TN2009000084A1 - Adenosine derivatives as a2a receptor agonists - Google Patents
Adenosine derivatives as a2a receptor agonistsInfo
- Publication number
- TN2009000084A1 TN2009000084A1 TN2009000084A TN2009000084A TN2009000084A1 TN 2009000084 A1 TN2009000084 A1 TN 2009000084A1 TN 2009000084 A TN2009000084 A TN 2009000084A TN 2009000084 A TN2009000084 A TN 2009000084A TN 2009000084 A1 TN2009000084 A1 TN 2009000084A1
- Authority
- TN
- Tunisia
- Prior art keywords
- receptor agonists
- adenosine derivatives
- stereoisomers
- compounds
- formula
- Prior art date
Links
- 101150051188 Adora2a gene Proteins 0.000 title 1
- 150000003835 adenosine derivatives Chemical class 0.000 title 1
- 239000000018 receptor agonist Substances 0.000 title 1
- 229940044601 receptor agonist Drugs 0.000 title 1
- 150000001875 compounds Chemical class 0.000 abstract 3
- 150000003839 salts Chemical class 0.000 abstract 2
- 102000007471 Adenosine A2A receptor Human genes 0.000 abstract 1
- 108010085277 Adenosine A2A receptor Proteins 0.000 abstract 1
- 208000027771 Obstructive airways disease Diseases 0.000 abstract 1
- 230000004913 activation Effects 0.000 abstract 1
- 208000027866 inflammatory disease Diseases 0.000 abstract 1
- 230000002757 inflammatory effect Effects 0.000 abstract 1
- 238000004519 manufacturing process Methods 0.000 abstract 1
- 230000001404 mediated effect Effects 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
Classifications
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D473/00—Heterocyclic compounds containing purine ring systems
-
- 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
- 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
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/08—Bronchodilators
-
- 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
- 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
- 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
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pulmonology (AREA)
- Immunology (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Dermatology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Saccharide Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Hydrogenated Pyridines (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP06120706A EP1903044A1 (fr) | 2006-09-14 | 2006-09-14 | Derivés de l'adénosine en tant qu' agonistes du récepteur A2A |
| PCT/EP2007/059666 WO2008031875A1 (fr) | 2006-09-14 | 2007-09-13 | Utilisation de dérivés de l'adénosine en tant qu'agonistes du récepteurs a2a |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| TN2009000084A1 true TN2009000084A1 (en) | 2010-08-19 |
Family
ID=37622170
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| TN2009000084A TN2009000084A1 (en) | 2006-09-14 | 2009-03-13 | Adenosine derivatives as a2a receptor agonists |
Country Status (30)
| Country | Link |
|---|---|
| US (1) | US8188100B2 (fr) |
| EP (2) | EP1903044A1 (fr) |
| JP (1) | JP2010503639A (fr) |
| KR (1) | KR20090040386A (fr) |
| CN (1) | CN101511831B (fr) |
| AR (1) | AR062768A1 (fr) |
| AT (1) | ATE481404T1 (fr) |
| AU (1) | AU2007296227A1 (fr) |
| BR (1) | BRPI0716936A2 (fr) |
| CA (1) | CA2662104A1 (fr) |
| CL (1) | CL2007002658A1 (fr) |
| CR (1) | CR10621A (fr) |
| CY (1) | CY1110990T1 (fr) |
| DE (1) | DE602007009272D1 (fr) |
| DK (1) | DK2066669T3 (fr) |
| ES (1) | ES2353141T3 (fr) |
| HR (1) | HRP20100694T1 (fr) |
| IL (1) | IL197153A0 (fr) |
| MA (1) | MA30722B1 (fr) |
| MX (1) | MX2009002811A (fr) |
| NO (1) | NO20091244L (fr) |
| PE (1) | PE20081151A1 (fr) |
| PL (1) | PL2066669T3 (fr) |
| PT (1) | PT2066669E (fr) |
| RU (1) | RU2009113668A (fr) |
| SI (1) | SI2066669T1 (fr) |
| TN (1) | TN2009000084A1 (fr) |
| TW (1) | TW200821324A (fr) |
| WO (1) | WO2008031875A1 (fr) |
| ZA (1) | ZA200901036B (fr) |
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| AU2002362443B2 (en) * | 2001-10-01 | 2008-05-15 | University Of Virginia Patent Foundation | 2-propynyl adenosine analogs having A2A agonist activity and compositions thereof |
| GT200500281A (es) * | 2004-10-22 | 2006-04-24 | Novartis Ag | Compuestos organicos. |
| US9512125B2 (en) | 2004-11-19 | 2016-12-06 | The Regents Of The University Of California | Substituted pyrazolo[3.4-D] pyrimidines as anti-inflammatory agents |
| GB0500785D0 (en) | 2005-01-14 | 2005-02-23 | Novartis Ag | Organic compounds |
| WO2007120972A2 (fr) * | 2006-02-10 | 2007-10-25 | University Of Virginia Patent Foundation | Procede permettant de traiter l'anemie a hematies falciformes |
| ES2423010T3 (es) | 2006-04-04 | 2013-09-17 | The Regents Of The University Of California | Derivados de pirazolopirimidina para su uso como antagonistas de cinasa |
| GB0607944D0 (en) * | 2006-04-21 | 2006-05-31 | Novartis Ag | Organic compounds |
| PT2013211E (pt) * | 2006-04-21 | 2012-06-21 | Novartis Ag | Derivados de purina para utilização como agonistas de receptores a2a de adenosina |
| GB0607950D0 (en) * | 2006-04-21 | 2006-05-31 | Novartis Ag | Organic compounds |
| GB0607953D0 (en) * | 2006-04-21 | 2006-05-31 | Novartis Ag | Organic compounds |
| US8188063B2 (en) | 2006-06-19 | 2012-05-29 | University Of Virginia Patent Foundation | Use of adenosine A2A modulators to treat spinal cord injury |
| AU2007263726A1 (en) * | 2006-06-27 | 2008-01-03 | Biovitrum Ab (Publ) | Novel 2',3'-methylidene acetyl adenosine prodrugs for use as prodrugs for adenosine receptor agonists |
| EP1889846A1 (fr) | 2006-07-13 | 2008-02-20 | Novartis AG | Dérivés de purine comme agonistes du recepteur A2a |
| KR20090087054A (ko) * | 2006-11-10 | 2009-08-14 | 노파르티스 아게 | 시클로펜텐 디올 모노아세테이트 유도체 |
| GB2467670B (en) | 2007-10-04 | 2012-08-01 | Intellikine Inc | Chemical entities and therapeutic uses thereof |
| EP2205601A1 (fr) * | 2007-10-17 | 2010-07-14 | Novartis Ag | Dérivés de purine comme ligands des récepteurs a1 à l'adénosine |
| US8058259B2 (en) | 2007-12-20 | 2011-11-15 | University Of Virginia Patent Foundation | Substituted 4-{3-[6-amino-9-(3,4-dihydroxy-tetrahydro-furan-2-yl)-9H-purin-2-yl]-prop-2-ynyl}-piperidine-1-carboxylic acid esters as A2AR agonists |
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| KR101660050B1 (ko) | 2008-01-04 | 2016-09-26 | 인텔리카인, 엘엘씨 | 특정 화학 물질, 조성물 및 방법 |
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| 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 |
| US20110224223A1 (en) | 2008-07-08 | 2011-09-15 | The Regents Of The University Of California, A California Corporation | MTOR Modulators and Uses Thereof |
| NZ590258A (en) | 2008-07-08 | 2013-10-25 | Intellikine Llc | Kinase inhibitors and methods of use |
| CA2738429C (fr) | 2008-09-26 | 2016-10-25 | Intellikine, Inc. | Inhibiteurs heterocycliques de kinases |
| EP2358720B1 (fr) | 2008-10-16 | 2016-03-02 | The Regents of The University of California | Inhibiteurs d'hétéroarylkinase à noyau fusionné |
| US8476431B2 (en) | 2008-11-03 | 2013-07-02 | Itellikine LLC | Benzoxazole kinase inhibitors and methods of use |
| CA2760791C (fr) | 2009-05-07 | 2017-06-20 | Intellikine, Inc. | Composes heterocycliques et leurs utilisations |
| EP2467141B1 (fr) | 2009-08-17 | 2018-10-31 | Intellikine, LLC | Composés hétérocycliques et leurs utilisations |
| WO2011047384A2 (fr) | 2009-10-16 | 2011-04-21 | The Regents Of The University Of California | Procédés d'inhibition de l'activité ire1 |
| ES2593256T3 (es) | 2010-05-21 | 2016-12-07 | Infinity Pharmaceuticals, Inc. | Compuestos químicos, composiciones y métodos para las modulaciones de cinasas |
| AU2011326427B2 (en) | 2010-11-10 | 2016-01-07 | Infinity Pharmaceuticals Inc. | Heterocyclic compounds and uses thereof |
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| CN103491962B (zh) | 2011-02-23 | 2016-10-12 | 因特利凯有限责任公司 | 激酶抑制剂的组合及其用途 |
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| CA2842190A1 (fr) | 2011-07-19 | 2013-01-24 | Infinity Pharmaceuticals Inc. | Composes heterocycliques et leurs utilisations |
| MX2014002542A (es) | 2011-08-29 | 2014-07-09 | Infinity Pharmaceuticals Inc | Compuestos heterociclicos y usos de los mismos. |
| CA2846496C (fr) | 2011-09-02 | 2020-07-14 | The Regents Of The University Of California | Pyrazolo[3,4-d]pyrimidines substituees et utilisations de celles-ci |
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| RU2015115631A (ru) | 2012-09-26 | 2016-11-20 | Дзе Риджентс Оф Дзе Юниверсити Оф Калифорния | Модулирование ire1 |
| PL2914296T5 (pl) | 2012-11-01 | 2022-01-17 | Infinity Pharmaceuticals, Inc. | Leczenie nowotworu z zastosowaniem modulatorów izoform kinazy PI3 |
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| KR101383228B1 (ko) | 2006-01-26 | 2014-04-09 | 더 가번먼트 오브 더 유나이티드 스테이츠 오브 아메리카, 레프리젠티드 바이 더 세크러터리, 디파트먼트 오브 헬쓰 앤드 휴먼 서비스즈 | A3 아데노신 수용체 알로스테릭 조절제 |
| DK1989206T3 (da) | 2006-02-02 | 2012-10-08 | Millennium Pharm Inc | E1-aktiveringsenzymhæmmere |
| US20080027022A1 (en) | 2006-02-08 | 2008-01-31 | Linden Joel M | Method to treat gastric lesions |
| GB0607945D0 (en) | 2006-04-21 | 2006-05-31 | Novartis Ag | Organic compounds |
| GB0607953D0 (en) | 2006-04-21 | 2006-05-31 | Novartis Ag | Organic compounds |
| PT2013211E (pt) | 2006-04-21 | 2012-06-21 | Novartis Ag | Derivados de purina para utilização como agonistas de receptores a2a de adenosina |
| GB0607951D0 (en) | 2006-04-21 | 2006-05-31 | Novartis Ag | Organic compounds |
| GB0607950D0 (en) * | 2006-04-21 | 2006-05-31 | Novartis Ag | Organic compounds |
| GB0607948D0 (en) | 2006-04-21 | 2006-05-31 | Novartis Ag | Organic compounds |
| GB0607954D0 (en) | 2006-04-21 | 2006-05-31 | Novartis Ag | Organic compounds |
| GB0607944D0 (en) | 2006-04-21 | 2006-05-31 | Novartis Ag | Organic compounds |
| EP1889846A1 (fr) | 2006-07-13 | 2008-02-20 | Novartis AG | Dérivés de purine comme agonistes du recepteur A2a |
| US8008307B2 (en) | 2006-08-08 | 2011-08-30 | Millennium Pharmaceuticals, Inc. | Heteroaryl compounds useful as inhibitors of E1 activating enzymes |
| KR20090087054A (ko) | 2006-11-10 | 2009-08-14 | 노파르티스 아게 | 시클로펜텐 디올 모노아세테이트 유도체 |
| WO2008124150A1 (fr) | 2007-04-09 | 2008-10-16 | University Of Virginia Patent Foundation | Méthode de traitement de l'entérite, d'une lésion intestinale et de la diarrhée provoquées par des bactéries c. difficile au moyen d'un agoniste du récepteur a2a de l'adénosine |
| US20080262001A1 (en) | 2007-04-23 | 2008-10-23 | Adenosine Therapeutics, Llc | Agonists of a2a adenosine receptors for treating recurrent tumor growth in the liver following resection |
| EP2170401A1 (fr) | 2007-06-29 | 2010-04-07 | Government of the United States of America, Represented by the Secretary, Department of Health and Human Services | Conjugués de dendrimère d'agonistes et d'antagonistes de la superfamille des gpcr |
| EP2205601A1 (fr) | 2007-10-17 | 2010-07-14 | Novartis Ag | Dérivés de purine comme ligands des récepteurs a1 à l'adénosine |
| US20090181934A1 (en) | 2007-10-17 | 2009-07-16 | Novartis Ag | Organic Compounds |
| WO2009061516A1 (fr) | 2007-11-08 | 2009-05-14 | New York University School Of Medicine | Implants médicaux contenant des agonistes du récepteur de l'adénosine et procédés pour inhiber un relâchement d'implant médical |
| BRPI0907248A2 (pt) | 2008-01-09 | 2019-02-26 | Pgxhealth, Llc | tratamento intratecal de dor neuropática com agonistas a2ar |
-
2006
- 2006-09-14 EP EP06120706A patent/EP1903044A1/fr not_active Ceased
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2007
- 2007-09-12 PE PE2007001224A patent/PE20081151A1/es not_active Application Discontinuation
- 2007-09-12 AR ARP070104040A patent/AR062768A1/es not_active Application Discontinuation
- 2007-09-13 DK DK07803477.4T patent/DK2066669T3/da active
- 2007-09-13 RU RU2009113668/04A patent/RU2009113668A/ru unknown
- 2007-09-13 EP EP07803477A patent/EP2066669B1/fr active Active
- 2007-09-13 AT AT07803477T patent/ATE481404T1/de active
- 2007-09-13 DE DE602007009272T patent/DE602007009272D1/de active Active
- 2007-09-13 CA CA002662104A patent/CA2662104A1/fr not_active Abandoned
- 2007-09-13 US US12/310,254 patent/US8188100B2/en not_active Expired - Fee Related
- 2007-09-13 WO PCT/EP2007/059666 patent/WO2008031875A1/fr active Application Filing
- 2007-09-13 PL PL07803477T patent/PL2066669T3/pl unknown
- 2007-09-13 BR BRPI0716936-1A2A patent/BRPI0716936A2/pt not_active IP Right Cessation
- 2007-09-13 SI SI200730448T patent/SI2066669T1/sl unknown
- 2007-09-13 MX MX2009002811A patent/MX2009002811A/es not_active Application Discontinuation
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- 2007-09-13 JP JP2009527828A patent/JP2010503639A/ja not_active Withdrawn
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- 2007-09-13 AU AU2007296227A patent/AU2007296227A1/en not_active Abandoned
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- 2007-09-13 KR KR1020097005251A patent/KR20090040386A/ko not_active Abandoned
- 2007-09-13 CN CN2007800333258A patent/CN101511831B/zh not_active Expired - Fee Related
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- 2007-09-13 ES ES07803477T patent/ES2353141T3/es active Active
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- 2009-02-13 ZA ZA200901036A patent/ZA200901036B/xx unknown
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- 2009-02-19 IL IL197153A patent/IL197153A0/en unknown
- 2009-03-13 TN TN2009000084A patent/TN2009000084A1/fr unknown
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- 2009-03-30 MA MA31736A patent/MA30722B1/fr unknown
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- 2010-12-15 CY CY20101101154T patent/CY1110990T1/el unknown
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