MA29170B1 - Derives puriniques agissant comme des agonistes du recepteur a2a - Google Patents
Derives puriniques agissant comme des agonistes du recepteur a2aInfo
- Publication number
- MA29170B1 MA29170B1 MA30103A MA30103A MA29170B1 MA 29170 B1 MA29170 B1 MA 29170B1 MA 30103 A MA30103 A MA 30103A MA 30103 A MA30103 A MA 30103A MA 29170 B1 MA29170 B1 MA 29170B1
- Authority
- MA
- Morocco
- Prior art keywords
- compounds
- purinic
- derivatives
- receptor agonists
- relates
- Prior art date
Links
- 239000000018 receptor agonist Substances 0.000 title 1
- 229940044601 receptor agonist Drugs 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
- 101150051188 Adora2a gene Proteins 0.000 abstract 1
- 239000002126 C01EB10 - Adenosine Substances 0.000 abstract 1
- 230000004913 activation Effects 0.000 abstract 1
- 229960005305 adenosine Drugs 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
- 208000035475 disorder Diseases 0.000 abstract 1
- 230000002757 inflammatory effect Effects 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 230000000414 obstructive effect Effects 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 208000023504 respiratory system disease Diseases 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
-
- 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
-
- 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
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/12—Antidiarrhoeals
-
- 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
-
- 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
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/12—Drugs for disorders of the urinary system of the kidneys
-
- 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
- A61P17/02—Drugs for dermatological disorders for treating wounds, ulcers, burns, scars, keloids, or the like
-
- 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
- A61P17/14—Drugs for dermatological disorders for baldness or alopecia
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P21/00—Drugs for disorders of the muscular or neuromuscular system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P21/00—Drugs for disorders of the muscular or neuromuscular system
- A61P21/04—Drugs for disorders of the muscular or neuromuscular system for myasthenia gravis
-
- 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
- A61P27/00—Drugs for disorders of the senses
- A61P27/02—Ophthalmic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P27/00—Drugs for disorders of the senses
- A61P27/02—Ophthalmic agents
- A61P27/06—Antiglaucoma agents or miotics
-
- 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
- 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
-
- 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
- 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
-
- 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
- A61P7/06—Antianaemics
-
- 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
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Pulmonology (AREA)
- Dermatology (AREA)
- Diabetes (AREA)
- Physical Education & Sports Medicine (AREA)
- Ophthalmology & Optometry (AREA)
- Neurology (AREA)
- Hematology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Urology & Nephrology (AREA)
- Biomedical Technology (AREA)
- Obesity (AREA)
- Immunology (AREA)
- Cardiology (AREA)
- Neurosurgery (AREA)
- Emergency Medicine (AREA)
- Endocrinology (AREA)
- Heart & Thoracic Surgery (AREA)
- Vascular Medicine (AREA)
- Rheumatology (AREA)
- Pain & Pain Management (AREA)
- Gastroenterology & Hepatology (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Saccharide Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
L'INVENTION CONCERNE DES COMPOSÉS REPRÉSENTÉS PAR LA FORMULE GÉNÉRALE (I) SOUS FORME SALINE OU LIBRE. DANS CETTE FORMULE, R1, R2 ET R3 DÉSIGNENT DES ÉLÉMENTS DÉFINIS DANS LA DESCRIPTION DE LA PRÉSENTE DEMANDE. CES COMPOSÉS SONT UTILES POUR LE TRAITEMENT DE TROUBLES INDUITS PAR L'ACTIVATION DU RÉCEPTEUR A2A DE L'ADÉNOSINE, EN PARTICULIER DES MALADIES INFLAMMATOIRES ET OBSTRUCTIVES DES VOIES RESPIRATOIRES. L'INVENTION CONCERNE ÉGALEMENT DES COMPOSITIONS PHARMACEUTIQUES CONTENANT LES COMPOSÉS DE L'INVENTION, AINSI QUE DES PROCÉDÉS DESTINÉS À LA PRÉPARATION DE CES COMPOSÉS.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GBGB0500785.1A GB0500785D0 (en) | 2005-01-14 | 2005-01-14 | Organic compounds |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MA29170B1 true MA29170B1 (fr) | 2008-01-02 |
Family
ID=34224620
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MA30103A MA29170B1 (fr) | 2005-01-14 | 2007-07-26 | Derives puriniques agissant comme des agonistes du recepteur a2a |
Country Status (31)
| Country | Link |
|---|---|
| US (1) | US8114877B2 (fr) |
| EP (1) | EP1841768B1 (fr) |
| JP (1) | JP2008526911A (fr) |
| KR (1) | KR20070093424A (fr) |
| CN (1) | CN101107249B (fr) |
| AR (1) | AR052659A1 (fr) |
| AT (1) | ATE414085T1 (fr) |
| AU (1) | AU2006205878B2 (fr) |
| BR (1) | BRPI0606324A2 (fr) |
| CA (1) | CA2593398A1 (fr) |
| CY (1) | CY1108752T1 (fr) |
| DE (1) | DE602006003628D1 (fr) |
| DK (1) | DK1841768T3 (fr) |
| ES (1) | ES2317483T3 (fr) |
| GB (1) | GB0500785D0 (fr) |
| GT (1) | GT200600013A (fr) |
| HR (1) | HRP20090061T3 (fr) |
| IL (1) | IL184149A0 (fr) |
| MA (1) | MA29170B1 (fr) |
| MX (1) | MX2007008557A (fr) |
| MY (1) | MY141727A (fr) |
| NO (1) | NO20074050L (fr) |
| PE (1) | PE20060833A1 (fr) |
| PL (1) | PL1841768T3 (fr) |
| PT (1) | PT1841768E (fr) |
| RU (1) | RU2400483C2 (fr) |
| SI (1) | SI1841768T1 (fr) |
| TN (1) | TNSN07268A1 (fr) |
| TW (1) | TW200637863A (fr) |
| WO (1) | WO2006074925A1 (fr) |
| ZA (1) | ZA200704743B (fr) |
Families Citing this family (23)
| 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 |
| GB0505219D0 (en) * | 2005-03-14 | 2005-04-20 | Novartis Ag | Organic compounds |
| EP2322525B1 (fr) | 2006-04-21 | 2013-09-18 | Novartis AG | Dérivés de purine comme agonistes des récepteurs de l'adénosine A2A |
| GB0607945D0 (en) * | 2006-04-21 | 2006-05-31 | Novartis Ag | Organic compounds |
| GB0607950D0 (en) | 2006-04-21 | 2006-05-31 | Novartis Ag | Organic compounds |
| GB0607951D0 (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 |
| GB0607948D0 (en) * | 2006-04-21 | 2006-05-31 | Novartis Ag | Organic compounds |
| GB0607954D0 (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 |
| CA2669108A1 (fr) * | 2006-11-10 | 2008-05-15 | Novartis Ag | Derives de monoacetate de cyclopentene diol |
| EP2132208A1 (fr) | 2007-03-28 | 2009-12-16 | NeuroSearch AS | Dérivés de purinyle et leur utilisation en tant que modulateurs des canaux potassiques |
| MX2010000424A (es) | 2007-07-09 | 2010-08-10 | Easter Virginia Medical School | Derivados de nucleosidos sustituidos con propiedades antivirales y antimicrobianas. |
| WO2009050199A1 (fr) * | 2007-10-17 | 2009-04-23 | Novartis Ag | Dérivés de purine comme ligands des récepteurs a1 à l'adénosine |
| HRP20150766T1 (hr) * | 2009-03-20 | 2015-08-14 | Sigma-Tau Industrie Farmaceutiche Riunite S.P.A. | Oksidirani derivati triazolilpurina, korisni kao ligandi adenozinskog receptora a2a, te namijenjeni upotrebi kao medikamenti |
| EA201270102A1 (ru) | 2009-06-30 | 2012-08-30 | Форест Лэборетериз Холдингз Лимитед | Соединения алкокси-карбонил-амино-алкинил-аденозина и их производные в качестве агонистов ar |
| WO2013144191A1 (fr) | 2012-03-29 | 2013-10-03 | Bayer Intellectual Property Gmbh | 2-amino-3-cyanopyridines substituées utilisées comme inhibiteurs de l'échange sodium-calcium et leurs utilisations dans le cas de maladies cardiovasculaires |
| CA2876780A1 (fr) | 2012-06-26 | 2014-01-03 | Saniona Aps | Derive de phenyle triazole et son utilisation pour moduler le complexe du recepteur gabaa |
| KR20190015492A (ko) * | 2016-06-08 | 2019-02-13 | 글락소스미스클라인 인털렉츄얼 프로퍼티 디벨로프먼트 리미티드 | 화학적 화합물 |
| WO2018160824A1 (fr) * | 2017-03-01 | 2018-09-07 | Prelude Therapeutics, Incorporated | Inhibiteurs sélectifs de la protéine arginine méthyltransférase 5 (prmt5) |
Family Cites Families (74)
| 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 |
| IL84414A0 (en) * | 1986-11-14 | 1988-04-29 | Ciba Geigy Ag | N9-cyclopentyl-substituted adenine derivatives |
| 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 |
| SG80526A1 (en) | 1990-09-25 | 2001-05-22 | Rhone Poulenc Rorer Int | Compounds having antihypertensive and anti- ischemic properies |
| IT1254915B (it) | 1992-04-24 | 1995-10-11 | Gloria Cristalli | Derivati di adenosina ad attivita' a2 agonista |
| GB9301000D0 (en) * | 1993-01-20 | 1993-03-10 | Glaxo Group Ltd | Chemical compounds |
| 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 |
| US5688744A (en) * | 1995-11-03 | 1997-11-18 | Rohm And Haas Company | Antimicrobial compounds with quick speed of kill |
| EA000884B1 (ru) * | 1996-01-02 | 2000-06-26 | Рон-Пуленк Рорер Фармасьютикалз Инк. | Способ получения 2,4-дигидроксипиридина и 2,4-дигидрокси-3-нитропиридина |
| 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 |
| 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 |
| AU750462B2 (en) * | 1998-06-23 | 2002-07-18 | Glaxo Group Limited | 2-(purin-9-yl)-tetrahydrofuran-3,4-diol derivatives |
| GB9813565D0 (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 |
| AU5879299A (en) | 1998-10-16 | 2000-05-08 | Monaghan, Sandra Marina | Adenine derivatives |
| CN1383427A (zh) * | 1998-12-31 | 2002-12-04 | 阿温蒂斯药物公司 | 制备n6-取代的脱氮杂一腺苷衍生物的方法 |
| US7427606B2 (en) * | 1999-02-01 | 2008-09-23 | University Of Virginia Patent Foundation | Method to reduce inflammatory response in transplanted tissue |
| GB9913932D0 (en) * | 1999-06-15 | 1999-08-18 | Pfizer Ltd | Purine derivatives |
| US6322771B1 (en) | 1999-06-18 | 2001-11-27 | University Of Virginia Patent Foundation | Induction of pharmacological stress with adenosine receptor agonists |
| US6403567B1 (en) | 1999-06-22 | 2002-06-11 | Cv Therapeutics, Inc. | N-pyrazole A2A adenosine receptor agonists |
| US6214807B1 (en) * | 1999-06-22 | 2001-04-10 | Cv Therapeutics, Inc. | C-pyrazole 2A A 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 |
| EP1434782A2 (fr) | 2001-10-01 | 2004-07-07 | University of Virginia Patent Foundation | Analogues de 2-propynyle adenosine presentant une activite agoniste de a2a et compositions en contenant |
| US7414036B2 (en) * | 2002-01-25 | 2008-08-19 | Muscagen Limited | Compounds useful as A3 adenosine receptor agonists |
| AU2003234716A1 (en) | 2002-04-10 | 2003-10-27 | Joel M. Linden | Use of a2a adenosine receptor agonists for the treatment of inflammatory diseases |
| DE602004006895T2 (de) * | 2003-12-29 | 2008-01-31 | Can-Fite Biopharma Ltd. | Verfahren zur behandlung von multipler sklerose |
| CA2557285A1 (fr) | 2004-03-05 | 2005-09-15 | Cambridge Biotechnology Limited | Composes therapeutiques |
| 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 |
| AR049384A1 (es) * | 2004-05-24 | 2006-07-26 | Glaxo Group Ltd | Derivados de purina |
| EP1778239B1 (fr) | 2004-07-28 | 2013-08-21 | Can-Fite Biopharma Ltd. | Agonistes du recepteur de l'adenosine a3 pour le traitement de troubles de l'oeil sec tels que le syndrome de sjogren |
| US7825102B2 (en) * | 2004-07-28 | 2010-11-02 | Can-Fite Biopharma Ltd. | Treatment of dry eye conditions |
| JP2008512457A (ja) * | 2004-09-09 | 2008-04-24 | アメリカ合衆国 | A3及びa1アデノシン受容体作用薬としてのプリン誘導体 |
| 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 |
| RS52458B (sr) * | 2005-02-04 | 2013-02-28 | Millennium Pharmaceuticals Inc. | Inhibitori e1 aktivirajućih enzima |
| GB0505219D0 (en) * | 2005-03-14 | 2005-04-20 | Novartis Ag | Organic compounds |
| GB0514809D0 (en) * | 2005-07-19 | 2005-08-24 | Glaxo Group Ltd | Compounds |
| JP5339916B2 (ja) * | 2005-11-30 | 2013-11-13 | キャン−ファイト・バイオファーマ・リミテッド | 骨関節炎の治療におけるa3アデノシン受容体アゴニストの使用 |
| CN101410114B (zh) * | 2006-01-26 | 2012-07-04 | 美国政府卫生与公共服务部 | A3腺苷受体别构调节剂 |
| EA024006B1 (ru) * | 2006-02-02 | 2016-08-31 | Миллениум Фармасьютикалз, Инк. | Ингибиторы е1 активирующих ферментов |
| WO2007092936A2 (fr) * | 2006-02-08 | 2007-08-16 | University Of Virginia Patent Foundation | Procédé pour traiter des lésions gastriques |
| GB0607944D0 (en) | 2006-04-21 | 2006-05-31 | Novartis Ag | Organic compounds |
| EP2322525B1 (fr) * | 2006-04-21 | 2013-09-18 | Novartis AG | Dérivés de purine comme agonistes des récepteurs de l'adénosine A2A |
| GB0607953D0 (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 |
| GB0607948D0 (en) | 2006-04-21 | 2006-05-31 | Novartis Ag | Organic compounds |
| GB0607945D0 (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 |
| EP1903044A1 (fr) | 2006-09-14 | 2008-03-26 | Novartis AG | Derivés de l'adénosine en tant qu' agonistes du récepteur A2A |
| CA2669108A1 (fr) * | 2006-11-10 | 2008-05-15 | Novartis Ag | Derives de monoacetate de cyclopentene diol |
| 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 |
| US20090181934A1 (en) | 2007-10-17 | 2009-07-16 | Novartis Ag | Organic Compounds |
| WO2009050199A1 (fr) * | 2007-10-17 | 2009-04-23 | Novartis Ag | Dérivés de purine comme ligands des récepteurs a1 à l'adénosine |
| 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 |
| JP2011509305A (ja) * | 2008-01-09 | 2011-03-24 | ピージーエックスヘルス、リミテッド、ライアビリティー、カンパニー | A2arアゴニストによる神経障害性疼痛の髄腔内治療 |
-
2005
- 2005-01-14 GB GBGB0500785.1A patent/GB0500785D0/en not_active Ceased
-
2006
- 2006-01-06 MY MYPI20060048A patent/MY141727A/en unknown
- 2006-01-11 GT GT200600013A patent/GT200600013A/es unknown
- 2006-01-12 PL PL06700452T patent/PL1841768T3/pl unknown
- 2006-01-12 JP JP2007550752A patent/JP2008526911A/ja active Pending
- 2006-01-12 ES ES06700452T patent/ES2317483T3/es not_active Expired - Lifetime
- 2006-01-12 US US11/722,835 patent/US8114877B2/en not_active Expired - Fee Related
- 2006-01-12 MX MX2007008557A patent/MX2007008557A/es active IP Right Grant
- 2006-01-12 WO PCT/EP2006/000217 patent/WO2006074925A1/fr not_active Ceased
- 2006-01-12 CN CN2006800024512A patent/CN101107249B/zh not_active Expired - Fee Related
- 2006-01-12 HR HR20090061T patent/HRP20090061T3/xx unknown
- 2006-01-12 AT AT06700452T patent/ATE414085T1/de active
- 2006-01-12 BR BRPI0606324-1A patent/BRPI0606324A2/pt not_active IP Right Cessation
- 2006-01-12 CA CA002593398A patent/CA2593398A1/fr not_active Abandoned
- 2006-01-12 AU AU2006205878A patent/AU2006205878B2/en not_active Ceased
- 2006-01-12 DK DK06700452T patent/DK1841768T3/da active
- 2006-01-12 AR ARP060100129A patent/AR052659A1/es not_active Application Discontinuation
- 2006-01-12 PT PT06700452T patent/PT1841768E/pt unknown
- 2006-01-12 KR KR1020077016098A patent/KR20070093424A/ko not_active Ceased
- 2006-01-12 DE DE602006003628T patent/DE602006003628D1/de not_active Expired - Lifetime
- 2006-01-12 SI SI200630194T patent/SI1841768T1/sl unknown
- 2006-01-12 EP EP06700452A patent/EP1841768B1/fr not_active Expired - Lifetime
- 2006-01-12 RU RU2007130802/04A patent/RU2400483C2/ru not_active IP Right Cessation
- 2006-01-13 PE PE2006000062A patent/PE20060833A1/es not_active Application Discontinuation
- 2006-01-13 TW TW095101304A patent/TW200637863A/zh unknown
-
2007
- 2007-06-20 ZA ZA200704743A patent/ZA200704743B/xx unknown
- 2007-06-21 IL IL184149A patent/IL184149A0/en unknown
- 2007-07-13 TN TNP2007000268A patent/TNSN07268A1/en unknown
- 2007-07-26 MA MA30103A patent/MA29170B1/fr unknown
- 2007-08-06 NO NO20074050A patent/NO20074050L/no not_active Application Discontinuation
-
2009
- 2009-02-05 CY CY20091100134T patent/CY1108752T1/el unknown
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| MA29170B1 (fr) | Derives puriniques agissant comme des agonistes du recepteur a2a | |
| MA30289B1 (fr) | Dérivés d'amines | |
| MA29692B1 (fr) | Derives de la xanthine en tant qu'agonistes selectifs du hm74a | |
| MA30696B1 (fr) | Derives de l'acide (3-amino-1,2,3,4-tetrahydro-9h-carbazol-9-yl)-acetique | |
| MA32466B1 (fr) | Derives de triazole utiles pour le traitement de maladies | |
| MA30411B1 (fr) | Derives de triazolopyrazine utiles comme agent anticancereux | |
| MA32070B1 (fr) | Dérivés hétérocycliques réunis par fusion et procédés d'utilisation associés | |
| TN2010000230A1 (fr) | Agonistes nouveaux des recepteurs de glucocorticoides | |
| TN2009000112A1 (fr) | Derives de sulfonamides servant d'agonistes adrenergiques et d'antagonistes muscariniques | |
| MA29772B1 (fr) | Benzimidazoles substitues et procedes de preparation | |
| MA28747B1 (fr) | Dérivés de pyridine | |
| MA27452A1 (fr) | Derives d'indole servant d'agonistes beta-2 | |
| MA30333B1 (fr) | Aminotetrahydropyranes utiles en tant qu'inhibiteurs de la dipeptidyle peptidase-iv pour le traitement ou la prevention du diabete. | |
| MA27883A1 (fr) | Derives de pyrido [2,1-a] isoquinoline utilises comme inhibiteurs de dpp-iv | |
| MA31949B1 (fr) | Dérivés d'aminotriazole comme agonistes d'alx | |
| MA29909B1 (fr) | Derives de pyridazine | |
| MA31087B1 (fr) | Derives d'amide et d'ester d'indazolyle pour traiter des troubles medies par le recepteur de glucocorticoïde. | |
| MA30722B1 (fr) | Utilisation de derives de l'adenosine en tant qu'agonistes du recepteurs a2a | |
| MA29926B1 (fr) | Derives de pyrazine | |
| MA27427A1 (fr) | Composes de benzimidazole-1-yl-thiophene utilises en cancerotherapie | |
| MA31766B1 (fr) | Composés organiques | |
| MA33119B1 (fr) | Derives de benzofuranyle utilises comme inhibiteurs de la glucokinase | |
| MA33730B1 (fr) | Procédés de synthèse pour des composés spiro-oxindoles | |
| MA30694B1 (fr) | Derives de n-(amino-heteroaryl)-1h-indole-2-carboxamides, leur preparation et leur application en therapeutique. | |
| TNSN04151A1 (fr) | Derives de nicotinamide utiles comme inhibiteurs de pde4 |