10, cicloalifático C3-10, arilo C6-10, heteroarilo de 5-10 miembros, heterociclilo de 3-10, alifático C1-6-cicloalifático C3-10, alifático C1-6-arilo C6-10, o alifático C1-6-(heteroarilo de 5-10 miembros), donde dicha R4 está opcionalmente sustituida con 0-5 J4; R8es H, un alifático C1-6, cicloalifático C3- 8, -C(O)R, -C(O)OR, o -C(O)NRR'; Cada J1 es independientemente haloalquilo de C1-6, halo, NO2, CN, Q, o - Z-Q, o dos J1 tomadas juntas pueden formar opcionalmente =O; Cada Z es independientemente un alifático C1-6 donde 0-3 unidades -CH2- en dicho alifático C1-6 están opcionalmente reemplazadas con -NR-, -O-, -S-, -C(O)-, C(=NR)-, C(=NOR)- , -S(O)-, o -S(O)2-, donde cualquiera de las unidades -CH2- no reemplazadas en dicho alifático C1-6 está opcionalmente sustituida con 0-2 Jz; Cada Q es independientemente H, alifático C1-6, un anillo monocíclico de 3-8 miembros aromático o no aromático que tiene 0-3 heteroátomos seleccionados independientemente entre O, N y S, o un anillo bicíclico de 8-12 miembros aromático o no aromático que tiene 0-5 heteroátomos seleccionados independientemente entre O, N y S, donde cada Q está independientemente sustituida con 0-5 JQ; Cada J2 y J3 es independientemente un alifático C1-6, cicloalifático C3-6, o -(alquilo C1-4)n-V1, donde n es 0 o 1, cada V1 es independientemente 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 entre un cicloalifático C3-6, fenilo, heteroarilo de 5-6 miembros, o heterociclilo de 3-6 miembros, donde dicho grupo cíclico está opcionalmente sustituido con 0-3 Jv; cada Rö es independientemente C1-4 insustituido, o dos de los mismos J2 y J3 ligados al mismo átomo, opcionalmente pueden formar juntos =O; cada Jz y Jv es independientemente halo, alifático C1- 6, cicloalifático C3-6, NO2, CN, OH, NH2, NH(alifático C1-4), N(alifático C1-4)2, -O(alifático C1-4), -CO2H, -CO2(alifático C1-4), -O(haloalifático C1-4, o halo(alifático C1-4); cada JQ, J4, y J23 es independientemente -M o -Y-M; cada Y es independientemente un alifático C1-6 insustituido donde 0-3 unidades -CH2- en dicho alifático C1-6 están opcionalmente reemplazadas con -NR-, -O-, -S-, -C(O)-, -S(O)-, o -S(O)2-; cada M es independientemente 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'; cada R es independientemente H o alifático C1-6 insustituido; y cada R' es alifático C1-6 insustituido, o dos grupos R', junto con el átomo al cual están ligados, forman un anillo monocíclico de 3-8 miembros saturado o parcialmente insaturado, insustituido que tiene 0-1 heteroátomos seleccionados independientemente entre O, N y S.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US79132706P | 2006-04-12 | 2006-04-12 | |
US83872006P | 2006-08-18 | 2006-08-18 |
Publications (1)
Publication Number | Publication Date |
---|---|
AR060432A1 true AR060432A1 (es) | 2008-06-18 |
Family
ID=38544378
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ARP070101560A AR060432A1 (es) | 2006-04-12 | 2007-04-12 | Tetrahidropteridinas utiles como inhibidores de las proteinas quinasas |
Country Status (17)
Country | Link |
---|---|
US (3) | US7763629B2 (es) |
EP (1) | EP2010542B1 (es) |
JP (1) | JP5313875B2 (es) |
KR (1) | KR101432316B1 (es) |
AR (1) | AR060432A1 (es) |
AT (1) | ATE542823T1 (es) |
AU (1) | AU2007238690B2 (es) |
CA (1) | CA2649324A1 (es) |
ES (1) | ES2381212T3 (es) |
HK (1) | HK1134486A1 (es) |
IL (1) | IL194699A (es) |
MX (1) | MX2008013110A (es) |
NO (1) | NO20084747L (es) |
NZ (1) | NZ571969A (es) |
RU (1) | RU2441006C2 (es) |
TW (1) | TW200808805A (es) |
WO (1) | WO2007120752A2 (es) |
Families Citing this family (22)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP5380447B2 (ja) * | 2007-08-15 | 2014-01-08 | 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 | 増殖性疾患の処置のための、ヒトタンパク質キナーゼplk1ないしplk4の阻害剤としての4−(9−(3,3−ジフルオロシクロペンチル)−5,7,7−トリメチル−6−オキソ−6,7,8,9−テトラヒドロ−5h−ピリミド[4,5−b[1,4]ジアゼパン−2−イルアミノ]−3−メトキシベンザミド誘導体 |
MX2010006457A (es) | 2007-12-19 | 2010-07-05 | Amgen Inc | Compuestos fusionados de piridina, pirimidina y triazina como inhibidores de ciclo celular. |
AU2009233951B2 (en) | 2008-04-07 | 2014-02-27 | Amgen Inc. | Gem-disubstituted and spirocyclic amino pyridines/pyrimidines as cell cycle inhibitors |
KR20110039278A (ko) * | 2008-06-23 | 2011-04-15 | 버텍스 파마슈티칼스 인코포레이티드 | 단백질 키나제 억제제 |
CN102076691A (zh) * | 2008-06-23 | 2011-05-25 | 维泰克斯制药公司 | 蛋白激酶抑制剂 |
CN103492391A (zh) * | 2009-09-25 | 2014-01-01 | 沃泰克斯药物股份有限公司 | 用于制备用作蛋白激酶抑制剂的嘧啶衍生物的方法 |
CA2773742C (en) | 2009-09-25 | 2017-12-05 | Vertex Pharmaceuticals Incorporated | Methods for preparing pyrimidine derivatives useful as protein kinase inhibitors |
MX2012007273A (es) | 2009-12-23 | 2012-12-17 | Elan Pharm Inc | Pteridinonas como inhibidores de la quinasa tipo polo. |
JP5850321B2 (ja) * | 2010-02-10 | 2016-02-03 | 公立大学法人横浜市立大学 | 神経選択的転写抑制因子NRSFに特異的に結合するmSin3Bに結合する化合物の利用 |
EP2588110B1 (en) | 2010-07-02 | 2018-10-17 | University Health Network | Methods of targeting pten mutant diseases and compositions therefor |
EP2661268A2 (en) * | 2010-10-08 | 2013-11-13 | Elan Pharmaceuticals Inc. | Inhibitors of polo-like kinase |
TW201307347A (zh) | 2010-11-01 | 2013-02-16 | Arqule Inc | 經取代苯並-咪唑並-吡啶並-二氮呯化合物 |
CA2830516C (en) | 2011-03-23 | 2017-01-24 | Amgen Inc. | Fused tricyclic dual inhibitors of cdk 4/6 and flt3 |
MD4300C1 (ro) * | 2012-12-28 | 2015-03-31 | Государственный Университет Молд0 | Inhibitor al proliferării celulelor HepG2 în cancerul hepatic în bază de cloro-[2-fenil(piridin-2-il)metanon-4-(3-metoxifenil)tiosemicarbazono]nichel |
WO2016183071A1 (en) | 2015-05-11 | 2016-11-17 | Incyte Corporation | Hetero-tricyclic compounds and their use for the treatment of cancer |
US9708333B2 (en) | 2015-08-12 | 2017-07-18 | Incyte Corporation | Fused bicyclic 1,2,4-triazine compounds as TAM inhibitors |
US10053465B2 (en) | 2015-08-26 | 2018-08-21 | Incyte Corporation | Pyrrolopyrimidine derivatives as TAM inhibitors |
RS65129B1 (sr) | 2016-03-28 | 2024-02-29 | Incyte Corp | Jedinjenja pirolotriazina kao inhibitori tam |
EP3988552A1 (en) | 2017-09-27 | 2022-04-27 | Incyte Corporation | Salts of pyrrolotriazine derivatives useful as tam inhibitors |
AU2019293618A1 (en) | 2018-06-29 | 2021-02-18 | Incyte Corporation | Formulations of an AXL/MER inhibitor |
CN109734809A (zh) * | 2019-02-27 | 2019-05-10 | 南方科技大学 | 治疗性的人Plk1蛋白单克隆抗体及其制备方法 |
MX2024001774A (es) * | 2021-08-10 | 2024-04-24 | Uppthera Inc | Compuesto inductor de la degradacion de plk1 novedoso. |
Family Cites Families (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
ZA973884B (en) * | 1996-05-23 | 1998-11-06 | Du Pont Merck Pharma | Tetrahydropteridines and pyridylpiperazines for treatment of neurological disorders |
US6184226B1 (en) * | 1998-08-28 | 2001-02-06 | Scios Inc. | Quinazoline derivatives as inhibitors of P-38 α |
WO2002076985A1 (en) * | 2001-03-23 | 2002-10-03 | Smithkline Beecham Corporation | Compounds useful as kinase inhibitors for the treatment of hyperproliferative diseases |
KR20110050745A (ko) | 2002-10-03 | 2011-05-16 | 탈자진 인코포레이티드 | 혈관항상성 유지제 및 그의 사용 방법 |
JP2006527257A (ja) | 2003-06-10 | 2006-11-30 | ファイザー・インク | 月経困難症の治療用のpde阻害剤及びバソプレッシン受容体アンタゴニストを含んでなる療法組合せ |
GB0315966D0 (en) * | 2003-07-08 | 2003-08-13 | Cyclacel Ltd | Compounds |
GB0400700D0 (en) | 2004-01-13 | 2004-02-18 | Pfizer Ltd | Compounds useful in therapy |
GB0412874D0 (en) | 2004-06-09 | 2004-07-14 | Pfizer Ltd | Novel pharmaceuticals |
DE102004029784A1 (de) * | 2004-06-21 | 2006-01-05 | Boehringer Ingelheim Pharma Gmbh & Co. Kg | Neue 2-Benzylaminodihydropteridinone, Verfahren zur deren Herstellung und deren Verwendung als Arzneimittel |
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2007
- 2007-04-12 AT AT07755318T patent/ATE542823T1/de active
- 2007-04-12 NZ NZ571969A patent/NZ571969A/en not_active IP Right Cessation
- 2007-04-12 WO PCT/US2007/009006 patent/WO2007120752A2/en active Application Filing
- 2007-04-12 TW TW096112918A patent/TW200808805A/zh unknown
- 2007-04-12 KR KR1020087027593A patent/KR101432316B1/ko not_active IP Right Cessation
- 2007-04-12 MX MX2008013110A patent/MX2008013110A/es active IP Right Grant
- 2007-04-12 EP EP07755318A patent/EP2010542B1/en not_active Not-in-force
- 2007-04-12 US US11/786,578 patent/US7763629B2/en not_active Expired - Fee Related
- 2007-04-12 AU AU2007238690A patent/AU2007238690B2/en not_active Ceased
- 2007-04-12 CA CA002649324A patent/CA2649324A1/en not_active Abandoned
- 2007-04-12 JP JP2009505472A patent/JP5313875B2/ja not_active Expired - Fee Related
- 2007-04-12 RU RU2008144584/04A patent/RU2441006C2/ru not_active IP Right Cessation
- 2007-04-12 ES ES07755318T patent/ES2381212T3/es active Active
- 2007-04-12 AR ARP070101560A patent/AR060432A1/es unknown
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2008
- 2008-10-12 IL IL194699A patent/IL194699A/en not_active IP Right Cessation
- 2008-11-10 NO NO20084747A patent/NO20084747L/no not_active Application Discontinuation
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2010
- 2010-01-08 HK HK10100194.2A patent/HK1134486A1/xx not_active IP Right Cessation
- 2010-06-08 US US12/796,174 patent/US8067417B2/en not_active Expired - Fee Related
-
2011
- 2011-10-05 US US13/253,196 patent/US8524902B2/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
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KR20080109919A (ko) | 2008-12-17 |
US7763629B2 (en) | 2010-07-27 |
AU2007238690B2 (en) | 2013-05-02 |
HK1134486A1 (en) | 2010-04-30 |
IL194699A0 (en) | 2009-08-03 |
JP2009536155A (ja) | 2009-10-08 |
US8524902B2 (en) | 2013-09-03 |
MX2008013110A (es) | 2009-03-06 |
WO2007120752A2 (en) | 2007-10-25 |
US20090062292A1 (en) | 2009-03-05 |
NO20084747L (no) | 2008-11-25 |
NZ571969A (en) | 2011-10-28 |
KR101432316B1 (ko) | 2014-08-29 |
US8067417B2 (en) | 2011-11-29 |
IL194699A (en) | 2014-07-31 |
EP2010542A2 (en) | 2009-01-07 |
ATE542823T1 (de) | 2012-02-15 |
ES2381212T3 (es) | 2012-05-24 |
RU2008144584A (ru) | 2010-05-20 |
JP5313875B2 (ja) | 2013-10-09 |
CA2649324A1 (en) | 2007-10-25 |
US20120277425A1 (en) | 2012-11-01 |
EP2010542B1 (en) | 2012-01-25 |
RU2441006C2 (ru) | 2012-01-27 |
US20110021519A1 (en) | 2011-01-27 |
WO2007120752A3 (en) | 2008-05-08 |
TW200808805A (en) | 2008-02-16 |
AU2007238690A1 (en) | 2007-10-25 |
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