MA27997A1 - Composes et compositions inhibiteurs de l'activite du recepteur tyrosine kinase - Google Patents
Composes et compositions inhibiteurs de l'activite du recepteur tyrosine kinaseInfo
- Publication number
- MA27997A1 MA27997A1 MA28818A MA28818A MA27997A1 MA 27997 A1 MA27997 A1 MA 27997A1 MA 28818 A MA28818 A MA 28818A MA 28818 A MA28818 A MA 28818A MA 27997 A1 MA27997 A1 MA 27997A1
- Authority
- MA
- Morocco
- Prior art keywords
- compounds
- tyrosine kinase
- receptor activity
- kinase receptor
- inhibiting tyrosine
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 title abstract 4
- 230000000694 effects Effects 0.000 title abstract 2
- 102000004278 Receptor Protein-Tyrosine Kinases Human genes 0.000 title 1
- 108090000873 Receptor Protein-Tyrosine Kinases Proteins 0.000 title 1
- 230000002401 inhibitory effect Effects 0.000 title 1
- 239000000203 mixture Substances 0.000 title 1
- 102100027842 Fibroblast growth factor receptor 3 Human genes 0.000 abstract 1
- 101710182396 Fibroblast growth factor receptor 3 Proteins 0.000 abstract 1
- 101150028321 Lck gene Proteins 0.000 abstract 1
- 101100272634 Mus musculus Bmx gene Proteins 0.000 abstract 1
- 101100335081 Mus musculus Flt3 gene Proteins 0.000 abstract 1
- 101150056950 Ntrk2 gene Proteins 0.000 abstract 1
- 108091000080 Phosphotransferase Proteins 0.000 abstract 1
- 230000006806 disease prevention Effects 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
- 208000035475 disorder Diseases 0.000 abstract 1
- 239000008194 pharmaceutical composition Chemical class 0.000 abstract 1
- 102000020233 phosphotransferase Human genes 0.000 abstract 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D473/00—Heterocyclic compounds containing purine ring systems
- C07D473/02—Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6
- C07D473/16—Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6 two nitrogen atoms
-
- 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
- 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
- A61P17/06—Antipsoriatics
-
- 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
- A61P17/16—Emollients or protectives, e.g. against radiation
-
- 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
- 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
-
- 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
- A61P7/02—Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D473/00—Heterocyclic compounds containing purine ring systems
- C07D473/02—Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6
- C07D473/18—Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6 one oxygen and one nitrogen atom, e.g. guanine
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D473/00—Heterocyclic compounds containing purine ring systems
- C07D473/26—Heterocyclic compounds containing purine ring systems with an oxygen, sulphur, or nitrogen atom directly attached in position 2 or 6, but not in both
- C07D473/32—Nitrogen atom
- C07D473/34—Nitrogen atom attached in position 6, e.g. adenine
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D473/00—Heterocyclic compounds containing purine ring systems
- C07D473/40—Heterocyclic compounds containing purine ring systems with halogen atoms or perhalogeno-alkyl radicals directly attached in position 2 or 6
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Dermatology (AREA)
- Hematology (AREA)
- Pulmonology (AREA)
- Cardiology (AREA)
- Vascular Medicine (AREA)
- Urology & Nephrology (AREA)
- Heart & Thoracic Surgery (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Oncology (AREA)
- Toxicology (AREA)
- Diabetes (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
L'invention concerne une nouvelle catégorie de composés, des compositions pharmaceutiques contenant ces composés et des méthodes pour utiliser ces composés dans le traitement ou la prévention de maladies ou de troubles associés à l'activité kinase cSRC, Lck, FGFR3, Flt3, TrkB, Bmx et/ou PFGFR$g(a).
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US49540603P | 2003-08-15 | 2003-08-15 | |
| US52435703P | 2003-11-21 | 2003-11-21 | |
| US56536704P | 2004-04-26 | 2004-04-26 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MA27997A1 true MA27997A1 (fr) | 2006-07-03 |
Family
ID=34198974
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MA28818A MA27997A1 (fr) | 2003-08-15 | 2006-02-17 | Composes et compositions inhibiteurs de l'activite du recepteur tyrosine kinase |
Country Status (16)
| Country | Link |
|---|---|
| US (2) | US20050124637A1 (fr) |
| EP (1) | EP1656378A4 (fr) |
| JP (1) | JP2007502776A (fr) |
| AU (2) | AU2004264419B2 (fr) |
| BR (1) | BRPI0413563A (fr) |
| CA (1) | CA2535620A1 (fr) |
| CO (1) | CO5680404A2 (fr) |
| EC (1) | ECSP066365A (fr) |
| IL (1) | IL173392A0 (fr) |
| IS (1) | IS8345A (fr) |
| MA (1) | MA27997A1 (fr) |
| MX (1) | MXPA06001758A (fr) |
| NO (1) | NO20061074L (fr) |
| SG (1) | SG145748A1 (fr) |
| TN (1) | TNSN06053A1 (fr) |
| WO (1) | WO2005016528A2 (fr) |
Families Citing this family (99)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1578722A4 (fr) * | 2001-10-12 | 2006-09-06 | Irm Llc | Squelettes d'inhibiteurs de kinase et leurs methodes de preparation |
| US7273864B2 (en) * | 2002-10-15 | 2007-09-25 | The Scripps Research Institute | Compositions and methods for inducing osteogenesis |
| AP2006003517A0 (en) * | 2003-09-25 | 2006-02-28 | Janssen Pharmaceutica Nv | Hiv replication purine derivatives. |
| US7256196B1 (en) | 2003-12-09 | 2007-08-14 | The Procter & Gamble Company | Purine cytokine inhibitors |
| US20070197559A1 (en) * | 2004-03-02 | 2007-08-23 | Rajagopal Bakthavatchalam | Aryl substituted purine analogues |
| EP1831225A2 (fr) | 2004-11-19 | 2007-09-12 | The Regents of the University of California | Pyrazolopyrimidines anti-inflammatoires |
| DE102005017259A1 (de) * | 2005-04-14 | 2006-10-19 | Merck Patent Gmbh | Purinderivate |
| DE602006019088D1 (de) | 2005-05-13 | 2011-02-03 | Irm Llc | Verbindungen und zusammensetzungen als proteinkinase-hemmer |
| WO2006136005A1 (fr) * | 2005-05-16 | 2006-12-28 | Prometic Biosciences Inc. | Derives de purine et utilisation de ceux-ci dans le traitement de maladies auto-immunes |
| CN100526315C (zh) * | 2005-06-16 | 2009-08-12 | 浙江医药股份有限公司新昌制药厂 | N2-喹啉或异喹啉取代的嘌呤衍生物及其制备方法和其用途 |
| WO2007024680A1 (fr) | 2005-08-22 | 2007-03-01 | Amgen Inc. | Composes de pyrazolopyridine et de pyrazolopyrimidine utilises comme modulateurs d'enzymes kinases |
| JP5400388B2 (ja) | 2005-12-15 | 2014-01-29 | ライジェル ファーマシューティカルズ, インコーポレイテッド | キナーゼインヒビターおよびその利用 |
| EA200870409A1 (ru) | 2006-04-04 | 2009-04-28 | Дзе Риджентс Оф Дзе Юниверсити Оф Калифорния | Антагонисты киназы pi3 |
| BRPI0722383A2 (pt) | 2006-12-08 | 2012-06-05 | Irm Llc | compostos inibidores de proteìna quinase, composições contendo os mesmos bem como seus usos |
| WO2008073687A2 (fr) * | 2006-12-08 | 2008-06-19 | Irm Llc | Composés et compositions inhibant la protéine kinase |
| MX2009007944A (es) * | 2007-01-26 | 2009-08-07 | Irm Llc | Compuestos y composiciones de purina como inhibidores de quinasa para el tratamiento de enfermedades relacionadas con plasmodium. |
| US20100105705A1 (en) * | 2007-03-28 | 2010-04-29 | Neurosearch A/S | Purinyl derivatives and their use as potassium channel modulators |
| EP2142547A1 (fr) * | 2007-03-28 | 2010-01-13 | NeuroSearch A/S | Dérivés de purinyle et leur utilisation en tant que modulateurs des canaux potassiques |
| CN101679422A (zh) * | 2007-03-28 | 2010-03-24 | 阵列生物制药公司 | 作为受体酪氨酸激酶抑制剂的咪唑并[1,2-a]吡啶化合物 |
| CN101289449A (zh) * | 2007-04-20 | 2008-10-22 | 浙江医药股份有限公司新昌制药厂 | 2,6-二含氮取代的嘌呤衍生物及其制备方法和应用 |
| WO2008135232A1 (fr) * | 2007-05-02 | 2008-11-13 | Riccardo Cortese | Utilisation et compositions de dérivés de purine pour le traitement de troubles prolifératifs |
| UA99459C2 (en) * | 2007-05-04 | 2012-08-27 | Астразенека Аб | 9-(pyrazol-3-yl)- 9h-purine-2-amine and 3-(pyraz0l-3-yl)-3h-imidazo[4,5-b]pyridin-5-amine derivatives and their use for the treatment of cancer |
| CZ302225B6 (cs) * | 2007-07-04 | 2010-12-29 | Univerzita Palackého v Olomouci | Substituované 6-anilinopurinové deriváty jako inhibitory cytokinin oxidasy a prípravky obsahující tyto slouceniny |
| FR2920776B1 (fr) * | 2007-09-12 | 2012-09-28 | Centre Nat Rech Scient | Utilisation de derives de purine pour la fabrication d'un medicament |
| GB2467670B (en) | 2007-10-04 | 2012-08-01 | Intellikine Inc | Chemical entities and therapeutic uses thereof |
| US8193182B2 (en) | 2008-01-04 | 2012-06-05 | Intellikine, Inc. | Substituted isoquinolin-1(2H)-ones, and methods of use thereof |
| CA2711558C (fr) | 2008-01-04 | 2016-12-13 | Intellikine, Inc. | Composes inhibitant la phosphatidyl-inositol-3 kinase |
| JP5547099B2 (ja) | 2008-03-14 | 2014-07-09 | インテリカイン, エルエルシー | キナーゼ阻害剤および使用方法 |
| US8993580B2 (en) | 2008-03-14 | 2015-03-31 | Intellikine Llc | Benzothiazole kinase inhibitors and methods of use |
| AU2013205510A1 (en) * | 2008-05-21 | 2013-05-16 | Ariad Pharmaceuticals, Inc. | Phosphorous derivatives as kinase inhibitors |
| EP2300013B2 (fr) * | 2008-05-21 | 2024-11-13 | Takeda Pharmaceutical Company Limited | Dérivés phosphorés servant d'inhibiteurs de kinase |
| US9273077B2 (en) | 2008-05-21 | 2016-03-01 | Ariad Pharmaceuticals, Inc. | Phosphorus derivatives as kinase inhibitors |
| WO2010006072A2 (fr) | 2008-07-08 | 2010-01-14 | The Regents Of The University Of California | Modulateurs de mtor et leurs utilisations |
| AU2009268611B2 (en) | 2008-07-08 | 2015-04-09 | Intellikine, Llc | Kinase inhibitors and methods of use |
| EP2320907A4 (fr) * | 2008-08-05 | 2012-09-05 | Merck Sharp & Dohme | Composés thérapeutiques |
| EP2344501A1 (fr) * | 2008-09-26 | 2011-07-20 | NeuroSearch A/S | Dérivés de purinyl-pyrazole substitués et leur utilisation en tant que modulateurs des canaux potassiques |
| JP5731978B2 (ja) | 2008-09-26 | 2015-06-10 | インテリカイン, エルエルシー | 複素環キナーゼ阻害剤 |
| US8268838B2 (en) * | 2008-09-26 | 2012-09-18 | Neurosearch A/S | Substituted purinyl-pyrazole derivatives and their use as potassium channel modulators |
| CA2740885C (fr) | 2008-10-16 | 2018-04-03 | The Regents Of The University Of California | Inhibiteurs d'heteroarylkinase a noyau fusionne |
| US8476282B2 (en) | 2008-11-03 | 2013-07-02 | Intellikine Llc | Benzoxazole kinase inhibitors and methods of use |
| WO2010059418A1 (fr) * | 2008-11-19 | 2010-05-27 | The Government Of The U.S.A. As Represented By The Secretary Of The Dept. Of Health & Human Services | Composés de triazine et de purine substituées, méthodes d'inhibition de cruzaïne et de rhodésaïne et méthodes de traitement de la maladie de chagas et de la trypanosomiase africaine |
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| WO2011047384A2 (fr) | 2009-10-16 | 2011-04-21 | The Regents Of The University Of California | Procédés d'inhibition de l'activité ire1 |
| US8759359B2 (en) | 2009-12-18 | 2014-06-24 | Incyte Corporation | Substituted heteroaryl fused derivatives as PI3K inhibitors |
| CA2790176A1 (fr) | 2010-02-18 | 2011-08-25 | Centro Nacional De Investigaciones Oncologicas (Cnio) | Composes bicycliques destines a etre utilises en tant qu'inhibiteurs de kinases |
| EP2558463A1 (fr) | 2010-04-14 | 2013-02-20 | Incyte Corporation | Dérivés condensés en tant qu'inhibiteurs de i3 |
| AU2011255218B2 (en) | 2010-05-21 | 2015-03-12 | Infinity Pharmaceuticals, Inc. | Chemical compounds, compositions and methods for kinase modulation |
| WO2011163195A1 (fr) | 2010-06-21 | 2011-12-29 | Incyte Corporation | Dérivés condensés de pyrrole en tant qu'inhibiteurs de pi3k |
| JP2013545749A (ja) | 2010-11-10 | 2013-12-26 | インフィニティー ファーマシューティカルズ, インコーポレイテッド | 複素環化合物及びその使用 |
| JP6000273B2 (ja) | 2010-11-29 | 2016-09-28 | オーエスアイ・ファーマシューティカルズ,エルエルシー | 大環状キナーゼ阻害剤 |
| TW201249844A (en) | 2010-12-20 | 2012-12-16 | Incyte Corp | N-(1-(substituted-phenyl)ethyl)-9H-purin-6-amines as PI3K inhibitors |
| AU2012205669B2 (en) | 2011-01-10 | 2015-08-20 | Infinity Pharmaceuticals Inc. | Processes for preparing isoquinolinones and solid forms of isoquinolinones |
| JP6130305B2 (ja) | 2011-02-23 | 2017-05-17 | インテリカイン, エルエルシー | キナーゼ阻害剤の組み合わせおよびそれらの使用 |
| WO2012119004A2 (fr) * | 2011-03-01 | 2012-09-07 | Sloan-Kettering Institute For Cancer Research | Analogues de l'hormone parathyroïdienne, compositions et utilisations connexes |
| WO2012125629A1 (fr) | 2011-03-14 | 2012-09-20 | Incyte Corporation | Dérivés diamino-pyrimidines et diamino-pyridines substituées en tant qu'inhibiteurs de pi3k |
| US9126948B2 (en) | 2011-03-25 | 2015-09-08 | Incyte Holdings Corporation | Pyrimidine-4,6-diamine derivatives as PI3K inhibitors |
| EP2704572B1 (fr) | 2011-05-04 | 2015-12-30 | Ariad Pharmaceuticals, Inc. | Composés permettant d'inhiber la prolifération cellulaire dans les cancers induits par l'egfr |
| WO2012172043A1 (fr) | 2011-06-15 | 2012-12-20 | Laboratoire Biodim | Dérivés de purine et leur utilisation comme produits pharmaceutiques pour prévenir ou traiter les infections bactériennes |
| JP6027610B2 (ja) | 2011-07-19 | 2016-11-16 | インフィニティー ファーマシューティカルズ, インコーポレイテッド | 複素環式化合物及びその使用 |
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| EP2751093A1 (fr) | 2011-08-29 | 2014-07-09 | Infinity Pharmaceuticals, Inc. | Composés hétérocycliques et leurs utilisations |
| MX370814B (es) | 2011-09-02 | 2020-01-08 | Univ California | Pirazolo[3,4-d]pirimidinas sustituidas y usos de las mismas. |
| UA121539C2 (uk) | 2011-09-02 | 2020-06-25 | Інсайт Холдинґс Корпорейшн | Гетероцикліламіни як інгібітори рі3к |
| US9493464B2 (en) | 2012-02-29 | 2016-11-15 | The Scripps Research Institute | Wee1 degradation inhibitors |
| AR090548A1 (es) | 2012-04-02 | 2014-11-19 | Incyte Corp | Azaheterociclobencilaminas biciclicas como inhibidores de pi3k |
| US8940742B2 (en) | 2012-04-10 | 2015-01-27 | Infinity Pharmaceuticals, Inc. | Heterocyclic compounds and uses thereof |
| JP6469567B2 (ja) | 2012-05-05 | 2019-02-13 | アリアド・ファーマシューティカルズ・インコーポレイテッド | Egfr発動性がんの細胞増殖阻害用化合物 |
| US8828998B2 (en) | 2012-06-25 | 2014-09-09 | Infinity Pharmaceuticals, Inc. | Treatment of lupus, fibrotic conditions, and inflammatory myopathies and other disorders using PI3 kinase inhibitors |
| KR20150033679A (ko) | 2012-06-26 | 2015-04-01 | 사니오나 에이피에스 | 페닐 트리아졸 유도체 및 이의 gabaa 수용체 복합체 조절용 용도 |
| MX2015003874A (es) | 2012-09-26 | 2015-12-16 | Univ California | Modulacion de ire1. |
| KR102229478B1 (ko) | 2012-11-01 | 2021-03-18 | 인피니티 파마슈티칼스, 인코포레이티드 | Pi3 키나아제 동형단백질 조절인자를 사용하는 암의 치료 |
| US9481667B2 (en) | 2013-03-15 | 2016-11-01 | Infinity Pharmaceuticals, Inc. | Salts and solid forms of isoquinolinones and composition comprising and methods of using the same |
| US9611283B1 (en) | 2013-04-10 | 2017-04-04 | Ariad Pharmaceuticals, Inc. | Methods for inhibiting cell proliferation in ALK-driven cancers |
| CN104418858B (zh) * | 2013-08-30 | 2018-12-11 | 浙江医药股份有限公司新昌制药厂 | 2,6-二含氮取代的嘌呤衍生物及其制备方法和其药物组合物与应用 |
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| US9751888B2 (en) | 2013-10-04 | 2017-09-05 | Infinity Pharmaceuticals, Inc. | Heterocyclic compounds and uses thereof |
| UA115388C2 (uk) | 2013-11-21 | 2017-10-25 | Пфайзер Інк. | 2,6-заміщені пуринові похідні та їх застосування в лікуванні проліферативних захворювань |
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| US20150320755A1 (en) | 2014-04-16 | 2015-11-12 | Infinity Pharmaceuticals, Inc. | Combination therapies |
| WO2015162518A1 (fr) | 2014-04-25 | 2015-10-29 | Pfizer Inc. | Composes hetero-aromatiques et leur utilisation comme ligands d1 de la dopamine |
| US10077277B2 (en) | 2014-06-11 | 2018-09-18 | Incyte Corporation | Bicyclic heteroarylaminoalkyl phenyl derivatives as PI3K inhibitors |
| US9708348B2 (en) | 2014-10-03 | 2017-07-18 | Infinity Pharmaceuticals, Inc. | Trisubstituted bicyclic heterocyclic compounds with kinase activities and uses thereof |
| UA122332C2 (uk) | 2015-02-27 | 2020-10-26 | Інсайт Корпорейшн | Солі інгібітора pi3k і способи їх отримання |
| CN104788387A (zh) * | 2015-04-17 | 2015-07-22 | 浙江海森药业有限公司 | 高纯度瑞舒伐他汀钙的制备方法 |
| WO2016183063A1 (fr) | 2015-05-11 | 2016-11-17 | Incyte Corporation | Formes cristallines d'un inhibiteur de pi3k |
| WO2016183060A1 (fr) | 2015-05-11 | 2016-11-17 | Incyte Corporation | Procédé de synthèse d'un inhibiteur de phospho-inositide 3-kinases |
| US10160761B2 (en) | 2015-09-14 | 2018-12-25 | Infinity Pharmaceuticals, Inc. | Solid forms of isoquinolinones, and process of making, composition comprising, and methods of using the same |
| WO2017161116A1 (fr) | 2016-03-17 | 2017-09-21 | Infinity Pharmaceuticals, Inc. | Isotopologues de composés isoquinolinone et quinazolinone et leurs utilisations comme inhibiteurs de la kinase pi3k |
| US10919914B2 (en) | 2016-06-08 | 2021-02-16 | Infinity Pharmaceuticals, Inc. | Heterocyclic compounds and uses thereof |
| MX391135B (es) | 2016-06-24 | 2025-03-21 | Infinity Pharmaceuticals Inc | Terapias de combinacion. |
| JP7082120B2 (ja) | 2016-10-21 | 2022-06-07 | ニンバス ラクシュミ, インコーポレイテッド | Tyk2阻害剤およびその使用 |
| CZ308029B6 (cs) * | 2017-03-20 | 2019-11-06 | Univerzita PalackĂ©ho v Olomouci | 2,6-Disubstituované-9-cyklopentyl-9H-puriny, jejich použití jako léčiva a farmaceutické přípravky |
| US11331313B2 (en) | 2017-05-22 | 2022-05-17 | Whitehead Institute For Biomedical Research | KCC2 expression enhancing compounds and uses thereof |
| MX2020012826A (es) | 2018-06-01 | 2021-03-09 | Incyte Corp | Regimen de dosificacion para el tratamiento de trastornos relacionados con fosfatidilinositol 3-cinasas (pi3k). |
| US12391694B2 (en) * | 2019-06-24 | 2025-08-19 | Merck Sharp & Dohme Llc | Process for the preparation of 2-fluoroadenine |
| KR20250121114A (ko) | 2022-12-16 | 2025-08-11 | 아스트라제네카 아베 | 2,6,9-삼치환된 퓨린 |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3041340A (en) * | 1962-06-26 | Method of preparing substituted | ||
| US3133065A (en) * | 1962-07-30 | 1964-05-12 | Abbott Lab | Purine derivatives |
| US4405781A (en) * | 1981-03-02 | 1983-09-20 | Polaroid Corporation | Method for preparing salts of 6-chloropurine |
| US5565566A (en) * | 1987-04-24 | 1996-10-15 | Discovery Therapeutics, Inc. | N6 -substituted 9-methyladenines: a new class of adenosine receptor antagonists |
| US5017578A (en) * | 1989-06-09 | 1991-05-21 | Hoechst-Roussel Pharmaceuticals Inc. | N-heteroaryl-purin-6-amines useful as analgesic and anticonvulsant agents |
| CA2174080A1 (fr) * | 1993-10-12 | 1995-04-20 | Paul Edward Aldrich | 1n-alkyle-n-arylpyrimidinamines et leurs derives |
| US5744424A (en) * | 1993-12-03 | 1998-04-28 | Caudill Seed Company, Inc. | Plant growth promoter composition comprising N-6-benzyladenine, an alcohol, and a metal hydroxide |
| EP0831829B1 (fr) * | 1995-06-07 | 2003-08-20 | Pfizer Inc. | Derives de pyrimidine heterocycliques a noyaux condenses |
| JPH10512896A (ja) * | 1995-11-14 | 1998-12-08 | フアルマシア・エ・アツプジヨン・エツセ・ピー・アー | アリールおよびヘテロアリールプリン化合物 |
| GB9613021D0 (en) * | 1996-06-21 | 1996-08-28 | Pharmacia Spa | Bicyclic 4-aralkylaminopyrimidine derivatives as tyrosine kinase inhibitors |
| US5866702A (en) * | 1996-08-02 | 1999-02-02 | Cv Therapeutics, Incorporation | Purine inhibitors of cyclin dependent kinase 2 |
| GB9903762D0 (en) * | 1999-02-18 | 1999-04-14 | Novartis Ag | Organic compounds |
| GB9918035D0 (en) * | 1999-07-30 | 1999-09-29 | Novartis Ag | Organic compounds |
| AU7323000A (en) * | 1999-08-26 | 2001-04-10 | Plant Research International B.V. | Conditional inhibition of vegetative propagation |
| OA12050A (en) * | 1999-09-30 | 2006-05-02 | Neurogen Corp | Certain alkylene diamine-substituted heterocycles. |
| EP1383767A1 (fr) * | 2001-02-08 | 2004-01-28 | Memory Pharmaceutical Corporation | Trifluoromethylpurines en tant qu'inhibiteurs de la phosphodiesterase 4 |
| CZ294535B6 (cs) * | 2001-08-02 | 2005-01-12 | Ústav Experimentální Botaniky Avčr | Heterocyklické sloučeniny na bázi N6-substituovaného adeninu, způsoby jejich přípravy, jejich použití pro přípravu léčiv, kosmetických přípravků a růstových regulátorů, farmaceutické přípravky, kosmetické přípravky a růstové regulátory tyto sloučeniny obsahující |
| JP2005506350A (ja) * | 2001-10-18 | 2005-03-03 | ベーリンガー インゲルハイム ファーマシューティカルズ インコーポレイテッド | サイトカイン阻害薬としての1,4−二置換ベンゾ−縮合尿素化合物 |
| US7273864B2 (en) * | 2002-10-15 | 2007-09-25 | The Scripps Research Institute | Compositions and methods for inducing osteogenesis |
| EP1444982A1 (fr) * | 2003-02-06 | 2004-08-11 | Merckle Gmbh | Utilisation des dérivés de purine comme inhibiteurs sélectifs de kinases |
| MX2009007944A (es) * | 2007-01-26 | 2009-08-07 | Irm Llc | Compuestos y composiciones de purina como inhibidores de quinasa para el tratamiento de enfermedades relacionadas con plasmodium. |
-
2004
- 2004-08-13 MX MXPA06001758A patent/MXPA06001758A/es not_active Application Discontinuation
- 2004-08-13 SG SG200806062-6A patent/SG145748A1/en unknown
- 2004-08-13 BR BRPI0413563-6A patent/BRPI0413563A/pt not_active IP Right Cessation
- 2004-08-13 US US10/917,578 patent/US20050124637A1/en not_active Abandoned
- 2004-08-13 AU AU2004264419A patent/AU2004264419B2/en not_active Ceased
- 2004-08-13 JP JP2006523409A patent/JP2007502776A/ja active Pending
- 2004-08-13 CA CA002535620A patent/CA2535620A1/fr not_active Abandoned
- 2004-08-13 WO PCT/US2004/026373 patent/WO2005016528A2/fr not_active Ceased
- 2004-08-13 EP EP04781114A patent/EP1656378A4/fr not_active Withdrawn
-
2006
- 2006-01-26 IL IL173392A patent/IL173392A0/en unknown
- 2006-02-14 TN TNP2006000053A patent/TNSN06053A1/en unknown
- 2006-02-14 EC EC2006006365A patent/ECSP066365A/es unknown
- 2006-02-17 MA MA28818A patent/MA27997A1/fr unknown
- 2006-02-20 CO CO06016491A patent/CO5680404A2/es not_active Application Discontinuation
- 2006-03-06 NO NO20061074A patent/NO20061074L/no not_active Application Discontinuation
- 2006-03-09 IS IS8345A patent/IS8345A/is unknown
-
2009
- 2009-04-15 AU AU2009201480A patent/AU2009201480A1/en not_active Abandoned
-
2010
- 2010-12-22 US US12/976,187 patent/US20110092491A1/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| AU2004264419B2 (en) | 2009-01-15 |
| WO2005016528A3 (fr) | 2005-05-12 |
| US20110092491A1 (en) | 2011-04-21 |
| NO20061074L (no) | 2006-03-06 |
| MXPA06001758A (es) | 2006-08-11 |
| SG145748A1 (en) | 2008-09-29 |
| ECSP066365A (es) | 2006-08-30 |
| US20050124637A1 (en) | 2005-06-09 |
| BRPI0413563A (pt) | 2006-10-17 |
| AU2009201480A1 (en) | 2009-05-14 |
| CA2535620A1 (fr) | 2005-02-24 |
| EP1656378A2 (fr) | 2006-05-17 |
| EP1656378A4 (fr) | 2011-05-11 |
| IS8345A (is) | 2006-03-09 |
| AU2004264419A1 (en) | 2005-02-24 |
| IL173392A0 (en) | 2006-06-11 |
| WO2005016528A2 (fr) | 2005-02-24 |
| CO5680404A2 (es) | 2006-09-29 |
| JP2007502776A (ja) | 2007-02-15 |
| TNSN06053A1 (en) | 2007-10-03 |
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