MA30693B1 - Derives de la purine utilises en tant qu'agonistes de l'a2a - Google Patents
Derives de la purine utilises en tant qu'agonistes de l'a2aInfo
- Publication number
- MA30693B1 MA30693B1 MA31615A MA31615A MA30693B1 MA 30693 B1 MA30693 B1 MA 30693B1 MA 31615 A MA31615 A MA 31615A MA 31615 A MA31615 A MA 31615A MA 30693 B1 MA30693 B1 MA 30693B1
- Authority
- MA
- Morocco
- Prior art keywords
- compounds
- agonists
- purine derivatives
- adenosin
- mediation
- Prior art date
Links
- 239000000556 agonist Substances 0.000 title 1
- 229940083251 peripheral vasodilators purine derivative Drugs 0.000 title 1
- 150000003212 purines Chemical class 0.000 title 1
- 150000001875 compounds Chemical class 0.000 abstract 4
- OIRDTQYFTABQOQ-KQYNXXCUSA-N adenosine Chemical compound C1=NC=2C(N)=NC=NC=2N1[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O OIRDTQYFTABQOQ-KQYNXXCUSA-N 0.000 abstract 2
- 230000004913 activation Effects 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
- 208000027866 inflammatory disease Diseases 0.000 abstract 1
- 230000000414 obstructive effect Effects 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 230000000241 respiratory effect Effects 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 208000011580 syndromic disease Diseases 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
-
- 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
- A61K31/52—Purines, e.g. adenine
-
- 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
- A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
-
- 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
- A61P11/02—Nasal agents, e.g. decongestants
-
- 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
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/14—Antitussive agents
-
- 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
- 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
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pulmonology (AREA)
- Immunology (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Dermatology (AREA)
- Otolaryngology (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
LA PRÉSENTE INVENTION CONCERNE DES COMPOSÉS DE FORMULE (I) OU DES STÉRÉOISOMÈRES OU ENCORE DES SELS DE CEUX-CI ACCEPTABLES SUR LE PLAN PHARMACEUTIQUE, W, R1, R2 ET R3 ÉTANT TELS QUE DÉFINIS DANS LE MÉMOIRE DESCRIPTIF, LESQUELS COMPOSÉS SONT UTILISABLES POUR LE TRAITEMENT DE TROUBLES À MÉDIATION PAR L'ACTIVATION DU RÉCEPTEUR A2A DE L'ADÉNOSINE, EN PARTICULIER DES MALADIES INFLAMMATOIRES OU DU SYNDROME RESPIRATOIRE OBSTRUCTIF. DES COMPOSITIONS PHARMACEUTIQUES CONTENANT CES COMPOSÉS ET UN PROCÉDÉ DE PRÉPARATION DE CES COMPOSÉS SONT ÉGALEMENT DÉCRITS.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP06117168A EP1889846A1 (fr) | 2006-07-13 | 2006-07-13 | Dérivés de purine comme agonistes du recepteur A2a |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MA30693B1 true MA30693B1 (fr) | 2009-09-01 |
Family
ID=37496423
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MA31615A MA30693B1 (fr) | 2006-07-13 | 2009-02-04 | Derives de la purine utilises en tant qu'agonistes de l'a2a |
Country Status (20)
| Country | Link |
|---|---|
| US (1) | US8071565B2 (fr) |
| EP (2) | EP1889846A1 (fr) |
| JP (1) | JP2009542753A (fr) |
| KR (1) | KR20090016017A (fr) |
| CN (1) | CN101479267B (fr) |
| AU (1) | AU2007271944A1 (fr) |
| BR (1) | BRPI0714216A2 (fr) |
| CA (1) | CA2656012A1 (fr) |
| CR (1) | CR10520A (fr) |
| EC (1) | ECSP099063A (fr) |
| ES (1) | ES2393931T3 (fr) |
| GT (1) | GT200900007A (fr) |
| IL (1) | IL196330A0 (fr) |
| MA (1) | MA30693B1 (fr) |
| MX (1) | MX2009000375A (fr) |
| NO (1) | NO20090664L (fr) |
| RU (1) | RU2009104764A (fr) |
| TN (1) | TNSN08544A1 (fr) |
| WO (1) | WO2008006563A1 (fr) |
| ZA (1) | ZA200810671B (fr) |
Families Citing this family (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GT200500281A (es) | 2004-10-22 | 2006-04-24 | Novartis Ag | Compuestos organicos. |
| GB0500785D0 (en) * | 2005-01-14 | 2005-02-23 | Novartis Ag | Organic compounds |
| GB0607950D0 (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 |
| 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 |
| EP1903044A1 (fr) | 2006-09-14 | 2008-03-26 | Novartis AG | Derivés de l'adénosine en tant qu' agonistes du récepteur 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 |
| 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 |
| GB2463151A (en) * | 2008-09-05 | 2010-03-10 | Acucela Inc | Amine derivative compounds for treating ophthalmic diseases and disorders |
| PE20100362A1 (es) * | 2008-10-30 | 2010-05-27 | Irm Llc | Derivados de purina que expanden las celulas madre hematopoyeticas |
| AU2019297361B2 (en) | 2018-07-05 | 2024-06-27 | Incyte Corporation | Fused pyrazine derivatives as A2A / A2B inhibitors |
| TWI829857B (zh) | 2019-01-29 | 2024-01-21 | 美商英塞特公司 | 作為a2a / a2b抑制劑之吡唑并吡啶及三唑并吡啶 |
| CN117069627B (zh) * | 2022-10-13 | 2025-08-26 | 上海康斯维克生物医药有限公司 | 4-(3-(3-氨磺酰基苯基)脲基)丁酸化合物、其荧光标记物、制备方法及用途 |
Family Cites Families (71)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1528382A (en) | 1974-12-26 | 1978-10-11 | Teijin Ltd | Cyclopentene diols and acyl esters thereof and processes for their preparation |
| US4738954A (en) | 1985-11-06 | 1988-04-19 | Warner-Lambert Company | Novel N6 -substituted-5'-oxidized adenosine analogs |
| US4873360A (en) | 1986-07-10 | 1989-10-10 | Board Of Governors Of Wayne State University | Process for the preparation of cyclopentanoids and novel intermediates produced thereby |
| EP0267878A1 (fr) | 1986-11-14 | 1988-05-18 | Ciba-Geigy Ag | Dérivés de l'adénine N9-substitués par le groupement cyclopentyle |
| US4954504A (en) | 1986-11-14 | 1990-09-04 | Ciba-Geigy Corporation | N9 -cyclopentyl-substituted adenine derivatives having adenosine-2 receptor stimulating activity |
| JP2586897B2 (ja) | 1987-03-09 | 1997-03-05 | 富士薬品工業株式会社 | 光学活性なシス−シクロペンテン−3,5−ジオ−ルモノエステルの製造法 |
| CA2092305C (fr) | 1990-09-25 | 2003-02-11 | Alfred P. Spada | Composes antihypertenseurs et anti-ischemiques |
| IT1254915B (it) | 1992-04-24 | 1995-10-11 | Gloria Cristalli | Derivati di adenosina ad attivita' a2 agonista |
| US5688774A (en) | 1993-07-13 | 1997-11-18 | The United States Of America As Represented By The Department Of Health And Human Services | A3 adenosine receptor agonists |
| US5691188A (en) | 1994-02-14 | 1997-11-25 | American Cyanamid Company | Transformed yeast cells expressing heterologous G-protein coupled receptor |
| CZ203998A3 (cs) | 1996-01-02 | 1999-11-17 | Rhone-Poulenc Rorer Pharmaceuticals Inc. | Způsob přípravy 2,4-dihydroxypyridinu a 2,4-dihydroxy-3-nitropyridinu |
| US6376472B1 (en) | 1996-07-08 | 2002-04-23 | Aventis Pharmaceuticals, Inc. | Compounds having antihypertensive, cardioprotective, anti-ischemic and antilipolytic properties |
| TW528755B (en) * | 1996-12-24 | 2003-04-21 | Glaxo Group Ltd | 2-(purin-9-yl)-tetrahydrofuran-3,4-diol derivatives |
| AU750322B2 (en) | 1997-05-09 | 2002-07-18 | Trustees Of The University Of Pennsylvania, The | Methods and compositions for reducing ischemic injury of the heart by administering adenosine receptor agonists and antagonists |
| YU44900A (sh) * | 1998-01-31 | 2003-01-31 | Glaxo Group Limited | Derivati 2-(purin-9-il)tetrahidrofuran-3,4-diola |
| EA200001224A1 (ru) * | 1998-06-23 | 2001-08-27 | Глаксо Груп Лимитед | Производные 2-(пурин-9-ил)-тетрагидрофуран-3,4-диола |
| GB9813554D0 (en) | 1998-06-23 | 1998-08-19 | Glaxo Group Ltd | Chemical compounds |
| GB9813540D0 (en) * | 1998-06-23 | 1998-08-19 | Glaxo Group Ltd | Chemical compounds |
| GB9813535D0 (en) | 1998-06-23 | 1998-08-19 | Glaxo Group Ltd | Chemical compounds |
| BR9914526A (pt) | 1998-10-16 | 2001-07-03 | Pfizer | Derivados de adenina |
| PT1140933E (pt) | 1998-12-31 | 2004-12-31 | Aventis Pharma Inc | Processo para preparar derivados n6-substituidos de desaza-adenosina |
| US7427606B2 (en) | 1999-02-01 | 2008-09-23 | University Of Virginia Patent Foundation | Method to reduce inflammatory response in transplanted tissue |
| US6322771B1 (en) | 1999-06-18 | 2001-11-27 | University Of Virginia Patent Foundation | Induction of pharmacological stress with adenosine receptor agonists |
| US6214807B1 (en) | 1999-06-22 | 2001-04-10 | Cv Therapeutics, Inc. | C-pyrazole 2A A receptor agonists |
| US6403567B1 (en) | 1999-06-22 | 2002-06-11 | Cv Therapeutics, Inc. | N-pyrazole A2A adenosine receptor agonists |
| US6586413B2 (en) | 1999-11-05 | 2003-07-01 | The United States Of America As Represented By The Department Of Health And Human Services | Methods and compositions for reducing ischemic injury of the heart by administering adenosine receptor agonists and antagonists |
| GB0003960D0 (en) | 2000-02-18 | 2000-04-12 | Pfizer Ltd | Purine derivatives |
| GB0022695D0 (en) | 2000-09-15 | 2000-11-01 | Pfizer Ltd | Purine Derivatives |
| JP4012070B2 (ja) | 2001-01-16 | 2007-11-21 | カン−フィテ・バイオファーマ・リミテッド | ウイルスの複製を阻害するためのアデノシンa3受容体アゴニストの使用 |
| GB2372741A (en) | 2001-03-03 | 2002-09-04 | Univ Leiden | C2,8-Disubstituted adenosine derivatives and their different uses |
| US20040162422A1 (en) | 2001-03-20 | 2004-08-19 | Adrian Hall | Chemical compounds |
| EP1258247A1 (fr) | 2001-05-14 | 2002-11-20 | Aventis Pharma Deutschland GmbH | Analogues d'adénosine pour le traitement de le diabete et de la resistance à l' insuline |
| SG176313A1 (en) | 2001-10-01 | 2011-12-29 | Univ Virginia Patent Found | 2-propynyl adenosine analogs having a2a agonist activity and compositions thereof |
| US7414036B2 (en) | 2002-01-25 | 2008-08-19 | Muscagen Limited | Compounds useful as A3 adenosine receptor agonists |
| EP1496911B1 (fr) | 2002-04-10 | 2007-12-19 | University Of Virginia Patent Foundation | Utilisation d'une combinaison comprenant un agoniste du recepteur d'adenosine a2a et un agent anti-pathogene dans le traitement de maladies inflammatoires |
| EP1699459B1 (fr) | 2003-12-29 | 2007-06-06 | Can-Fite Biopharma Ltd. | Methode de traitement de la sclerose en plaques |
| MXPA06010075A (es) | 2004-03-05 | 2007-04-10 | Cambridge Biotechnology Ltd | Compuestos terapeuticos. |
| WO2005107463A1 (fr) | 2004-05-03 | 2005-11-17 | University Of Virginia Patent Foundation | Agonistes de recepteurs de l'adenosine a2a servant au traitement d'une nephropathie diabetique |
| PE20060272A1 (es) | 2004-05-24 | 2006-05-22 | Glaxo Group Ltd | (2r,3r,4s,5r,2'r,3'r,4's,5's)-2,2'-{trans-1,4-ciclohexanodiilbis-[imino(2-{[2-(1-metil-1h-imidazol-4-il)etil]amino}-9h-purin-6,9-diil)]}bis[5-(2-etil-2h-tetrazol-5-il)tetrahidro-3,4-furanodiol] como agonista a2a |
| US7825102B2 (en) | 2004-07-28 | 2010-11-02 | Can-Fite Biopharma Ltd. | Treatment of dry eye conditions |
| ES2432113T3 (es) | 2004-07-28 | 2013-11-29 | Can-Fite Biopharma Ltd. | Agonistas del receptor de adenosina A3 para el tratamiento de trastornos del ojo seco, incluido el síndrome de Sjogren |
| EP1794162A1 (fr) | 2004-09-09 | 2007-06-13 | The Government of the United States of America, as repres. by the Secretary of Health and Human Services, Nat. Inst. of Health | Derives de purine comme agonistes du recepteur d'adenosine a3 et a1 |
| 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 |
| GB0607954D0 (en) | 2006-04-21 | 2006-05-31 | Novartis Ag | Organic compounds |
| 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 |
| 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 |
| 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 |
| EP1903044A1 (fr) | 2006-09-14 | 2008-03-26 | Novartis AG | Derivés de l'adénosine en tant qu' agonistes du récepteur 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 |
| 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
- 2006-07-13 EP EP06117168A patent/EP1889846A1/fr not_active Withdrawn
-
2007
- 2007-07-11 CN CN2007800240198A patent/CN101479267B/zh not_active Expired - Fee Related
- 2007-07-11 BR BRPI0714216-1A patent/BRPI0714216A2/pt not_active IP Right Cessation
- 2007-07-11 RU RU2009104764/04A patent/RU2009104764A/ru not_active Application Discontinuation
- 2007-07-11 AU AU2007271944A patent/AU2007271944A1/en not_active Abandoned
- 2007-07-11 CA CA002656012A patent/CA2656012A1/fr not_active Abandoned
- 2007-07-11 ES ES07765174T patent/ES2393931T3/es active Active
- 2007-07-11 JP JP2009518788A patent/JP2009542753A/ja active Pending
- 2007-07-11 MX MX2009000375A patent/MX2009000375A/es not_active Application Discontinuation
- 2007-07-11 EP EP07765174A patent/EP2044070B1/fr active Active
- 2007-07-11 US US12/308,637 patent/US8071565B2/en not_active Expired - Fee Related
- 2007-07-11 WO PCT/EP2007/006156 patent/WO2008006563A1/fr not_active Ceased
- 2007-07-11 KR KR1020097000552A patent/KR20090016017A/ko not_active Ceased
-
2008
- 2008-12-18 ZA ZA200810671A patent/ZA200810671B/xx unknown
- 2008-12-18 CR CR10520A patent/CR10520A/es not_active Application Discontinuation
- 2008-12-31 TN TNP2008000544A patent/TNSN08544A1/en unknown
-
2009
- 2009-01-01 IL IL196330A patent/IL196330A0/en unknown
- 2009-01-12 GT GT200900007A patent/GT200900007A/es unknown
- 2009-01-13 EC EC2009009063A patent/ECSP099063A/es unknown
- 2009-02-04 MA MA31615A patent/MA30693B1/fr unknown
- 2009-02-11 NO NO20090664A patent/NO20090664L/no not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| TNSN08544A1 (en) | 2010-04-14 |
| EP1889846A1 (fr) | 2008-02-20 |
| AU2007271944A1 (en) | 2008-01-17 |
| RU2009104764A (ru) | 2010-08-20 |
| NO20090664L (no) | 2009-02-11 |
| BRPI0714216A2 (pt) | 2013-01-29 |
| GT200900007A (es) | 2009-11-30 |
| US8071565B2 (en) | 2011-12-06 |
| EP2044070B1 (fr) | 2012-08-22 |
| ECSP099063A (es) | 2009-02-27 |
| EP2044070A1 (fr) | 2009-04-08 |
| MX2009000375A (es) | 2009-01-27 |
| WO2008006563A1 (fr) | 2008-01-17 |
| CR10520A (es) | 2009-03-19 |
| US20100240680A1 (en) | 2010-09-23 |
| CA2656012A1 (fr) | 2008-01-17 |
| CN101479267A (zh) | 2009-07-08 |
| CN101479267B (zh) | 2012-05-02 |
| ES2393931T3 (es) | 2013-01-02 |
| KR20090016017A (ko) | 2009-02-12 |
| JP2009542753A (ja) | 2009-12-03 |
| ZA200810671B (en) | 2009-11-25 |
| IL196330A0 (en) | 2009-09-22 |
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