MA30722B1 - Utilisation de derives de l'adenosine en tant qu'agonistes du recepteurs a2a - Google Patents
Utilisation de derives de l'adenosine en tant qu'agonistes du recepteurs a2aInfo
- Publication number
- MA30722B1 MA30722B1 MA31736A MA31736A MA30722B1 MA 30722 B1 MA30722 B1 MA 30722B1 MA 31736 A MA31736 A MA 31736A MA 31736 A MA31736 A MA 31736A MA 30722 B1 MA30722 B1 MA 30722B1
- Authority
- MA
- Morocco
- Prior art keywords
- receptor agonists
- compounds
- adenosine derivatives
- adenosine
- formula
- Prior art date
Links
- 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 4
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 2
- 102000007471 Adenosine A2A receptor Human genes 0.000 abstract 1
- 108010085277 Adenosine A2A receptor Proteins 0.000 abstract 1
- 230000004913 activation Effects 0.000 abstract 1
- 201000010099 disease Diseases 0.000 abstract 1
- 230000002757 inflammatory effect Effects 0.000 abstract 1
- 230000000414 obstructive effect Effects 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 150000003839 salts Chemical class 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)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (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)
- Public Health (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)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Hydrogenated Pyridines (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Abstract
LA PRÉSENTE INVENTION CONCERNE UN COMPOSÉ DE FORMULE (I), OU DES STÉRÉO-ISOMÈRES OU DES SELS PHARMACEUTIQUEMENT ACCEPTABLES DE CE DERNIER. DANS LADITE FORMULE, A, U1, U2, R1A, R1B, R2 ET R3 SONT TELS QUE DÉFINIS DANS LA DESCRIPTION. LESDITS COMPOSÉS SONT UTILES POUR TRAITER DES TROUBLES INDUITS PAR L'ACTIVATION DU RÉCEPTEUR DE L'ADÉNOSINE A2A, EN PARTICULIER DES MALADIES INFLAMMATOIRES OU OBSTRUCTIVES DES VOIES AÉRIENNES. L'INVENTION A ÉGALEMENT TRAIT À DES COMPOSITIONS PHARMACEUTIQUES QUI CONTIENNENT LES COMPOSÉS SELON L'INVENTION, ET À UN PROCÉDÉ DE PRÉPARATION DESDITS COMPOSÉS.
Applications Claiming Priority (1)
| 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 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MA30722B1 true MA30722B1 (fr) | 2009-09-01 |
Family
ID=37622170
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MA31736A MA30722B1 (fr) | 2006-09-14 | 2009-03-30 | Utilisation de derives de l'adenosine en tant qu'agonistes du recepteurs a2a |
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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| SG176313A1 (en) * | 2001-10-01 | 2011-12-29 | Univ Virginia Patent Found | 2-propynyl adenosine analogs having a2a agonist activity and compositions thereof |
| GT200500281A (es) * | 2004-10-22 | 2006-04-24 | Novartis Ag | Compuestos organicos. |
| EP1831225A2 (fr) | 2004-11-19 | 2007-09-12 | The Regents of the University of California | Pyrazolopyrimidines anti-inflammatoires |
| GB0500785D0 (en) | 2005-01-14 | 2005-02-23 | Novartis Ag | Organic compounds |
| US8178509B2 (en) * | 2006-02-10 | 2012-05-15 | University Of Virginia Patent Foundation | Method to treat sickle cell disease |
| EA200870409A1 (ru) | 2006-04-04 | 2009-04-28 | Дзе Риджентс Оф Дзе Юниверсити Оф Калифорния | Антагонисты киназы pi3 |
| GB0607944D0 (en) * | 2006-04-21 | 2006-05-31 | Novartis Ag | Organic compounds |
| ATE549337T1 (de) | 2006-04-21 | 2012-03-15 | Novartis Ag | Purinderivate zur verwendung als adenosin-a2a- rezeptoragonisten |
| 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 |
| ES2361886T3 (es) * | 2006-06-27 | 2011-06-24 | Cbt Development Limited | Profármacos adenosina acetil 2',3'-metilideno novedosos para uso como profármacos para agonistas del receptor adenosina. |
| EP1889846A1 (fr) | 2006-07-13 | 2008-02-20 | Novartis AG | Dérivés de purine comme agonistes du recepteur A2a |
| JP2010508835A (ja) * | 2006-11-10 | 2010-03-25 | ノバルティス アーゲー | シクロペンテンジオールモノアセテート誘導体 |
| GB2467670B (en) | 2007-10-04 | 2012-08-01 | Intellikine Inc | Chemical entities and therapeutic uses thereof |
| CN101827847A (zh) * | 2007-10-17 | 2010-09-08 | 诺瓦提斯公司 | 用作腺苷a1受体配体的嘌呤衍生物 |
| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
| EP2427195B1 (fr) | 2009-05-07 | 2019-05-01 | Intellikine, LLC | Composés hétérocycliques et leurs utilisations |
| MY162604A (en) | 2009-08-17 | 2017-06-30 | Intellikine Llc | Heterocyclic compounds and uses thereof |
| WO2011047384A2 (fr) | 2009-10-16 | 2011-04-21 | The Regents Of The University Of California | Procédés d'inhibition de l'activité ire1 |
| AU2011255218B2 (en) | 2010-05-21 | 2015-03-12 | Infinity Pharmaceuticals, Inc. | Chemical compounds, compositions and methods for kinase modulation |
| 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 |
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| 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 |
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| MX370814B (es) | 2011-09-02 | 2020-01-08 | Univ California | Pirazolo[3,4-d]pirimidinas sustituidas y usos de las mismas. |
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| KR102229478B1 (ko) | 2012-11-01 | 2021-03-18 | 인피니티 파마슈티칼스, 인코포레이티드 | Pi3 키나아제 동형단백질 조절인자를 사용하는 암의 치료 |
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| GT200500281A (es) * | 2004-10-22 | 2006-04-24 | Novartis Ag | Compuestos organicos. |
| US20080051364A1 (en) * | 2004-11-08 | 2008-02-28 | Pninna Fishman | Therapeutic Treatment of Accelerated Bone Resorption |
| GB0500785D0 (en) * | 2005-01-14 | 2005-02-23 | Novartis Ag | Organic compounds |
| JP5048520B2 (ja) * | 2005-02-04 | 2012-10-17 | ミレニアム ファーマシューティカルズ, インコーポレイテッド | E1活性化酵素の阻害剤 |
| GB0505219D0 (en) * | 2005-03-14 | 2005-04-20 | Novartis Ag | Organic compounds |
| GB0514809D0 (en) * | 2005-07-19 | 2005-08-24 | Glaxo Group Ltd | Compounds |
| EP1959939B1 (fr) * | 2005-11-30 | 2012-01-11 | Can-Fite Biopharma Ltd. | Utilisation de l'agoniste des recepteurs de l'adenosine a3 dans le traitement de l'osteoarthrite |
| EP1983990B1 (fr) * | 2006-01-26 | 2011-03-23 | Government of the United States of America, Represented by the Secretary, Department of Health and Human Services | Modulateurs allostériques du récepteur de l adénosine a3 |
| SG169369A1 (en) * | 2006-02-02 | 2011-03-30 | Millennium Pharm Inc | Inhibitors of e1 activating enzymes |
| US20080027022A1 (en) * | 2006-02-08 | 2008-01-31 | Linden Joel M | Method to treat gastric lesions |
| GB0607948D0 (en) | 2006-04-21 | 2006-05-31 | Novartis Ag | Organic compounds |
| GB0607945D0 (en) | 2006-04-21 | 2006-05-31 | Novartis Ag | Organic compounds |
| ATE549337T1 (de) | 2006-04-21 | 2012-03-15 | Novartis Ag | Purinderivate zur verwendung als adenosin-a2a- rezeptoragonisten |
| GB0607953D0 (en) * | 2006-04-21 | 2006-05-31 | Novartis Ag | Organic compounds |
| GB0607944D0 (en) * | 2006-04-21 | 2006-05-31 | Novartis Ag | Organic compounds |
| GB0607951D0 (en) * | 2006-04-21 | 2006-05-31 | Novartis Ag | Organic compounds |
| GB0607954D0 (en) | 2006-04-21 | 2006-05-31 | Novartis Ag | Organic compounds |
| GB0607950D0 (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 |
| JP2010508835A (ja) * | 2006-11-10 | 2010-03-25 | ノバルティス アーゲー | シクロペンテンジオールモノアセテート誘導体 |
| 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 |
| AU2008270735C1 (en) * | 2007-06-29 | 2014-03-06 | Government Of The United States Of America, Represented By The Secretary, Department Of Health And Human Services | Dendrimer conjugates of agonists and antagonists of the GPCR superfamily |
| US20090181934A1 (en) * | 2007-10-17 | 2009-07-16 | Novartis Ag | Organic Compounds |
| CN101827847A (zh) * | 2007-10-17 | 2010-09-08 | 诺瓦提斯公司 | 用作腺苷a1受体配体的嘌呤衍生物 |
| US8183225B2 (en) * | 2007-11-08 | 2012-05-22 | New York University | Inhibition of bone resorption using medical implants containing adenosine receptor antagonists |
| AU2009204084A1 (en) * | 2008-01-09 | 2009-07-16 | Trovis Pharmaceuticals Llc | Intrathecal treatment of neuropathic pain with A2AR agonists |
-
2006
- 2006-09-14 EP EP06120706A patent/EP1903044A1/fr not_active Ceased
-
2007
- 2007-09-12 AR ARP070104040A patent/AR062768A1/es not_active Application Discontinuation
- 2007-09-12 PE PE2007001224A patent/PE20081151A1/es not_active Application Discontinuation
- 2007-09-13 US US12/310,254 patent/US8188100B2/en not_active Expired - Fee Related
- 2007-09-13 RU RU2009113668/04A patent/RU2009113668A/ru unknown
- 2007-09-13 AT AT07803477T patent/ATE481404T1/de active
- 2007-09-13 CA CA002662104A patent/CA2662104A1/fr not_active Abandoned
- 2007-09-13 WO PCT/EP2007/059666 patent/WO2008031875A1/fr not_active Ceased
- 2007-09-13 CN CN2007800333258A patent/CN101511831B/zh not_active Expired - Fee Related
- 2007-09-13 DE DE602007009272T patent/DE602007009272D1/de active Active
- 2007-09-13 MX MX2009002811A patent/MX2009002811A/es not_active Application Discontinuation
- 2007-09-13 DK DK07803477.4T patent/DK2066669T3/da active
- 2007-09-13 PL PL07803477T patent/PL2066669T3/pl unknown
- 2007-09-13 CL CL200702658A patent/CL2007002658A1/es unknown
- 2007-09-13 BR BRPI0716936-1A2A patent/BRPI0716936A2/pt not_active IP Right Cessation
- 2007-09-13 JP JP2009527828A patent/JP2010503639A/ja not_active Withdrawn
- 2007-09-13 PT PT07803477T patent/PT2066669E/pt unknown
- 2007-09-13 AU AU2007296227A patent/AU2007296227A1/en not_active Abandoned
- 2007-09-13 ES ES07803477T patent/ES2353141T3/es active Active
- 2007-09-13 TW TW096134289A patent/TW200821324A/zh unknown
- 2007-09-13 EP EP07803477A patent/EP2066669B1/fr active Active
- 2007-09-13 SI SI200730448T patent/SI2066669T1/sl unknown
- 2007-09-13 HR HR20100694T patent/HRP20100694T1/hr unknown
- 2007-09-13 KR KR1020097005251A patent/KR20090040386A/ko not_active Abandoned
-
2009
- 2009-02-13 ZA ZA200901036A patent/ZA200901036B/xx unknown
- 2009-02-19 IL IL197153A patent/IL197153A0/en unknown
- 2009-02-19 CR CR10621A patent/CR10621A/es not_active Application Discontinuation
- 2009-03-13 TN TN2009000084A patent/TN2009000084A1/fr unknown
- 2009-03-25 NO NO20091244A patent/NO20091244L/no not_active Application Discontinuation
- 2009-03-30 MA MA31736A patent/MA30722B1/fr unknown
-
2010
- 2010-12-15 CY CY20101101154T patent/CY1110990T1/el unknown
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